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European Neurology|January 1, 1984
Centronuclear myopathy with special consideration of the adult formH H Goebel, H M Meinck, M Reinecke, et al.European Journal of Pediatrics|November 1, 1979
Clinical, morphological, and biochemical investigations on a patient with an unusual form of neuronal ceroid-lipofuscinosisK Becker, H H Goebel, L Svennerholm, et al.Dementia and Geriatric Cognitive Disorders|February 20, 1998
Reduced intraneuronal lipofuscin content in dementia with Lewy bodies compared with Alzheimer's disease and controlsL M Drach, J Bohl, S Wach, et al.American Journal of Medical Genetics|June 5, 1995
Pigment variant of neuronal ceroid-lipofuscinosisH H Goebel, F Gullotta, T Bajanowski, et al.Neuromuscular Disorders : NMD|May 1, 1997
Congenital myopathy with excess of thin myofilamentsH H Goebel, J R Anderson, C Hübner, et al.Muscle & Nerve|December 1, 1993
Focal myositis of the temporal muscleM Naumann, K V Toyka, H H Goebel, et al.Journal of Neuroscience Research|August 24, 2000
Long-term culture and characterization of human neurofibroma-derived Schwann cellsT Rosenbaum, C Rosenbaum, U Winner, et al.Rofo : Fortschritte Auf Dem Gebiete Der Rontgenstrahlen Und Der Nuklearmedizin|June 1, 1989
[Space-occupying lesions in the pineal region--MRT using Gd-DTPA]T Kahn, G Fürst, N Roosen, 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.Pageof 33