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Brain Research
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October 21, 1999
Apolipoprotein E and beta-amyloid levels in the hippocampus and frontal cortex of Alzheimer's disease subjects are disease-related and apolipoprotein E genotype dependent
U Beffert, J S Cohn, C Petit-Turcotte, et al.
Human Genetics
|
October 1, 1991
X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus
L Van Maldergem, M Espeel, F Roels, et al.
Journal of Medical Genetics
|
October 5, 2001
Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene
M Mustapha, N Salem, V Delague, et al.
Blood
|
August 1, 1997
Even individuals considered as long-term nonprogressors show biological signs of progression after 10 years of human immunodeficiency virus infection
J J Lefrère, L Morand-Joubert, M Mariotti, et al.
Nature
|
February 1, 2013
Magnetic ratchet for three-dimensional spintronic memory and logic
Reinoud Lavrijsen, Ji-Hyun Lee, Amalio Fernández-Pacheco, et al.
Journal of Medical Economics
|
July 17, 2023
Reply to letter by Hadigal et al. regarding the cost-effectiveness of high dose quadrivalent vaccine in three European countries
F P Alvarez, H Bricout, C Marques, et al.
Protein Science : a Publication of the Protein Society
|
April 1, 1996
Solution structure and lipid binding of a nonspecific lipid transfer protein extracted from maize seeds
J Gomar, M C Petit, P Sodano, et al.
BMC Musculoskeletal Disorders
|
May 27, 2010
Impregnation of bone chips with antibiotics and storage of antibiotics at different temperatures: an in vitro study
Nina M C Mathijssen, Pieter L C Petit, Peter Pilot, et al.
Neuroradiology
|
January 17, 2002
Hemangioma of the porus acusticus. Impact of imaging studies: case reports
M C Petit-Lacour, K Marsot-Dupuch, M Hadj-Rabia, et al.
Human Molecular Genetics
|
January 1, 1997
A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21
H Chaïb, J Kaplan, S Gerber, et al.
Page
of 57
Search research articles
Search
Showing results (391-400 of 563) with videos related to
Sort By:
Page
of 57
Brain Research
|
October 21, 1999
Apolipoprotein E and beta-amyloid levels in the hippocampus and frontal cortex of Alzheimer's disease subjects are disease-related and apolipoprotein E genotype dependent
U Beffert, J S Cohn, C Petit-Turcotte, et al.
Human Genetics
|
October 1, 1991
X-linked recessive chondrodysplasia punctata with XY translocation in a stillborn fetus
L Van Maldergem, M Espeel, F Roels, et al.
Journal of Medical Genetics
|
October 5, 2001
Autosomal recessive non-syndromic hearing loss in the Lebanese population: prevalence of the 30delG mutation and report of two novel mutations in the connexin 26 (GJB2) gene
M Mustapha, N Salem, V Delague, et al.
Blood
|
August 1, 1997
Even individuals considered as long-term nonprogressors show biological signs of progression after 10 years of human immunodeficiency virus infection
J J Lefrère, L Morand-Joubert, M Mariotti, et al.
Nature
|
February 1, 2013
Magnetic ratchet for three-dimensional spintronic memory and logic
Reinoud Lavrijsen, Ji-Hyun Lee, Amalio Fernández-Pacheco, et al.
Journal of Medical Economics
|
July 17, 2023
Reply to letter by Hadigal et al. regarding the cost-effectiveness of high dose quadrivalent vaccine in three European countries
F P Alvarez, H Bricout, C Marques, et al.
Protein Science : a Publication of the Protein Society
|
April 1, 1996
Solution structure and lipid binding of a nonspecific lipid transfer protein extracted from maize seeds
J Gomar, M C Petit, P Sodano, et al.
BMC Musculoskeletal Disorders
|
May 27, 2010
Impregnation of bone chips with antibiotics and storage of antibiotics at different temperatures: an in vitro study
Nina M C Mathijssen, Pieter L C Petit, Peter Pilot, et al.
Neuroradiology
|
January 17, 2002
Hemangioma of the porus acusticus. Impact of imaging studies: case reports
M C Petit-Lacour, K Marsot-Dupuch, M Hadj-Rabia, et al.
Human Molecular Genetics
|
January 1, 1997
A newly identified locus for Usher syndrome type I, USH1E, maps to chromosome 21q21
H Chaïb, J Kaplan, S Gerber, et al.
Page
of 57