31 results on '"Enrico Valerio"'
Search Results
2. Surgical management of large scalp infantile hemangioma in 30-month-old infant
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Cosimo Bleve, Maria Luisa Conighi, Enrico Valerio, Mario Cutrone, Giuseppe Iannucci, Alessandro Segna, and Salvatore Fabio Chiarenza
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Infantile hemangioma ,surgical management ,magnetic resonance imaging propranolol ,scalp ,Pediatrics ,RJ1-570 ,Surgery ,RD1-811 - Abstract
Infantile Hemangiomas (IH) are the most common benign tumor of infancy, occurring in over 10% of newborns. The head and neck is the most frequently affected area (60%), and the scalp is a typical site for such large lesions. Scalp-IHs are usually focal lesions that can be both disfiguring and may lead to complications such as ulceration and bleeding. We describe a case of a 30-months old female who presented a large scalp-IH at birth that rapidly grew in the first year of life. Topical and systemic treatments (with timolol ointment and oral propranolol, respectively) were not effective in reducing dimensions of the hemangioma. After vascular imaging study, the patient underwent surgical resection of the IH and primary closure with excellent cosmetic outcome. When medical therapy is ineffective or cosmetic and functional integrity is threatened, early surgery allows to completely removing large scalp-IHs, with good cosmetic results.
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- 2022
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3. Urinary metabotypes of newborns with perinatal asphyxia undergoing therapeutic hypothermia.
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Enrico Valerio, Veronica Mardegan, Matteo Stocchero, Maria Elena Cavicchiolo, Paola Pirillo, Gabriele Poloniato, Gianluca D'Onofrio, Luca Bonadies, Giuseppe Giordano, and Eugenio Baraldi
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Medicine ,Science - Abstract
Perinatal asphyxia (PA) still occurs in about three to five per 1,000 deliveries in developed countries; 20% of these infants show hypoxic-ischemic encephalopathy (HIE) on brain magnetic resonance imaging (MRI). The aim of our study was to apply metabolomic analysis to newborns undergoing therapeutic hypothermia (TH) after PA to identify a distinct metabotype associated with the development of HIE on brain MRI. We enrolled 53 infants born at >35 weeks of gestation with PA: 21 of them showed HIE on brain MRI (the "HIE" group), and 32 did not (the "no HIE" group). Urine samples were collected at 24, 48 and 72 hours of TH. Metabolomic data were acquired using high-resolution mass spectrometry and analyzed with univariate and multivariate methods. Considering the first urines collected during TH, untargeted analysis found 111 relevant predictors capable of discriminating between the two groups. Of 35 metabolites showing independent discriminatory power, four have been well characterized: L-alanine, Creatine, L-3-methylhistidine, and L-lysine. The first three relate to cellular energy metabolism; their involvement suggests a multimodal derangement of cellular energy metabolism during PA/HIE. In addition, seven other metabolites with a lower annotation level (proline betaine, L-prolyl-L-phenylalanine, 2-methyl-dodecanedioic acid, S-(2-methylpropionyl)-dihydrolipoamide-E, 2,6 dimethylheptanoyl carnitine, Octanoylglucuronide, 19-hydroxyandrost-4-ene-3,17-dione) showed biological consistency with the clinical picture of PA. Moreover, 4 annotated metabolites (L-lysine, L-3-methylhistidine, 2-methyl-dodecanedioic acid, S-(2-methylpropionyl)-dihydrolipoamide-E) retained a significant difference between the "HIE" and "no HIE" groups during all the TH treatment. Our analysis identified a distinct urinary metabotype associated with pathological findings on MRI, and discovered 2 putative markers (L-lysine, L-3-methylhistidine) which may be useful for identifying neonates at risk of developing HIE after PA.
