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D Hilton-Jones

Showing results (41-50 of 58) with videos related to

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Brain : a Journal of Neurology|February 27, 2001
Oculopharyngeal muscular dystrophy: phenotypic and genotypic studies in a UK populationM E Hill, G A Creed, T F McMullan, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|April 26, 2012
Fracture rate in patients with myasthenia gravis: the general practice research databaseS Pouwels, A de Boer, M K Javaid, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 20, 2002
Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth diseaseM-J Lee, I Nelson, H Houlden, et al.
Human Molecular Genetics|July 1, 1997
Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophyL Metzinger, D J Blake, M V Squier, et al.
Journal of Medical Genetics|September 11, 1998
Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangementsS W Horsley, S J Knight, J Nixon, et al.
The British Journal of Radiology|April 1, 1987
The study of human organs by phosphorus-31 topical magnetic resonance spectroscopyR D Oberhaensli, G J Galloway, D Hilton-Jones, et al.
Neuromuscular Disorders : NMD|March 16, 2013
Longitudinal observational study of sporadic inclusion body myositis: implications for clinical trialsA Cortese, P Machado, J Morrow, et al.
Journal of the Neurological Sciences|December 1, 1987
An unusual metabolic myopathy: a malate-aspartate shuttle defectD J Hayes, D J Taylor, P J Bore, et al.
European Journal of Neurology|April 21, 2010
Guidelines for treatment of autoimmune neuromuscular transmission disordersG O Skeie, S Apostolski, A Evoli, et al.
Neurology|September 25, 2003
Rapsyn mutations in hereditary myasthenia: distinct early- and late-onset phenotypesG Burke, J Cossins, S Maxwell, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Brain : a Journal of Neurology|February 27, 2001
Oculopharyngeal muscular dystrophy: phenotypic and genotypic studies in a UK populationM E Hill, G A Creed, T F McMullan, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|April 26, 2012
Fracture rate in patients with myasthenia gravis: the general practice research databaseS Pouwels, A de Boer, M K Javaid, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 20, 2002
Six novel connexin32 (GJB1) mutations in X-linked Charcot-Marie-Tooth diseaseM-J Lee, I Nelson, H Houlden, et al.
Human Molecular Genetics|July 1, 1997
Dystrobrevin deficiency at the sarcolemma of patients with muscular dystrophyL Metzinger, D J Blake, M V Squier, et al.
Journal of Medical Genetics|September 11, 1998
Del(18p) shown to be a cryptic translocation using a multiprobe FISH assay for subtelomeric chromosome rearrangementsS W Horsley, S J Knight, J Nixon, et al.
The British Journal of Radiology|April 1, 1987
The study of human organs by phosphorus-31 topical magnetic resonance spectroscopyR D Oberhaensli, G J Galloway, D Hilton-Jones, et al.
Neuromuscular Disorders : NMD|March 16, 2013
Longitudinal observational study of sporadic inclusion body myositis: implications for clinical trialsA Cortese, P Machado, J Morrow, et al.
Journal of the Neurological Sciences|December 1, 1987
An unusual metabolic myopathy: a malate-aspartate shuttle defectD J Hayes, D J Taylor, P J Bore, et al.
European Journal of Neurology|April 21, 2010
Guidelines for treatment of autoimmune neuromuscular transmission disordersG O Skeie, S Apostolski, A Evoli, et al.
Neurology|September 25, 2003
Rapsyn mutations in hereditary myasthenia: distinct early- and late-onset phenotypesG Burke, J Cossins, S Maxwell, et al.
Pageof 6