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Mark Davis

Showing results (261-270 of 318) with videos related to

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Neuromuscular Disorders : NMD|August 10, 2022
A genetic basis is identified in 74% cases of paediatric hyperCKaemia without weakness presenting to a tertiary paediatric neuromuscular centreWui-Kwan Wong, Samantha J Bryen, Adam Bournazos, et al.
Brain, Behavior, and Immunity|March 24, 2006
Ibuprofen use, endotoxemia, inflammation, and plasma cytokines during ultramarathon competitionDavid C Nieman, Dru A Henson, Charles L Dumke, et al.
Allergy and Asthma Proceedings|February 26, 2015
Before and after, the impact of available on-demand treatment for HAESandra C Christiansen, Anette Bygum, Aleena Banerji, et al.
Cell Reports|November 21, 2015
Adenoviral Vector Vaccination Induces a Conserved Program of CD8(+) T Cell Memory Differentiation in Mouse and ManBeatrice Bolinger, Stuart Sims, Leo Swadling, et al.
Neuromuscular Disorders : NMD|March 13, 2013
A novel mutation expands the genetic and clinical spectrum of MYH7-related myopathiesNigel F Clarke, Kimberly Amburgey, James Teener, et al.
NPJ Genomic Medicine|November 21, 2017
Cost-effectiveness of massively parallel sequencing for diagnosis of paediatric muscle diseasesDeborah Schofield, Khurshid Alam, Lyndal Douglas, et al.
The New Phytologist|March 18, 2009
Quantitative genetic analysis of biomass and wood chemistry of Populus under different nitrogen levelsEvandro Novaes, Luis Osorio, Derek R Drost, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 10, 2018
Patient with ALS with a novel TBK1 mutation, widespread brain involvement, behaviour changes and metabolic dysfunctionPamela A McCombe, Shyuan T Ngo, Christine Cong Guo, et al.
Journal of Medical Genetics|March 18, 2020
A homozygous <i>UBA5</i> pathogenic variant causes a fatal congenital neuropathyMacarena Cabrera-Serrano, David Joseph Coote, Dimitar Azmanov, et al.
The Journal of Allergy and Clinical Immunology. in Practice|September 8, 2020
US HAEA Medical Advisory Board 2020 Guidelines for the Management of Hereditary AngioedemaPaula J Busse, Sandra C Christiansen, Marc A Riedl, et al.
Pageof 32

Showing results (261-270 of 318) with videos related to

Sort By:
Pageof 32
Neuromuscular Disorders : NMD|August 10, 2022
A genetic basis is identified in 74% cases of paediatric hyperCKaemia without weakness presenting to a tertiary paediatric neuromuscular centreWui-Kwan Wong, Samantha J Bryen, Adam Bournazos, et al.
Brain, Behavior, and Immunity|March 24, 2006
Ibuprofen use, endotoxemia, inflammation, and plasma cytokines during ultramarathon competitionDavid C Nieman, Dru A Henson, Charles L Dumke, et al.
Allergy and Asthma Proceedings|February 26, 2015
Before and after, the impact of available on-demand treatment for HAESandra C Christiansen, Anette Bygum, Aleena Banerji, et al.
Cell Reports|November 21, 2015
Adenoviral Vector Vaccination Induces a Conserved Program of CD8(+) T Cell Memory Differentiation in Mouse and ManBeatrice Bolinger, Stuart Sims, Leo Swadling, et al.
Neuromuscular Disorders : NMD|March 13, 2013
A novel mutation expands the genetic and clinical spectrum of MYH7-related myopathiesNigel F Clarke, Kimberly Amburgey, James Teener, et al.
NPJ Genomic Medicine|November 21, 2017
Cost-effectiveness of massively parallel sequencing for diagnosis of paediatric muscle diseasesDeborah Schofield, Khurshid Alam, Lyndal Douglas, et al.
The New Phytologist|March 18, 2009
Quantitative genetic analysis of biomass and wood chemistry of Populus under different nitrogen levelsEvandro Novaes, Luis Osorio, Derek R Drost, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|September 10, 2018
Patient with ALS with a novel TBK1 mutation, widespread brain involvement, behaviour changes and metabolic dysfunctionPamela A McCombe, Shyuan T Ngo, Christine Cong Guo, et al.
Journal of Medical Genetics|March 18, 2020
A homozygous <i>UBA5</i> pathogenic variant causes a fatal congenital neuropathyMacarena Cabrera-Serrano, David Joseph Coote, Dimitar Azmanov, et al.
The Journal of Allergy and Clinical Immunology. in Practice|September 8, 2020
US HAEA Medical Advisory Board 2020 Guidelines for the Management of Hereditary AngioedemaPaula J Busse, Sandra C Christiansen, Marc A Riedl, et al.
Pageof 32