G de Michele - JoVE Visualize

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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.

Neuroscience Letters|August 24, 1999

The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's diseaseB S Harhangi, M J Farrer, S Lincoln, 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.

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.

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.

Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003

PARK6 is a common cause of familial parkinsonismE M Valente, F Brancati, V Caputo, 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.

Annals of Neurology|February 16, 1999

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotesM Cossée, A Dürr, M Schmitt, et al.

Neurology|January 28, 2004

Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosumC Casali, E M Valente, E Bertini, et al.

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Showing results (111-120 of 123) with videos related to

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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.

Neuroscience Letters|August 24, 1999

The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's diseaseB S Harhangi, M J Farrer, S Lincoln, 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.

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.

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.

Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003

PARK6 is a common cause of familial parkinsonismE M Valente, F Brancati, V Caputo, 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.

Annals of Neurology|February 16, 1999

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotesM Cossée, A Dürr, M Schmitt, et al.

Neurology|January 28, 2004

Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosumC Casali, E M Valente, E Bertini, et al.

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