115 results on '"Shanklin DR"'
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2. Factors influencing the transport of sea water cations across the ectoderm of Fundulus heteroclitus
- Author
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Shanklin Dr
- Subjects
animal structures ,Multidisciplinary ,biology ,Chemistry ,Zoology ,Fundulidae ,Ectoderm ,Biological Transport ,biology.organism_classification ,Fundulus ,Fishery ,medicine.anatomical_structure ,Distilled water ,Cations ,embryonic structures ,medicine ,Osmotic pressure ,Animals ,Seawater ,Hardiness (plants) - Abstract
IN 1913 George G. Scott reviewed the then existing literature and added experiments of his own on the remarkable ability of adult Fundulus heteroclitus to withstand wide variations in the osmotic pressure of their environment1. The significance of his conclusions is retold in the easily observed hardiness of these teleosts. The survivors of such changes appear to function adequately to gross observations. Similarly the Fundulus embryos, although less than 2 mm. in diameter, and with tissues that are readily torn with sharp glass needles, will develop in extremes of distilled water and sea water with salts or sucrose added up to twice the normal osmotic pressure.
- Published
- 1956
3. On the pulmonary toxicity of oxygen. 5. Electronic structure and the paramagnetic property of oxygen.
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Shanklin DR
- Subjects
- Animals, Animals, Newborn, Disease Models, Animal, Electron Spin Resonance Spectroscopy, Female, Longevity, Lung pathology, Lung Injury metabolism, Lung Injury pathology, Male, Mice, Molecular Structure, Rabbits, Respiratory Mechanics, Lung drug effects, Lung Injury chemically induced, Oxygen chemistry, Oxygen toxicity
- Abstract
Oxygen uptake by the pulmonary circulation is a chemical reaction. The physicochemical attributes of oxygen are critical when studying pulmonary oxygen toxicity. Extent of lung injury depends on the percentage of oxygen in an oxygen-nitrogen mix in polybaric circumstances (Shanklin, 1969). Further change in extent of lesion follows when other gases are used in the inhalant mix instead of nitrogen (Shanklin and Lester, 1972), with oxygen at 21-100% of the mix. Comparative subatmospheric oxygen levels down to 3% in hydrogen, helium, nitrogen, argon, or sulfur hexafluoride, were run with and without ventilatory distress by the Farber (1937) model, bilateral cervical vagotomy (BCV). This yielded coherent results indicating a need to consider molecular characteristics at the atomic level. Molecular mass and size, gas viscosity, and thermal conductivity yielded no obvious correlates to lung injury. Saturation of the outer electron shells of the diluents fit the empiric data, prospectively an interaction between oxygen and nitrogen from their electronegativity and closely approximate molecular mass, size, and shape. The lesion is essentially eliminated at 7% oxygen in nitrogen. At 3% oxygen, the least lesion is found with N(2), H(2), and SF(6), all gases with incomplete outer electron shells, allowing for transient, possibly polarized, covalent bonding with oxygen as the significant minority component in the mix. Argon and helium do not interfere with oxygen. With 3% oxygen in argon without BCV, the experiments ran so long (>70hours) they were terminated once the point had been made. 3% oxygen in argon after BCV yielded a mean survival more than twice that of BCV in air, indicating a remarkable degree of nitrogen interference with oxygen in the respiratory medium of terrestrial animal life. Argon displayed other advantages for the lung compared to nitrogen. Hydrogen, nitrogen, and oxygen are diatomic molecules, a feature which does relate to the extent of lung injury, but only oxygen is paramagnetic. Magnetic effects on lesion formation were tested: [1] with ventilatory distress induced in newborn rabbits, and [2] in young adult female white mice exposed to 100% oxygen without added mechanical distress. A noninvasive model for ventilatory distress, thoracic restraint (TR), with longer mean survivals of 40-50hours, was employed rather than the Farber model. Parallel runs with TR, one subset receiving 100% oxygen in a plastic chamber resting on six strong ring magnets with measured fields up to +1200 gauss, the other plain 100% oxygen, were performed. Both subsets developed moderate metabolic acidosis with average weight losses circa 25%, but over different time courses, 82.89±4.91hours in magnetized oxygen, 55.4% longer than the 53.34±9.82hours in plain oxygen (p<0.001). The longer survival in magnetized oxygen meant extensive lung injury (99.57±0.42% pleural surface, versus 83.86±14.03%), but the rate of lesion formation was 30.89% faster in plain oxygen (1.5722% per hour) than in magnetized oxygen (1.2012% per hour), a difference significant at p<0.001. The effect of oxygen without mechanical ventilatory distress was examined in female adult white mice exposed to oxygen or magnetized oxygen. Similar survivals and weight losses were achieved. The rate of lung lesion formation was different, 1.2617% per hour in plain oxygen, 46.13% faster than 0.8634% per hour in magnetized oxygen. A variable magnetic field, with animals moving and breathing in chambers flooded with oxygen, has both systemic and pulmonary effects which alter the rate of lesion formation due to oxygen toxicity. Paramagnetic oxygen in a magnetic field influences the effect of oxygen toxicity on the lung but at these strengths of field it does not overcome significant mechanical disturbance., (Copyright © 2012 Elsevier Inc. All rights reserved.)
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- 2012
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4. On the pulmonary toxicity of oxygen. 4. The thyroid arena.
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Shanklin DR
- Subjects
- Animals, Animals, Newborn, Birth Weight, Blood Proteins analysis, Female, Fetus, Gestational Age, Humans, Hyaline Membrane Disease pathology, Infant, Newborn, Infant, Premature blood, Infant, Premature metabolism, Lung drug effects, Lung growth & development, Male, Oxygen metabolism, Pregnancy, Rabbits, Respiratory Distress Syndrome, Newborn pathology, Thyroid Gland metabolism, Thyroid Gland pathology, Thyrotropin blood, Thyroxine administration & dosage, Thyroxine blood, Thyroxine metabolism, Triiodothyronine blood, Weight Loss, Hyaline Membrane Disease etiology, Infant, Premature physiology, Lung pathology, Oxygen toxicity, Respiratory Distress Syndrome, Newborn etiology, Thyroid Gland physiology
- Abstract
Normally developed thyroid function is critical to the transition from fetal to neonatal life with the onset of independent thermoregulation, the most conspicuous of the many ways in which thyroid secretions act throughout the body. A role for thyroid secretions in growth and maturation of the lungs as part of the preparation for the onset of breathing has been recognized for some time but how this contributes to tissue and cell processes and defenses under the duress of respiratory distress has not been well examined. Extensive archival autopsy material was searched for thyroid and adrenal weights, first by gestational age, and then for changes during the first hours after birth as ratios to body weight. After a gestational age of 22 weeks the fetal thyroid and adrenal glands at autopsy in those with hyaline membrane disease are persistently half the size of those in "normal" infants dying with other disorders. When the thyroid is examined shortly after birth it reveals a post natal loss of mass per body weight of similar orders of magnitude which does not occur in the control group. A clinical sample of premature infants with (12) and without (14) hyaline membrane disease was tested for T(4), TSH, TBG, and total serum protein. The results also demonstrate a special subset with lower birth weights at the same gestational age, and lower serum T(4) and total serum protein. Ventilatory distress in newborn rabbits was induced by bilateral cervical vagotomy at 24 h post natal following earlier injection of thyroxine (T(4)) or thyroid stimulating hormone (TSH) and comparisons were made with untreated animals and by dose. Early life thyroidectomy was performed followed by exposure to either air or 100% oxygen. A final experiment in air was vagotomy after thyroidectomy. Composite analysis of these methods indicates that thyroid factors are both operative and important in the newborn animal with ventilatory distress. This work and the archival data indicate those infants destined to develop hyaline membrane disease through respiratory distress are a distinct developmental and clinical subset with the point of departure from otherwise normal development and maturation in the second or early third trimester. This interval is known to be a period of marked variation in the overview indicators of fetal progress through gestational time. The initiating factor or circumstance which then separates this special subset from normal future development is placed by these observations firmly into the period when human fetal TSH dramatically rises 7-fold (17.5-25.5 weeks) followed by a lesser 3 to 4-fold increase in T(4) which is extended into the early third trimester. The earlier part of this interval is characterized by the thyrotrophic action of chorionic gonadotropin (hCG). The possibility that abnormalities in the intrauterine environment secondary to maternal infection play a role within this time frame is indicated by the demonstration that interleukin-2 (IL-2) induces an anterior pituitary release of TSH. Since IL-2 has this property and is not an acute phase cytokine, some form of chronic infection or an immunopathic process seems more likely as a possible active factor in pathogenesis., (Copyright © 2011 Elsevier Inc. All rights reserved.)
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- 2012
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5. On the pulmonary toxicity of oxygen: III. The induction of oxygen dependency by oxygen use.
