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Malaria Journal
|
December 25, 2015
An ultrasensitive reverse transcription polymerase chain reaction assay to detect asymptomatic low-density Plasmodium falciparum and Plasmodium vivax infections in small volume blood samples
Matthew Adams, Sudhaunshu N Joshi, Gillian Mbambo, et al.
Molecular Genetics and Metabolism
|
January 30, 2019
Recessive GM3 synthase deficiency: Natural history, biochemistry, and therapeutic frontier
Lauren E Bowser, Millie Young, Olivia K Wenger, et al.
Ophthalmology
|
January 18, 2011
A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome
Brian G Mohney, Jose S Pulido, Noralane M Lindor, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 27, 2004
Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function
Erik G Puffenberger, Diane Hu-Lince, Jennifer M Parod, et al.
The Journal of Infectious Diseases
|
February 8, 2024
Recombinant Full-length Plasmodium falciparum Circumsporozoite Protein-Based Vaccine Adjuvanted With Glucopyranosyl Lipid A-Liposome Quillaja saponaria 21: Results of Phase 1 Testing With Malaria Challenge
DeAnna J Friedman-Klabanoff, Andrea A Berry, Mark A Travassos, et al.
Sports Medicine (Auckland, N.Z.)
|
May 10, 2026
Methodological Considerations for Studies in Sport and Exercise Science with Women as Participants Part II: Guidance for Applied Studies in Elite Female Athletes
Kirsty J Elliott-Sale, Richard J Burden, Kathryn E Ackerman, et al.
American Journal of Human Genetics
|
September 16, 2020
De Novo and Inherited Variants in GBF1 are Associated with Axonal Neuropathy Caused by Golgi Fragmentation
Natalia Mendoza-Ferreira, Mert Karakaya, Nur Cengiz, et al.
Translational Psychiatry
|
September 19, 2019
Clinical and genetic validity of quantitative bipolarity
Heather A Bruce, Peter Kochunov, Braxton Mitchell, et al.
Brain : a Journal of Neurology
|
March 12, 2014
Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood
Joanne Ng, Juan Zhen, Esther Meyer, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 21, 2019
Decreased Aerobic Exercise Capacity After Long-Term Remission From Cushing Syndrome: Exploration of Mechanisms
Sean H P P Roerink, Matthew S Cocks, Margreet A E M Wagenmakers, et al.
Page
of 46
Search research articles
Search
Showing results (411-420 of 453) with videos related to
Sort By:
Page
of 46
Malaria Journal
|
December 25, 2015
An ultrasensitive reverse transcription polymerase chain reaction assay to detect asymptomatic low-density Plasmodium falciparum and Plasmodium vivax infections in small volume blood samples
Matthew Adams, Sudhaunshu N Joshi, Gillian Mbambo, et al.
Molecular Genetics and Metabolism
|
January 30, 2019
Recessive GM3 synthase deficiency: Natural history, biochemistry, and therapeutic frontier
Lauren E Bowser, Millie Young, Olivia K Wenger, et al.
Ophthalmology
|
January 18, 2011
A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome
Brian G Mohney, Jose S Pulido, Noralane M Lindor, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
July 27, 2004
Mapping of sudden infant death with dysgenesis of the testes syndrome (SIDDT) by a SNP genome scan and identification of TSPYL loss of function
Erik G Puffenberger, Diane Hu-Lince, Jennifer M Parod, et al.
The Journal of Infectious Diseases
|
February 8, 2024
Recombinant Full-length Plasmodium falciparum Circumsporozoite Protein-Based Vaccine Adjuvanted With Glucopyranosyl Lipid A-Liposome Quillaja saponaria 21: Results of Phase 1 Testing With Malaria Challenge
DeAnna J Friedman-Klabanoff, Andrea A Berry, Mark A Travassos, et al.
Sports Medicine (Auckland, N.Z.)
|
May 10, 2026
Methodological Considerations for Studies in Sport and Exercise Science with Women as Participants Part II: Guidance for Applied Studies in Elite Female Athletes
Kirsty J Elliott-Sale, Richard J Burden, Kathryn E Ackerman, et al.
American Journal of Human Genetics
|
September 16, 2020
De Novo and Inherited Variants in GBF1 are Associated with Axonal Neuropathy Caused by Golgi Fragmentation
Natalia Mendoza-Ferreira, Mert Karakaya, Nur Cengiz, et al.
Translational Psychiatry
|
September 19, 2019
Clinical and genetic validity of quantitative bipolarity
Heather A Bruce, Peter Kochunov, Braxton Mitchell, et al.
Brain : a Journal of Neurology
|
March 12, 2014
Dopamine transporter deficiency syndrome: phenotypic spectrum from infancy to adulthood
Joanne Ng, Juan Zhen, Esther Meyer, et al.
The Journal of Clinical Endocrinology and Metabolism
|
December 21, 2019
Decreased Aerobic Exercise Capacity After Long-Term Remission From Cushing Syndrome: Exploration of Mechanisms
Sean H P P Roerink, Matthew S Cocks, Margreet A E M Wagenmakers, et al.
Page
of 46