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Showing results (131-140 of 276) with videos related to

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Pediatric Endocrinology Reviews : PER|October 28, 2014
State of the art review in hypospadias: challenges in diagnosis and medical managementMin-Jye Chen, Lefkothea P Karaviti, Charles G Macias, et al.
JIMD Reports|March 4, 2016
Chronic Oral L-Carnitine Supplementation Drives Marked Plasma TMAO Elevations in Patients with Organic Acidemias Despite Dietary Meat RestrictionsMarcus J Miller, Bret L Bostwick, Adam D Kennedy, et al.
The Journal of Clinical Endocrinology and Metabolism|January 20, 2023
Approach to the Patient: Pharmacological Therapies for Fracture Risk Reduction in Adults With Osteogenesis ImperfectaWinnie Liu, Brendan Lee, Sandesh C S Nagamani, et al.
Molecular Genetics and Metabolism|June 4, 2014
Improved standards for prenatal diagnosis of citrullinemiaMarcus J Miller, Claudia R Soler-Alfonso, Jaime E Grund, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|April 17, 2016
Inoculation site leprosy in a tattoo as a paradoxical reaction following tuberculosis treatmentP Branagan, B Moran, M Fitzgibbon, et al.
American Journal of Medical Genetics. Part A|September 18, 2009
A genome-wide screen for copy number alterations in Aicardi syndromeXiaoling Wang, V Reid Sutton, Tanya N Eble, et al.
JIMD Reports|December 1, 2016
Expansion of the Phenotypic Spectrum of Propionic Acidemia with Isolated Elevated PropionylcarnitineGerarda Cappuccio, Paldeep S Atwal, Taraka R Donti, et al.
European Journal of Medical Genetics|December 30, 2018
Oro-dental and cranio-facial characteristics of osteogenesis imperfecta type VJean-Marc Retrouvey, Doaa Taqi, Faleh Tamimi, et al.
Cell Reports|December 4, 2014
A rare human syndrome provides genetic evidence that WNT signaling is required for reprogramming of fibroblasts to induced pluripotent stem cellsJason Ross, Julia Busch, Ellen Mintz, et al.
Molecular Genetics and Metabolism|July 15, 2025
Effective algorithm to differentiate NBS MCADD cases from carriers and non-carriers and an assessment of the utility of the second newborn screen for MCADDMatthew T Snyder, Kristian Divin, Ning Liu, et al.
Pageof 28

Showing results (131-140 of 276) with videos related to

Sort By:
Pageof 28
Pediatric Endocrinology Reviews : PER|October 28, 2014
State of the art review in hypospadias: challenges in diagnosis and medical managementMin-Jye Chen, Lefkothea P Karaviti, Charles G Macias, et al.
JIMD Reports|March 4, 2016
Chronic Oral L-Carnitine Supplementation Drives Marked Plasma TMAO Elevations in Patients with Organic Acidemias Despite Dietary Meat RestrictionsMarcus J Miller, Bret L Bostwick, Adam D Kennedy, et al.
The Journal of Clinical Endocrinology and Metabolism|January 20, 2023
Approach to the Patient: Pharmacological Therapies for Fracture Risk Reduction in Adults With Osteogenesis ImperfectaWinnie Liu, Brendan Lee, Sandesh C S Nagamani, et al.
Molecular Genetics and Metabolism|June 4, 2014
Improved standards for prenatal diagnosis of citrullinemiaMarcus J Miller, Claudia R Soler-Alfonso, Jaime E Grund, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|April 17, 2016
Inoculation site leprosy in a tattoo as a paradoxical reaction following tuberculosis treatmentP Branagan, B Moran, M Fitzgibbon, et al.
American Journal of Medical Genetics. Part A|September 18, 2009
A genome-wide screen for copy number alterations in Aicardi syndromeXiaoling Wang, V Reid Sutton, Tanya N Eble, et al.
JIMD Reports|December 1, 2016
Expansion of the Phenotypic Spectrum of Propionic Acidemia with Isolated Elevated PropionylcarnitineGerarda Cappuccio, Paldeep S Atwal, Taraka R Donti, et al.
European Journal of Medical Genetics|December 30, 2018
Oro-dental and cranio-facial characteristics of osteogenesis imperfecta type VJean-Marc Retrouvey, Doaa Taqi, Faleh Tamimi, et al.
Cell Reports|December 4, 2014
A rare human syndrome provides genetic evidence that WNT signaling is required for reprogramming of fibroblasts to induced pluripotent stem cellsJason Ross, Julia Busch, Ellen Mintz, et al.
Molecular Genetics and Metabolism|July 15, 2025
Effective algorithm to differentiate NBS MCADD cases from carriers and non-carriers and an assessment of the utility of the second newborn screen for MCADDMatthew T Snyder, Kristian Divin, Ning Liu, et al.
Pageof 28