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Y. Agid

Showing results (471-480 of 483) with videos related to

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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.
Human Molecular Genetics|May 1, 1997
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 familiesG Cancel, A Dürr, O Didierjean, et al.
Human Molecular Genetics|March 11, 1999
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseN Abbas, C B Lücking, S Ricard, et al.
Human Molecular Genetics|July 1, 1996
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrantR Sherrington, S Froelich, S Sorbi, et al.
American Journal of Human Genetics|February 1, 1997
Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sexH Bickeböller, D Campion, A Brice, et al.
Human Molecular Genetics|July 1, 1996
Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeatS Igarashi, Y Takiyama, G Cancel, et al.
Pageof 49

Showing results (471-480 of 483) with videos related to

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Pageof 49
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.
Human Molecular Genetics|May 1, 1997
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 familiesG Cancel, A Dürr, O Didierjean, et al.
Human Molecular Genetics|March 11, 1999
A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseN Abbas, C B Lücking, S Ricard, et al.
Human Molecular Genetics|July 1, 1996
Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrantR Sherrington, S Froelich, S Sorbi, et al.
American Journal of Human Genetics|February 1, 1997
Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sexH Bickeböller, D Campion, A Brice, et al.
Human Molecular Genetics|July 1, 1996
Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJD1) is affected by the genotype of the normal chromosome: implications for the molecular mechanisms of the instability of the CAG repeatS Igarashi, Y Takiyama, G Cancel, et al.
Pageof 49