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European Journal of Human Genetics : EJHG|June 15, 2000
Importance of searching for associated mitochondrial DNA alterations in patients with multiple deletionsR Paul, C Desnuelle, J Pouget, et al.Neurology|June 14, 2006
The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type VO Dubourg, H Azzedine, R Ben Yaou, et al.Neurology|May 5, 1998
Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetranceE Plassart-Schiess, A Gervais, B Eymard, et al.Journal of Medical Genetics|March 21, 1998
Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2pO Heinzlef, C Paternotte, F Mahieux, et al.Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders : Official Publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases|June 19, 2004
A longitudinal study of the evolution of cognitive function and affective state in patients with amyotrophic lateral sclerosisM Kilani, J Micallef, C Soubrouillard, et al.Revue Neurologique|May 26, 1999
[Superficial siderosis of the central nervous system]A Durieux, F Flocard, A Ferreira, et al.Multiple Sclerosis (Houndmills, Basingstoke, England)|January 21, 2009
Motor evoked potentials in clinically isolated syndrome suggestive of multiple sclerosisA Rico, B Audoin, J Franques, et al.Revue Neurologique|January 1, 1981
[Neuropathy in angioimmunoblastic lymphadenopathy (author's transl)]P Brunet, J L Binet, H de Saxce, et al.Revue Neurologique|January 1, 1993
[Treatment of immune deficient neuropathies with intravenous polyvalent immunoglobulins. An open study of 16 cases]K Hoang-Xuan, J M Léger, A Ben Younes-Chennoufi, et al.Nephrologie|January 1, 1994
[Crescentic glomerulonephritis and primary Gougerot-Sjögren syndrome]B Dussol, M Tsimaratos, G Bolla, et al.Pageof 36