34 results on '"Ehlers-Danlos Syndrome classification"'
Search Results
2. Updates in Clinical and Genetics Aspects of Hypermobile Ehlers Danlos Syndrome.
- Author
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Forghani, Irman
- Subjects
EHLERS-Danlos syndrome ,GENETICS ,MEDICAL personnel ,DISEASE management ,SYMPTOMS ,RESEARCH personnel ,DIAGNOSIS ,THERAPEUTICS - Abstract
Efforts on recognition, diagnosis, and management of the presumed, most common connective tissue disorder hypermobile Ehlers-Danlos syndrome have been an ongoing challenge, even decades after the description of this condition. A recent international consortium proposed a revised Ehlers-Danlos syndrome classification, an update much needed since Villefranche nosology, in 1998. Hypermobile Ehlers-Danlos syndrome is the only subtype in these groups of syndromes with no known genetic cause(s). This effort brought significant attention to this often underappreciated condition. This review provides an update of the clinical and genetic aspects of hypermobile Ehlers-Danlos syndrome for clinicians and researchers. [ABSTRACT FROM AUTHOR]
- Published
- 2019
- Full Text
- View/download PDF
3. Neuro-ophthalmic manifestations of Ehlers--Danlos syndrome.
- Author
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Rachapudi, Sruti S., Laylani, Noor A., Davila-Siliezar, Pamela A., and Lee, Andrew G.
- Published
- 2023
- Full Text
- View/download PDF
4. The Importance of Physical Therapy Intervention in Improving the Quality of Life in a Patient with Ehlers-Danlos Syndrome.
- Author
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Camelia, Şlicaru Adina and Ionela, Cerchez
- Subjects
EHLERS-Danlos syndrome ,PHYSICAL therapy ,QUALITY of life ,RANGE of motion of joints ,WOMEN patients - Abstract
Copyright of Gymnasium: Scientific Journal of Education, Sports & Health is the property of Alma Mater and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2023
- Full Text
- View/download PDF
5. Growing rods for early-onset scoliosis in Ehlers-Danlos disease.
- Author
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Toumia, Mohamed Laroussi, Mohseni, Ahmed Amine, Nessib, Mohamed Nabil, Boussetta, Rim, Yacoub-Youssef, Houda, and Bouchoucha, Sami
- Published
- 2023
- Full Text
- View/download PDF
6. Occupational Therapy Interventions for Clients with Ehlers-Danlos Syndrome (EDS) in the Presence of Postural Orthostatic Tachycardia Syndrome (POTS).
- Author
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Levine, David, Work, Brittany, McDonald, Susan, Harty, Nicole, Mabe, Carolee, Powell, Alison, and Sanford, Graceline
- Subjects
EHLERS-Danlos syndrome ,ONLINE information services ,CINAHL database ,OCCUPATIONAL roles ,MYALGIA ,PATIENT participation ,DIZZINESS ,POSTURAL orthostatic tachycardia syndrome ,EVIDENCE-based medicine ,PATIENT-centered care ,HEALTH status indicators ,SLEEP hygiene ,HABIT ,MENTAL health ,ENERGY conservation ,JOB involvement ,OCCUPATIONAL therapy services ,HEALTH ,QUALITY of life ,ACCIDENTAL falls ,FATIGUE (Physiology) ,MEDLINE ,ORTHOPEDIC apparatus ,EXERCISE therapy - Abstract
Postural orthostatic tachycardia syndrome (POTS) is often seen in clients with Ehlers-Danlos syndrome (EDS), primarily hypermobile EDS. Research has shown clients with EDS and POTS may experience limitations affecting not only their physical function, but also their social, emotional, and mental well-being. Using a client-centered approach, occupational therapy practitioners assess health, well-being, symptomatology (fatigue, muscle pain, dizziness, etc.), participation and engagement in occupation, and provide interventions to improve quality of life. This paper will address occupational therapy interventions to treat common symptomatology for clients with EDS in the presence of POTS, including environmental modifications, use of adaptive equipment and orthoses, exercise and fall prevention, energy conservation and pacing, sleep hygiene, and routine and habit development to promote optimal engagement in meaningful occupations. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
7. Haploinsufficiency of Col5a1 causes intrinsic lung and respiratory changes in a mouse model of classical Ehlers‐Danlos syndrome.