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- 2022
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4. Exstrophy–Epispadias Complex in a Newborn: Case Report and Review of the Literature
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Enrico Valerio, Valentina Vanzo, Patrizia Zaramella, Sabrina Salvadori, Marco Castagnetti, and Eugenio Baraldi
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exstrophy–epispadias complex ,neonatology ,newborn ,congenital disease ,urology ,Gynecology and obstetrics ,RG1-991 - Abstract
Abstract Aim The aim of this report is to present a brief review of the current literature on the management of EEC. Case Report A term male neonate presented at birth with classic bladder exstrophy, a variant of the exstrophy-epispadias complex (EEC). The defect was covered with sterile silicon gauzes and waterproof dressing; at 72 hours of life, primary closure without osteotomy of bladder, pelvis, and abdominal wall was successfully performed. Discussion EEC incidence is approximately 2.15 per 1,00,000 live births; several urological, musculocutaneous, spinal, orthopedic, gastrointestinal, and gynecological anomalies may be associated to EEC. Initial medical management includes use of occlusive dressings to prevent air contact and dehydration of the open bladder template. Umbilical catheters should not be positioned. Surgical repair stages include initial closure of the bladder and abdominal wall with or without osteotomy, followed by epispadias repair at 6 to 12 months, and bladder neck repair around 5 years of life. Those who fail to attain continence eventually undergo bladder augmentation and placement of a catheterizable conduit. Conclusion Modern-staged repair of EEC guarantees socially acceptable urinary continence in up to 80% of cases; sexual function can be an issue in the long term, but overall quality of life can be good.
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- 2015
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5. Ankyloblepharon Filiforme Adnatum in a Newborn
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Giulia Bordin, Enrico Valerio, and Mario Cutrone
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ankyloblepharon filiforme adnatum ,neonatology ,ophthalmology ,congenital malformations ,Gynecology and obstetrics ,RG1-991 - Abstract
Abstract Ankyloblepharon filiforme adnatum (AFA) is a rare congenital anomaly consisting of a partial or complete fusion of the eyelid margins. It is usually an isolated and benign malformation but its presence should alert the neonatologist because it can be rarely associated to other important multisystemic disorders. We report a case of a newborn presenting with isolated AFA at birth, treated in the first day of life.
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- 2015
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6. Harlequin Color Change: Neonatal Case Series and Brief Literature Review
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Enrico Valerio, Alessia Barlotta, Eleonora Lorenzon, Livio Antonazzo, and Mario Cutrone
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harlequin color change ,preterm ,neonate ,infant ,dermatology ,Gynecology and obstetrics ,RG1-991 - Abstract
Abstract First clinical report of Harlequin color change (HCC) phenomenon came in 1952 from Neligan and Strang. Since then, HCC has been described in a fairly broad number of clinical reports involving neonates, infants, children, and adult patients. We here present a small case series of HCC occurring in neonates, pointing out three of the different possible presentations (hemifacial, patchy scattered across the whole body, and hemiscrotal) of this phenomenon. A brief discussion and literature review encompassing epidemiology, clinical features, physiopathology, associated conditions, and differential diagnoses of HCC is then presented. In most cases, HCC represents a benign, idiopathic, and rapidly autoresolutive phenomenon, with no need for treatment. Some drugs (especially anesthetics and prostaglandin E) are thought to enhance HCC expression through their influence on the capillary tone in the peripheral vascular bed; this effect is anyway promptly reversible with drug withdrawal. Only in rare circumstances, HCC may act as a clue for serious central nervous system disorders (e.g., meningitis; hypothalamic, brain stem, or sympathetic nervous system lesions); anyway, in these rare occurrences HCC always represents an epiphenomenon of the disease, never acting as the sole sign of the underlying disorder.
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- 2015
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7. Infantile Perineal Protrusion in Two Monochorionic Twins
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Paola Cavicchioli, Enrico Valerio, and Mario Cutrone
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infantile perineal protrusion ,monochorionic twins ,congenital disease ,neonatology ,Gynecology and obstetrics ,RG1-991 - Abstract
Abstract Case Report Two female monochorionic-monoamniotic twins showed the same kind of infantile perineal protrusion (IPP) at birth. Lesions in both twins progressively healed until resolution in 6 weeks' time; none of the twins have manifested, till date, alvus disturbances. Discussion and Literature Review A literature review numbers approximately 100 reports of IPP. This condition has been classically classified into three categories: congenital/familiar (i.e., female sex, positive parental history of IPP), acquired (mainly due to constipation), and associated with lichen sclerosus et atrophicus. Conclusions and Final Remarks This case report describes, for the first time, the presence of IPP in monochorionic-monoamniotic twins, supporting the existence of hereditary/genetic factors in the developing of this condition.