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Shanklin DR
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- Animals, Animals, Newborn, Environmental Exposure, Female, Lung Injury metabolism, Lung Injury pathology, Oxygen metabolism, Pregnancy, Rabbits, Respiratory Insufficiency metabolism, Respiratory Insufficiency pathology, Respiratory Mechanics, Survival Rate, Vagotomy, Lung Injury chemically induced, Oxygen toxicity, Respiratory Insufficiency etiology
- Abstract
Oxygen is central to the development of neonatal lung injury. The increase in oxygen exposure of the neonatal lung during the onset of extrauterine air breathing is an order of magnitude, from a range of 10-12 to 110-120Torr. The contributions of oxygen and the volume and pressure relationships of ventilatory support to lung injury are not easily distinguished in the clinical setting. Sequential changes in inspired air or 100% oxygen were studied in 536 newborn rabbits without ventilatory support. Bilateral cervical vagotomies (BCV) were performed at 24h post natal to induce ventilatory distress which eventuates in hyaline membrane disease. The sequences applied yielded evidence for an induced state of oxygen dependency from oxygen use which was reflected in differences in survival and the extent of pulmonary injury. The median survival for animals kept in air throughout was 3h. Oxygen before vagotomy or during the first 3h afterwards extended the survival significantly but produced more extensive, more severe, and more rapid lung lesions. Returning animals to air after prior oxygen exposure reduced the number of survivors past 10h and shortened the maximum survival in those groups. These features indicate the development of a dependency of the defense mechanisms on the availability of oxygen at the higher level for metabolic and possibly other aspects of the pulmonary and systemic response to injury, beyond the usual physiological need. Subset analysis revealed additive and latent effects of oxygen and demonstrated a remarkable rapidity in onset of severe lesions under some circumstances, illustrating the toxicity of oxygen per se., (Copyright 2010 Elsevier Inc. All rights reserved.)
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- 2010
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6. Cerebropulmonary dysgenetic syndrome.
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Shanklin DR, Mullins AC, and Baldwin HS
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- Bronchopulmonary Dysplasia pathology, Fatal Outcome, Heterozygote, Humans, Infant, Newborn, Mutation, Respiratory Distress Syndrome, Newborn genetics, Respiratory Distress Syndrome, Newborn metabolism, Syndrome, ATP-Binding Cassette Transporters genetics, Bronchopulmonary Dysplasia genetics, Infant, Premature, Diseases genetics, Pulmonary Surfactants therapeutic use, Respiratory Distress Syndrome, Newborn drug therapy
- Abstract
Ventilatory treatment of neonatal respiratory distress often results in bronchopulmonary dysplasia from congenital surfactant deficiency due to mutants of transporter protein ABCA3. Association of this condition with other severe disorders in premature newborns has not heretofore been reported. A neonatal autopsy included an in vivo whole blood sample for genetic testing. Autopsy revealed severe interstitial pulmonary fibrosis at age 8 days with heterozygotic mutation p.E292V of ABCA3 and severe dystrophic retardation of cerebral cortex and cerebellum. Subsequently, 1300 archival neonatal autopsies, 1983-2006, were reviewed for comparable concurrent findings and bronchopulmonary dysplasia or retarded cerebral dystrophy lacking the other principal feature of this syndrome. Archival review revealed four similar cases and eight less so, without gene analysis. Further review for bronchopulmonary dysplasia revealed 59 cases, 1983-2006. Several other examples of similar retarded migration of germinal matrix and underdevelopment of cortical mantle, without pulmonary lesions of this type, were identified. The determination of an ABCA3 mutation in one case of severe pulmonary fibrosis with significant dystrophy of the brain and the identification of four highly similar archival cases and eight others with partial pathological findings supports the designation of an independent disorder, here referred to as the cerebropulmonary dysgenetic syndrome.
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- 2008
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7. Cellular magnesium acquisition: an anomaly in embryonic cation homeostasis.
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Shanklin DR
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- Animals, Calcium metabolism, Female, Fundulidae, Humans, Kinetics, Magnesium blood, Models, Biological, Ovum physiology, Potassium metabolism, Sodium metabolism, Solutions, Embryonic Development physiology, Magnesium metabolism
- Abstract
The intracellular dominance of magnesium ion makes clinical assessment difficult despite the critical role of Mg(++) in many key functions of cells and enzymes. There is general consensus that serum Mg(++) levels are not representative of the growing number of conditions for which magnesium is known to be important. There is no consensus method or sample source for testing for clinical purposes. High intracellular Mg(++) in vertebrate embryos results in part from interactions of cations which influence cell membrane transport systems. These are functionally competent from the earliest stages, at least transiently held over from the unfertilized ovum. Kinetic studies with radiotracer cations, osmolar variations, media lacking one or more of the four biological cations, Na(+), Mg(++), K(+), and Ca(++), and metabolic poison 0.05 mEq/L NaF, demonstrated that: (1) all four cations influence the behavior of the others, and (2) energy is required for uptake and efflux on different time scales, some against gradient. Na(+) uptake is energy dependent against an efflux gradient. The rate of K(+) loss is equal with or without fluoride, suggesting a lack of an energy requirement at these stages. Ca(++) efflux took twice as long in the presence of fluoride, likely due in part to intracellular binding. Mg(++) is anomalous in that early teleost vertebrate embryos have an intracellular content exceeding the surrounding sea water, an isolated unaffected yolk compartment, and a clear requirement for energy for both uptake and efflux. The physiological, pathological, and therapeutic roles of magnesium are poorly understood. This will change: (1) when (28)Mg is once again generally available at a reasonable cost for both basic research and clinical assessment, and (2) when serum or plasma levels are determined simultaneously with intracellular values, preferably as part of complete four cation profiles. Atomic absorption spectrophotometry, energy-dispersive x-ray analysis, and inductively coupled plasma emission spectroscopy on sublingual mucosal and peripheral blood samples are potential methods of value for coordinated assessments.
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- 2007
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8. Neonate with a single umbilical vessel: a case report.
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Shanklin DR and Zhang J
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- Congenital Abnormalities, Fatal Outcome, Female, Humans, Infant, Newborn, Placenta pathology, Pregnancy, Umbilical Cord pathology, Umbilical Veins pathology, Gastroschisis complications, Umbilical Cord abnormalities, Umbilical Veins abnormalities
- Abstract
Background: The respiratory, metabolic and excretory functions of the placenta provide maintenance of fetuses in utero even in the presence of severe malformations that preclude postnatal survival., Case: A 17-year-old secundigravida delivered a 1,075-g liveborn in the 30th week of gestation. The infant was severely malformed, with gastroschisis and a short umbilical cord, and survived for 62 minutes after birth. The placenta was examined pathologically, and a complete an autopsy was performed. The cord measured 13.0 cm long, the limit for absolute shortness. An 8.0-cm segment was found to contain only 1 umbilical vessel, basically a vein, with segmental arterial pads., Conclusion: The concurrence in a liveborn infant of malformations so severe it could not be sustained, a segment of umbilical cord with only 1 vessel and postnatal survival of 62 minutes emphasizes the biologic distinction between existence and vitality.
- Published
- 2007
9. Kinetics of T lymphocyte responses to persistent antigens.
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Shanklin DR and Smalley DL
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- Cytokines biosynthesis, Female, Humans, Immunologic Memory, Interleukin-2 biosynthesis, Interleukin-2 immunology, Mathematics, Time Factors, Antigens immunology, Breast Implants, Cytokines immunology, Models, Immunological, Silicone Gels, T-Lymphocytes immunology
- Abstract
Long term sequential study of immune responses in the same individuals is difficult from the time commitment required and the problem of maintaining enough subjects to provide for comparative analysis. We closely studied one hundred women with silicone mammary devices through cross sectional analysis up to 26 years post implantation and a similar sample of women to 6 years post explantation. The T cell index, calculated from tritiated thymidine incorporation during lymphoblast transformation, rose to a post implant peak at 10.5-12.0 years, falling progressively over the next 14.0-15.5 years to values indicative of probable immune quiescence. Post explantation, the index rose over the first 3 years and then sharply declined to within the range for unexposed controls. The shape of these time curves contains considerable information referent cell dynamics for both stimulatory and inhibitory factors and for demonstrating net group effects, appropriate to analysis in the cross sectional perspective. When a subset of four women was studied frequently and sequentially up to 8 years, an internal oscillatory pattern emerged, focusing attention on both the stimulatory and the inhibitory aspects of long term clonal expansion. IL-2 has stimulatory and inhibitory properties at different levels of production and is considered a prime candidate as the essential cytokine. The equations have details, however, which require exploration beyond any such provisional conclusion. The analytic process was aided by normalization of oscillatory data to eliminate subject variability and by Pareto optimization to assess the trend shown by normalization. Pareto analysis revealed two minimally coordinated oscillations, one over time and the other along net clonal expansion or decline of the siloxane specific T lymphocyte clone. The segments of the time related oscillation greatly exceeded the reaction times of cytokines currently known to be active in T cell regulation. Although the ultimate controlling factor(s) may be cytokine or chemokine combinations, the data are compatible with some more basic regulatory factor(s) of cell integrity, including limits on the number of cell divisions which can be sustained in long term immunopathic lesions, among other processes.
