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European Journal of Pediatrics|September 1, 1986
Hearing loss in facioscapulohumeral dystrophyT Voit, A Lamprecht, H G Lenard, et al.Pediatric Research|January 1, 1989
B1 variant of GM2 gangliosidosis in a 12-year-old patientH H Goebel, G Stolte, B Kustermann-Kuhn, et al.Research in Experimental Medicine. Zeitschrift Fur Die Gesamte Experimentelle Medizin Einschliesslich Experimenteller Chirurgie|December 15, 1977
Muscle capillary basement membrane thickness in lipoatrophic diabetesF D Goebel, H Dörfler, H H Goebel, et al.Journal of Neurology|January 1, 1981
Tumor-like amyloid formation (amyloidoma) in the brainF W Spaar, H H Goebel, E Volles, et al.Annals of Neurology|May 1, 1985
Hereditary motor sensory neuropathy type II with neurofilament accumulation: new finding or new disorder?P Vogel, M Gabriel, H H Goebel, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|January 1, 1988
Electrophysiological findings of neuronal ceroid lipofuscinosis in heterozygotesI Gottlob, K P Leipert, A Kohlschütter, et al.Revue Neurologique|January 1, 1991
Spheroid-cytoplasmic complexes in a congenital myopathyL Halbig, H H Goebel, H C Hopf, et al.Neuromuscular Disorders : NMD|March 1, 1996
A mild adult myopathic variant of type IV glycogenosisA Bornemann, R Besser, Y S Shin, et al.Muscle & Nerve|April 1, 1997
Familial mixed congenital myopathy with rigid spine phenotypeH Reichmann, H H Goebel, C Schneider, et al.Journal of the Neurological Sciences|July 1, 1982
Congenital muscular dystrophy (CMD) - a collagen formative disease?A Fidzianska, H H Goebel, H G Lenard, et al.Pageof 29