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Muscle & Nerve|December 1, 1993
Focal myositis of the temporal muscleM Naumann, K V Toyka, H H Goebel, et al.Acta Neuropathologica|January 1, 1988
Ultrastructural pathology in emetine-induced myopathyL Halbig, L Gutmann, H H Goebel, et al.Archives of Neurology|October 21, 1998
Alcohol-related acute axonal polyneuropathy: a differential diagnosis of Guillain-Barré syndromeJ C Wöhrle, K Spengos, W Steinke, et al.Journal of Neurology|February 1, 1996
Glucocorticoid-sensitive hereditary inclusion body myositisM Naumann, H Reichmann, H H Goebel, et al.Neuropediatrics|September 10, 1999
Autosomal recessive micrencephaly with simplified gyral pattern, abnormal myelination and arthrogryposisL Sztriha, L I Al-Gazali, E Várady, et al.Der Nervenarzt|November 11, 1999
[Indications for simultaneous origin of a German and American family with type II hereditary amyloid neuropathy]S Seddigh, N Dahmen, H H Goebel, et al.Journal of Child Neurology|January 1, 1997
Infantile intranuclear rod myopathyH H Goebel, A Piirsoo, I Warlo, et al.European Journal of Pediatrics|January 1, 1985
A case of lipogranulomatosis Farber: some clinical and ultrastructural aspectsU Burck, H W Moser, H H Goebel, et al.Journal of Neurology, Neurosurgery, and Psychiatry|December 1, 1982
The forearm ischaemic work test--hazardous to McArdle patients?H M Meinck, H H Goebel, K W Rumpf, et al.Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|December 1, 1987
[Leigh's subacute necrotizing encephalomyelopathy due to decreased activity of the pyruvate dehydrogenase complex]H Siemes, H H Goebel, R C Sengers, et al.Pageof 29