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- 2006
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10. Ureaplasma urealyticum binds mannose-binding lectin.
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Benstein BD, Ourth DD, Crouse DT, and Shanklin DR
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- Animals, Autopsy, Guinea Pigs, Humans, Infant, Lung immunology, Lung metabolism, Lung Diseases immunology, Lung Diseases microbiology, Mannose-Binding Lectin genetics, Mannose-Binding Lectin immunology, Mice, Protein Binding, Rabbits, Ureaplasma Infections immunology, Ureaplasma Infections metabolism, Ureaplasma Infections microbiology, Lung microbiology, Lung Diseases metabolism, Mannose-Binding Lectin metabolism, Ureaplasma urealyticum metabolism
- Abstract
Mannose-binding C-type lectin (MBL) is an important component of innate immunity in mammals. Mannose-binding lectin (MBL), an acute phase protein, acts as an opsonin for phagocytosis and also activates the mannan-binding lectin complement pathway. It may play a particularly significant role during infancy before adequate specific protection can be provided by the adaptive immune system. Ureaplasma urealyticum has been linked to several diseases including pneumonia and chronic lung disease (CLD) in premature infants. We therefore investigated the ability of U. urealyticum to bind MBL. A guinea pig IgG anti-rabbit-MBL antiserum was produced. An immunoblot (dot-blot) assay done on nitrocellulose membrane determined that the anti-MBL antibody had specificity against both rabbit and human MBL. Pure cultures of U. urealyticum, serotype 3, were used to make slide preparations. The slides containing the organisms were then incubated with nonimmune rabbit serum containing MBL. Ureaplasma was shown to bind rabbit MBL with an immunocytochemical assay using the guinea pig IgG anti-rabbit MBL antiserum. Horseradish peroxidase (HRP)-labeled anti-guinea pig IgG was used to localize the reaction. The anti-MBL antiserum was also used in an immunocytochemical assay to localize U. urealyticum in histological sections of lungs from mice specifically infected with this organism. The same method also indicated binding of MBL by ureaplasma in human lung tissue obtained at autopsy from culture positive infants. Our results demonstrate that ureaplasma has the capacity to bind MBL. The absence of MBL may play a role in the predisposition of diseases related to this organism.
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- 2004
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11. Neonatal adrenal failure due to congenital lipoid hyperplasia of cortex.
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Shanklin DR, Smalley DL, and Handorf CR
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- Adrenal Hyperplasia, Congenital complications, Anemia etiology, Fatal Outcome, Female, Humans, Hydrops Fetalis etiology, Infant, Newborn, Adrenal Cortex pathology, Adrenal Hyperplasia, Congenital diagnosis, Lipidoses pathology
- Published
- 2004
12. Ureaplasma in lung. 2. Association with bronchopulmonary dysplasia in premature newborns.
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Benstein BD, Crouse DT, Shanklin DR, and Ourth DD
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- Birth Weight, Bronchopulmonary Dysplasia pathology, Female, Gestational Age, Humans, In Situ Hybridization, Incidence, Infant, Infant, Newborn, Lung microbiology, Lung pathology, Risk Factors, Ureaplasma Infections pathology, Bronchopulmonary Dysplasia microbiology, Infant, Premature, Ureaplasma Infections microbiology, Ureaplasma urealyticum isolation & purification
- Abstract
Infants with Ureaplasma urealyticum in the lower respiratory tract are at risk for chronic lung disease (CLD) or bronchopulmonary dysplasia (BPD) but causality has been difficult to prove. The goal of this study was to identify ureaplasma in human neonatal lung tissue using the in situ hybridization (ISH) procedure described in Part 1 (Exp. Mol. Pathol., in press) of this report. By correlating their presence with the histopathologic findings, it may be possible to provide further evidence of the pathogenicity of ureaplasmas and their association with BPD. Lung autopsy tissue from seven infants with positive cultures and seven infants with negative cultures for ureaplasma were included in the study. All culture-positive infants were positive for ureaplasma on ISH and all had histopathologic evidence of BPD. Two of the seven infants with negative cultures were positive for ureaplasma with ISH. Of interest, these two infants were also found to have BPD at autopsy. The other five infants with negative cultures were also negative for ureaplasma on ISH and had no evidence of BPD. This study correlates the presence of U. urealyticum by ISH with the finding of BPD on histopathologic evaluation and provides evidence that it has a role in the development of CLD.
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- 2003
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13. Ureaplasma in lung. 1. Localization by in situ hybridization in a mouse model.
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Benstein BD, Crouse DT, Shanklin DR, and Ourth DD
- Subjects
- Administration, Intranasal, Animals, Animals, Newborn, Bronchopulmonary Dysplasia pathology, DNA, Viral analysis, Humans, Immunoenzyme Techniques, In Situ Hybridization, Infant, Newborn, Lung microbiology, Lung ultrastructure, Mice, Polymerase Chain Reaction, Ureaplasma Infections pathology, Ureaplasma urealyticum genetics, Ureaplasma urealyticum ultrastructure, Bronchopulmonary Dysplasia microbiology, Disease Models, Animal, Ureaplasma Infections microbiology, Ureaplasma urealyticum isolation & purification
- Abstract
Ureaplasma urealyticum is a common inhabitant of mucosal surfaces but is also associated with a higher incidence of pneumonia and bronchopulmonary dysplasia in preterm infants. Culture and polymerase chain reaction demonstrate high isolation rates of ureaplasma in clinical specimens documenting their presence but do not associate the organism directly with the diseased tissue. In this study, lung tissue samples from newborn mice inoculated intranasally with U. urealyticum were used to develop an in situ hybridization (ISH) test for the organism. In situ hybridization allows the localization of gene expression for visualization within the context of tissue morphology. New techniques which use biotinyl-tyramide based signal amplification have been able to greatly enhance the sensitivity of ISH. Using the Dako GenPoint Catalyzed Signal Amplification system to detect a biotinylated DNA probe specific for an internal nucleotide sequence within the urease gene of U. urealyticum, the organism was detected within the infected murine lung tissues. Electron microscopy was used to verify the presence of the organisms in the positive ISH areas. The ISH procedure developed in this study can be used to analyze the presence of ureaplasma in human neonatal lung tissue with the corresponding histopathology.
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- 2003
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14. Is pathology examination useful after early surgical abortion?
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Shanklin DR
- Subjects
- Female, Fetus pathology, Humans, Pregnancy, Abortion, Induced
- Published
- 2002
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15. Pathogenetic and diagnostic aspects of siliconosis.
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Shanklin DR and Smalley DL
- Subjects
- Autoantibodies blood, Blotting, Western, Contraceptive Devices, Female, Dose-Response Relationship, Immunologic, Epitope Mapping, Humans, Silicon immunology, Autoimmune Diseases diagnosis, Autoimmune Diseases pathology, Siloxanes adverse effects, Siloxanes chemistry
- Abstract
Silicones have an adverse effect on human health well beyond that suggested by the recent superficial public controversy. The evidence for immune responses to injected/implanted silicones is extensive, detailed, often very specific, and not at all new. Comprehending the immunopathogenicity, realized and potential, of silicone has grown as our general understanding of the immune system has developed. Several major issues in furthering this comprehension pertain to the nature of the essential epitope, special risk of silicones to women, and definition of the chronic disease complex so evident clinically, one defying classification within currently traditional disease categories and states. The commentary presented here emphasizes the immunopathic evidence, explores the question of the essential epitope, estimates the minimal threshold of silicone load for immune reactivity, presents a profile of autoantibodies for siliconosis, and calls attention to specific silicone-based female contraceptive modalities. The silicone content of personal care products, not always revealed by retail package labeling, is explored as a potential sensitizing factor in the environment.
- Published
- 2002
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16. Environmental immunogens and T-cell-mediated responses in fibromyalgia: evidence for immune dysregulation and determinants of granuloma formation.
