El objetivo del estudio fue describir el comportamiento de los casos de colestasis del lactante atendidos en el Servicio de Hepatología del. El diagnóstico de sospecha se establece con la cifra baja de alfaantitripsina en sangre (menor de mg/dl); Confirmación mediante. Transcript of COLESTASIS NEONATAL. COLESTASIS NEONATAL Lactante de 7 meses, AF: hermana hipotiroidea y celíaca. Madre con CIA.
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Implications for neonatal screening. Gastroenterology, 80eh. Continuing navigation will be considered as acceptance of this use. Pediatr Clin North Am, 43pp.
Si continua navegando, consideramos que acepta su uso. Gastroenterol Clin North Am, 28pp. Sem Liver Dis, 20pp.
Continuing navigation will be considered as acceptance of this use. Diagnostic approach to the child with hepatobiliary disease. The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years.
Hospital Universitario 12 de Octubre. Gastrointestinal complication and gene therapy. An Esp Pediatr, 28pp. We present the case of an infant with cystic fibrosis whose primary clinical manifestation was cholestasis and liver failure at the age of 6 weeks. Are you a health professional able to prescribe or dispense drugs? You can change the settings or obtain more information by clicking here. SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact.
Niemann-Pick disease in neonatal cholestasis at a North American center. Recommendations for management of liver and biliary tract disease in Cystic Fibrosis. This item has received. A retrospective and descriptive study was conducted.
Genetics defects in hepatocanalicular transport. Liver disease in infancy: Neonatal cholestasis and liver failure as a clinical manifestation of cystic fibrosis.
COLESTASIS NEONATAL by Mariana dos Santos on Prezi
Gut, 32pp. The Spanish Association of Pediatrics has as one of its main objectives the dissemination of rigorous and updated scientific information on the different areas of pediatrics. Neonatal cholestasis as the presenting feature in cystic fibrosis.
Gastrointest End, 45pp. Previous article Next article. J Med Genet, 12pp. A review on statistical grounds. J Pediatr Gastroenterol Nutr, 28pp. Sem Liver Dis, 18pp. Ursodeoxycholic acid improves cholestasis in infants with cystic fibrosis. Alpha-feto-protein during development and in disease. The incidence of anemia, hypoproteinemia, and edema in infants as presenting symptoms of Cystic Fibrosis: We present the case of an infant with cystic fibrosis whose primary clinical manifestation was cholestasis and liver failure at the age of 6 weeks.
The magazine, referring to the Spanish-speaking pediatric, indexed in major international databases: SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field. Am Pharmacother, 31pp.
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Causes and consequences of impaired bile formation. Pediatr Clin North Am, 35pp. Subscribe to our Newsletter.