- Author
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Fett, Jordan, Dimori, Milena, Carroll, John L., and Morello, Roy
- Subjects
EHLERS-Danlos syndrome ,LABORATORY mice ,RESPIRATORY mechanics ,ANIMAL disease models ,RESPIRATORY organs - Abstract
The Ehlers‐Danlos syndromes (EDS) are inherited connective tissue diseases with primary manifestations that affect the skin and the musculoskeletal system. However, the effects of EDS on the respiratory system are not well understood and are described in the literature as sporadic case reports. We performed histological, histomorphometric, and the first in‐depth characterization of respiratory system function in a mouse model of classical EDS (cEDS) with haploinsufficiency of type V collagen (Col5a1+/−). In young adult male and female mice, lung histology showed reduced alveolar density, reminiscent of emphysematous‐like changes. Respiratory mechanics showed a consistent increase in respiratory system compliance accompanied by increased lung volumes in Col5a1+/− compared to control mice. Flow–volume curves, generated to mimic human spirometry measurements, demonstrated larger volumes throughout the expiratory limb of the flow volume curves in Col5a1+/− compared to controls. Some parameters showed a sexual dimorphism with significant changes in male but not female mice. Our study identified a clear respiratory phenotype in the Col5a1+/− mouse model of EDS and indicated that intrinsic respiratory and lung changes may exist in cEDS patients. Their potential impact on the respiratory function during lung infections, other respiratory disease processes, or insults may be significant and justify further clinical evaluation. [ABSTRACT FROM AUTHOR]
- Published
- 2022
- Full Text
- View/download PDF
8. Updates in Clinical and Genetics Aspects of Hypermobile Ehlers Danlos Syndrome
- Author
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Irman Forghani
- Subjects
Ehlers-Danlos syndrome ,classification ,joint hypermobility ,hypermobility spectrum disorder ,Medicine - Abstract
Efforts on recognition, diagnosis, and management of the presumed, most common connective tissue disorder hypermobile Ehlers-Danlos syndrome have been an ongoing challenge, even decades after the description of this condition. A recent international consortium proposed a revised Ehlers-Danlos syndrome classification, an update much needed since Villefranche nosology, in 1998. Hypermobile Ehlers-Danlos syndrome is the only subtype in these groups of syndromes with no known genetic cause(s). This effort brought significant attention to this often underappreciated condition. This review provides an update of the clinical and genetic aspects of hypermobile Ehlers-Danlos syndrome for clinicians and researchers.
- Published
- 2019
- Full Text
- View/download PDF
9. Az Ehlers–Danlos-szindrómák korszerű osztályozása és multidiszciplináris tünettana.
- Author
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Ralovich, Fanni Virág, Kiss, Norbert, Horváth, Krisztina, Kárpáti, Sarolta, and Medvecz, Márta
- Abstract
Copyright of Hungarian Medical Journal / Orvosi Hetilap is the property of Akademiai Kiado and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2019
- Full Text
- View/download PDF
10. Diagnosis andmanagement of floppy pouch complex.
- Author
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Khan, Freeha, Hull, Tracy L, and Shen, Bo
- Published
- 2018
- Full Text
- View/download PDF
11. Ehlers-Danlos syndrome: how to diagnose and when to perform genetic tests.
- Author
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Sobey, Glenda
- Subjects
EHLERS-Danlos syndrome ,GENETIC research ,CONNECTIVE tissue diseases in children ,GENETICS ,MEDICAL screening - Abstract
The term Ehlers-Danlos syndrome (EDS) encompasses a group of inherited connective tissue disorders. The manifestations of EDS can be seen in skin, joints, blood vessels and internal organs and vary from mild to severe and life threatening. Each subtype is a separate and different condition. The genetic basis of many subtypes has now been elucidated, confirming heterogeneity. An awareness of the different conditions within this group is the starting point towards accurate diagnosis. Accurate elicitation of history and clinical signs is vital in selecting the correct confirmatory investigation. Skin biopsy with electron microscopy can be helpful in the decision process of whether and when to perform genetic testing. Correct diagnosis within the EDSs allows targeted management, family screening and prenatal diagnosis. [ABSTRACT FROM AUTHOR]
- Published
- 2015
- Full Text
- View/download PDF
12. Aneurysmal Disease.
- Author
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White, Rodney A. and Hollier, Larry H.
