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David Hilton

Showing results (101-110 of 130) with videos related to

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Annals of the New York Academy of Sciences|June 24, 2008
Myasthenia gravis seronegative for acetylcholine receptor antibodiesAngela Vincent, Maria Isabel Leite, Maria Elena Farrugia, et al.
Journal of Neurology|May 11, 2016
Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registryTeresinha Evangelista, Libby Wood, Roberto Fernandez-Torron, et al.
Neuromuscular Disorders : NMD|February 1, 2020
Paediatric myasthenia gravis: Prognostic factors for drug free remissionDomizia Vecchio, Sithara Ramdas, Pinki Munot, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|June 20, 2017
IgG-specific cell-based assay detects potentially pathogenic MuSK-Abs in seronegative MGSaif Huda, Patrick Waters, Mark Woodhall, et al.
Clinical Rehabilitation|November 19, 2013
A multicentre postal survey investigating the contribution of illness perceptions, coping and optimism to quality of life and mood in adults with muscle diseaseChristopher D Graham, John Weinman, Reza Sadjadi, et al.
Muscle & Nerve|October 21, 2017
Chronic pain has a strong impact on quality of life in facioscapulohumeral muscular dystrophyGermán Morís, Libby Wood, Roberto FernáNdez-Torrón, et al.
Clinical Rehabilitation|March 9, 2011
Supported community exercise in people with long-term neurological conditions: a phase II randomized controlled trialCharlotte Elsworth, Charlotte Winward, Cath Sackley, et al.
Neuromuscular Disorders : NMD|November 18, 2005
Sub-cellular localisation of fukutin related protein in different cell lines and in the muscle of patients with MDC1C and LGMD2ISilvia Torelli, Susan C Brown, Martin Brockington, et al.
Pharmacological Research|July 22, 2015
A novel quantitative assay of mitophagy: Combining high content fluorescence microscopy and mitochondrial DNA load to quantify mitophagy and identify novel pharmacological tools against pathogenic heteroplasmic mtDNAAlan Diot, Alex Hinks-Roberts, Tiffany Lodge, et al.
Journal of Neuromuscular Diseases|November 18, 2016
Mortality and Causes of Death in Patients with Sporadic Inclusion Body Myositis: Survey Study Based on the Clinical Experience of Specialists in Australia, Europe and the USAMark A Price, Victoria Barghout, Olivier Benveniste, et al.
Pageof 13

Showing results (101-110 of 130) with videos related to

Sort By:
Pageof 13
Annals of the New York Academy of Sciences|June 24, 2008
Myasthenia gravis seronegative for acetylcholine receptor antibodiesAngela Vincent, Maria Isabel Leite, Maria Elena Farrugia, et al.
Journal of Neurology|May 11, 2016
Design, set-up and utility of the UK facioscapulohumeral muscular dystrophy patient registryTeresinha Evangelista, Libby Wood, Roberto Fernandez-Torron, et al.
Neuromuscular Disorders : NMD|February 1, 2020
Paediatric myasthenia gravis: Prognostic factors for drug free remissionDomizia Vecchio, Sithara Ramdas, Pinki Munot, et al.
Neurology(R) Neuroimmunology & Neuroinflammation|June 20, 2017
IgG-specific cell-based assay detects potentially pathogenic MuSK-Abs in seronegative MGSaif Huda, Patrick Waters, Mark Woodhall, et al.
Clinical Rehabilitation|November 19, 2013
A multicentre postal survey investigating the contribution of illness perceptions, coping and optimism to quality of life and mood in adults with muscle diseaseChristopher D Graham, John Weinman, Reza Sadjadi, et al.
Muscle & Nerve|October 21, 2017
Chronic pain has a strong impact on quality of life in facioscapulohumeral muscular dystrophyGermán Morís, Libby Wood, Roberto FernáNdez-Torrón, et al.
Clinical Rehabilitation|March 9, 2011
Supported community exercise in people with long-term neurological conditions: a phase II randomized controlled trialCharlotte Elsworth, Charlotte Winward, Cath Sackley, et al.
Neuromuscular Disorders : NMD|November 18, 2005
Sub-cellular localisation of fukutin related protein in different cell lines and in the muscle of patients with MDC1C and LGMD2ISilvia Torelli, Susan C Brown, Martin Brockington, et al.
Pharmacological Research|July 22, 2015
A novel quantitative assay of mitophagy: Combining high content fluorescence microscopy and mitochondrial DNA load to quantify mitophagy and identify novel pharmacological tools against pathogenic heteroplasmic mtDNAAlan Diot, Alex Hinks-Roberts, Tiffany Lodge, et al.
Journal of Neuromuscular Diseases|November 18, 2016
Mortality and Causes of Death in Patients with Sporadic Inclusion Body Myositis: Survey Study Based on the Clinical Experience of Specialists in Australia, Europe and the USAMark A Price, Victoria Barghout, Olivier Benveniste, et al.
Pageof 13