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Acta Neuropathologica
|
January 23, 2013
Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: genetic, clinical and neuropathological analysis
Carol Dobson-Stone, Agnes A Luty, Elizabeth M Thompson, et al.
Science (New York, N.Y.)
|
March 17, 2018
Environmental dynamics during the onset of the Middle Stone Age in eastern Africa
Richard Potts, Anna K Behrensmeyer, J Tyler Faith, et al.
Molecular Biology of the Cell
|
December 9, 2020
Costameric integrin and sarcoglycan protein levels are altered in a <i>Drosophila</i> model for Limb-girdle muscular dystrophy type 2H
Simranjot Bawa, Samantha Gameros, Kenny Baumann, et al.
Journal of Clinical Medicine
|
August 12, 2022
Recovering or Persisting: The Immunopathological Features of SARS-CoV-2 Infection in Children
Danilo Buonsenso, Piero Valentini, Cristina De Rose, et al.
Journal of Neuroinflammation
|
August 22, 2008
Association of alleles carried at TNFA -850 and BAT1 -22 with Alzheimer's disease
Anastazija Gnjec, Katarzyna J D'Costa, Simon M Laws, et al.
Plos One
|
February 26, 2013
C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patients
Carol Dobson-Stone, Marianne Hallupp, Clement T Loy, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases
|
October 17, 2025
Active surveillance for emerging influenza A virus: findings from a one health study in Vietnam's live bird markets
Vuong N Bui, Judith U Oguzie, Tung D Dao, et al.
Space Science Reviews
|
February 6, 2026
Geodetic Investigations of the Europa Clipper Mission
G Steinbrügge, R S Park, J H Roberts, et al.
Neuroreport
|
April 14, 1997
Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype
J B Kwok, K Taddei, M Hallupp, et al.
Orphanet Journal of Rare Diseases
|
June 27, 2020
ERNICA guidelines for the management of rectosigmoid Hirschsprung's disease
Kristiina Kyrklund, Cornelius E J Sloots, Ivo de Blaauw, et al.
Page
of 73
Search research articles
Search
Showing results (631-640 of 728) with videos related to
Sort By:
Page
of 73
Acta Neuropathologica
|
January 23, 2013
Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: genetic, clinical and neuropathological analysis
Carol Dobson-Stone, Agnes A Luty, Elizabeth M Thompson, et al.
Science (New York, N.Y.)
|
March 17, 2018
Environmental dynamics during the onset of the Middle Stone Age in eastern Africa
Richard Potts, Anna K Behrensmeyer, J Tyler Faith, et al.
Molecular Biology of the Cell
|
December 9, 2020
Costameric integrin and sarcoglycan protein levels are altered in a <i>Drosophila</i> model for Limb-girdle muscular dystrophy type 2H
Simranjot Bawa, Samantha Gameros, Kenny Baumann, et al.
Journal of Clinical Medicine
|
August 12, 2022
Recovering or Persisting: The Immunopathological Features of SARS-CoV-2 Infection in Children
Danilo Buonsenso, Piero Valentini, Cristina De Rose, et al.
Journal of Neuroinflammation
|
August 22, 2008
Association of alleles carried at TNFA -850 and BAT1 -22 with Alzheimer's disease
Anastazija Gnjec, Katarzyna J D'Costa, Simon M Laws, et al.
Plos One
|
February 26, 2013
C9ORF72 repeat expansion in Australian and Spanish frontotemporal dementia patients
Carol Dobson-Stone, Marianne Hallupp, Clement T Loy, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases
|
October 17, 2025
Active surveillance for emerging influenza A virus: findings from a one health study in Vietnam's live bird markets
Vuong N Bui, Judith U Oguzie, Tung D Dao, et al.
Space Science Reviews
|
February 6, 2026
Geodetic Investigations of the Europa Clipper Mission
G Steinbrügge, R S Park, J H Roberts, et al.
Neuroreport
|
April 14, 1997
Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype
J B Kwok, K Taddei, M Hallupp, et al.
Orphanet Journal of Rare Diseases
|
June 27, 2020
ERNICA guidelines for the management of rectosigmoid Hirschsprung's disease
Kristiina Kyrklund, Cornelius E J Sloots, Ivo de Blaauw, et al.
Page
of 73