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Clinical Ophthalmology (Auckland, N.Z.)|August 12, 2009
Ocular myositis: diagnostic assessment, differential diagnoses, and therapy of a rare muscle disease - five new cases and reviewBenedikt G H SchoserSeminars in Pediatric Neurology|October 10, 2006
Myotonic dystrophies type 1 and 2: a summary on current aspectsUlrike Schara, Benedikt G H SchoserStrabismus|June 9, 2006
Extraocular mitochondrial myopathies and their differential diagnosesBenedikt G H Schoser, Dieter PongratzClinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|January 7, 2004
Motor excitability in myopathyJoachim Liepert, Benedikt G H Schoser, Cornelius WeillerNeurological Research|September 15, 2005
Evoked potentials during active horizontal head rotations in patients with vertigoBenedikt G H Schoser, Juergen Lorenz, Wolfgang H ZangemeisterNeuro Endocrinology Letters|May 2, 2006
Age related profiles of free amino acids in human skeletal muscleHans Joerg Stuerenburg, Birgit Stangneth, Benedikt G H SchoserMuscle & Nerve|January 11, 2007
A large German kindred with cold-aggravated myotonia and a heterozygous A1481D mutation in the SCN4A geneBenedikt G H Schoser, J Michael Schröder, Timo Grimm, et al.Journal of Child Neurology|September 25, 2002
Rippling muscle disease in childhoodUlrike Schara, Matthias Vorgerd, Nikola Popovic, et al.Annals of Neurology|March 24, 2005
Commonality of TRIM32 mutation in causing sarcotubular myopathy and LGMD2HBenedikt G H Schoser, Patrick Frosk, Andrew G Engel, et al.Brain : a Journal of Neurology|July 3, 2004
Homozygosity for CCTG mutation in myotonic dystrophy type 2Benedikt G H Schoser, Wolfram Kress, Maggie C Walter, et al.Pageof 2