- Published
- 2005
- Full Text
- View/download PDF
13. Ehlers-Danlos syndrome: case report and an electron microscopy study.
- Author
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Carlesimo, M., Cortesi, G., Gamba, A., Narcisi, A., Turturro, F., Raffa, S., Torrisi, M., and Camplone, G.
- Subjects
CASE studies ,EHLERS-Danlos syndrome ,ELECTRON microscopy ,OSTEOARTHRITIS ,JOINT hypermobility ,SHOULDER dislocations ,DISEASES in women - Abstract
Ehlers-Danlos syndrome (EDS) type III is a inherited connective tissue disorders characterized by extensibility of the skin, hypermobility of the joints, chronic pain, tissue fragility, easy bruising, and delayed wound healing with result of atrophic scars. The patients report commonly a history of recurrent dislocations of the shoulders and knees after low-impact trauma, chronic joint pain, and early osteoarthritis, which lead to diagnosis. The pathogenesis of this condition is unknown, and the diagnosis is generally made in adult age, based only on clinical criteria. In this report, we describe a case of a 50-year-old woman with a 30-year history of recurrent dislocations and atrophic scars. We performed diagnosis of EDS type III after a complete clinical and instrumental evaluation, comprising of histological and electron microscopic studies, that highlighted collagen abnormalities. [ABSTRACT FROM AUTHOR]
- Published
- 2012
- Full Text
- View/download PDF
14. A CASE WITH BILATERAL SUPPLEMENTAL MAXILLARY LATERAL INCISORS.
- Published
- 2010
15. Genetics of ehlers-danlos syndrome
- Author
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E. I. Auerkari, M. Rosita, and I. R.N. Alima
- Subjects
History ,medicine.medical_specialty ,Ehlers–Danlos syndrome ,business.industry ,medicine ,medicine.disease ,business ,Dermatology ,Computer Science Applications ,Education - Abstract
Ehlers-Danlos Syndrome (EDS) is a genetic condition characterized characterized by join hypermobility, skin hyperextension, and tissue fragility that affects the connective tissue and collagen structures in the human body. The prevalence has been reported as in 1 in 5000 births and affects equally in both sexes. EDS has no racial proportions. There are several types of EDS, that are based on the 2017 International Ehlers-Danlos Syndrome Classification. Thin and fragile mucosa, bleeding tendency, periodontal tissue injuries, and also tongue ghorlin syndrome has been reported as the intraoral manifestations in EDS. Another manifestation is hypermobile temporomandibular joint with high incidence of subluxation and dislocation. The mechanism of Ehlers-Danlos Syndrome is connected to collagen biosyhntesis, originating with nucleus transcription to aggregate collagen heterotrimers into large fibrils. Mutations have been found in collagen-encoding genes for several of these forms, or in genes encoding collagen-modifying enzymes. One of the most common type of EDS is classical EDS which is having type V collagen deficiency. This is caused by mutation in type V collagen-encoding gene, COL5A1 dan COL5A2. Type V collagen is a regulatory collagen fibril that forms the basis of the fibrils in bony, cartilaginous, fibrous, and tubular structures. The majority of mutations have been reported are nonsense mutations; splice site mutations leading to exon skips, missense mutations causing glycine substitutions, and frameshift mutation. As a clinician, the knowledge about the etiology, clinical sign, oral manifestation, and the genetic aspect of this syndrome is crucial for making correct diagnoses and proper treatment planning. In this review, the author will explain further about the genetic aspects of Ehlers-Danlos Syndrome.
