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Mark Roberts

Showing results (181-190 of 189) with videos related to

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The Lancet. Neurology|November 20, 2021
Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trialJordi Diaz-Manera, Priya S Kishnani, Hani Kushlaf, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2026
A 5' UTR CCG expansion in <i>TBC1D7</i> causes oculopharyngodistal myopathyLiedewei Van de Vondel, Riccardo Curro, Stefano Facchini, et al.
Journal of American College Health : J of ACH|January 3, 2023
SARS-CoV-2 control on a large urban college campus without mass testingChristopher O'Donnell, Katherine Brownlee, Elise Martin, et al.
Brain : a Journal of Neurology|December 20, 2021
Forecasting stroke-like episodes and outcomes in mitochondrial diseaseYi Shiau Ng, Nichola Z Lax, Alasdair P Blain, et al.
Genome Research|June 28, 2008
Comparative genome analysis of Salmonella Enteritidis PT4 and Salmonella Gallinarum 287/91 provides insights into evolutionary and host adaptation pathwaysNicholas R Thomson, Debra J Clayton, Daniel Windhorst, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|January 14, 2017
Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis SpectrumSimon Rothwell, Robert G Cooper, Ingrid E Lundberg, et al.
The New England Journal of Medicine|April 5, 2018
Outpatient Talc Administration by Indwelling Pleural Catheter for Malignant EffusionRahul Bhatnagar, Emma K Keenan, Anna J Morley, et al.
Journal of Cachexia, Sarcopenia and Muscle|April 25, 2025
Myo-Guide: A Machine Learning-Based Web Application for Neuromuscular Disease Diagnosis With MRIJose Verdu-Diaz, Carla Bolano-Díaz, Alejandro Gonzalez-Chamorro, et al.
Human Mutation|April 23, 2013
ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutationAnna Sarkozy, Debbie Hicks, Judith Hudson, et al.
Pageof 19

Showing results (181-190 of 189) with videos related to

Sort By:
Pageof 19
You have reached the last page of results.This site can display upto 189 results.
The Lancet. Neurology|November 20, 2021
Safety and efficacy of avalglucosidase alfa versus alglucosidase alfa in patients with late-onset Pompe disease (COMET): a phase 3, randomised, multicentre trialJordi Diaz-Manera, Priya S Kishnani, Hani Kushlaf, et al.
Medrxiv : the Preprint Server for Health Sciences|April 10, 2026
A 5' UTR CCG expansion in <i>TBC1D7</i> causes oculopharyngodistal myopathyLiedewei Van de Vondel, Riccardo Curro, Stefano Facchini, et al.
Journal of American College Health : J of ACH|January 3, 2023
SARS-CoV-2 control on a large urban college campus without mass testingChristopher O'Donnell, Katherine Brownlee, Elise Martin, et al.
Brain : a Journal of Neurology|December 20, 2021
Forecasting stroke-like episodes and outcomes in mitochondrial diseaseYi Shiau Ng, Nichola Z Lax, Alasdair P Blain, et al.
Genome Research|June 28, 2008
Comparative genome analysis of Salmonella Enteritidis PT4 and Salmonella Gallinarum 287/91 provides insights into evolutionary and host adaptation pathwaysNicholas R Thomson, Debra J Clayton, Daniel Windhorst, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|January 14, 2017
Immune-Array Analysis in Sporadic Inclusion Body Myositis Reveals HLA-DRB1 Amino Acid Heterogeneity Across the Myositis SpectrumSimon Rothwell, Robert G Cooper, Ingrid E Lundberg, et al.
The New England Journal of Medicine|April 5, 2018
Outpatient Talc Administration by Indwelling Pleural Catheter for Malignant EffusionRahul Bhatnagar, Emma K Keenan, Anna J Morley, et al.
Journal of Cachexia, Sarcopenia and Muscle|April 25, 2025
Myo-Guide: A Machine Learning-Based Web Application for Neuromuscular Disease Diagnosis With MRIJose Verdu-Diaz, Carla Bolano-Díaz, Alejandro Gonzalez-Chamorro, et al.
Human Mutation|April 23, 2013
ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutationAnna Sarkozy, Debbie Hicks, Judith Hudson, et al.
Pageof 19