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Shanklin DR, Stevens MV, Hall MF, and Smalley DL
- Subjects
- Adult, Aged, Antigens, Case-Control Studies, Concanavalin A pharmacology, Female, Granuloma etiology, Humans, In Vitro Techniques, Lymphocyte Activation, Male, Middle Aged, Siloxanes adverse effects, Fibromyalgia etiology, Fibromyalgia immunology, Granuloma immunology, Metals adverse effects, Metals immunology, T-Lymphocytes immunology
- Abstract
Thirty-nine patients with fibromyalgia syndrome (FMS) according to American College of Rheumatology criteria were studied for cell-mediated sensitivity to environmental chemicals. Lymphocytes were tested by standard [(3)H]thymidine incorporation in vitro for T cell memory to 11 chemical substances. Concanavalin A (Con A) was used to demonstrate T cell proliferation. Controls were 25 contemporaneous healthy adults and 252 other concurrent standard controls without any aspect of FMS. Significantly higher (P < 0.01) stimulation indexes (SI) were found in FMS for aluminum, lead, and platinum; borderline higher (0.05 > P > 0.02) SI were found for cadmium and silicon. FMS patients showed sporadic responses to the specific substances tested, with no high-frequency result (>50%) and no obvious pattern. Mitogenic responses to Con A indicated some suppression of T cell functionality in FMS. Possible links between mitogenicity and immunogenic T cell proliferation, certain electrochemical specifics of granuloma formation, maintenance of connective tissue, and the fundamental nature of FMS are considered., (Copyright 2000 Academic Press.)
- Published
- 2000
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17. Dynamics of wound healing after silicone device implantation.
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Shanklin DR and Smalley DL
- Subjects
- Breast Diseases immunology, Breast Diseases pathology, Cicatrix etiology, Cicatrix immunology, Cicatrix pathology, Female, Foreign-Body Reaction immunology, Foreign-Body Reaction pathology, Humans, Hypersensitivity, Delayed immunology, Hypersensitivity, Delayed pathology, Immunologic Memory immunology, Lymphocyte Activation, Polyurethanes adverse effects, T-Lymphocytes, Helper-Inducer immunology, Breast Diseases etiology, Breast Implantation adverse effects, Breast Implants adverse effects, Foreign-Body Reaction etiology, Hypersensitivity, Delayed etiology, Silicone Gels adverse effects, Wound Healing
- Abstract
A large surgical wound is required for implantation of silicone mammary devices. Formation of capsules around silicone devices follows wound healing processes except that the healing is conformed and significantly delayed by the physical presence of the implant. Multilayered capsules are thicker and lymphocytic and plasmalymphocytic vasculitis, markers for delayed hypersensitivity, also correlate with thicker capsules. Polyurethane-coated devices induce very thick capsules that remain so for over 20 years. By contrast, gel and saline content devices show maximum thickness at 6. 5 years. Active T(H) lymphocyte memory does not differ by implant type for individuals with devices in place and that for gel content devices peaks at 10.5 years. There was a significant decrease in T cell indexes only after the removal of saline content devices. Comparison of the rate of formation of the periprosthetic capsule with the healing time of large wounds of similar size indicates that silicone devices interfere with the healing process, requiring substantially more time. This extended period has the potential for enhancing autoimmune conversion as a consequence of persistent delayed hypersensitivity., (Copyright 1999 Academic Press.)
- Published
- 1999
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18. Additional surgery after breast device implantation.
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Shanklin DR and Smalley DL
- Subjects
- Adolescent, Adult, Aged, Female, Humans, Middle Aged, Postoperative Complications etiology, Surgery, Plastic adverse effects, Breast Implants adverse effects, Postoperative Complications surgery, Silicones adverse effects
- Published
- 1998
19. Risk of connective tissue disease among women with breast implants. Study adds nothing to knowledge of processes of tissue injury induced by silicone.
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Shanklin DR and Smalley DL
- Subjects
- Data Interpretation, Statistical, Female, Humans, Prosthesis Failure, Risk Factors, T-Lymphocytes immunology, Breast Implants adverse effects, Connective Tissue Diseases etiology
- Published
- 1998
20. The immunopathology of siliconosis. History, clinical presentation, and relation to silicosis and the chemistry of silicon and silicone.
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Shanklin DR and Smalley DL
- Subjects
- Equipment Failure, Female, Histocompatibility Antigens Class II, Humans, Immunity, Cellular, Immunologic Memory, Major Histocompatibility Complex, Silicosis, Siloxanes, Superantigens, Autoimmune Diseases pathology, Breast Implants adverse effects, Silicon immunology, Silicones adverse effects
- Abstract
Recent evidence confirms the fundamental involvement of the human immune system in the reaction to implantation of silicone-based medical devices. An as yet-to-be particularized epitope of many complex substances sharing siloxane structures is presented through the MHC-II apparatus with development and retention of T cell memory. This memory can be tested for in practical terms using one or more forms of silica, which links the immuno-histopathology and autoimmune attributes of "silicosis" with those of "siliconosis." The lesions of siliconosis are typical of those for persistent antigens and delayed, cell mediated hypersensitivity. The basic descriptive pathology of the reaction to silicone has been known since soon after introduction of silicones in medical procedures, with the exception of some details related to the more recent discoveries on the role of cytokines in the immunopathic process. The clinical consequences of siliconosis are common and can be severe in some individuals implanted with silicone devices.
- Published
- 1998
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21. Monocyte-dependent stimulation of human T cells by silicon dioxide.
- Author
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Smalley DL, Shanklin DR, and Hall MF
- Subjects
- Antibodies, Monoclonal pharmacology, Cell Communication, Concanavalin A pharmacology, Female, HLA-DP Antigens immunology, HLA-DQ Antigens immunology, HLA-DR Antigens immunology, Humans, In Vitro Techniques, Lymphocyte Activation drug effects, Silicon Dioxide immunology, Breast Implants adverse effects, Monocytes immunology, Silicon Dioxide adverse effects, T-Lymphocytes drug effects, T-Lymphocytes immunology
- Abstract
Mononuclear cells were isolated by Ficoll-Hypaque density gradient centrifugation from randomly selected silicone breast implant recipients for testing. Restricted antibody to HLA-DR (28-33 kD) depleted the concanavalin A mitogenic response which was expected but failed to inhibit the proliferative response to silicon dioxide. Further testing with monoclonal antibodies to HLA-DP, -DQ, and a second -DR with specificity for the NS1 region of the MHC class II genome, all markedly inhibited proliferation of T cells despite otherwise adequate stimulation by concanavalin A or silicon dioxide. Monoclonal antibodies directed against B7-1 also inhibited proliferation of T cells following stimulation with concanavalin A or silicon dioxide. These results confirm the T-cell response to silicon dioxide is monocyte-dependent and not a superantigen as has been speculated.
- Published
- 1998
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22. Analytic review of the scientific literature on silicone immune responses: comment on the article by Marcus.
- Author
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Smalley DL and Shanklin DR
- Subjects
- Animals, Breast Implants, Databases, Bibliographic, Female, Humans, Immune System, Silicon Dioxide immunology, Antibody Formation immunology, Silicones
- Published
- 1997
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23. T-cell-specific response to silicone gel.
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Smalley DL and Shanklin DR
- Subjects
- Drug Hypersensitivity immunology, Humans, Immunity, Cellular, Drug Hypersensitivity etiology, Hypersensitivity, Delayed chemically induced, Silicones, T-Lymphocytes immunology
- Published
- 1996
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24. T cell-mediated immune response to silica in silicone breast implant patients.
- Author
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Shanklin DR, Smalley DL, Hall MF, and Stevens MV
- Subjects
- Female, Humans, Interleukin-2 physiology, Retrospective Studies, Breast Implants adverse effects, Silicon Dioxide immunology, Silicones adverse effects, T-Lymphocytes immunology
- Published
- 1996
- Full Text
- View/download PDF
25. Microscopic techniques and histologic findings in silicone mammary implant capsules and regional paranodal tissues.
- Author
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Shanklin DR and Smalley DL
- Subjects
- Female, Granuloma pathology, Humans, Silicon Dioxide analysis, Breast Implants adverse effects, Silicones adverse effects
