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P St George-Hyslop

Showing results (41-50 of 85) with videos related to

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Annals of Neurology|November 1, 1990
A comparison of neurological, metabolic, structural, and genetic evaluations in persons at risk for Huntington's diseaseS T Grafton, J C Mazziotta, J J Pahl, et al.
Genomics|March 20, 1995
The human NACP/alpha-synuclein gene: chromosome assignment to 4q21.3-q22 and TaqI RFLP analysisX Chen, H A de Silva, M J Pettenati, et al.
Neurology|June 1, 1995
Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patientsK Young, C K Jones, P Piccardo, et al.
Genetika|March 1, 1994
[Mapping the gene for palmoplantar hyperkeratosis (thylosis) to chromosome 17 in the 17q12-q24 region]E I Rogaev, E A Rogaeva, E K Ginter, et al.
Archives of Neurology|November 1, 1992
Serial changes of cerebral glucose metabolism and caudate size in persons at risk for Huntington's diseaseS T Grafton, J C Mazziotta, J J Pahl, et al.
American Journal of Human Genetics|October 1, 1993
Polymorphic microsatellites and Wilson disease (WD)E A Stewart, A White, J Tomfohrde, et al.
Neurobiology of Disease|September 25, 1998
Additive effects of PS1 and APP mutations on secretion of the 42-residue amyloid beta-proteinM Citron, C B Eckman, T S Diehl, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|August 24, 2000
Comparison of clinical and pathological phenotypes in two ethnically and geographically unrelated pedigrees segregating an equivalent presenilin 1 mutationR Jorge, C Mangone, E Castano, et al.
Neurology|September 15, 2005
LRRK2 gene in Parkinson disease: mutation analysis and case control association studyC Paisán-Ruíz, A E Lang, T Kawarai, et al.
Human Molecular Genetics|May 23, 1998
Analysis of the butyrylcholinesterase gene and nearby chromosome 3 markers in Alzheimer diseaseN Brindle, Y Song, E Rogaeva, et al.
Pageof 9

Showing results (41-50 of 85) with videos related to

Sort By:
Pageof 9
Annals of Neurology|November 1, 1990
A comparison of neurological, metabolic, structural, and genetic evaluations in persons at risk for Huntington's diseaseS T Grafton, J C Mazziotta, J J Pahl, et al.
Genomics|March 20, 1995
The human NACP/alpha-synuclein gene: chromosome assignment to 4q21.3-q22 and TaqI RFLP analysisX Chen, H A de Silva, M J Pettenati, et al.
Neurology|June 1, 1995
Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patientsK Young, C K Jones, P Piccardo, et al.
Genetika|March 1, 1994
[Mapping the gene for palmoplantar hyperkeratosis (thylosis) to chromosome 17 in the 17q12-q24 region]E I Rogaev, E A Rogaeva, E K Ginter, et al.
Archives of Neurology|November 1, 1992
Serial changes of cerebral glucose metabolism and caudate size in persons at risk for Huntington's diseaseS T Grafton, J C Mazziotta, J J Pahl, et al.
American Journal of Human Genetics|October 1, 1993
Polymorphic microsatellites and Wilson disease (WD)E A Stewart, A White, J Tomfohrde, et al.
Neurobiology of Disease|September 25, 1998
Additive effects of PS1 and APP mutations on secretion of the 42-residue amyloid beta-proteinM Citron, C B Eckman, T S Diehl, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|August 24, 2000
Comparison of clinical and pathological phenotypes in two ethnically and geographically unrelated pedigrees segregating an equivalent presenilin 1 mutationR Jorge, C Mangone, E Castano, et al.
Neurology|September 15, 2005
LRRK2 gene in Parkinson disease: mutation analysis and case control association studyC Paisán-Ruíz, A E Lang, T Kawarai, et al.
Human Molecular Genetics|May 23, 1998
Analysis of the butyrylcholinesterase gene and nearby chromosome 3 markers in Alzheimer diseaseN Brindle, Y Song, E Rogaeva, et al.
Pageof 9