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B Singleton

Showing results (181-190 of 477) with videos related to

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Journal of Neurology|November 13, 2010
Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9pJustin P Pearson, Nigel M Williams, Elisa Majounie, et al.
Journal of Medical Genetics|December 1, 2019
Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson's diseaseHampton Leonard, Cornelis Blauwendraat, Lynne Krohn, et al.
Parkinsonism & Related Disorders|October 15, 2017
Genetic risk factors in Finnish patients with Parkinson's diseaseSusanna Ylönen, Ari Siitonen, Michael A Nalls, et al.
Pharmacogenetics|April 20, 1999
CYP2D6 is associated with Parkinson's disease but not with dementia with Lewy Bodies or Alzheimer's diseaseA Atkinson, A B Singleton, A Steward, et al.
Neurology|February 11, 2000
Lack of association of the alpha2-macroglobulin locus on chromosome 12 in ADA M Gibson, A B Singleton, G Smith, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|March 13, 2012
Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorderThomas G Schulze, Nirmala Akula, René Breuer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndromeJanel O Johnson, Giovanni Stevanin, Joyce van de Leemput, et al.
Neurology. Genetics|January 31, 2018
Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+)Mira Mäkelä, Karri Kaivola, Miko Valori, et al.
Biological Psychiatry|July 17, 2012
Alzheimer risk variant CLU and brain function during agingMadhav Thambisetty, Lori L Beason-Held, Yang An, et al.
Neurobiology of Aging|April 7, 2020
Comprehensive assessment of PINK1 variants in Parkinson's diseaseLynne Krohn, Francis P Grenn, Mary B Makarious, et al.
Pageof 48

Showing results (181-190 of 477) with videos related to

Sort By:
Pageof 48
Journal of Neurology|November 13, 2010
Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9pJustin P Pearson, Nigel M Williams, Elisa Majounie, et al.
Journal of Medical Genetics|December 1, 2019
Genetic variability and potential effects on clinical trial outcomes: perspectives in Parkinson's diseaseHampton Leonard, Cornelis Blauwendraat, Lynne Krohn, et al.
Parkinsonism & Related Disorders|October 15, 2017
Genetic risk factors in Finnish patients with Parkinson's diseaseSusanna Ylönen, Ari Siitonen, Michael A Nalls, et al.
Pharmacogenetics|April 20, 1999
CYP2D6 is associated with Parkinson's disease but not with dementia with Lewy Bodies or Alzheimer's diseaseA Atkinson, A B Singleton, A Steward, et al.
Neurology|February 11, 2000
Lack of association of the alpha2-macroglobulin locus on chromosome 12 in ADA M Gibson, A B Singleton, G Smith, et al.
The World Journal of Biological Psychiatry : the Official Journal of the World Federation of Societies of Biological Psychiatry|March 13, 2012
Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorderThomas G Schulze, Nirmala Akula, René Breuer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndromeJanel O Johnson, Giovanni Stevanin, Joyce van de Leemput, et al.
Neurology. Genetics|January 31, 2018
Alzheimer risk loci and associated neuropathology in a population-based study (Vantaa 85+)Mira Mäkelä, Karri Kaivola, Miko Valori, et al.
Biological Psychiatry|July 17, 2012
Alzheimer risk variant CLU and brain function during agingMadhav Thambisetty, Lori L Beason-Held, Yang An, et al.
Neurobiology of Aging|April 7, 2020
Comprehensive assessment of PINK1 variants in Parkinson's diseaseLynne Krohn, Francis P Grenn, Mary B Makarious, et al.
Pageof 48