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Revue Neurologique|October 1, 1977
[Eaton-Lambert myasthenic syndrome: clinical, electrophysiologic, histological and ultrastructural study]P Castaigne, P Rondot, M Fardeau, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Clinical assessment of olfactory dysfunction in Parkinson's diseaseC Potagas, G Dellatolas, M Ziegler, et al.
Revue Neurologique|January 1, 1989
[X-ray computed tomography of lumbosacral roots and primary hypertrophic neuritis (Dejerine-Sottas disease)]J L Mas, D Buthiau, C Fallet-Bianco, et al.
Journal of Neuro-Oncology|October 1, 1991
Intravascular lymphomatosis (neoplastic angioendotheliosis) of the central nervous system: case report and literature reviewD Smadja, J L Mas, C Fallet-Bianco, et al.
Revue Neurologique|March 1, 1997
[Juvenile GM2 gangliosidosis with progressive spinal muscular atrophy onset]P Rondot, R Navon, B Eymard, et al.
Annales De Genetique|January 1, 1986
Rearrangement of chromosome 21 in Alzheimer's diseaseJ M Delabar, Y Lamour, A Gegonne, et al.
Annales De Biologie Clinique|February 27, 2003
[Apolipoprotein E and bleomycin hydrolase. Polymorphisms: association with neurodegenerative diseases]V Nivet-Antoine, M-P Coulhon, C Le Denmat, et al.
Annals of Human Genetics|March 14, 2001
Four novel mutations in the tyrosine hydroxylase gene in patients with infantile parkinsonismR J Swaans, P Rondot, W O Renier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 1, 1991
(99mTc)-HM-PAO SPECT and cognitive impairment in Parkinson's disease: a comparison with dementia of the Alzheimer typeU Spampinato, M O Habert, J L Mas, et al.
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