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European Journal of Pediatrics|November 9, 2002
Severe Fusobacteria infections (Lemierre syndrome) in two boysLars Klinge, Udo Vester, Jörg Schaper, et al.Chemosphere|December 28, 2010
Effects of bioturbation on the fate of oil in coastal sandy sediments--an in situ experimentKaren Timmermann, Gary T Banta, Lars Klinge, et al.Pediatric Neurology|December 4, 2003
Reversible infantile hypoglycorrhachia: possible transient disturbance in glucose transport?Jörg Klepper, Darryl C De Vivo, David W Webb, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 17, 2007
From T-tubule to sarcolemma: damage-induced dysferlin translocation in early myogenesisLars Klinge, Steve Laval, Sharon Keers, et al.Neuromuscular Disorders : NMD|August 29, 2006
Severe phenotype in infantile facioscapulohumeral muscular dystrophyLars Klinge, Michelle Eagle, Irene D Haggerty, et al.Journal of Neuroscience Research|January 19, 2012
Motor performance of young dystrophic mdx mice treated with long-circulating prednisolone liposomesCharlotte Weller, Jana Zschüntzsch, Gregor Makosch, et al.Neuromuscular Disorders : NMD|November 11, 2008
Sarcoglycanopathies: can muscle immunoanalysis predict the genotype?Lars Klinge, Gabriele Dekomien, Ahmed Aboumousa, et al.Journal of Neurochemistry|August 1, 2015
Treatment with human immunoglobulin G improves the early disease course in a mouse model of Duchenne muscular dystrophyJana Zschüntzsch, Yaxin Zhang, Florian Klinker, et al.Mitochondrion|January 14, 2015
From ventriculomegaly to severe muscular atrophy: expansion of the clinical spectrum related to mutations in AIFM1Matthias Kettwig, Max Schubach, Franz A Zimmermann, et al.American Journal of Medical Genetics. Part A|January 17, 2012
A de novo interstitial deletion of 2p23.3-24.3 in a boy presenting with intellectual disability, overgrowth, dysmorphic features, skeletal myopathy, dilated cardiomyopathyMoneef Shoukier, Julia Schröder, Barbara Zoll, et al.Pageof 2