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Molecular and Cellular Pediatrics|February 3, 2016
Towards understanding microvillus inclusion diseaseGeorg F Vogel, Michael W Hess, Kristian Pfaller, et al.Wiener Klinische Wochenschrift|October 19, 2007
CFTR gene mutations in pancreatitis: Frequency and clinical manifestations in an Austrian patient cohortHeinz Zoller, Margit Egg, Ivo Graziadei, et al.Orphanet Journal of Rare Diseases|September 8, 2019
The cardiovascular phenotype of adult patients with phenylketonuriaAline Azabdaftari, Markus van der Giet, Mirjam Schuchardt, et al.Lipids in Health and Disease|December 14, 2011
Vitamin A metabolism is changed in donors after living-kidney transplantation: an observational studyAndrea Henze, Jens Raila, Caroline Kempf, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 2, 2010
Prematurity, small for gestational age and perinatal parameters in children with congenital, hereditary and acquired chronic kidney diseaseDoris Franke, Sina Völker, Sanny Haase, et al.Pediatric Nephrology (Berlin, Germany)|March 12, 2004
NPHS2 mutation associated with recurrence of proteinuria after transplantationHeiko Billing, Dominik Müller, Rainer Ruf, et al.Pediatric Nephrology (Berlin, Germany)|September 3, 2013
Birth parameters and parental height predict growth outcome in children with chronic kidney diseaseDoris Franke, Hülya Alakan, Leo Pavičić, et al.Journal of Hepatology|August 10, 2010
Ferroportin disease: a systematic meta-analysis of clinical and molecular findingsRoman Mayr, Andreas R Janecke, Melanie Schranz, et al.The Journal of Pediatrics|February 5, 2004
Joubert-like syndrome unlinked to known candidate lociAndreas R Janecke, Thomas Müller, Ingmar Gassner, et al.Journal of Human Genetics|January 30, 2010
Identification of a 4.9-kilo base-pair Alu-mediated founder SDHD deletion in two extended paraganglioma families from AustriaAndreas R Janecke, Joan E Willett-Brozick, Christoph Karas, et al.Pageof 25