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Brain : a Journal of Neurology|July 9, 2004
Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR studyL Guerrini, F Lolli, A Ginestroni, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2000
Accuracy of clinical diagnostic criteria for Friedreich's ataxiaA Filla, G De Michele, G Coppola, et al.Bioorganic & Medicinal Chemistry Letters|December 20, 2003
Substituted furo[3,2-b]pyridines: novel bioisosteres of 5-HT 1F receptor agonistsBrian M Mathes, Kevin J Hudziak, John M Schaus, et al.European Journal of Neurology|October 2, 2019
The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian familiesM Lieto, V Riso, D Galatolo, et al.Journal of Medicinal Chemistry|June 27, 2003
Novel potent 5-HT(1F) receptor agonists: structure-activity studies of a series of substituted N-[3-(1-methyl-4-piperidinyl)-1H-pyrrolo[3,2-b]pyridin-5-yl]amidesSandra A Filla, Brian M Mathes, Kirk W Johnson, et al.Neurology|April 26, 2006
Ataxia with oculomotor apraxia type 2: a clinical, pathologic, and genetic studyC Criscuolo, L Chessa, S Di Giandomenico, et al.Journal of Medical Genetics|December 14, 2004
Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's diseaseM Martinez, A Brice, J R Vaughan, et al.American Journal of Human Genetics|June 23, 1998
Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study Group, and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseJ Tassin, A Dürr, T de Broucker, et al.Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|August 7, 2001
The parkin gene and its phenotype. Italian PD Genetics Study Group, French PD Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseV Bonifati, G De Michele, C B Lücking, et al.Neurogenetics|December 6, 2003
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locusM Muglia, C Criscuolo, A Magariello, et al.Pageof 13