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- 2014
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8. The association of biomarkers with pain and function in acute and subacute low back pain: a secondary analysis of an RCT
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Tonelli Enrico, Valerio, Schneider, Michael, Haas, Mitchell, Vo, Nam, Huang, Wan, McFarland, Christine, Weber, Nick, and Sowa, Gwendolyn
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- 2022
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9. Assessing Diet and Musculoskeletal Pain in Adults: Results From a Cross-Sectional Analysis of the National Health and Nutrition Examination Survey (NHANES)
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Tonelli Enrico, Valerio, primary, Hébert, James R., additional, Mugford, Gerald, additional, Gao, Zhiwei, additional, Wang, Peter, additional, Shivappa, Nitin, additional, and Sowa, Gwendolyn, additional
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- 2023
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10. Neurosteroid pathway derangement in asphyctic infants treated with hypothermia: an untargeted metabolomic approach
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Enrico Valerio, Matteo Stocchero, Paola Pirillo, Ignazio D’Errico, Luca Bonadies, Alfonso Galderisi, Giuseppe Giordano, and Eugenio Baraldi
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General Medicine ,General Biochemistry, Genetics and Molecular Biology - Published
- 2023
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11. Influenza-associated hemolytic uremic syndrome: The pathogenic role of the virus
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Luisa Murer, Enrico Valerio, Gianluca D'Onofrio, Giulia Rubin, Enrico Vidal, and Valeria Silecchia
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Hemolytic anemia ,Oseltamivir ,medicine.diagnostic_test ,business.industry ,Stool test ,medicine.medical_treatment ,pathogenesis ,H1N1 ,Acute kidney injury ,Complete blood count ,Case Report ,medicine.disease ,Complement system ,chemistry.chemical_compound ,Upper respiratory tract infection ,chemistry ,Nephrology ,Immunology ,medicine ,hemolytic uremic syndrome ,complement ,Geriatrics and Gerontology ,business ,Dialysis - Abstract
A 3-year-old girl came to our attention for fever and upper respiratory tract infection associated with thrombocytopenia, non-immune hemolytic anemia, and acute kidney injury (AKI). Complete blood count and renal function slowly normalized, with no need for dialysis. She was always normotensive with valid diuresis; her neurological status also rapidly improved. Nasal swab turned out positive for influenza A H1N1; stool test was negative for Shiga toxin-producing Escherichia coli (STEC). The patient was treated with oseltamivir for 5 days with a favorable outcome. Association between hemolytic uremic syndrome (HUS) and H1N1 influenza is poorly reported in literature [1, 2, 3, 4]. The pathogenic role of the virus in causing HUS is still controversial and debated [1, 2, 3, 4]. In our patient, complement activity markers (serum C3 and C5b-9) alteration suggested a transient, virus-mediated complement activation.
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- 2021
12. Review of: 'Transcriptional evaluation of the ductus arteriosus at the single-cell level uncovers a requirement for vimentin for complete closure'
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Enrico Valerio
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medicine.medical_specialty ,medicine.anatomical_structure ,biology ,business.industry ,Internal medicine ,Ductus arteriosus ,medicine ,Cardiology ,biology.protein ,Closure (topology) ,Vimentin ,Cellular level ,business - Published
- 2021
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13. Contact Dermatitis from Jamon Serrano
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Gina Grimalt, Enrico Valerio, Mario Cutrone, and Ramon Grimalt
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medicine.medical_specialty ,business.industry ,Medicine ,business ,medicine.disease ,Contact dermatitis ,Dermatology - Published
- 2021
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14. Unilateral hypertrophy of the inner lip
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Enrico Valerio, Ramon Grimalt, and Mario Cutrone
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Vulva--Malalties ,Genitalia, Female--Surgery ,Aparato genital femenino -- Cirugía ,business.industry ,Unilateral hypertrophy ,Vulva -- Enfermedades ,Medicine ,Anatomy ,Vulva--Diseases ,Aparell genital femení--Cirurgia ,business - Abstract
Variations on normality on the vulvar aspect have generated many difficulties among general pediatricians.The great amount of aesthetical perfection has led to an increasing number of adolescents seeking for vulvar correction. Here we describe a common alteration and provide some clues on the eventual surgical managing of the condition. info:eu-repo/semantics/acceptedVersion
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- 2019
15. Subcutaneous fat necrosis of the newborn
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Francesco Morandi, Enrico Valerio, Mario Cutrone, Giulia Rubin, and Giulia Spagnut
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medicine.medical_specialty ,congenital, hereditary, and neonatal diseases and abnormalities ,Case Report ,Case Reports ,Gastroenterology ,Lethargy ,Polyuria ,Meconium ,newborn ,Internal medicine ,subcutaneous fat necrosis ,medicine ,perinatal asphyxia ,business.industry ,General Medicine ,medicine.disease ,female genital diseases and pregnancy complications ,Hypotonia ,Perinatal asphyxia ,Surgery ,Vomiting ,Hypercalcemia ,Subcutaneous fat necrosis of the newborn ,medicine.symptom ,business ,Polydipsia - Abstract
Key Clinical Message Subcutaneous fat necrosis (SCFN) is a rare fat tissue inflammation of the newborn. Risk factors include cord prolapse, perinatal asphyxia, therapeutic hypothermia, meconium aspiration, and sepsis. When present, hypercalcemia comes with lethargy, hypotonia, irritability, vomiting, polyuria, polydipsia, constipation, and dehydration. Kidney injury must be avoided. SCFN is often completely autoresolutive.