- Published
- 1996
- Full Text
- View/download PDF
26. Biology of the congenitally hypothyroid hyt/hyt mouse.
- Author
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Biesiada E, Adams PM, Shanklin DR, Bloom GS, and Stein SA
- Subjects
- Animals, Disease Models, Animal, Humans, Mice, Mice, Mutant Strains, Receptors, Thyrotropin genetics, Congenital Hypothyroidism, Genes, Recessive, Hypothyroidism genetics
- Abstract
The hyt/hyt mouse has an autosomal recessive, fetal onset, characterized by severe hypothyroidism that persists throughout life and is a reliable model of human sporadic congenital hypothyroidism. The hypothyroidism in the hyt/hyt mouse reflects the hyporesponsiveness of the thyroid gland to thyrotropin (TSH). This is attributable to a point mutation of C to T at nucleotide position 1666, resulting in the replacement of a Pro with Leu at position 556 in transmembrane domain IV of the G protein-linked TSH receptor. This mutation leads to a reduction in all cAMP-regulated events, including thyroid hormone synthesis. The diminution in T3/T4 in serum and other organs, including the brain, also leads to alterations in the level and timing of expression of critical brain molecules, i.e. selected tubulin isoforms (M beta 5, M beta 2, and M alpha 1), microtubule associated proteins (MAPs), and myelin basic protein, as well as to changes in important neuronal cytoskeletal events, i.e. microtubule assembly and SCa and SCb axonal transport. In the hyt/hyt mouse, fetal hypothyroidism leads to reductions in M beta 5, M beta 2, and M alpha 1 mRNAs, important tubulin isoforms, and M beta 5 and M beta 2 proteins, which comprise the microtubules. These molecules are localized to layer V pyramidal neurons in the sensorimotor cortex, a site of differentiating neurons, as well as a site for localization of specific thyroid hormone receptors. These molecular abnormalities in specific cells and at specific times of development or maturation may contribute to the observed neuroanatomical abnormalities, i.e. altered neuronal process growth and maintenance, synaptogenesis, and myelination, in hypothyroid brain. Abnormal neuroanatomical development in selected brain regions may be the factor underlying the abnormalities in reflexive, locomotor, and adaptive behavior seen in the hyt/hyt mouse and other hypothyroid animals.
- Published
- 1996
- Full Text
- View/download PDF
27. Lymphocyte response to silica among offspring of silicone breast implant recipients.
- Author
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Smalley DL, Levine JJ, Shanklin DR, Hall MF, and Stevens MV
- Subjects
- Adolescent, Adult, Child, Child, Preschool, Female, Humans, Male, Mothers, Pregnancy, T-Lymphocytes immunology, Breast Implants adverse effects, Lymphocyte Activation drug effects, Maternal-Fetal Exchange drug effects, Silicon Dioxide pharmacology, Silicone Elastomers pharmacology, T-Lymphocytes drug effects
- Abstract
The current study evaluated immune response to silicon dioxide in children born to women with silicone breast implants. In part one of the study, the T lymphocytes of 21 of 24 such children were significantly stimulated by silicon dioxide (silica). Part two consisted of eleven children, four born preimplantation and seven born postimplantation. None of the preimplant offspring showed T cell responses to silica; five of the seven postimplant children were positive for T cell memory for silica. Part three was a blinded study based on statistically significant differences in T cell stimulation with silicon dioxide between postimplant children and controls. These findings indicate a common immune reaction, that of T cell memory, occurs in mothers and their children born after exposure to silicone mammary implants placed prior to pregnancy. Since not all such children were breast fed the result favors transplacental passage of immunogens such as silicone oligomers or through maternofetal cellular traffic.
- Published
- 1996
- Full Text
- View/download PDF
28. Placental metastasis from maternal carcinoma. A report of three cases.
- Author
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Eltorky M, Khare VK, Osborne P, and Shanklin DR
- Subjects
- Adult, Female, Humans, Pregnancy, Adenocarcinoma secondary, Breast Neoplasms pathology, Carcinoma, Ductal, Breast secondary, Pancreatic Neoplasms pathology, Placenta Diseases pathology, Pregnancy Complications, Neoplastic pathology
- Abstract
Metastasis of a maternal neoplasm to the products of conception is extremely rare. Of the 54 reported cases in the world literature, only 14 (25%) showed fetal metastasis. More than 50% of the reported cases were not examined grossly or had no visually apparent tumor deposits. Malignant melanoma is the most common malignant maternal neoplasm to metastasize to the products of conception. We report three unusual maternal malignant neoplasms (one pancreatic and two breast cancer) with evidence of placental metastasis and discuss the risk factors for fetal involvement in these cases.
- Published
- 1995
29. Immunologic stimulation of T lymphocytes by silica after use of silicone mammary implants.
- Author
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Smalley DL, Shanklin DR, Hall MF, Stevens MV, and Hanissian A
- Subjects
- Adult, Female, Humans, Male, Middle Aged, Rheumatic Diseases immunology, Breast Implants adverse effects, Lymphocyte Activation drug effects, Silicon Dioxide immunology, Silicones adverse effects, T-Lymphocytes immunology
- Abstract
Difficulties in showing the biologic activity of silicones in vitro have contributed to the controversy over effects of silicone mammary implants in vivo. We adapted a standard lymphocyte stimulation test to detect evidence of cellular immunity in patients with silicone gel implants. Initially, lymphocytes were harvested from 70 implant patients, 76 normal controls without implants or symptoms, and 18 patients with classic rheumatic disorders and without a history of silicone implants. The harvested lymphocytes were stimulated with PWM, PHA, Con A, and pharmaceutical grade colloidal silicon dioxide (silica). Implant patients showed increased SI compared to controls and those with rheumatic disorders. The mean SI of implant patients was 195.0 +/- 19.3, 18-fold that of normal controls (< 0.0001). Patients with rheumatic disease showed the same SI as controls (P = 0.3577). A follow-up study included 220 normal controls without implants, 942 silicone gel implant patients with demonstrable rheumatic symptoms, and 34 implant patients without symptoms at the time of the study. The average SI for the 220 normal controls was 10.0 +/- 0.41. Among the symptomatic implant women, 860 (91.3%) had SI significantly above those of the normal controls. Of these, 171 (18.2%) had SI between 25 and 50, 316 (33.5%) had SI between 50 and 100, and 373 (39.6%) had SI over 100. The data presented confirms that silicone implant patients respond immunologically to the silicon dioxide contained in mammary prostheses.
- Published
- 1995
- Full Text
- View/download PDF
30. Light/dye microvascular injury selectively eliminates hypercapnia-induced pial arteriolar dilation in newborn pigs.
- Author
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Leffler CW, Mirro R, Shanklin DR, Armstead WM, and Shibata M
- Subjects
- Animals, Animals, Newborn, Arterioles drug effects, Arterioles ultrastructure, Carbon Dioxide blood, Fluorescein, Hypercapnia blood, Hypercapnia pathology, Iloprost pharmacology, Isoproterenol pharmacology, Muscle, Smooth, Vascular physiopathology, Muscle, Smooth, Vascular ultrastructure, Nitroprusside pharmacology, Oxygen blood, Parietal Lobe drug effects, Parietal Lobe ultrastructure, Partial Pressure, Swine, Arterioles pathology, Fluoresceins toxicity, Hypercapnia physiopathology, Light adverse effects, Muscle, Smooth, Vascular pathology, Pia Mater blood supply, Vasodilation drug effects
- Abstract
Cerebral vasodilation in response to hypercapnia involves prostanoids in newborn pigs. This study examines the hypothesis that endothelial injury in vivo inhibits cerebral vasodilation and prostacyclin synthesis in response to hypercapnia, thus suggesting prostacyclin is a primary endothelium-derived vasodilating factor in newborn pig cerebral circulation. Anesthetized piglets with closed cranial windows were studied before and after injury caused by light/dye or before and after dye-only sham control. Light/dye injury was produced by injecting sodium fluorescein intravenously and passing filtered light from a mercury arc lamp through the cranial window. Ultrastructural changes to endothelium of pial vessels were produced that were characterized by surface pits, vacuolar cytoplasmic inclusions, and mitochondrial injury. After the light/dye injury, dilation to hypercapnia was absent while dilations to iloprost, isoproterenol, and sodium nitroprusside and constrictions to norepinephrine and acetylcholine were retained. Before light/dye treatment, hypercapnia increased cortical periarachnoid 6-keto prostaglandin F1 alpha concentration approximately threefold. However, after treatment, 6-keto-prostaglandin F1 alpha was not increased significantly in response to hypercapnia. These findings are consistent with the hypothesis that endothelial prostacyclin synthesis induced by hypercapnia participates in dilation of adjacent smooth muscle.
- Published
- 1994
- Full Text
- View/download PDF
31. Effects of intrauterine growth on intestinal length in the human fetus.
- Author
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Shanklin DR and Cooke RJ
- Subjects
- Birth Weight, Fetal Growth Retardation pathology, Gestational Age, Humans, Infant, Newborn, Reference Values, Embryonic and Fetal Development, Fetus anatomy & histology, Intestines embryology
- Abstract
Standards for human fetal intestinal length are not well established but have important implications for the care of the preterm and intra-uterine growth-retarded (IUGR) infant. Our purpose was to examine the relationship between intra-uterine growth and intestinal length in the human fetus. One hundred infants were studied. Birth weight and gestational age ranged from 76 to 4,385 g and from 12 to 42 weeks, respectively. Twenty-one infants were noted to be IUGR. Intestinal length (total, small, large) increased (p < 0.0001) with birth weight, gestational age, and crown-heel length but was reduced in IUGR infants. The ratio of body weight to intestinal length increased with gestation but was also reduced in IUGR infants. In conclusion, a reduced functional mass, as suggested by decreased intestinal length or body weight:intestinal length ratio, may contribute to the poor weight sometimes seen in the very-low-birth weight or IUGR infant.
