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Showing results (111-120 of 117) 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|January 28, 2003
Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7V Bonifati, M C J Dekker, N Vanacore, 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.
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.
Neurology|May 9, 2007
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson diseaseA Di Fonzo, H F Chien, M Socal, et al.
Journal of Medical Genetics|November 8, 2005
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestorS Goldwurm, A Di Fonzo, E J Simons, et al.
Neurology|July 13, 2005
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypesV Bonifati, C F Rohé, G J Breedveld, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 29, 2005
The European Multiple System Atrophy-Study Group (EMSA-SG)F Geser, K Seppi, M Stampfer-Kountchev, et al.
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Showing results (111-120 of 117) with videos related to

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Pageof 12
You have reached the last page of results.This site can display upto 117 results.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|January 28, 2003
Autosomal recessive early onset parkinsonism is linked to three loci: PARK2, PARK6, and PARK7V Bonifati, M C J Dekker, N Vanacore, 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.
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.
Neurology|May 9, 2007
ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson diseaseA Di Fonzo, H F Chien, M Socal, et al.
Journal of Medical Genetics|November 8, 2005
The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestorS Goldwurm, A Di Fonzo, E J Simons, et al.
Neurology|July 13, 2005
Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypesV Bonifati, C F Rohé, G J Breedveld, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 29, 2005
The European Multiple System Atrophy-Study Group (EMSA-SG)F Geser, K Seppi, M Stampfer-Kountchev, et al.
Pageof 12