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P Rizzu

Showing results (21-30 of 31) with videos related to

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Journal of Neurology|August 11, 2014
Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohortP E Cohn-Hokke, T H Wong, P Rizzu, et al.
Neurology|March 2, 2011
Sporadic COL4A1 mutations with extensive prenatal porencephaly resembling hydranencephalyM E C Meuwissen, L S de Vries, H A Verbeek, et al.
Neuroscience Letters|October 26, 1999
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian casesV Bonifati, M Joosse, D J Nicholl, et al.
Genomics|September 16, 1999
Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21S Froelich, H Houlden, P Rizzu, et al.
Neurology|August 16, 2008
Distinct genetic forms of frontotemporal dementiaH Seelaar, W Kamphorst, S M Rosso, 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.
BMC Medical Genetics|July 20, 2015
Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcomeW Kelmemi, M E Teeuw, Z Bochdanovits, et al.
Neuroscience Letters|March 17, 1999
Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutationsH Houlden, P Rizzu, M Stevens, et al.
Human Molecular Genetics|July 20, 2010
Loss of the Parkinson's disease-linked gene DJ-1 perturbs mitochondrial dynamicsI Irrcher, H Aleyasin, E L Seifert, et al.
Nature|June 26, 1998
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17M Hutton, C L Lendon, P Rizzu, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Journal of Neurology|August 11, 2014
Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohortP E Cohn-Hokke, T H Wong, P Rizzu, et al.
Neurology|March 2, 2011
Sporadic COL4A1 mutations with extensive prenatal porencephaly resembling hydranencephalyM E C Meuwissen, L S de Vries, H A Verbeek, et al.
Neuroscience Letters|October 26, 1999
The tau gene in progressive supranuclear palsy: exclusion of mutations in coding exons and exon 10 splice sites, and identification of a new intronic variant of the disease-associated H1 haplotype in Italian casesV Bonifati, M Joosse, D J Nicholl, et al.
Genomics|September 16, 1999
Construction of a detailed physical and transcript map of the FTDP-17 candidate region on chromosome 17q21S Froelich, H Houlden, P Rizzu, et al.
Neurology|August 16, 2008
Distinct genetic forms of frontotemporal dementiaH Seelaar, W Kamphorst, S M Rosso, 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.
BMC Medical Genetics|July 20, 2015
Determining the genome-wide kinship coefficient seems unhelpful in distinguishing consanguineous couples with a high versus low risk for adverse reproductive outcomeW Kelmemi, M E Teeuw, Z Bochdanovits, et al.
Neuroscience Letters|March 17, 1999
Apolipoprotein E genotype does not affect the age of onset of dementia in families with defined tau mutationsH Houlden, P Rizzu, M Stevens, et al.
Human Molecular Genetics|July 20, 2010
Loss of the Parkinson's disease-linked gene DJ-1 perturbs mitochondrial dynamicsI Irrcher, H Aleyasin, E L Seifert, et al.
Nature|June 26, 1998
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17M Hutton, C L Lendon, P Rizzu, et al.
Pageof 4