- Published
- 2021
- Full Text
- View/download PDF
16. Fetal and Neonatal Physiology E-Book
- Author
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Richard Polin, Steven H. Abman, David H. Rowitch, William Benitz, Richard Polin, Steven H. Abman, David H. Rowitch, and William Benitz
- Subjects
- Fetus--Physiology, Newborn infants--Physiology
- Abstract
Offering the comprehensive, authoritative information needed for effective diagnosis, treatment, and management of sick and premature infants, Fetal and Neonatal Physiology, 6th Edition, is an invaluable resource for board review, clinical rounds, scientific research, and day-to-day practice. This trusted two-volume text synthesizes recent advances in the field into definitive guidance for today's busy practitioner, focusing on the basic science needed for exam preparation and key information required for full-time practice. It stands alone as the most complete text available in this complex and fast-changing field, yet is easy to use for everyday application. - Offers definitive guidance on how to effectively manage the many health problems seen in newborn and premature infants. - Contains new chapters on Pathophysiology of Genetic Neonatal Disease, Genetic Variants and Neonatal Disease, and Developmental Biology of Lung Stem Cells, as well as significantly revised chapters on Cellular Mechanisms of Neonatal Brain Injury, Neuroprotective Therapeutic Hypothermia, Enteric Nervous System Development and Gastrointestinal Motility, and Physiology of Twin-Twin Transfusion. - Features 1,000 full-color diagrams, graphs and anatomic illustrations, 170+ chapters, and more than 350 global contributors. - Includes chapters devoted to clinical correlation that help explain the implications of fetal and neonatal physiology, as well as clinical applications boxes throughout. - Provides summary boxes at the end of each chapter and extensive cross-referencing between chapters for quick reference and review. - Allows you to apply the latest insights on genetic therapy, intrauterine infections, brain protection and neuroimaging, and much more.
- Published
- 2022
17. Syndromes: Rapid Recognition and Perioperative Implications, 2nd Edition
- Author
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Bruno Bissonnette and Bruno Bissonnette
- Abstract
Publisher's Note: Products purchased from Third Party sellers are not guaranteed by the publisher for quality, authenticity, or access to any online entitlements included with the product. The ULTIMATE reference about syndromes to have on hand to facilitate rapid recognition and perioperative implications --- in full color Syndromes: Rapid Recognition and Perioperative Implications, Second Edition, is the ultimate reference for anesthesiologists, surgeons, internists, pediatricians, emergency physicians and nurses caring for patients affected with special operative needs and acute medical care. This updated book provides a complete A-to-Z encyclopedic clinical presentation of more than 2,200 syndromes. Extensive cross-referencing of international synonyms, classifications, and other conditions to be considered in the differential diagnosis further expands coverage to more than 5,000 entries. It is the most comprehensive reference on the subject. Syndromes: Rapid Recognition and Perioperative Implications, Second Edition, is enhanced by 200 high-quality photographs, in addition to tables, classifications and clinical management considerations. The addition of color tabs, a new feature, improve consultation and speed information retrieval. Each syndrome, listed in alphabetical order, is described as follows: •“At a glance” description•Synonyms•Incidence•Genetic Inheritance•Pathophysiology•Diagnosis•Clinical Aspects•Precautions Before Anesthesia•Anesthetic Considerations•Pharmacological Implications•Other conditions to be considered•References Health care providers, fellows and residents in training will find this textbook to be an essential reference to improve patient care in this highly demanding medical and surgical environment.
- Published
- 2019
18. Endovascular Aortic Repair : Current Techniques with Fenestrated, Branched and Parallel Stent-Grafts
- Author
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Gustavo S. Oderich and Gustavo S. Oderich
- Subjects
- Blood-vessels--Endoscopic surgery, Aortic valve--Surgery
- Abstract
This text provides a comprehensive, state-of-the art review of complex endovascular aortic techniques. It will serve as a valuable resource for vascular and cardiovascular surgeons, interventionalists, cardiologists, clinicians, bioengineers and researchers with an interest in complex aortic diseases. The book reviews imaging modalities, diagnostic work up and novel endovascular approaches. Technical aspects are provided by experts in the field, with over 600 illustrations and photographs of key steps for each type of procedure. Results of epidemiologic studies and national databases are summarized, as well as large institutional experiences. An evidence-based approach is used for recommendations regarding best therapies. Other highlights of this unique text include: A new, state-of-the-art review on fenestrated, branched and parallel stent-graft techniques from procedure planning to stent design and implantation. A text dedicated to a topic that has been increasingly recognized by vascular specialists as a priority area in aortic management. An updated overview of current designs and future developments. Special attention to technical details of the procedures with use of illustrations. Technical tips on how to get out of problems during these challenging procedures. Endovascular Aortic Repair: Current Techniques with Fenestrated, Branched and Parallel Stent-Grafts will serve as a very useful resource for physicians and researchers dealing with and interested in complex aortic diseases. It will provide a concise yet comprehensive summary of the current status of the field that will help guide patient management and stimulate investigative efforts. All chapters are written by experts in their fields and include the most up to date scientific and clinical information.
