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International Journal of Geriatric Psychiatry
|
March 17, 2023
Psychometric approaches to defining cognitive phenotypes in the Old Order Amish
Andrew Zaman, Laura Caywood, Michael Prough, et al.
The Journal of Infectious Diseases
|
December 16, 2015
Frequent Malaria Drives Progressive Vδ2 T-Cell Loss, Dysfunction, and CD16 Up-regulation During Early Childhood
Lila A Farrington, Prasanna Jagannathan, Tara I McIntyre, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Clinical Manifestations
Olufisayo Oluyinka Elugbadebo, Olusegun Baiyewu, Hephzibah Oyedapo-Ishola, et al.
Stem Cell Research
|
February 29, 2024
Generation of an induced pluripotent stem cell line (UMi043-A) from an African American patient with Alzheimer's disease carrying an ABCA7 deletion (p.Arg578Alafs)
Holly N Cukier, Shaina A Simon, Eugene Tang, et al.
American Journal of Human Genetics
|
April 12, 2003
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V
Anthony Antonellis, Rachel E Ellsworth, Nyamkhishig Sambuughin, et al.
Neurology. Genetics
|
August 13, 2019
Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease
Juan I Young, Sathesh K Sivasankaran, Lily Wang, et al.
Neurogenetics
|
March 25, 2000
Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia
W K Scott, P C Gaskell, F Lennon, et al.
Neurogenetics
|
September 13, 2000
Genetic studies in autistic disorder and chromosome 15
M P Bass, M M Menold, C M Wolpert, et al.
Neurogenetics
|
May 17, 2001
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia
A Ashley-Koch, E R Bonner, P C Gaskell, et al.
Science (New York, N.Y.)
|
November 3, 1995
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy
S Noguchi, E M McNally, K Ben Othmane, et al.
Page
of 43
Search research articles
Search
Showing results (271-280 of 428) with videos related to
Sort By:
Page
of 43
International Journal of Geriatric Psychiatry
|
March 17, 2023
Psychometric approaches to defining cognitive phenotypes in the Old Order Amish
Andrew Zaman, Laura Caywood, Michael Prough, et al.
The Journal of Infectious Diseases
|
December 16, 2015
Frequent Malaria Drives Progressive Vδ2 T-Cell Loss, Dysfunction, and CD16 Up-regulation During Early Childhood
Lila A Farrington, Prasanna Jagannathan, Tara I McIntyre, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Clinical Manifestations
Olufisayo Oluyinka Elugbadebo, Olusegun Baiyewu, Hephzibah Oyedapo-Ishola, et al.
Stem Cell Research
|
February 29, 2024
Generation of an induced pluripotent stem cell line (UMi043-A) from an African American patient with Alzheimer's disease carrying an ABCA7 deletion (p.Arg578Alafs)
Holly N Cukier, Shaina A Simon, Eugene Tang, et al.
American Journal of Human Genetics
|
April 12, 2003
Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V
Anthony Antonellis, Rachel E Ellsworth, Nyamkhishig Sambuughin, et al.
Neurology. Genetics
|
August 13, 2019
Genome-wide brain DNA methylation analysis suggests epigenetic reprogramming in Parkinson disease
Juan I Young, Sathesh K Sivasankaran, Lily Wang, et al.
Neurogenetics
|
March 25, 2000
Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia
W K Scott, P C Gaskell, F Lennon, et al.
Neurogenetics
|
September 13, 2000
Genetic studies in autistic disorder and chromosome 15
M P Bass, M M Menold, C M Wolpert, et al.
Neurogenetics
|
May 17, 2001
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegia
A Ashley-Koch, E R Bonner, P C Gaskell, et al.
Science (New York, N.Y.)
|
November 3, 1995
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy
S Noguchi, E M McNally, K Ben Othmane, et al.
Page
of 43