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A Nicholson

Showing results (991-1000 of 1,065) with videos related to

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International Journal of Oral and Maxillofacial Surgery|August 28, 2023
Management of the neck in T1 and T2 buccal squamous cell carcinomaO A Nicholson, C G F Van Lanschot, B N van den Besselaar, et al.
Scientific Reports|June 6, 2019
Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expressionIngrid S Tarr, Emily P McCann, Beben Benyamin, et al.
BMJ Military Health|March 23, 2025
Influence of military preventive policy for recruit training on COVID-19 seroconversion: the IMPACT-COVID-19 studyMichael John Stacey, P Ferentinos, F Koivula, et al.
Brain : a Journal of Neurology|November 16, 2022
Novel gene-intergenic fusion involving ubiquitin E3 ligase UBE3C causes distal hereditary motor neuropathyAnthony N Cutrupi, Ramesh K Narayanan, Gonzalo Perez-Siles, et al.
Plos Genetics|July 21, 2016
Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3Megan H Brewer, Rabia Chaudhry, Jessica Qi, et al.
Zebrafish|October 10, 2018
Motor Neuron Abnormalities Correlate with Impaired Movement in Zebrafish that Express Mutant Superoxide Dismutase 1Katherine J Robinson, Kristy C Yuan, Emily K Don, et al.
Headache|June 1, 2005
Guidelines for trials of behavioral treatments for recurrent headache, first edition: American Headache Society Behavioral Clinical Trials WorkgroupDonald B Penzien, Frank Andrasik, Brian M Freidenberg, et al.
World Journal for Pediatric & Congenital Heart Surgery|July 17, 2019
Impact of High-Risk Characteristics in Hypoplastic Left Heart SyndromeGananjay G Salve, Gauri M Datar, Gopinath Perumal, et al.
Neurogenetics|April 24, 2019
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian familyShelisa Tey, Nortina Shahrizaila, Alexander P Drew, et al.
Acta Chirurgica Belgica|February 27, 2010
The Immediate Management of the Patient with Rupture: Open Versus Endovascular repair (IMPROVE) aneurysm trial--ISRCTN 48334791 IMPROVE trialists, J T Powell, S G Thompson, et al.
Pageof 107

Showing results (991-1000 of 1,065) with videos related to

Sort By:
Pageof 107
International Journal of Oral and Maxillofacial Surgery|August 28, 2023
Management of the neck in T1 and T2 buccal squamous cell carcinomaO A Nicholson, C G F Van Lanschot, B N van den Besselaar, et al.
Scientific Reports|June 6, 2019
Monozygotic twins and triplets discordant for amyotrophic lateral sclerosis display differential methylation and gene expressionIngrid S Tarr, Emily P McCann, Beben Benyamin, et al.
BMJ Military Health|March 23, 2025
Influence of military preventive policy for recruit training on COVID-19 seroconversion: the IMPACT-COVID-19 studyMichael John Stacey, P Ferentinos, F Koivula, et al.
Brain : a Journal of Neurology|November 16, 2022
Novel gene-intergenic fusion involving ubiquitin E3 ligase UBE3C causes distal hereditary motor neuropathyAnthony N Cutrupi, Ramesh K Narayanan, Gonzalo Perez-Siles, et al.
Plos Genetics|July 21, 2016
Whole Genome Sequencing Identifies a 78 kb Insertion from Chromosome 8 as the Cause of Charcot-Marie-Tooth Neuropathy CMTX3Megan H Brewer, Rabia Chaudhry, Jessica Qi, et al.
Zebrafish|October 10, 2018
Motor Neuron Abnormalities Correlate with Impaired Movement in Zebrafish that Express Mutant Superoxide Dismutase 1Katherine J Robinson, Kristy C Yuan, Emily K Don, et al.
Headache|June 1, 2005
Guidelines for trials of behavioral treatments for recurrent headache, first edition: American Headache Society Behavioral Clinical Trials WorkgroupDonald B Penzien, Frank Andrasik, Brian M Freidenberg, et al.
World Journal for Pediatric & Congenital Heart Surgery|July 17, 2019
Impact of High-Risk Characteristics in Hypoplastic Left Heart SyndromeGananjay G Salve, Gauri M Datar, Gopinath Perumal, et al.
Neurogenetics|April 24, 2019
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian familyShelisa Tey, Nortina Shahrizaila, Alexander P Drew, et al.
Acta Chirurgica Belgica|February 27, 2010
The Immediate Management of the Patient with Rupture: Open Versus Endovascular repair (IMPROVE) aneurysm trial--ISRCTN 48334791 IMPROVE trialists, J T Powell, S G Thompson, et al.
Pageof 107