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Neuroreport
|
April 20, 1999
The -491AA polymorphism in the APOE gene is associated with increased plasma apoE levels in Alzheimer's disease
S M Laws, K Taddei, G Martins, et al.
Plos One
|
September 30, 2014
Genome-wide investigation of DNA methylation marks associated with FV Leiden mutation
Dylan Aïssi, Jessica Dennis, Martin Ladouceur, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists
|
August 30, 2021
BCOR Internal Tandem Duplication Associated Uterine Sarcoma: Expanding the Clinicopathologic Spectrum
Sakinah A Thiryayi, Helen Ettler, Emily A Goebel, et al.
Proceedings. Symposium on Computer Applications in Medical Care
|
January 1, 1994
Building a cooperative institutional model of IAIMS at the Yale-New Haven Medical Center
P L Miller, J A Paton, N K Roderer, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
April 22, 2026
Assessing the significance of cytomegalovirus reactivation in recipients of allogeneic hematopoietic stem cell transplantation: a cohort study
L P de Oliveira, E J A Paton, M F Giovanardi, et al.
Molecular Psychiatry
|
August 23, 2002
APOE-epsilon4 and APOE -491A polymorphisms in individuals with subjective memory loss
S M Laws, R M Clarnette, K Taddei, et al.
Pediatric Transplantation
|
November 19, 2015
The genetic diversity of Epstein-Barr virus in the setting of transplantation relative to non-transplant settings: A feasibility study
Upton D Allen, Pingzhao Hu, Sergio L Pereira, et al.
The Journal of Urology
|
December 1, 1983
Small center kidney transplantation
G E Brannen, R J Correa, R P Gibbons, et al.
Journal of Alzheimer'S Disease : JAD
|
September 1, 2005
Neurological soft signs are associated with APOE genotype, age and cognitive performance
N T Lautenschlager, Jing-Shan Wu, S M Laws, et al.
Journal of Medical Genetics
|
October 9, 2014
OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium
Ajoy Vincent, Nicole Forster, Jason T Maynes, et al.
Page
of 20
Search research articles
Search
Showing results (171-180 of 198) with videos related to
Sort By:
Page
of 20
Neuroreport
|
April 20, 1999
The -491AA polymorphism in the APOE gene is associated with increased plasma apoE levels in Alzheimer's disease
S M Laws, K Taddei, G Martins, et al.
Plos One
|
September 30, 2014
Genome-wide investigation of DNA methylation marks associated with FV Leiden mutation
Dylan Aïssi, Jessica Dennis, Martin Ladouceur, et al.
International Journal of Gynecological Pathology : Official Journal of the International Society of Gynecological Pathologists
|
August 30, 2021
BCOR Internal Tandem Duplication Associated Uterine Sarcoma: Expanding the Clinicopathologic Spectrum
Sakinah A Thiryayi, Helen Ettler, Emily A Goebel, et al.
Proceedings. Symposium on Computer Applications in Medical Care
|
January 1, 1994
Building a cooperative institutional model of IAIMS at the Yale-New Haven Medical Center
P L Miller, J A Paton, N K Roderer, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas
|
April 22, 2026
Assessing the significance of cytomegalovirus reactivation in recipients of allogeneic hematopoietic stem cell transplantation: a cohort study
L P de Oliveira, E J A Paton, M F Giovanardi, et al.
Molecular Psychiatry
|
August 23, 2002
APOE-epsilon4 and APOE -491A polymorphisms in individuals with subjective memory loss
S M Laws, R M Clarnette, K Taddei, et al.
Pediatric Transplantation
|
November 19, 2015
The genetic diversity of Epstein-Barr virus in the setting of transplantation relative to non-transplant settings: A feasibility study
Upton D Allen, Pingzhao Hu, Sergio L Pereira, et al.
The Journal of Urology
|
December 1, 1983
Small center kidney transplantation
G E Brannen, R J Correa, R P Gibbons, et al.
Journal of Alzheimer'S Disease : JAD
|
September 1, 2005
Neurological soft signs are associated with APOE genotype, age and cognitive performance
N T Lautenschlager, Jing-Shan Wu, S M Laws, et al.
Journal of Medical Genetics
|
October 9, 2014
OTX2 mutations cause autosomal dominant pattern dystrophy of the retinal pigment epithelium
Ajoy Vincent, Nicole Forster, Jason T Maynes, et al.
Page
of 20