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Physical Review. E
|
June 17, 2021
Enhancements in laser-generated hot-electron production via focusing cone targets at short pulse and high contrast
D R Rusby, P M King, A Pak, et al.
Pediatrics
|
May 3, 2006
Controlled clinical trial of dichloroacetate for treatment of congenital lactic acidosis in children
Peter W Stacpoole, Douglas S Kerr, Carie Barnes, et al.
Cell Metabolism
|
October 13, 2016
NAD<sup>+</sup> Replenishment Improves Lifespan and Healthspan in Ataxia Telangiectasia Models via Mitophagy and DNA Repair
Evandro Fei Fang, Henok Kassahun, Deborah L Croteau, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
May 11, 2021
Cardiovascular Safety of Hydroxychloroquine in US Veterans With Rheumatoid Arthritis
Charles Faselis, Qing Zeng-Treitler, Yan Cheng, et al.
Comprehensive Psychiatry
|
August 30, 2023
Mental health outcomes in frontline healthcare workers in Brazil during the COVID-19 epidemic: Results of an online survey in four regions using respondent-driven sampling (RDS)
Mírian Cohen, Ricardo B Cardoso, Ligia R F S Kerr, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
May 1, 2014
Periodontitis and Porphyromonas gingivalis in patients with rheumatoid arthritis
Ted R Mikuls, Jeffrey B Payne, Fang Yu, et al.
Rheumatology (Oxford, England)
|
January 18, 2026
Heterogeneity in the association of genetic risk for rheumatoid arthritis and resultant rheumatoid arthritis phenotypes
Thomas R Riley, Austin M Wheeler, Bryant R England, et al.
Molecular Genetics and Metabolism
|
March 2, 2010
Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders Consortium
Jennifer Seminara, Mendel Tuchman, Lauren Krivitzky, et al.
The Journal of Pathology. Clinical Research
|
September 12, 2023
Accounting for intensity variation in image analysis of large-scale multiplexed clinical trial datasets
Anja L Frei, Anthony McGuigan, Ritik Rak Sinha, et al.
Molecular Genetics and Metabolism
|
May 28, 2014
Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivity
David R Adams, Hongjie Yuan, Todd Holyoak, et al.
Page
of 68
Search research articles
Search
Showing results (641-650 of 671) with videos related to
Sort By:
Page
of 68
Physical Review. E
|
June 17, 2021
Enhancements in laser-generated hot-electron production via focusing cone targets at short pulse and high contrast
D R Rusby, P M King, A Pak, et al.
Pediatrics
|
May 3, 2006
Controlled clinical trial of dichloroacetate for treatment of congenital lactic acidosis in children
Peter W Stacpoole, Douglas S Kerr, Carie Barnes, et al.
Cell Metabolism
|
October 13, 2016
NAD<sup>+</sup> Replenishment Improves Lifespan and Healthspan in Ataxia Telangiectasia Models via Mitophagy and DNA Repair
Evandro Fei Fang, Henok Kassahun, Deborah L Croteau, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
May 11, 2021
Cardiovascular Safety of Hydroxychloroquine in US Veterans With Rheumatoid Arthritis
Charles Faselis, Qing Zeng-Treitler, Yan Cheng, et al.
Comprehensive Psychiatry
|
August 30, 2023
Mental health outcomes in frontline healthcare workers in Brazil during the COVID-19 epidemic: Results of an online survey in four regions using respondent-driven sampling (RDS)
Mírian Cohen, Ricardo B Cardoso, Ligia R F S Kerr, et al.
Arthritis & Rheumatology (Hoboken, N.J.)
|
May 1, 2014
Periodontitis and Porphyromonas gingivalis in patients with rheumatoid arthritis
Ted R Mikuls, Jeffrey B Payne, Fang Yu, et al.
Rheumatology (Oxford, England)
|
January 18, 2026
Heterogeneity in the association of genetic risk for rheumatoid arthritis and resultant rheumatoid arthritis phenotypes
Thomas R Riley, Austin M Wheeler, Bryant R England, et al.
Molecular Genetics and Metabolism
|
March 2, 2010
Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders Consortium
Jennifer Seminara, Mendel Tuchman, Lauren Krivitzky, et al.
The Journal of Pathology. Clinical Research
|
September 12, 2023
Accounting for intensity variation in image analysis of large-scale multiplexed clinical trial datasets
Anja L Frei, Anthony McGuigan, Ritik Rak Sinha, et al.
Molecular Genetics and Metabolism
|
May 28, 2014
Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivity
David R Adams, Hongjie Yuan, Todd Holyoak, et al.
Page
of 68