- Published
- 1993
- Full Text
- View/download PDF
32. Hepatic histopathologic condition does not correlate with laboratory abnormalities in HELLP syndrome (hemolysis, elevated liver enzymes, and low platelet count)
- Author
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Barton JR, Riely CA, Adamec TA, Shanklin DR, Khoury AD, and Sibai BM
- Subjects
- Adolescent, Adult, Female, HELLP Syndrome blood, HELLP Syndrome metabolism, Hemorrhage pathology, Humans, Liver enzymology, Liver Diseases pathology, Pregnancy, HELLP Syndrome pathology, Liver pathology
- Abstract
Objective: Our objective was to categorize the histologic findings in the liver in patients with HELLP syndrome (hemolysis, elevated liver enzymes, and low platelet count) and to correlate these findings with the severity of clinical laboratory abnormalities., Study Design: Eleven patients with laboratory criteria for HELLP syndrome who required cesarean delivery underwent needle biopsy of the liver under direct visualization., Results: Eight patients had periportal hemorrhage, and six had fibrin deposition. Fatty infiltration was seen in four, one with large-droplet fat, three with microvesicular fat. There was no statistically significant correlation between the severity of the histologic findings of periportal hemorrhage and fibrin deposition and the clinical laboratory findings. Fatty infiltration did not correlate with the severity of the HELLP syndrome's histologic condition, but, in contrast, did correlate with thrombocytopenia and aminotransferase elevations., Conclusions: Laboratory abnormalities do not accurately reflect the severity of the underlying histopathologic condition in HELLP syndrome. We propose that all patients with HELLP syndrome, regardless of the degree of their laboratory abnormalities, be treated aggressively, primarily with delivery.
- Published
- 1992
- Full Text
- View/download PDF
33. Polyethylene glycol superoxide dismutase and catalase attenuate increased blood-brain barrier permeability after ischemia in piglets.
- Author
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Armstead WM, Mirro R, Thelin OP, Shibata M, Zuckerman SL, Shanklin DR, Busija DW, and Leffler CW
- Subjects
- Animals, Animals, Newborn, Blood Vessels ultrastructure, Brain metabolism, Brain Ischemia pathology, Cerebrovascular Circulation drug effects, Free Radical Scavengers, Microcirculation, Nitroblue Tetrazolium, Reperfusion, Swine, Urea pharmacokinetics, Blood-Brain Barrier drug effects, Brain Ischemia physiopathology, Capillary Permeability drug effects, Catalase pharmacology, Polyethylene Glycols pharmacology, Superoxide Dismutase pharmacology
- Abstract
Background and Purpose: Transport of urea across the blood-brain barrier is increased during postischemic cerebral reperfusion in the piglet. Ischemia/reperfusion also has been observed to increase apparent superoxide anion generation on the surface of the brain. The present study was designed to address the hypothesis that the increased transfer of urea into the brain after ischemia/reperfusion could be due to superoxide anion-induced alterations in blood-brain barrier permeability., Methods: Blood-to-brain transfer of carbon-14-labeled urea was measured in four groups (n = 7 each) of newborn pigs: 1) control (no ischemia, no pretreatment), 2) pretreatment with polyethylene glycol superoxide dismutase (1,000 IU/kg) and polyethylene glycol catalase (10,000 IU/kg i.v.) but no ischemia, 3) no pretreatment and 20 minutes of ischemia followed by 2 hours of reperfusion, and 4) pretreatment with polyethylene glycol superoxide dismutase and polyethylene glycol catalase in addition to ischemia/reperfusion. The following brain regions were investigated: cerebrum, caudate, midbrain, pons, medulla, and cerebellum., Results: Polyethylene glycol superoxide dismutase inhibited generation of superoxide anion by the brain during reperfusion after ischemia. Regional transfer of [14C]urea from blood to brain increased at 2 hours' reperfusion. This ischemia-induced increase in blood-to-brain transfer of [14C]urea was attenuated by pretreatment with polyethylene glycol superoxide dismutase and polyethylene glycol catalase: e.g., cerebrum Kin was 28 +/- 2 in the control group, 26 +/- 3 in the pretreated/no ischemia group, 67 +/- 5 in the untreated/ischemia group, and 40 +/- 2 ml.g-1.s-1.10(6) in the pretreated/ischemia group. After ischemia/reperfusion, cerebral blood flow was unchanged by pretreatment with polyethylene glycol superoxide dismutase and polyethylene glycol catalase., Conclusions: These data suggest that production of a partially reduced species of oxygen contributes to the increased urea transfer across the blood-brain barrier after ischemia in the newborn pig.
- Published
- 1992
- Full Text
- View/download PDF
34. The pathology of maternal mortality.
- Author
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Shanklin DR, Sommers SC, Brown DA, Driscoll SG, and Jewett JF
- Subjects
- Adult, Female, Humans, Infant Mortality, Infant, Newborn, Massachusetts, Pregnancy, Pregnancy Complications classification, Pregnancy Complications etiology, Pregnancy Complications mortality, Retrospective Studies, Cause of Death, Maternal Mortality, Pregnancy Complications pathology
- Published
- 1991
- Full Text
- View/download PDF
35. The site of the molecular defect in the thyroid gland of the hyt/hyt mouse: abnormalities in the TSH receptor-G protein complex.
- Author
-
Stein SA, Zakarija M, McKenzie JM, Shanklin DR, Palnitkar MB, and Adams PM
- Subjects
- Adenylyl Cyclases metabolism, Animals, Base Sequence, Blotting, Northern, Cyclic AMP biosynthesis, Mice, Mice, Inbred Strains, Molecular Sequence Data, Nucleic Acid Hybridization, RNA, Messenger analysis, Thyroglobulin blood, Thyrotropin blood, GTP-Binding Proteins physiology, Hypothyroidism genetics, Receptors, Thyrotropin physiology, Thyroid Gland metabolism
- Abstract
The hyt/hyt mouse has a severe and pervasive primary inherited hypothyroidism with significantly depressed serum T4, elevated serum and pituitary TSH, and reduced thyroid gland iodide uptake. Previous ultrastructural and histologic analysis of the hyt/hyt thyroid gland along with these biochemical abnormalities support an inherited defect in TSH responsiveness of the hyt/hyt thyroid gland. In order to evaluate the potential site of the defect in the hyt/hyt mouse, we have studied the hyt/hyt gland and hyt/hyt TSH from a biochemical and molecular standpoint. Based on demonstrated bioactivity of hyt/hyt serum in the McKenzie bioassay, this reduced responsiveness to TSH in the hyt/hyt mouse is not due to reduced bioactivity of hyt/hyt TSH or a major structural abnormality in the hyt/hyt TSH molecule. In comparison to hyt/ + euthyroid littermates and +/+ BALB/cBY progenitor strain mice, the hyt/hyt mouse demonstrates a twofold reduction in thyroid gland basal cAMP and a markedly diminished response of adenylyl cyclase to exogenous TSH. However, hyt/hyt cAMP production is equivalent to the euthyroid mice after stimulation of thyroid glands by forskolin, cholera toxin, PGE1, and isoproterenol. These results support a defect in the TSH-G protein-adenylyl cyclase system in the hyt/hyt thyroid gland. Specifically, these findings suggest that the hyt/hyt mouse has a defect in TSH responsivity due to an inherited defect in the thyroid gland TSH receptor molecule. Since the hyt/hyt gland makes T3 and T4 but at diminished levels, the proposed defect in the TSH receptor would still impart partial function. Both hyt/hyt and euthyroid hyt/ + littermates make TSH receptor mRNAs of 5500 and 2400 base pairs. This suggests that the receptor defect does not represent a major structural abnormality of the gene. The receptor defect could represent a reduction in receptor number, receptor-TSH affinity, or TSH receptor-G protein coupling. The specificity of this effect on adenylyl cyclase-cAMP is shown by the reduction of TSH-cAMP regulated thyroid peroxidase (TPO) and thyroglobulin mRNAs in the hyt/hyt thyroid gland. Given the importance of TPO and thyroglobulin in normal thyroid hormone synthesis, the reductions in TPO and thyroglobulin mRNAs in the hyt/hyt thyroid gland may underlie the significant decrease in thyroid hormone production by the hyt/hyt mouse.
- Published
- 1991
- Full Text
- View/download PDF
36. Isolation of skeletal muscle mitochondria from hamsters using an ionic medium containing ethylenediaminetetraacetic acid and nagarse.
