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Revue Neurologique|April 1, 1975
[Familial case of myotonia with muscular hypertrophy, weakness corrected by effort and atrophy of type II fibers]B Pépin, M Haguenau, J MikolRevue Neurologique|January 1, 1994
[GM2-Gangliosidosis variant B1 disclosed during adolescence by an isolated multi-systemic involvement of the central and peripheral nervous systems]P Le Coz, E Assouline, M T Vanier, et al.Revue Neurologique|December 1, 1976
[Familial form of centronuclear myopathy in the adult]B Pépin, J Mikol, B Goldstein, et al.Revue Neurologique|March 1, 1975
[Glioma of the posterior limbic system revealed by transient global amnesia. Anatomic-clinical observations of 1 case]G Boudin, B Pépin, J Mikol, et al.Journal of the Neurological Sciences|January 1, 1986
Familial juvenile parkinsonism with multiple systems degenerations. A clinicopathological studyJ M Mayer, J Mikol, M Haguenau, et al.Annales De Medecine Interne|January 1, 1996
[Hypothermia and the nervous system. Review of the literature apropos of 4 cases]P Mouton, F Woimant, O Ille, et al.Revue Neurologique|January 1, 1984
[Sex-linked familial form of progressive spinal amyotrophy in adults]A Schanen, J Mikol, C Guiziou, et al.Revue Neurologique|January 1, 1988
[Cerebral ischemic accidents and chronic disseminated intravascular coagulation of cancerous origin]F Woimant, L Moulinier, P Lecoz, et al.Neuropathology and Applied Neurobiology|April 1, 1991
Granulomatous angiitis and cerebral amyloid angiopathy presenting as a mass lesionP Le Coz, J Mikol, J Ferrand, et al.Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|April 30, 1999
Neuropathology of prion diseasesJ MikolPageof 32