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Deutsches Arzteblatt International|September 7, 2016
Organ-Protective Intensive Care in Organ DonorsKlaus Hahnenkamp, Klaus Böhler, Heiner Wolters, et al.Annals of Hepatology|August 6, 2016
Early initiation of MARS® dialysis in Amanita phalloides-induced acute liver injury prevents liver transplantationMike Hendrik Pillukat, Tina Schomacher, Peter Baier, et al.The American Journal of Case Reports|August 25, 2016
Successful Anti-HCV Therapy of a Former Intravenous Drug User with Sofosbuvir and Daclatasvir in a Peritranspant Setting: A Case ReportLeon Louis Seifert, Hauke Heinzow, Iyad Kabar, et al.Deutsche Medizinische Wochenschrift (1946)|March 16, 2018
[Transthyretin Familial Amyloid Polyneuropathy - Disease Profile of a Multisystem Disorder]Christoph Niemietz, Christoph Röcken, Matthias Schilling, et al.Archives of Neurology|February 15, 2002
Reduction of plasma 24S-hydroxycholesterol (cerebrosterol) levels using high-dosage simvastatin in patients with hypercholesterolemia: evidence that simvastatin affects cholesterol metabolism in the human brainSandra Locatelli, Dieter Lütjohann, Hartmut H J Schmidt, et al.Journal of Neurochemistry|April 27, 2011
Neuroinflammatory and behavioural changes in the Atp7B mutant mouse model of Wilson's diseaseDick Terwel, Yi-Na Löschmann, Hartmut H-J Schmidt, et al.Muscle & Nerve|June 9, 2016
Management of asymptomatic gene carriers of transthyretin familial amyloid polyneuropathyHartmut H-J Schmidt, Fabio Barroso, Alejandra González-Duarte, et al.World Journal of Gastroenterology|November 1, 2012
Dietary copper triggers onset of fulminant hepatitis in the Long-Evans cinnamon rat modelRamsi Siaj, Vanessa Sauer, Sandra Stöppeler, et al.Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology|April 8, 2014
Small bowel transplantation complicated by cytomegalovirus tissue invasive disease without viremiaYesim Avsar, Vito R Cicinnati, Iyad Kabar, et al.Annals of Human Genetics|April 5, 2013
Wilson disease mutation pattern with genotype-phenotype correlations from Western India: confirmation of p.C271* as a common Indian mutation and identification of 14 novel mutationsAnnu Aggarwal, Gursimran Chandhok, Theodor Todorov, et al.Pageof 7