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Cardiology in the Young|June 7, 2014
Scimitar syndrome in a case with VACTERL associationChristian J Fritz, Heiko M Reutter, Ulrike Herberg
Orphanet Journal of Rare Diseases|April 10, 2021
Currarino syndrome: a comprehensive genetic review of a rare congenital disorderGabriel C Dworschak, Heiko M Reutter, Michael Ludwig
Genes|September 28, 2021
The Role of De Novo Variants in Formation of Human Anorectal MalformationsGabriel C Dworschak, Iris A L M van Rooij, Heiko M Reutter
Scientific Reports|July 18, 2018
Circulating microRNAs are associated with Pulmonary Hypertension and Development of Chronic Lung Disease in Congenital Diaphragmatic HerniaMarisol Herrera-Rivero, Rong Zhang, Stefanie Heilmann-Heimbach, et al.
Journal of the American Society of Nephrology : JASN|April 5, 2014
Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tractStefan Kohl, Daw-Yang Hwang, Gabriel C Dworschak, et al.
Kidney International|January 17, 2014
Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tractDaw-Yang Hwang, Gabriel C Dworschak, Stefan Kohl, et al.
Cells|January 22, 2024
PKD1L1 Is Involved in Congenital ChylothoraxJonathan B Whitchurch, Sophia Schneider, Alina C Hilger, et al.
Frontiers in Pediatrics|June 9, 2020
Treatment Strategies and Outcome of the Exstrophy-Epispadias Complex in Germany: Data From the German CURE-NetAnne-Karoline Ebert, Nadine Zwink, Heiko M Reutter, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 25, 2016
Targeted sequencing of 96 renal developmental microRNAs in 1213 individuals from 980 families with congenital anomalies of the kidney and urinary tractStefan Kohl, Jing Chen, Asaf Vivante, et al.
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