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Revue Neurologique|January 1, 1989
[Myasthenia and pregnancy: a clinical and immunologic study of 42 cases (21 neonatal myasthenia cases)]B Eymard, E Morel, O Dulac, et al.
Neurology|March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.
European Journal of Nuclear Medicine|January 1, 1991
A comparative technetium 99m hexamethylpropylene amine oxime SPET study in different types of dementiaM O Habert, U Spampinato, J L Mas, et al.
Annals of Neurology|May 1, 1997
Juvenile-onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA geneR Navon, R Khosravi, J Melki, et al.
Brain : a Journal of Neurology|June 1, 1993
Linkage analysis in British and French families with idiopathic torsion dystoniaT T Warner, N A Fletcher, M B Davis, et al.
Revue Neurologique|January 1, 1993
[Positron-emission tomographic study of the dopaminergic system in a case of secondary unilateral tremor after mesencephalic hematoma]A De Recondo, P Rondot, C Loc'h, et al.
American Journal of Human Genetics|January 1, 1996
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM intervalA Ducros, T Nagy, S Alamowitch, et al.
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