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- 2015
16. Congenital isolated Iso–Kikuchi syndrome in a newborn
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Ilaria Mattei, Enrico Valerio, Francesca Favot, and Mario Cutrone
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Pediatrics ,medicine.medical_specialty ,business.industry ,Iso-Kikuchi syndrome ,Case Reports ,Iso–Kikuchi syndrome ,General Medicine ,medicine.disease ,Onychodysplasia ,dermatology ,Anonychia ,newborn ,Nail disease ,medicine ,Family history ,business ,onychodysplasia - Abstract
Key Clinical Message Classic CO (also called Iso–Kikuchi syndrome) represents a benign, isolated condition associated with normal patient outcome. Nevertheless, clinical follow-up and/or further clinically-based tests are needed to exclude other nail diseases associated with multisystem pathology; complete family history is also important to determine sporadic or hereditary transmission of such condition.
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- 2015
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17. Tissue Doppler Imaging in the evaluation of abdominal aortic pulsatility: a useful tool for the neonatologist
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Alessandra Grison, Massimo Bellettato, Paola Ferrarese, Anna Capretta, Enrico Valerio, and Rosanna Golin
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Aortic arch ,medicine.medical_specialty ,Pulsatile flow ,030204 cardiovascular system & hematology ,Doppler imaging ,Aortic Coarctation ,030218 nuclear medicine & medical imaging ,03 medical and health sciences ,symbols.namesake ,0302 clinical medicine ,Neonatologists ,Internal medicine ,medicine.artery ,Internal Medicine ,medicine ,Humans ,Radiology, Nuclear Medicine and imaging ,Aorta, Abdominal ,business.industry ,Abdominal aorta ,Infant, Newborn ,Ultrasonography, Doppler ,General Medicine ,Blood flow ,Echocardiography ,Parasternal line ,Pulsatile Flow ,Descending aorta ,Intensive Care, Neonatal ,cardiovascular system ,symbols ,Cardiology ,Pictorial Essay ,Radiology ,business ,Doppler effect - Abstract
Sonographic cardiac evaluation of newborns with suspected aortic coarctation (AoC) should tend to demonstrate a good phasic and pulsatile flow and the absence of pressure gradient along a normally conformed aortic arch from the modified left parasternal and suprasternal echocardiographic views; these findings, however, may not necessarily rule out a more distal coarctation in the descending aorta. For this reason, the sonographic exam of newborns with suspected AoC should always include a Doppler evaluation of abdominal aortic blood flow from the subcostal view. Occasionally, however, a clearly pulsatile Doppler flow trace in abdominal aorta may be difficult to obtain due to the bad insonation angle existing between the probe and the vessel. In such suboptimal ultrasonic alignment situation, the use of Tissue Doppler Imaging instead of classic Doppler flow imaging may reveal a preserved aortic pulsatility by sampling the aortic wall motion induced by normal flow. We propose to take advantage of the TDI pattern as a surrogate of a normal pulsatile Doppler flow trace in abdominal aorta when the latter is difficult to obtain due to malalignment with the insonated vessel.La valutazione ecocardiografica del neonato con sospetta coartazione aortica deve poter dimostrare, dalle proiezioni parasternale sinistra alta e soprasternale, un arco aortico normoconformato con traccia Doppler normale (flusso fasico) in assenza di gradiente transistmico; tali rilievi, tuttavia, non escludono la possibilità di una coartazione aortica più distale, sita in aorta discendente toracica. Per tale motivo, la valutazione ecografica neonatale nel sospetto di coartazione aortica deve sempre includere un’analisi Doppler del flusso in aorta discendente, visualizzata tramite approccio sottocostale. Talvolta, tuttavia, l’angolo che si viene a creare tra il fascio ultrasonoro e il vaso a questo livello