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Showing results (851-860 of 994) with videos related to

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Pilot and Feasibility Studies|May 2, 2018
Developing and feasibility testing of data collection methods for an economic evaluation of a supported selfmanagement programme for adults with a learning disability and type 2 diabetesJohn L O'Dwyer, Amy M Russell, Louise D Bryant, et al.
Pediatric Blood & Cancer|October 18, 2016
Renal cell carcinoma harboring somatic TSC2 mutations in a child with methylmalonic acidemiaSamara L Potter, Rajkumar Venkatramani, Scott Wenderfer, et al.
Molecular Genetics and Metabolism|July 20, 2014
Mitochondrial myopathy, lactic acidosis, and sideroblastic anemia (MLASA) plus associated with a novel de novo mutation (m.8969G>A) in the mitochondrial encoded ATP6 geneLindsay C Burrage, Sha Tang, Jing Wang, et al.
World Journal of Surgery|October 4, 2022
Parathyroidectomy for Normocalcemic Primary Hyperparathyroidism is Associated with Improved Bone Mineral Density Regardless of Postoperative Parathyroid Hormone LevelsMichael S Lui, Uriel Clemente-Gutierrez, Danica M Vodopivec, et al.
Health Technology Assessment (Winchester, England)|March 14, 2018
A pragmatic randomised controlled trial and economic evaluation of family therapy versus treatment as usual for young people seen after second or subsequent episodes of self-harm: the Self-Harm Intervention - Family Therapy (SHIFT) trialDavid J Cottrell, Alex Wright-Hughes, Michelle Collinson, et al.
Plos Genetics|June 23, 2017
Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouseMichael F Wangler, Yu-Hsin Chao, Vafa Bayat, et al.
Journal of the American Academy of Dermatology|March 6, 2020
Dupilumab treatment results in early and sustained improvements in itch in adolescents and adults with moderate to severe atopic dermatitis: Analysis of the randomized phase 3 studies SOLO 1 and SOLO 2, AD ADOL, and CHRONOSJonathan I Silverberg, Gil Yosipovitch, Eric L Simpson, et al.
Molecular Genetics and Metabolism|August 7, 2023
Specifications of the ACMG/AMP guidelines for ACADVL variant interpretationMay Flowers, Alexa Dickson, Marcus J Miller, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
Critical Care Medicine|January 22, 2002
Increased adenosine in cerebrospinal fluid after severe traumatic brain injury in infants and children: association with severity of injury and excitotoxicityC L Robertson, M J Bell, P M Kochanek, et al.
Pageof 100

Showing results (851-860 of 994) with videos related to

Sort By:
Pageof 100
Pilot and Feasibility Studies|May 2, 2018
Developing and feasibility testing of data collection methods for an economic evaluation of a supported selfmanagement programme for adults with a learning disability and type 2 diabetesJohn L O'Dwyer, Amy M Russell, Louise D Bryant, et al.
Pediatric Blood & Cancer|October 18, 2016
Renal cell carcinoma harboring somatic TSC2 mutations in a child with methylmalonic acidemiaSamara L Potter, Rajkumar Venkatramani, Scott Wenderfer, et al.
Molecular Genetics and Metabolism|July 20, 2014
Mitochondrial myopathy, lactic acidosis, and sideroblastic anemia (MLASA) plus associated with a novel de novo mutation (m.8969G>A) in the mitochondrial encoded ATP6 geneLindsay C Burrage, Sha Tang, Jing Wang, et al.
World Journal of Surgery|October 4, 2022
Parathyroidectomy for Normocalcemic Primary Hyperparathyroidism is Associated with Improved Bone Mineral Density Regardless of Postoperative Parathyroid Hormone LevelsMichael S Lui, Uriel Clemente-Gutierrez, Danica M Vodopivec, et al.
Health Technology Assessment (Winchester, England)|March 14, 2018
A pragmatic randomised controlled trial and economic evaluation of family therapy versus treatment as usual for young people seen after second or subsequent episodes of self-harm: the Self-Harm Intervention - Family Therapy (SHIFT) trialDavid J Cottrell, Alex Wright-Hughes, Michelle Collinson, et al.
Plos Genetics|June 23, 2017
Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouseMichael F Wangler, Yu-Hsin Chao, Vafa Bayat, et al.
Journal of the American Academy of Dermatology|March 6, 2020
Dupilumab treatment results in early and sustained improvements in itch in adolescents and adults with moderate to severe atopic dermatitis: Analysis of the randomized phase 3 studies SOLO 1 and SOLO 2, AD ADOL, and CHRONOSJonathan I Silverberg, Gil Yosipovitch, Eric L Simpson, et al.
Molecular Genetics and Metabolism|August 7, 2023
Specifications of the ACMG/AMP guidelines for ACADVL variant interpretationMay Flowers, Alexa Dickson, Marcus J Miller, et al.
Genome Medicine|February 7, 2013
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndromeMatthew N Bainbridge, Hao Hu, Donna M Muzny, et al.
Critical Care Medicine|January 22, 2002
Increased adenosine in cerebrospinal fluid after severe traumatic brain injury in infants and children: association with severity of injury and excitotoxicityC L Robertson, M J Bell, P M Kochanek, et al.
Pageof 100