- Published
- 2017
19. Textbook of Pediatric Rheumatology
- Author
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Ross E. Petty, Ronald M. Laxer, Carol B Lindsley, Lucy Wedderburn, Ross E. Petty, Ronald M. Laxer, Carol B Lindsley, and Lucy Wedderburn
- Subjects
- Children, Connective tissues--Diseases, Vasculitis, Arthritis, Pediatric rheumatology, Rheumatism in children, Rheumatism
- Abstract
Matchless in reputation, content, and usefulness, Textbook of Pediatric Rheumatology, 7th Edition, is a must-have for any physician caring for children with rheumatic diseases. It provides an up-to-date, global perspective on every aspect of pediatric rheumatology, reflecting the changes in diagnosis, monitoring, and management that recent advances have made possible – all enhanced by a full-color design that facilitates a thorough understanding of the science that underlies rheumatic disease. Get an authoritative, balanced view of the field with a comprehensive and coherent review of both basic science and clinical practice. Apply the knowledge and experience of a who's who of international experts in the field. Examine the full spectrum of rheumatologic diseases and non-rheumatologic musculoskeletal disorders in children and adolescents, including the presentation, differential diagnosis, course, management, and prognosis of every major condition. Diagnose and treat effectively through exhaustive reviews of the complex symptoms and signs and lab abnormalities that characterize these clinical disorders. Keep current with the latest information on small molecule treatment, biologics, biomarkers, epigenetics, biosimilars, and cell-based therapies. Increase your knowledge with three all-new chapters on laboratory investigations, CNS vasculitis, and other vasculitides. Understand the evolving globalization of pediatric rheumatology, especially as it is reflected in the diagnosis and management of childhood rheumatic diseases in the southern hemisphere. Choose treatment protocols based on the best scientific evidence available today.
- Published
- 2016
20. Fetal and Neonatal Physiology E-Book
- Author
-
Richard Polin, Steven H. Abman, David H. Rowitch, William Benitz, Richard Polin, Steven H. Abman, David H. Rowitch, and William Benitz
- Subjects
- Fetus--Physiology, Newborn infants--Physiology
- Abstract
Fetal & Neonatal Physiology provides neonatologist fellows and physicians with the essential information they need to effectively diagnose, treat, and manage sick and premature infants. Fully comprehensive, this resource continues to serve as an excellent reference tool, focusing on the basic science needed for exam preparation and the key information required for full-time practice. The 5th edition is the most substantially updated and revised edition ever. In the 5 years since the last edition published, there have been thousands of publications on various aspects of development of health and disease; Fetal and Neonatal Physiology synthesizes this knowledge into definitive guidance for today's busy practitioner. Offers definitive guidance on how to effectively manage the many health problems seen in newborn and premature infants. Chapters devoted to clinical correlation help explain the implications of fetal and neonatal physiology. Allows you to apply the latest insights on genetic therapy, intrauterine infections, brain protection and neuroimaging, and much more. Expert Consult eBook version included with purchase. This enhanced eBook experience allows you to search all of the text, figures, images, and references from the book on a variety of devices. Features a fantastic new 4-color design with 1,000 illustrations, 170+ chapters, and over 350 contributors. 16 new chapters cover such hot topics as Epigenetics; Placental Function in Intrauterine Growth Restriction; Regulation of Pulmonary Circulation; The Developing Microbiome of the Fetus and Newborn; Hereditary Contribution to Neonatal Hyperbilirubinemia; Mechanistic Aspects of Phototherapy for Neonatal Hyperbilirubinemia; Cerebellar Development; Pathophysiology of Neonatal Sepsis; Pathophysiology of Persistent Pulmonary Hypertension of the Newborn; Pathophysiology of Meconium Aspiration Syndrome; Pathophysiology of Ventilator Dependent Infants; Pathophysiology of Hypoxic-Ischemic Brain Injury; Pathophysiology of Neonatal White Matter Injury; Pathophysiology of Meningitis; Pathophysiology of Preeclampsia; and Pathophysiology of Chorioamnionitis. New Pathophysiology of Neonatal Diseases section highlights every process associated with a disease or injury, all in one place. In-depth information, combined with end-of-chapter summaries, enables deep or quick use of the text.