può risultare subottimale ai fini di un adeguato campionamento Doppler che dimostri la presenza di flusso fasico e privo di run-off diastolico in aorta addominale. In tale situazione di allineamento non ottimale per l’analisi Doppler classica, la metodica TDI (Tissue Doppler Imaging) può rivelare una preservata pulsatilità aortica tramite l’analisi della motilità di parete del vaso indotta dal normale flusso fasico. Tale metodica di valutazione della pulsatilità di parete aortica potrebbe, se validata attraverso studi di numerosità adeguata sul neonato sano, rappresentare un adeguato surrogato di una traccia Doppler normale in aorta addominale nei casi in cui quest’ultima fosse difficoltosa da ottenere a causa di un malallineamento tra il vaso ed il fascio ultrasonoro esplorante.La valutazione ecocardiografica del neonato con sospetta coartazione aortica deve poter dimostrare, dalle proiezioni parasternale sinistra alta e soprasternale, un arco aortico normoconformato con traccia Doppler normale (flusso fasico) in assenza di gradiente transistmico; tali rilievi, tuttavia, non escludono la possibilità di una coartazione aortica più distale, sita in aorta discendente toracica. Per tale motivo, la valutazione ecografica neonatale nel sospetto di coartazione aortica deve sempre includere un’analisi Doppler del flusso in aorta discendente, visualizzata tramite approccio sottocostale. Talvolta, tuttavia, l’angolo che si viene a creare tra il fascio ultrasonoro e il vaso a questo livello può risultare subottimale ai fini di un adeguato campionamento Doppler che dimostri la presenza di flusso fasico e privo di run-off diastolico in aorta addominale. In tale situazione di allineamento non ottimale per l’analisi Doppler classica, la metodica TDI (Tissue Doppler Imaging) può rivelare una preservata pulsatilità aortica tramite l’analisi della motilità di parete del vaso indotta dal normale flusso fasico. Tale metodica di valutazione della pulsatilità di parete aortica potrebbe, se validata attraverso studi di numerosità adeguata sul neonato sano, rappresentare un adeguato surrogato di una traccia Doppler normale in aorta addominale nei casi in cui quest’ultima fosse difficoltosa da ottenere a causa di un malallineamento tra il vaso ed il fascio ultrasonoro esplorante.
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- 2017
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18. Severe asymptomatic maternal antepartum hyponatremia leading to neonatal seizures: prevention is better than cure
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Margherita Fantinato, Irene Giovannini, Lino Chiandetti, Enrico Valerio, and Eugenio Baraldi
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Pediatrics ,medicine.medical_specialty ,Fetus ,Neonatal intensive care unit ,business.industry ,Case Report ,Neonatal seizures ,Hyponatremia ,Intensive care ,Neonatology ,Newborn ,Obstetrics ,medicine.disease ,Asymptomatic ,Bolus (medicine) ,medicine ,Phenobarbital ,medicine.symptom ,business ,medicine.drug - Abstract
Background Pre-delivery maternal electrolyte derangements may reflect themselves in the newborn, since placental homeostasis determines electrolyte equilibrium between mother and fetus. Case presentation A term newborn, transferred to our Neonatal Intensive Care Unit 1 h after birth for an apnoea episode, presented with initially left-sided, and subsequently generalized tonic-clonic seizures due to severe hyponatremia (119 mmol/L). Seizures rapidly ceased after electrolyte correction plus a phenobarbital bolus. Deep hyponatremia was also detected in the mother (123 mmol/L). Conclusions As placental homeostasis determines electrolytes equilibrium between mother and fetus, obstetrics and neonatologists should be aware that any maternal dyselectrolytemia will reflect itself in the newborn; hence, it is fundamental to detect possible maternal electrolyte imbalances before delivery, in order to be prepared to timely correction of electrolyte derangements in the newborn.
