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Neuromuscular Disorders : NMD
|
June 28, 2008
Caveolinopathy--new mutations and additional symptoms
Ahmed 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 segment
Ayush 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 group
Fiona 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 gene
Anna 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 myositis
Gina 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 two
Benedikt 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 Ireland
Boglarka Bansagi, Thalia Antoniadi, Sarah Burton-Jones, et al.
Brain : a Journal of Neurology
|
October 14, 2011
Long-term observational study of sporadic inclusion body myositis
Olivier 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 Gravis
Pedro M Rodríguez Cruz, Michal Al-Hajjar, Saif Huda, et al.
Page
of 8
Search research articles
Search
Showing results (41-50 of 79) with videos related to
Sort By:
Page
of 8
Neuromuscular Disorders : NMD
|
June 28, 2008
Caveolinopathy--new mutations and additional symptoms
Ahmed 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 segment
Ayush 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 group
Fiona 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 gene
Anna 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 myositis
Gina 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 two
Benedikt 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 Ireland
Boglarka Bansagi, Thalia Antoniadi, Sarah Burton-Jones, et al.
Brain : a Journal of Neurology
|
October 14, 2011
Long-term observational study of sporadic inclusion body myositis
Olivier 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 Gravis
Pedro M Rodríguez Cruz, Michal Al-Hajjar, Saif Huda, et al.
Page
of 8