Showing results (301-310 of 330) with videos related to
Sort By:
Pageof 33
Acta Neuropathologica|June 1, 1997
Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patientA Larnaout, S Belal, M Zouari, et al.Strabismus|September 13, 2008
Eye movement involvement in Parry-Romberg Syndrome: a clinicopathologic case reportA A Zubcov-Iwantscheff, F Thomke, H H Goebel, et al.Journal of Neurosurgery|August 10, 2000
Multiple intracranial juvenile xanthogranulomas. Case reportJ Boström, G Janssen, M Messing-Jünger, et al.Neuromuscular Disorders : NMD|January 5, 2000
Immunosuppressive treatment of rippling muscles in patients with myasthenia gravisW Müller-Felber, C F Ansevin, K Ricker, et al.Neurology|February 1, 1995
The syndrome of autosomal recessive pontocerebellar hypoplasia, microcephaly, and extrapyramidal dyskinesia (pontocerebellar hypoplasia type 2): compiled data from 10 pedigreesP G Barth, G Blennow, H G Lenard, et al.Klinische Padiatrie|July 1, 1991
[Treatment of non-testicular germ cell tumors in children and adolescents with BEP and VIP: initial results of the MAKEI 89 therapy study]U Göbel, M Bamberg, J Engert, et al.Muscle & Nerve|September 1, 1997
Spheroid body myopathy revisitedH H Goebel, A N D'Agostino, J Wilson, et al.Klinische Padiatrie|July 1, 1993
[Improved prognosis of intracranial germ cell tumors by intensified therapy: results of the MAKEI 89 therapy protocol]U Göbel, M Bamberg, G Calaminus, et al.Neurology|January 5, 2002
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutationM Vorgerd, K Ricker, F Ziemssen, et al.Annals of the New York Academy of Sciences|March 27, 1995
X-linked dilated cardiomyopathy. Novel mutation of the dystrophin geneW M Franz, M Cremer, R Herrmann, et al.Pageof 33