- Published
- 2016
21. Basic Ophthalmology
- Author
-
Jogi, Renu and Jogi, Renu
- Subjects
- Ophthalmology
- Abstract
• Extensively revised and updated edition • Written as per syllabi of Indian universities • Presents the basic aspects as well as recent advances in ophthalmology comprehensively • Addition of new clinical photographs, flowcharts, and tables to facilitate quick learning • Covers more than 500 MCQs with answers for easy recall of the subject • Useful for graduate and postgraduate students and teachers as well as practising ophthalmologists.
- Published
- 2016
22. Frontiers in Neurosurgery Volume 3
- Author
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Editors: Simone Peschillo and Editors: Simone Peschillo
- Subjects
- Brain--Congestion, Cerebrovascular disease
- Abstract
Stroke is thought to be the second biggest killer worldwide, and is responsible for over 5 million deaths per year. Several strategies have been developed to enhance treatment of stroke patients. Multimodal neuroimaging allows physicians to diagnose and e
- Published
- 2016
23. Landmark Papers in Rheumatology
- Author
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Richard A. Watts, David G. I. Scott, Richard A. Watts, and David G. I. Scott
- Subjects
- Adolescent rheumatology, Pediatric rheumatology, Rheumatology
- Abstract
Rheumatic disease is a major cause of morbidity and disability in the Western world. There have been major developments in our understanding of the causes of rheumatic disease and in their treatment during the last half-century, and there are relatively few papers which can be regarded as truly'landmark'in their construction and subsequent findings. Part of the Landmark Papers in series, this book provides a detailed review of the seminal papers that have paved the way for breakthroughs in the clinical management of the entire spectrum of rheumatic diseases.
- Published
- 2015
24. A-Z of Neurological Practice : A Guide to Clinical Neurology
- Author
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Andrew J. Larner, Alasdair J Coles, Neil J. Scolding, Roger A Barker, Andrew J. Larner, Alasdair J Coles, Neil J. Scolding, and Roger A Barker
- Subjects
- Neurology, Nervous system--Diseases
- Abstract
The Second Edition of A-Z of Neurological Practice builds on the previous edition with revised and updated information in a high density but easily accessible format to provide a quick and ready reference for busy clinicians of all degrees of experience. Entries for specific neurological conditions are uniformly structured indicating: Pathophysiology; Clinical Features; Investigations and Diagnosis; Differential Diagnosis; Treatment and Prognosis. Key references are cited throughout and all entries are cross referenced. A-Z of Neurological Practice, Second Edition is a practical, authoritative guide that will become an invaluable resource for neurologists in clinical practice, neurology trainees and all those involved with the treatment of neurological disorders.
- Published
- 2011
25. Fetal and Neonatal Physiology
- Author
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Richard A. Polin, William W. Fox, Steven H. Abman, Richard A. Polin, William W. Fox, and Steven H. Abman
- Subjects
- Newborn infants--Physiology, Fetus--Physiology
- Abstract
Fetal and Neonatal Physiology, edited by Drs. Polin, Fox, and Abman, focuses on physiologic developments of the fetus and newborn and their impact on the clinical practice of neonatology. A must for practice, this 4th edition brings you the latest information on genetic therapy, intrauterine infections, brain protection and neuroimaging, and much more. Gain a comprehensive, state-of-the-art understanding of normal and abnormal physiology, and its relationship to disease in the fetus and newborn premature infant, from Dr. Richard Polin and other acknowledged worldwide leaders in the field. Understand the implications of fetal and neonatal physiology through chapters devoted to clinical correlation. Apply the latest insights on genetic therapy, intrauterine infections, brain protection and neuroimaging, and much more. Effectively manage the consequences of intrauterine infections with three new chapters covering intrauterine infection and preterm birth, intrauterine infection and brain injury, and intrauterine infection and chronic lung disease.