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- 2015
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19. Tinea Incognito
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Giulia Paloni, Enrico Valerio, Irene Berti, and Mario Cutrone
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Diagnosis, Differential ,Male ,Tinea ,Pediatrics, Perinatology and Child Health ,Humans ,Infant ,Skin - Published
- 2015
20. Multi-district coronary tree involvement in a 17-year-old girl with Williams-Beuren syndrome
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Enrico Valerio, Tiziana Serena, Biagio Castaldi, Ornella Milanesi, and Elena Reffo
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medicine.medical_specialty ,Williams–Beuren syndrome ,Pediatric cardiology ,Multi-district coronary artery disease ,Myocardial infarction ,Supravalvular aortic stenosis ,Multidisciplinary ,Chest pain ,Cardiac magnetic resonance imaging ,medicine.artery ,Internal medicine ,Ascending aorta ,medicine ,Past medical history ,Ejection fraction ,medicine.diagnostic_test ,Case Study ,business.industry ,medicine.disease ,Stenosis ,Cardiology ,cardiovascular system ,medicine.symptom ,business - Abstract
We describe a case of 17-year-old Chinese girl referred to our Pediatric Cardiology Unit for asthenia, reduced exercise tolerance, and dyspnea. Past medical history was relevant for multiple chest pain episodes in childhood and several syncopal episodes, for which the patient had been never evaluated. Clinical examination, electrocardiogram, and echocardiography were compatible with Williams–Beuren syndrome; such condition was later confirmed by genetic analysis. Cardiac magnetic resonance imaging showed transmural fibrosis of the apex with impaired left ventricular ejection fraction (29 %), severe stenosis of aortic sinotubular junction with left and right coronary ostia involvement; more importantly, the whole coronary artery tree beyond ostia was affected by multiple stenosis and aneurysmatic tracts. Ascending aorta proved hypoplastic, with post-stenotic dilation and multiple aneurysms. At the end of the diagnostic process, surgical risk was considered too high to proceed with the correction. The presented case is of educational value since it provides good iconographical illustration of diffuse, multiple-site coronary artery tree involvement, a rather rare co-morbidity in Williams–Beuren syndrome. Electronic supplementary material The online version of this article (doi:10.1186/s40064-015-1231-0) contains supplementary material, which is available to authorized users.
- Published
- 2015
21. P495Wolff-Parkinson-White: clinical management and follow up of symptomatic and asymptomatic pediatric patients
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Enrico Valerio, Sonia Ferretto, F. Pellizzari, Loira Leoni, and Ornella Milanesi
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Pediatrics ,medicine.medical_specialty ,White (horse) ,business.industry ,Physiology (medical) ,medicine ,medicine.symptom ,Cardiology and Cardiovascular Medicine ,business ,Asymptomatic - Published
- 2017
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22. Two-dimensional, M-mode and Doppler-derived echocardiographic parameters in sedated healthy growing female sheep
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Helen Poser, Gabriele Gerardi, Andrea Semplicini, Enrico Valerio, Nicola Maschietto, Daniele Bernardini, Barbara Contiero, L. Semplicini, G. M. De Benedictis, and Ornella Milanesi
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medicine.medical_specialty ,Cardiovascular investigation ,Time Factors ,Midazolam ,Cardiovascular research ,symbols.namesake ,Animal model ,Reference Values ,Internal medicine ,Medicine ,Animals ,Hypnotics and Sedatives ,Infusions, Intravenous ,Propofol ,Echocardiography, Doppler, Pulsed ,Sheep ,General Veterinary ,business.industry ,Ultrasound ,Heart ,Butorphanol ,Echocardiography ,Reference values ,symbols ,Cardiology ,Animal Science and Zoology ,Female ,business ,Doppler effect - Abstract
Despite the fact that sheep are a widely used animal model in cardiovascular research, reference values for transthoracic echocardiography in normal growing animals are not available. Eight healthy female lambs underwent two-dimensional, M-mode and pulsed wave Doppler echocardiographic examination at 100 days of age and every three months thereafter over a 12-month period. The study was conducted under sedation with midazolam, butorphanol and constant rate infusion of intravenous propofol. Their growth phase was completed at about one year of age. All the echocardiographic parameters considered were significantly correlated with body weight and age class except for the left ventricular systolic and diastolic diameters. Functional indices were not correlated to body weight or age except for the E-point to septal separation distance (EPSS). Doppler-derived parameters were not influenced by independent variables. Transthoracic echocardiography can be considered an applicable method for cardiovascular research using a growing lamb animal model after appropriate adjustments for age and body size.