- Author
-
Bhattacharya SK, Thakar JH, Johnson PL, and Shanklin DR
- Subjects
- Animals, Cell Fractionation methods, Cricetinae, Male, Oxidative Phosphorylation, Edetic Acid, Mitochondria metabolism, Mitochondria ultrastructure, Muscles ultrastructure, Subtilisins
- Abstract
An improved procedure is reported for the isolation of skeletal muscle mitochondria from hamsters and compared with our previous method. This procedure utilizes 20 mg% Nagarse in an ionic medium containing 100 mM sucrose, 10 mM EDTA, 100 mM Tris-HCl, 46 mM KCl, and 0.5% bovine serum albumin (BSA), at pH 7.4 (medium-B). Oxidative phosphorylation was studied by measuring ADP/O ratio and respiratory control ratio (RCR) using NAD(+)-linked pyruvate-malate (PM), as well as FAD-linked succinate (SUCC) as substrates. The mitochondria isolated in medium-B exhibited high RCR and high ADP phosphorylation capacity, and were superior to those prepared by our previous method. Electron micrographs of organelles isolated in medium-B revealed intact mitochondrial membrane and structural integrity, whereas those isolated with medium-A containing 50 mg% Nagarse depicted considerable damage including swelling, ruptured membrane, and loss of intramitochondrial matrix. Previously, we used a nonionic medium containing 210 mM mannitol, 70 mM sucrose, 0.1 mM EDTA, 10 mM Tris-HCl, 50 mg% Nagarse, and 0.5% BSA, at pH 7.4 (medium-A). Mitochondria isolated with medium-B yielded mean RCR values of 7.3 to 8.3 with PM, and values of 3.7 to 4.7 with SUCC as substrates, compared to 1.6 and 1.8 with PM, and 1.4 and 1.7 with SUCC for the organelles isolated using medium-A, respectively. Likewise, the ADP/O ratios were 2.6 to 2.7 with PM, and 1.6 to 1.7 with SUCC for medium-B preparations, compared to 1.5 and 1.8 with PM and 1.0 and 1.2 with SUCC for medium-A preparations, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)
- Published
- 1991
- Full Text
- View/download PDF
37. Pathologic studies of fetal thyroid development.
- Author
-
Shanklin DR
- Subjects
- Brain embryology, Embryonic and Fetal Development physiology, Humans, Infant, Newborn growth & development, Organ Size physiology, Thyroid Gland growth & development, Thyroid Gland pathology, Thyroid Gland embryology
- Published
- 1991
- Full Text
- View/download PDF
38. Thyroid hormone control of brain and motor development: molecular, neuroanatomical, and behavioral studies.
- Author
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Stein SA, Adams PM, Shanklin DR, Mihailoff GA, and Palnitkar MB
- Subjects
- Animals, Brain embryology, Cerebral Palsy physiopathology, Child, Preschool, Humans, Intellectual Disability physiopathology, Learning Disabilities physiopathology, Mice, Brain growth & development, Developmental Disabilities physiopathology, Nervous System anatomy & histology, Psychomotor Performance physiology, Thyroid Hormones physiology
- Published
- 1991
- Full Text
- View/download PDF
39. Hypothyroidism reduces the rate of slow component A (SCa) axonal transport and the amount of transported tubulin in the hyt/hyt mouse optic nerve.
- Author
-
Stein SA, Kirkpatrick LL, Shanklin DR, Adams PM, and Brady ST
- Subjects
- Actins analysis, Animals, Cytoskeleton ultrastructure, Hypothyroidism genetics, Intermediate Filament Proteins metabolism, Mice, Models, Neurological, Neurofilament Proteins, Thyroxine blood, Axonal Transport physiology, Cytoskeleton physiology, Hypothyroidism physiopathology, Mice, Mutant Strains physiology, Optic Nerve physiopathology, Tubulin metabolism
- Abstract
Thyroid hormone deficiency in the developing brain leads to disorders of neuronal process growth. This is evidenced by reduced axonal and dendritic size and complexity (Garza et al.: Developmental Brain Research 43:287-297, 1988; Ruiz-Marcos: Iodine and the Brain. New York: Plenum Press, pp 91-102, 1989). These findings may be related to alterations in the neuronal cytoskeleton in hypothyroidism, such as reduced or abnormal microtubular number and density (Faivre et al.: Developmental Brain Research 8: 21-30, 1983), and altered assembly, stabilization, and composition of microtubule protein in the hypothyroid brain. Neurofilaments also contribute to axonal caliber and process stability. Similar to microtubules, certain properties of neurofilaments are altered in developing hypothyroid axons (Marc and Rabie: International Journal of Developmental Neuroscience 3: 353-358, 1985; Faivre et al.: Developmental Brain Research 8:21-30, 1983) that may affect axonal caliber and process stability. Normal process growth is predicted on formation of appropriate numbers of microtubules and on the normal synthesis and axonal transport of cytoskeletal components [tubulin, microtubule associated proteins (MAPs), and neurofilament proteins]. Hypothyroidism might alter the neuronal cytoskeleton and neuronal growth either by affecting the developmental programs for expression of specific isoforms of cytoskeletal proteins or by changing the delivery of cytoskeletal proteins via slow axonal transport, particularly slow component a (SCa). Previous studies had demonstrated changes in the amount of specific microtubule protein isoforms and mRNAs (Stein et al.: Iodine and the Brain. New York: Plenum Press, pp 59-78, 1989a). To further elucidate the molecular basis for process growth abnormalities in the hypothyroid brain, we investigated slow axonal transport in the mouse to determine the effects of thyroid hormone deficiency on the rate and composition of SCa. Comparisons of SCa in the optic nerve of hyt/hyt hypothyroid mouse and euthyroid hyt/+ littermates and euthyroid progenitor strain, BALB/cBY +/+ mice, indicated that the velocity of SCa was significantly reduced in hyt/hyt optic nerve relative to hyt/+ and +/+. The axonal transport rate for tubulin, which is carried in SCa, was 0.118 mm/day in the hyt/hyt optic nerves. This rate was significantly different for the tubulin rates for the hyt/+ optic nerves (0.127 mm/day) and for the +/+ optic nerves (0.138 mm/day). Neurofilament proteins, as measured by the 140,000 daltons component, NFM, also appeared to be reduced in velocity in the hyt/hyt versus the hyt/+ and +/+ optic nerves.(ABSTRACT TRUNCATED AT 400 WORDS)
- Published
- 1991
- Full Text
- View/download PDF
40. Activated oxygen and arachidonate effects on newborn cerebral arterioles.
- Author
-
Leffler CW, Busija DW, Armstead WM, Shanklin DR, Mirro R, and Thelin O
- Subjects
- Animals, Arachidonic Acid, Arterioles drug effects, Arterioles ultrastructure, Cerebral Cortex metabolism, Hypercapnia physiopathology, Pia Mater blood supply, Prostaglandins metabolism, Swine, Vasodilation, Animals, Newborn physiology, Arachidonic Acids pharmacology, Cerebrovascular Circulation drug effects, Oxygen pharmacology
- Abstract
We have observed that pial arteriolar dilation in response to hypercapnia and hypotension is abolished after cerebral ischemia in newborn pigs. We determined whether direct generation of activated oxygen on the brain surface (OX: xanthine oxidase, hypoxanthine, FeCl3, and FeSO4) or topical arachidonate altered pial arteriolar responsiveness in a manner similarly to cerebral ischemia. OX, which generated more brain surface superoxide than reperfusion after ischemia, dilated pial arterioles. This dilation was reversed within 10 min of the end of exposure. OX produced ultrastructural changes in pial vessel endothelium and appeared to cause intravascular aggregation of granulocytes. After OX, prostanoid-dependent pial arteriolar dilations in response to hypercapnia and hypotension were attenuated, whereas constrictor responses to norepinephrine and acetylcholine and dilator responses to prostaglandin E2 and isoproterenol were not affected. After OX, hypercapnia increased cortical periarachnoid cerebrospinal fluid prostanoids modestly, whereas acetylcholine produced the normal strong stimulation of prostanoid synthesis. Arachidonate (10(-4) M and 7 x 10(-4) M) also caused reversible pial arteriolar dilation but did not alter subsequent pial arteriolar responses. Therefore, although arachidonate did not mimic the effects of ischemia-reperfusion on pial arteriolar reactivity, OX produced alterations that are qualitatively similar, although quantitatively less, than those produced by ischemia.
