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Revue Neurologique|April 3, 2001
[Familial orthochromatic leukodystrophy: clinicopathological study of two cases]F Chrétien, J Servan, D Elghozi, et al.
Journal of Clinical Pharmacy and Therapeutics|October 1, 1996
Determination of clozapine in serum by radioreceptor assay versus high-performance liquid chromatography: possible detection of hydroxy-metabolitesP Odou, B Frimat, B Fontaine, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|March 11, 1998
Identification of a Val 145 Ile substitution in the human myelin oligodendrocyte glycoprotein: lack of association with multiple sclerosis. The Réseau de Recherche Clinique INSERM sur la Susceptibilité Génétique à la Sclérose en PlaquesD Rodriguez, B Della Gaspera, B Zalc, et al.
Journal of Neurology|October 20, 1999
Novel mutations in the muscle chloride channel CLCN1 gene causing myotonia congenita in Spanish familiesC de Diego, J Gámez, E Plassart-Schiess, 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.
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.
Neuroscience|April 2, 2008
Decreased expression of the mitochondrial matrix proteases Lon and ClpP in cells from a patient with hereditary spastic paraplegia (SPG13)J Hansen, T J Corydon, J Palmfeldt, et al.
Archives of Neurology|April 30, 1998
Systemic autoimmune features and multiple sclerosis: a 5-year follow-up studyA Tourbah, A Clapin, O Gout, et al.
Neuroscience Letters|February 12, 2000
No evidence for long CAG/CTG repeats in families with spastic paraplegia linked to chromosome 2p21-24C Zander, Q P Yuan, K Lindblad, et al.
Annales De Cardiologie Et D'Angeiologie|November 11, 1998
[Acute post-traumatic aortic insufficiency: transesophageal echocardiography in the diagnosis and therapy of the lesions]P Brandstätt, R Carlioz, B Fontaine, et al.
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