- Published
- 2013
23. 216-22: Head To Head Comparison Between Transesophageal And Intracardiac Electrophysiologic Study In Pediatric Patients With Supraventricular Tachycardia Or Manifest Accessory Pathway
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Nicola Maschietto, Enrico Valerio, Sonia Ferretto, Marta Rotella, Loira Leoni, Elena Reffo, Alessia Cerutti, Roberta Biffanti, Sabino Iliceto, Biagio Castaldi, and Ornella Milanesi
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medicine.medical_specialty ,Head to head ,business.industry ,Accessory pathway ,medicine.disease ,Intracardiac injection ,Physiology (medical) ,Internal medicine ,Cardiology ,medicine ,Electrophysiologic study ,Supraventricular tachycardia ,Cardiology and Cardiovascular Medicine ,business - Published
- 2016
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24. Ankyloblepharon Filiforme Adnatum in a Newborn
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Giulia Bordin, Enrico Valerio, and Mario Cutrone
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medicine.medical_specialty ,Pediatrics ,business.industry ,Day of life ,Obstetrics and Gynecology ,Congenital malformations ,Ankyloblepharon filiforme adnatum ,lcsh:Gynecology and obstetrics ,neonatology ,Article ,ophthalmology ,medicine.anatomical_structure ,Pediatrics, Perinatology and Child Health ,parasitic diseases ,medicine ,Neonatology ,Eyelid ,business ,lcsh:RG1-991 ,congenital malformations ,ankyloblepharon filiforme adnatum - Abstract
Ankyloblepharon filiforme adnatum (AFA) is a rare congenital anomaly consisting of a partial or complete fusion of the eyelid margins. It is usually an isolated and benign malformation but its presence should alert the neonatologist because it can be rarely associated to other important multisystemic disorders. We report a case of a newborn presenting with isolated AFA at birth, treated in the first day of life.
- Published
- 2014
25. Ages and metallicities of Globular Clusters in M33
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Enrico Valerio Held, Alberto Moretti, and Alessia Moretti
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Physics ,Space and Planetary Science ,Globular cluster ,Local Group ,Astronomy and Astrophysics ,Astrophysics - Published
- 2006
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26. Commissione per la gestione dei database e della riduzione dati: Rapporto finale
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GARILLI, BIANCA MARIA ROSA, FONTANA, Adriano, GIALLONGO, Emanuele, Longo, Giuseppe, HELD, Enrico Valerio, NONINO, Mario, Pasian Fabio, and RADOVICH, MARIO
- Published
- 2003
27. Stellar populations in the Phoenix dwarf galaxy
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Enrico Valerio Held, Saviane, I., and Momany, Y.
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Astrophysics (astro-ph) ,FOS: Physical sciences ,Astrophysics - Abstract
We have obtained deep BVI CCD photometry of Phoenix, a galaxy considered a transition case between dwarf spheroidal and dwarf irregular galaxies. A comparison of our data with the RGBs of Galactic globular clusters gives a mean metal abundance [Fe/H] = -1.81+/-0.10 dex. The presence of an intrinsic color dispersion in the upper red RGB suggests an abundance range of about 0.5 dex, although a range in age may also affect the RGB width. For the first time, a HB has been revealed at V~23.8. The HB is predominantly red yet moderately extended to the blue, which indicates the presence of a significant population with age comparable to that of old halo GGCs. This HB morphology in a metal-poor system indicates a mild "second parameter" effect. From the mean level of the HB we derived a true distance modulus 23.21+/-0.08, in good agreement with the distance modulus 23.04+/-0.07 estimated from the cutoff of the RGB at I~23.1. We find a radial gradient in the HB morphology, and our CMDs show a small number of stars above the RGB tip, that most likely are AGB stars of an intermediate age population. Their number indicates that the fraction of intermediate age population in Phoenix is approximately 30-40%. A young stellar population is definitely present in Phoenix, consistent with a star formation episode started at least 0.6 Gyr ago, up to 1x10^{8} yr ago. Both young stars and AGB stars are centrally concentrated, which indicates that recent star formation preferentially occurred in the inner galaxy regions. In many respects, Phoenix appears not dissimilar from dwarf spheroidal galaxies in the Local Group., 14 pages, 13 figures, accepted for publication in Astronomy and Astrophysics (main journal)