- Published
- 2011
26. Orthopaedic Pathology
- Author
-
Peter G. Bullough and Peter G. Bullough
- Subjects
- Musculoskeletal system--Diseases--Atlases
- Abstract
Orthopaedic Pathology, 5th Edition, by Peter G. Bullough, MB, ChB, presents a unique, lavishly illustrated account of the pathology of arthritic disorders, metabolic disturbances, and soft tissue and bone tumors. Nearly 2,000 high-quality pathologic slides, diagnostic images, and gross specimens-side-by-side-depict the appearance of a wide range of conditions and correlate orthopaedic pathology to clinical practice for greater diagnostic accuracy. It's the ideal resource for the orthopaedic surgeon and radiologist as well as the trainee and practicing pathologist. Provides extensive coverage of arthritic disorders, metabolic disturbances, soft tissue tumors, bone tumors, and rare disorders-not just tumors, which most books emphasize-for guidance on the most commonly seen conditions. Uses nearly 2000 high-quality illustrations-including pathology, histology, radiologic imaging, and schematic line diagrams-that present a clear visual correlation between pathology and clinical images to aid in diagnosis. Includes a chapter on imaging techniques, interpretation, and strategies that provides a foundation of knowledge in radiology. Features brief text, including bulleted lists of key points and information, that makes reference quick and learning easy. Offers updated coverage of immunohistochemistry and molecular pathology-along with examples from the latest imaging and pathologic techniques-to help you recognize the presentation of disorders using these approaches. Features discussions of some rare conditions, equipping you to diagnose even the least common orthopaedic disorders.
- Published
- 2010
27. AAOS Comprehensive Orthopaedic Review
- Author
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Jay R. Lieberman, MD and Jay R. Lieberman, MD
- Subjects
- Orthopedic surgery, Musculoskeletal system--Diseases, Orthopedics
- Abstract
'This book is accompanied by a booklet containing hundreds of study questions that have been validated and created for this text and other AAOS publications'--Pref.
- Published
- 2009
28. Principles of Molecular Medicine
- Author
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Marschall S. Runge, Cam Patterson, Marschall S. Runge, and Cam Patterson
- Subjects
- Gene therapy, Medical genetics, Pathology, Molecular, Molecular biology
- Abstract
The concept of molecular medicine dates back to Linus means that there are many new opportunities and challenges Pauling, who in the late 1940s and early 1950s generalized for clinical medicine. One of the effects of the completion of from the ideas that came from the study of the sickle cell the Human Genome Project is the increasing application of hemoglobin molecule. With the first cloning of human genes the fields of molecular biology and genetics to the und- about 1976, molecular genetics took the molecular perspec- standing and management of common diseases. Assimi- tive on disease to the level of DNA. The term molecular tion of the new developments since the first edition has been medicine achieved wide currency in the 1980s with the ably accomplished by Drs. Runge and Patterson with the assignment of this designation to journals, at least one soci- help of their many knowledgeable authors. ety, institutes, and academic divisions of departments of in- As was evident in the firstedition, molecular genetics is ternal medicine. Undoubtedly, molecular medicine has been involved in every specialty of medicine. A recurrent theme abetted by the Human Genome Project, which has aided in that edition, perhaps even more striking in the present one, greatly in the molecular characterization of disease.
