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C Gallagher

Showing results (561-570 of 572) with videos related to

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Open Forum Infectious Diseases|November 30, 2018
Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant <i>Pseudomonas aeruginosa</i> Infections: A Multicenter StudyJason C Gallagher, Michael J Satlin, Abdulrahman Elabor, et al.
Nature Medicine|August 12, 2020
The role of exome sequencing in newborn screening for inborn errors of metabolismAashish N Adhikari, Renata C Gallagher, Yaqiong Wang, et al.
JIMD Reports|April 22, 2014
Lysine-Restricted Diet as Adjunct Therapy for Pyridoxine-Dependent Epilepsy: The PDE Consortium Consensus RecommendationsClara D M van Karnebeek, Sylvia Stockler-Ipsiroglu, Sravan Jaggumantri, et al.
Molecular Genetics and Metabolism|March 2, 2010
Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders ConsortiumJennifer Seminara, Mendel Tuchman, Lauren Krivitzky, et al.
Annals of Joint|February 21, 2025
Expert consensus on vitamin D in osteoporosisSha Lei, Xiaoya Zhang, Lige Song, et al.
NPJ Genomic Medicine|May 26, 2023
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
NPJ Genomic Medicine|October 23, 2023
Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
European Journal of Medical Genetics|August 2, 2005
Clinical and mutational spectrum of Mowat-Wilson syndromeChristiane Zweier, Christian T Thiel, Andreas Dufke, et al.
American Journal of Human Genetics|July 22, 2020
De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial DysmorphismMaria J Guillen Sacoto, Iva A Tchasovnikarova, Erin Torti, et al.
Nature Communications|October 5, 2018
Pathogenic variants in glutamyl-tRNA<sup>Gln</sup> amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorderMarisa W Friederich, Sharita Timal, Christopher A Powell, et al.
Pageof 58

Showing results (561-570 of 572) with videos related to

Sort By:
Pageof 58
Open Forum Infectious Diseases|November 30, 2018
Ceftolozane-Tazobactam for the Treatment of Multidrug-Resistant <i>Pseudomonas aeruginosa</i> Infections: A Multicenter StudyJason C Gallagher, Michael J Satlin, Abdulrahman Elabor, et al.
Nature Medicine|August 12, 2020
The role of exome sequencing in newborn screening for inborn errors of metabolismAashish N Adhikari, Renata C Gallagher, Yaqiong Wang, et al.
JIMD Reports|April 22, 2014
Lysine-Restricted Diet as Adjunct Therapy for Pyridoxine-Dependent Epilepsy: The PDE Consortium Consensus RecommendationsClara D M van Karnebeek, Sylvia Stockler-Ipsiroglu, Sravan Jaggumantri, et al.
Molecular Genetics and Metabolism|March 2, 2010
Establishing a consortium for the study of rare diseases: The Urea Cycle Disorders ConsortiumJennifer Seminara, Mendel Tuchman, Lauren Krivitzky, et al.
Annals of Joint|February 21, 2025
Expert consensus on vitamin D in osteoporosisSha Lei, Xiaoya Zhang, Lige Song, et al.
NPJ Genomic Medicine|May 26, 2023
Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
NPJ Genomic Medicine|October 23, 2023
Author Correction: Diagnostic yield of pediatric and prenatal exome sequencing in a diverse populationAnne Slavotinek, Shannon Rego, Nuriye Sahin-Hodoglugil, et al.
European Journal of Medical Genetics|August 2, 2005
Clinical and mutational spectrum of Mowat-Wilson syndromeChristiane Zweier, Christian T Thiel, Andreas Dufke, et al.
American Journal of Human Genetics|July 22, 2020
De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial DysmorphismMaria J Guillen Sacoto, Iva A Tchasovnikarova, Erin Torti, et al.
Nature Communications|October 5, 2018
Pathogenic variants in glutamyl-tRNA<sup>Gln</sup> amidotransferase subunits cause a lethal mitochondrial cardiomyopathy disorderMarisa W Friederich, Sharita Timal, Christopher A Powell, et al.
Pageof 58