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David Hilton-Jones

Showing results (41-50 of 79) with videos related to

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Neuromuscular Disorders : NMD|June 28, 2008
Caveolinopathy--new mutations and additional symptomsAhmed Aboumousa, Jessica Hoogendijk, Richard Charlton, et al.
Muscle & Nerve|May 27, 2003
Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c-terminal alpha-helical segmentAyush Dagvadorj, Bertrand Goudeau, David Hilton-Jones, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 13, 2013
Myasthenia in pregnancy: best practice guidelines from a U.K. multispecialty working groupFiona Norwood, Mandish Dhanjal, Marguerite Hill, et al.
European Journal of Human Genetics : EJHG|June 2, 2011
Phenotypic heterogeneity in British patients with a founder mutation in the FHL1 geneAnna Sarkozy, Christian Windpassinger, Judith Hudson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 14, 2021
Longitudinal observational study investigating outcome measures for clinical trials in inclusion body myositisGina Sangha, Bohao Yao, Daniel Lunn, et al.
Neuromuscular Disorders : NMD|February 12, 2009
Immune-mediated rippling muscle disease with myasthenia gravis: a report of seven patients with long-term follow-up in twoBenedikt Schoser, Saiju Jacob, David Hilton-Jones, et al.
Journal of Neurology|June 3, 2015
Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and IrelandBoglarka Bansagi, Thalia Antoniadi, Sarah Burton-Jones, et al.
Brain : a Journal of Neurology|October 14, 2011
Long-term observational study of sporadic inclusion body myositisOlivier Benveniste, Marguerite Guiguet, Jane Freebody, et al.
JIMD Reports|September 6, 2021
Energy metabolism during exercise in patients with β-enolase deficiency (GSDXIII)Astrid Emilie Buch, Olimpia Musumeci, Ralph Wigley, et al.
JAMA Neurology|April 21, 2015
Clinical Features and Diagnostic Usefulness of Antibodies to Clustered Acetylcholine Receptors in the Diagnosis of Seronegative Myasthenia GravisPedro M Rodríguez Cruz, Michal Al-Hajjar, Saif Huda, et al.
Pageof 8

Showing results (41-50 of 79) with videos related to

Sort By:
Pageof 8
Neuromuscular Disorders : NMD|June 28, 2008
Caveolinopathy--new mutations and additional symptomsAhmed Aboumousa, Jessica Hoogendijk, Richard Charlton, et al.
Muscle & Nerve|May 27, 2003
Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin c-terminal alpha-helical segmentAyush Dagvadorj, Bertrand Goudeau, David Hilton-Jones, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 13, 2013
Myasthenia in pregnancy: best practice guidelines from a U.K. multispecialty working groupFiona Norwood, Mandish Dhanjal, Marguerite Hill, et al.
European Journal of Human Genetics : EJHG|June 2, 2011
Phenotypic heterogeneity in British patients with a founder mutation in the FHL1 geneAnna Sarkozy, Christian Windpassinger, Judith Hudson, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 14, 2021
Longitudinal observational study investigating outcome measures for clinical trials in inclusion body myositisGina Sangha, Bohao Yao, Daniel Lunn, et al.
Neuromuscular Disorders : NMD|February 12, 2009
Immune-mediated rippling muscle disease with myasthenia gravis: a report of seven patients with long-term follow-up in twoBenedikt Schoser, Saiju Jacob, David Hilton-Jones, et al.
Journal of Neurology|June 3, 2015
Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and IrelandBoglarka Bansagi, Thalia Antoniadi, Sarah Burton-Jones, et al.
Brain : a Journal of Neurology|October 14, 2011
Long-term observational study of sporadic inclusion body myositisOlivier Benveniste, Marguerite Guiguet, Jane Freebody, et al.
JIMD Reports|September 6, 2021
Energy metabolism during exercise in patients with β-enolase deficiency (GSDXIII)Astrid Emilie Buch, Olimpia Musumeci, Ralph Wigley, et al.
JAMA Neurology|April 21, 2015
Clinical Features and Diagnostic Usefulness of Antibodies to Clustered Acetylcholine Receptors in the Diagnosis of Seronegative Myasthenia GravisPedro M Rodríguez Cruz, Michal Al-Hajjar, Saif Huda, et al.
Pageof 8