- Published
- 2006
29. Vascular Surgery : Basic Science and Clinical Correlations
- Author
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Rodney A. White, MD, Larry H. Hollier, Rodney A. White, MD, and Larry H. Hollier
- Subjects
- Blood-vessels--Surgery, Blood-vessels--Pathophysiology, Blood-vessels--Physiology
- Abstract
This second edition of a very successful vascular surgery text was developed in order to address significant changes that have occurred in contemporary vascular surgery and to highlight new information that has developed regarding vascular imaging, interventional and endovascular procedures. The overall length of the text is slightly shorter than the first edition with relevant core chapters being retained to emphasize the basic science nature of the text, with approximately 60% of the material undergoing major revisions or being new chapters. The significant change from the first text is an emphasis on vascular pathology and physiology that is relevant to current practice including information that is currently included on the vascular board examinations. A new emphasis on endovascular therapies has been added by including five chapters on endovascular techniques and an additional section with six chapters comparing conventional vascular reconstruction to endovascular methods. These new chapters address the most important issue in contemporary vascular surgery, i.e., the role of endovascular methods in treating vascular lesions and the impact that this has on training and credentialing. A unique aspect of this book differentiating it from other texts is a comparison of conventional methods with the endovascular techniques. Overall the text provides a comprehensive perspective of contemporary vascular surgery and future perspectives. The authors are preeminent in the field and are most capable for addressing the assigned topics with the goals being to provide an updated and forward looking text that accommodates the needs of practicing and training vascular surgeons.
- Published
- 2005
30. The Ehlers–Danlos syndromes
- Author
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Malfait, Fransiska, Castori, Marco, Francomano, Clair A., Giunta, Cecilia, Kosho, Tomoki, and Byers, Peter H.
- Published
- 2020
- Full Text
- View/download PDF
31. Small Animal Dermatology Secrets
- Author
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Karen L. Campbell and Karen L. Campbell
- Subjects
- Veterinary dermatology
- Abstract
This full-color dermatology text provides essential, practical information for solving dermatological problems commonly encountered in small animals. Organized by disorder type, the popular question-and-answer format and detailed index make it easy to find vital information. In more than 50 chapters, the expert contributors propose key questions and provide authoritative answers about the diagnosis and treatment of dermatologic conditions relevant to small animal veterinary practice.
- Published
- 2004
32. Gait Retraining in Patients With Joint Hypermobility Syndrome/Hypermobile Ehlers Danlos Syndrome
- Subjects
Physical fitness ,Biofeedback ,Health ,University of South Florida - Abstract
2018 JUL 21 (NewsRx) -- By a News Reporter-Staff News Editor at Obesity, Fitness & Wellness Week -- Staff editors report on the newly launched clinical trial, NCT03575182, which has [...]
- Published
- 2018
33. Principles of Molecular Rheumatology
- Author
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George C. Tsokos and George C. Tsokos
- Subjects
- Arthritis--Molecular aspects, Rheumatism--Molecular aspects, Arthritis--Pathophysiology, Rheumatism--Pathophysiology
- Abstract
George Tsokos and a panel of authoritative clinicians and researchers synthesize the latest findings from across cell and molecular biology with the basic principles of rheumatology to create the first textbook of molecular rheumatology. These established experts describe the biochemical mechanisms by which apoptosis, cell signaling, complement, lipids, and viruses contribute to disease expression, and detail both immune and nonimmune cell function in rheumatic diseases. Their review of the major rheumatic diseases integrates the cellular, biochemical, and molecular biological mechanisms that are important in rheumatic disease pathogenesis. Path-breaking and illuminating, Principles of Molecular Rheumatology expands the envelope of clinical understanding to reveal the biological roots underlying rheumatologic disease, as well as the nature and roles of the powerful new therapeutics now emerging for its optimal treatment.
- Published
- 2000
34. Studies Conducted at University of Miami on Ehlers-Danlos Syndrome Recently Reported (Updates in Clinical and Genetics Aspects of Hypermobile Ehlers Danlos Syndrome)
- Subjects
Ehlers-Danlos syndrome ,Consortia ,Editors ,Health - Abstract
2019 AUG 16 (NewsRx) -- By a News Reporter-Staff News Editor at Health & Medicine Week -- Data detailed on Diseases and Conditions - Ehlers-Danlos Syndrome have been presented. According [...]
- Published
- 2019
Catalog
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