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V Bonifati

Showing results (61-70 of 78) with videos related to

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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.
Human Genetics|October 5, 2006
The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidenceE K Tan, Y Zhao, L Skipper, et al.
Neurology|February 12, 2004
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson diseaseK Hedrich, A Djarmati, N Schäfer, et al.
Neurology|September 24, 2008
Hyposmia in G2019S LRRK2-related parkinsonism: clinical and pathologic dataL Silveira-Moriyama, L C Guedes, A Kingsbury, 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
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.
Neurology|November 29, 2008
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndromeA Di Fonzo, M C J Dekker, P Montagna, et al.
Pageof 8

Showing results (61-70 of 78) with videos related to

Sort By:
Pageof 8
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.
Human Genetics|October 5, 2006
The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidenceE K Tan, Y Zhao, L Skipper, et al.
Neurology|February 12, 2004
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson diseaseK Hedrich, A Djarmati, N Schäfer, et al.
Neurology|September 24, 2008
Hyposmia in G2019S LRRK2-related parkinsonism: clinical and pathologic dataL Silveira-Moriyama, L C Guedes, A Kingsbury, 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
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.
Neurology|November 29, 2008
FBXO7 mutations cause autosomal recessive, early-onset parkinsonian-pyramidal syndromeA Di Fonzo, M C J Dekker, P Montagna, et al.
Pageof 8