- Published
- 1999
28. Evolution of black-hole intermediate-mass X-ray binaries
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Enrico Valerio Held, Luigi Bedin, Marco Gullieuszik, and Yazan Al Momany
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Physics ,Angular momentum ,Astrophysics::High Energy Astrophysical Phenomena ,Astronomy ,Rotational transition ,Astronomy and Astrophysics ,Azimuthal quantum number ,Black hole ,General Relativity and Quantum Cosmology ,Rotating black hole ,Space and Planetary Science ,Total angular momentum quantum number ,Angular momentum coupling ,Astrophysics::Earth and Planetary Astrophysics ,Circumbinary planet - Abstract
We propose a plausible mechanism for orbital angular momentum loss in black-hole intermediate-mass X-ray binaries, assuming that a small fraction of the transferred mass form a circumbinary disc. The disc can effectively drain orbital angular momentum from the binary, leading to the formation of compact black-hole low-mass X-ray binaries. This scenario also suggests the possible existence of luminous, persistent black hole low-mass X-ray binaries.
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- 2006
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29. P7.05 AORTIC STENT IMPLANTATION IN THE ISTHMIC REGION IN AN ANIMAL MODEL
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Daniele Bernardini, L. Semplicini, Ornella Milanesi, Helen Poser, Nicola Maschietto, Giulio Ceolotto, T. Pilla, G. M. De Benedictis, Andrea Semplicini, Gabriele Gerardi, S. Basso, Enrico Valerio, Federica Stella, Ilaria Iacopetti, and L. Aresu
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medicine.medical_specialty ,Animal model ,RC581-951 ,business.industry ,RC666-701 ,medicine ,Specialties of internal medicine ,Diseases of the circulatory (Cardiovascular) system ,General Medicine ,business ,Aortic stent ,Surgery - Published
- 2010
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30. Young Galactic globular clusters II. The case of Palomar 12
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Rosenberg, A., Saviane, I., Piotto, G., and Enrico Valerio Held
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Astrophysics (astro-ph) ,FOS: Physical sciences ,Astrophysics - Abstract
We present broadband V,I CCD photometry for ca. 1700 stars towards the Galactic globular cluster Palomar 12, covering a field of 10.7' x 10.7'. From these data, a color-magnitude diagram from the red giant branch tip to ca. 2 mag below the cluster's turn-off is obtained. From a comparison with the color magnitude diagrams of 47 Tuc and M5, and using different theoretical models, we confirm that Pal 12 is younger, finding an age 68% +/- 10% that of both template clusters. Revised structural parameters are also obtained: r(c) = 37.8 +/- 0.6 and c = 1.08 +/- 0.02., 10 pages, 7 figures, to be published in Astronomy & Astrophysics, vol. 339
31. Metallicities and alpha-to-iron ratios in globular clusters stars in a homogeneous scale - Search for multiple populations
- Author
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Dias, B., Saviane, I., Barbuy, B., Enrico Valerio Held, Da Costa, G., Ortolani, S., ITA, AUS, BRA, and CHL
- Abstract
We are carrying out a survey of 51 poorly studied globular clusters, by means of spectroscopy of ̃20 red giants per cluster. Optical spectra (4600-5800 Å) were obtained with the FORS2@VLT/ESO, at a resolution Delta lambda ̃ 2.5 Å. We are using ETOILE code to derive [Fe/H], T_eff, log g for each star, by finding the best fitting spectrum among a grid of ̃ 2000 stars of the ELODIE library. These parameters represent the initial guess for HALO, which finds [Mg/Fe] values by comparing the observed spectrum to a grid of 4000 synthetic spectra. The main contributions of this work are: to provide a homogeneous scale of [Fe/H], [Mg/Fe], and radial velocities for the 51 clusters -- in particular for the 29 distant and/or highly reddened ones -- to provide a catalogue of confirmed member stars for each cluster, as well as to find interesting cases for follow-up with high resolution (like M 22, and NGC 5824, for which we found a spread in [Fe/H]).
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