- Published
- 1990
- Full Text
- View/download PDF
41. Ultrastructural aspects of preeclampsia. II. Mitochondrial changes.
- Author
-
Shanklin DR and Sibai BM
- Subjects
- Cell Survival, Endothelium, Vascular ultrastructure, Female, Humans, Liver ultrastructure, Mitochondria, Muscle ultrastructure, Myometrium ultrastructure, Pre-Eclampsia genetics, Pregnancy, Skin ultrastructure, Mitochondria ultrastructure, Pre-Eclampsia pathology
- Abstract
Biopsy specimens were obtained under direct vision at the time of cesarean section from 47 patients (35 with preeclampsia and 12 normotensive patients) and from four women with cesarean section hysterectomies (all normotensive) as an extension of previous work. Tissues were obtained from the myometrium near the placental bed and from the opposite side of the uterus. Skin biopsies were also obtained from eight women with preeclampsia and liver biopsies were obtained from two patients with acute microvesicular fatty change of pregnancy (one with and one without concomitant preeclampsia). Specimens were examined histologically and by electron microscopy. Mitochondrial changes in small vessels, principally venules, in myometrial smooth muscle, myometrial interstitial cells, circulating leukocytes, epidermal and dermal cells, and hepatocytes were examined and compared between women with preeclamptic and normotensive pregnancies. These findings were then compared with mitochondria from 500 biopsies over the same 3-year interval to assess the possible role of delay in tissue fixation. There were 12 other biopsies from nonpregnant women of childbearing age. As further control on artifact, other specimens were initially sampled immediately in the operating room and then serially for up to 2 hours later. Artifact as a basis for the mitochondrial changes was ruled out by these procedures. Normal mitochondria undergo a morphologic conformational sequence with physiologic changes in substrate, oxygen consumption, adenosine diphosphate, and respiratory rate. The mitochondria of preeclamptic tissues show a central disruption that is outside this normal sequence or cycle. This disruption occurs more often and is more severe in preeclampsia than in normotensive pregnancies. In addition, the hypertrophic smooth muscle of the pregnant uterus has a complex of cytoplasmic organelles in a paranuclear location, usually apical, that contains a variable mixture of glycogen, the Golgi apparatus, endoplasmic reticulum, mitochondria, and small unidentified microvesicles. This complex has the location and appearance suggestive of a myometrial "power pack" of significance in metabolism and contraction. The presence of similar mitochondrial changes in a limited sample of nonuterine tissues is suggestive of a systemic metabolic disorder as an important feature of preeclampsia.
- Published
- 1990
- Full Text
- View/download PDF
42. Recurrent acute fatty liver of pregnancy.
- Author
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Barton JR, Sibai BM, Mabie WC, and Shanklin DR
- Subjects
- Acute Disease, Adult, Biopsy, Female, Humans, Microscopy, Electron, Pregnancy, Recurrence, Fatty Liver pathology, Liver ultrastructure, Pregnancy Complications pathology
- Abstract
The first reported case of recurrent acute fatty liver of pregnancy confirmed by biopsy is described. In this case a high index of suspicion led to an early diagnosis and intervention with resultant improved maternal and fetal outcome. Electron microscopic examination of a liver biopsy specimen proved more beneficial in confirmation of the diagnosis compared with routine microscopic examination.
- Published
- 1990
- Full Text
- View/download PDF
43. Dilation and evacuation for second-trimester genetic pregnancy termination.
- Author
-
Shulman LP, Ling FW, Meyers CM, Shanklin DR, Simpson JL, and Elias S
- Subjects
- Congenital Abnormalities diagnosis, Dilatation methods, Extraction, Obstetrical methods, Female, Fetal Diseases diagnosis, Humans, Pregnancy, Pregnancy Trimester, Second, Abortion, Eugenic methods, Abortion, Induced methods
- Abstract
Dilation and evacuation (D&E) is the most common procedure for second-trimester pregnancy termination currently used by United States obstetrician-gynecologists. Although this method carries morbidity and mortality rates significantly lower than methods requiring labor induction, the procedure most commonly used for second-trimester genetic terminations seems to be labor induction (eg, vaginal prostaglandin suppositories). Many geneticists appear reluctant to recommend D&E over induction methods of pregnancy termination because they perceive that fetal abnormalities cannot be consistently confirmed by evaluation of the products of conception obtained by D&E. We report here 60 consecutive patients who underwent D&E (14-22 weeks' gestation) after detection of fetal abnormalities. The prenatal diagnoses were confirmed in all cases. Our experience thus indicates that D&E is reliable in confirming most prenatal diagnoses and should be the procedure of choice when second-trimester pregnancy termination is chosen because of fetal abnormalities.
- Published
- 1990
44. Effect of exogenous surfactant on the development of bronchopulmonary dysplasia in a baboon hyaline membrane disease model.
- Author
-
Maeta H, Raju TN, Vidyasagar D, Bhat R, Esterly J, Matsuda H, Shimada S, Krukenkamp IB, and Shanklin DR
- Subjects
- Animals, Bronchopulmonary Dysplasia etiology, Bronchopulmonary Dysplasia pathology, Humans, Hyaline Membrane Disease complications, Hyaline Membrane Disease drug therapy, Hyaline Membrane Disease physiopathology, Infant, Newborn, Lung pathology, Lung Compliance, Papio, Pulmonary Gas Exchange, Bronchopulmonary Dysplasia prevention & control, Hyaline Membrane Disease pathology, Pulmonary Surfactants therapeutic use
- Abstract
To test the effect of exogenous surfactant on the evolution of histopathologic changes of bronchopulmonary dysplasia (BPD), we conducted a study in a premature baboon hyaline membrane disease model. One hundred mg/kg bovine surfactant sonicated in saline or 3 ml/kg saline placebo was instilled via the trachea at about 10 min of age. The clinical status and physiologic changes were monitored for 9 days, and pulmonary histopathology was evaluated after death. Compared to the control, the surfactant-treated animals showed a significant improvement in arterial/alveolar oxygen ratio and pulmonary compliance, facilitating rapid weaning from assisted ventilation. Lung histology revealed that pulmonary parenchyma expanded 70% to 95% without features of early BPD. Dysplastic maturation, air trapping, or cellular atypia was not seen. In contrast, lung histology in the control group revealed alveolar expansion less than or equal to 50%, basal cell hyperplasia in the bronchial and bronchiolar epithelium, dysplastic maturation with cellular atypia, extensive epithelial erosion, and type II cell hyperplasia, all features of early BPD. The results of this study suggest that in the premature baboon model, exogenous surfactant therapy improves pulmonary functional abnormalities and lessens the histologic features of BPD, perhaps because of rapid weaning and reduced barotrauma.
- Published
- 1990
- Full Text
- View/download PDF
45. Private consulting forensic pathology.
- Author
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Shanklin DR
- Subjects
- Adult, Consultants, Female, Homicide, Humans, Male, Middle Aged, United States, Forensic Medicine, Private Practice
- Published
- 1987
46. Editorial: It is time to take a stand.
- Author
-
Shanklin DR
- Subjects
- Physical Examination, Prenatal Care, Prenatal Diagnosis, United States, Abortion, Legal, Gestational Age, Jurisprudence
- Published
- 1975
47. Detection of intrauterine growth retardation.
- Author
-
Shanklin DR
- Subjects
- Female, Humans, Pregnancy, Prenatal Diagnosis, Fetal Growth Retardation diagnosis, Ultrasonics
- Published
- 1982
48. The peripheral hypoechoic rim of the fetal heart.
- Author
-
Brown DL, Cartier MS, Emerson DS, Shanklin DR, Smith WC, and Felker RE
- Subjects
- Diagnosis, Differential, Female, Gestational Age, Heart Septum pathology, Heart Ventricles pathology, Humans, Infant, Newborn, Myocardium pathology, Pregnancy, Fetal Heart pathology, Pericardial Effusion diagnosis, Pericardium pathology, Prenatal Diagnosis, Ultrasonography
- Abstract
The purpose of this study is to determine the origin of the hypoechoic rim around the fetal heart; this rim has been noted previously but there is disagreement as to its origin. Of 314 fetuses scanned, a four-chamber view was obtained in 290; a hypoechoic rim was present in 94% of these. In all cases in which a short-axis view could be obtained, the rim continued circumferentially through the ventricular septum. Because the rim continues through the septum, it cannot be pericardial fluid but is instead part of the myocardium. The presence as well as the origin of this normal hypoechoic rim around the fetal cardiac ventricles should be considered before diagnosing small pericardial effusions.
- Published
- 1989
- Full Text
- View/download PDF
49. Editorial: Better is the end of a thing than the beginning thereof.
- Author
-
Shanklin DR
- Subjects
- Abortion, Legal history, Female, Gynecology history, History, 20th Century, Humans, Nutritional Sciences history, Social Change, United States, Obstetrics history
- Published
- 1975
50. Editorial: Of protein and pregnancy.
- Author
-
Shanklin DR
- Subjects
- Female, Humans, Prenatal Care, Scotland, Dietary Proteins, Pregnancy
- Published
- 1974
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