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Neurology|July 1, 1997
What are the obstacles for an accurate clinical diagnosis of Pick's disease? A clinicopathologic studyI Litvan, Y Agid, N Sastry, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 7, 2006
Parkinson's disease with camptocormiaF Bloch, J L Houeto, S Tezenas du Montcel, 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.Human Molecular Genetics|December 1, 1996
Screening for proteins with polyglutamine expansions in autosomal dominant cerebellar ataxiasG Stevanin, Y Trottier, G Cancel, et al.Nature Genetics|September 1, 1997
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansionG David, N Abbas, G Stevanin, 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.Annals of Neurology|August 26, 1998
The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's DiseaseJ Vaughan, A Durr, J Tassin, et al.American Journal of Human Genetics|February 17, 2001
Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effectsM Periquet, C Lücking, J Vaughan, et al.The Journal of Comparative Neurology|March 10, 2001
Parkin immunoreactivity in the brain of human and non-human primates: an immunohistochemical analysis in normal conditions and in Parkinsonian syndromesM Zarate-Lagunes, W J Gu, V Blanchard, et al.Neurology|April 23, 2003
New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonismN Rawal, M Periquet, E Lohmann, et al.Pageof 56