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Journal of Hepatology|August 31, 2010
Hepatic but not brain iron is rapidly chelated by deferasirox in aceruloplasminemia due to a novel gene mutationArmin Finkenstedt, Elisabeth Wolf, Elmar Höfner, et al.Plos One|November 16, 2016
Reduced Microvascular Density in Omental Biopsies of Children with Chronic Kidney DiseaseDorothea Burkhardt, Maria Bartosova, Betti Schaefer, et al.Human Mutation|September 8, 2016
Chondroitin Sulfate N-acetylgalactosaminyltransferase-1 (CSGalNAcT-1) Deficiency Results in a Mild Skeletal Dysplasia and Joint LaxityJulia Vodopiutz, Shuji Mizumoto, Ekkehart Lausch, et al.American Journal of Medical Genetics. Part A|September 17, 2015
The phenotype of the musculocontractural type of Ehlers-Danlos syndrome due to CHST14 mutationsAndreas R Janecke, Ben Li, Manfred Boehm, et al.Journal of Neurology|September 6, 2011
SNP array-based whole genome homozygosity mapping as the first step to a molecular diagnosis in patients with Charcot-Marie-Tooth diseaseCarina Fischer, Slave Trajanoski, Lea Papić, et al.Scientific Reports|February 25, 2016
Quantitative Histomorphometry of the Healthy PeritoneumBetti Schaefer, Maria Bartosova, Stephan Macher-Goeppinger, et al.BMJ Open|October 13, 2018
Initial treatment of steroid-sensitive idiopathic nephrotic syndrome in children with mycophenolate mofetil versus prednisone: protocol for a randomised, controlled, multicentre trial (INTENT study)Rasmus Ehren, Marcus R Benz, Jorg Doetsch, et al.The Journal of Pediatrics|August 10, 2010
A hospital-based intermittent nocturnal hemodialysis program for children and adolescentsAnne Hoppe, Christina von Puttkamer, Ursula Linke, et al.JCI Insight|July 21, 2017
Disrupted apical exocytosis of cargo vesicles causes enteropathy in FHL5 patients with Munc18-2 mutationsGeorg F Vogel, Jorik M van Rijn, Iris M Krainer, et al.Journal of Hepatology|January 28, 2003
The canine copper toxicosis gene MURR1 does not cause non-Wilsonian hepatic copper toxicosisThomas Müller, Bart van de Sluis, Alexandra Zhernakova, et al.Pageof 25