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The American Journal of Cardiology
|
March 23, 2002
Haptoglobin phenotype and the risk of restenosis after coronary artery stent implantation
Ariel Roguin, Flavio Ribichini, Valeria Ferrero, et al.
Clinical Case Reports
|
October 14, 2017
Developmental progression of intellectual disability, autism, and epilepsy in a child with an IQSEC2 gene mutation
Rachelle Zipper, Sherri D Baine, Jacob Genizi, et al.
Translational Psychiatry
|
March 23, 2021
Structural and functional brain-wide alterations in A350V Iqsec2 mutant mice displaying autistic-like behavior
Daniela Lichtman, Eyal Bergmann, Alexandra Kavushansky, et al.
Atherosclerosis
|
March 17, 2004
Haptoglobin phenotype and prevalent coronary heart disease in the Framingham offspring cohort
Andrew P Levy, Martin G Larson, Diane Corey, et al.
American Journal of Ophthalmology
|
November 5, 2003
Haptoglobin phenotype in age-related macular degeneration patients
Nir Seider, Itzchak Beiran, Rachel Miller-Lotan, et al.
European Journal of Applied Physiology
|
April 7, 2009
Haptoglobin genotype and endothelial function in diabetes mellitus: a pilot study
Lior Dayan, Andrew P Levy, Shany Blum, et al.
World Journal of Nephrology
|
November 21, 2013
Vitamin E and diabetic nephropathy in mice model and humans
Nakhoul Farid, Dahan Inbal, Nakhoul Nakhoul, et al.
International Journal of Molecular Sciences
|
June 26, 2019
IQSEC2-Associated Intellectual Disability and Autism
Nina S Levy, George K E Umanah, Eli J Rogers, et al.
Journal of the American College of Cardiology
|
June 11, 2013
Currently available versions of genome-wide association studies cannot be used to query the common haptoglobin copy number variant
Leah E Cahill, Majken K Jensen, Daniel I Chasman, et al.
Diabetes Care
|
October 27, 2004
The effect of vitamin E supplementation on cardiovascular risk in diabetic individuals with different haptoglobin phenotypes
Andrew P Levy, Hertzel C Gerstein, Rachel Miller-Lotan, et al.
Page
of 14
Search research articles
Search
Showing results (61-70 of 134) with videos related to
Sort By:
Page
of 14
The American Journal of Cardiology
|
March 23, 2002
Haptoglobin phenotype and the risk of restenosis after coronary artery stent implantation
Ariel Roguin, Flavio Ribichini, Valeria Ferrero, et al.
Clinical Case Reports
|
October 14, 2017
Developmental progression of intellectual disability, autism, and epilepsy in a child with an IQSEC2 gene mutation
Rachelle Zipper, Sherri D Baine, Jacob Genizi, et al.
Translational Psychiatry
|
March 23, 2021
Structural and functional brain-wide alterations in A350V Iqsec2 mutant mice displaying autistic-like behavior
Daniela Lichtman, Eyal Bergmann, Alexandra Kavushansky, et al.
Atherosclerosis
|
March 17, 2004
Haptoglobin phenotype and prevalent coronary heart disease in the Framingham offspring cohort
Andrew P Levy, Martin G Larson, Diane Corey, et al.
American Journal of Ophthalmology
|
November 5, 2003
Haptoglobin phenotype in age-related macular degeneration patients
Nir Seider, Itzchak Beiran, Rachel Miller-Lotan, et al.
European Journal of Applied Physiology
|
April 7, 2009
Haptoglobin genotype and endothelial function in diabetes mellitus: a pilot study
Lior Dayan, Andrew P Levy, Shany Blum, et al.
World Journal of Nephrology
|
November 21, 2013
Vitamin E and diabetic nephropathy in mice model and humans
Nakhoul Farid, Dahan Inbal, Nakhoul Nakhoul, et al.
International Journal of Molecular Sciences
|
June 26, 2019
IQSEC2-Associated Intellectual Disability and Autism
Nina S Levy, George K E Umanah, Eli J Rogers, et al.
Journal of the American College of Cardiology
|
June 11, 2013
Currently available versions of genome-wide association studies cannot be used to query the common haptoglobin copy number variant
Leah E Cahill, Majken K Jensen, Daniel I Chasman, et al.
Diabetes Care
|
October 27, 2004
The effect of vitamin E supplementation on cardiovascular risk in diabetic individuals with different haptoglobin phenotypes
Andrew P Levy, Hertzel C Gerstein, Rachel Miller-Lotan, et al.
Page
of 14