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Auteur Swash M

Documents disponibles écrits par cet auteur (25)

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Article

Handbook of clinical neurology, 195. Upper and lower motor neuron neurophysiology and motor control

De Carvalho M ; Swash M | 2023

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En ligne

Article

Journal of neurology, neurosurgery and psychiatry, 88, 7. Six issues in muscle disease

Swash M, Auteur | 2017

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En ligne

Article

Journal of neurology, neurosurgery and psychiatry, 87, 6. Brown-Vialetto-Van Laere syndrome: a 28-year follow-up

Davis A, Auteur ; Josifova D ; Lloyd-Oven S ; Radunovic A ; Swash M | 2016

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Article

Neuromuscular disorders : NMD, 23, 2. Congenital myopathy with focal loss of cross-striations revisited

Voermans NC ; Jungbluth H ; Aronica E ; Monnier N ; Lunardi J ; Swash M ; de Visser M | 2013

Accès au résumé PubMed / to PubMed abstract

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Article

Neuromuscular disorders : NMD, 18, 9-10. Late-onset axial myopathy with cores due to a novel dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene (Poster)

Collectif ; Jungbluth H ; Lillis S ; Zhou H ; Abbs S ; Swash M ; Muntoni F | 2008

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Article

Brain, 130, 8. Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies

Zhou H ; Jungbluth H ; Sewry CA ; Feng L ; Bertini E ; Bushby K ; Straub V ; Roper H ; Rose MR ; Brockington M ; Kinali M ; Manzur A ; Robb S ; Appleton R ; Messina S ; D'Amico A ; Quinlivan R ; Swash M ; Müller CR ; Brown S ; Treves S ; Muntoni F | 2007

Accès au résumé PubMed / to PubMed abstract

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Article

Neurology, 68, 12. Homozygous mutation in MYH7 in myosin storage myopathy and cardiomyopathy

Tajsharghi H ; Oldfors A ; Macleod DP ; Swash M | 2007

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Article

Amyotrophic lateral sclerosis and other motor neuron disorders, 6, 1. Neurophysiological measures in amyotrophic lateral sclerosis: markers of progression in clinical trials

Chio A ; Dengler R ; Hecht M ; Weber M ; Swash M | 2005

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Article

Neurology, 65, 12. Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene

Jungbluth H ; Zhou H ; Hartley C ; Halliger-Keller B ; Messina S ; Longman C ; Brockington M ; Robb SA ; Straub V ; Voit T ; Swash M ; Ferreiro A ; Bydder G ; Sewry CA ; Muller C ; Muntoni F ; Hartley L | 2005

Accès au résumé PubMed / to PubMed abstract

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Article

Muscle & Nerve, 28. Clinical and neurophysiological evaluation of progression in amyotrophic lateral sclerosis

Carvalho M ; Scotto M ; Lopes J ; Swash M | 11/2003

Accès au résumé Pubmed/to pubmed abstract

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Article

Journal of neurology, neurosurgery and psychiatry, 68, 2. Quantitative measure of fatiguability in myasthenia gravis

Proceedings of the Association of British Neurologists (15-17 Sept. 1999; Londres) ; Househam E ; Swash M | 2000

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Article

Journal of neurology, neurosurgery and psychiatry, 64, 1. Faecal incontinence in myotonic dystrophy

Abercrombie JF ; Rogers J ; Swash M | 1998

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Article

Neuromuscular disorders : NMD, 6, 3. HTLV-1 polymyositis

Caldwell CJ ; Barrett WY ; Breuer J ; Farmer SF ; Swash M | 1996

Description du cas d'une femme jamaïcaine séropositive au HTLV-1 (Human T-cell lymphocyte virus) présentant les signes cliniques d'une polymyosite et d'une myélopathie. Analyse des observations faites à la biopsie musculaire, à l'immunocytochimi[...]

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Article

Human molecular genetics, 4, 7. Two novel mutations in the gene for copper zinc superoxide dismutase in UK families with amyotrophic lateral sclerosis

Enayat ZE ; Orrell RW ; Claus A ; Ludolph AC ; Bachus R ; Brockmuller J ; Ray-Chaudhuri K ; Radunovic A ; Shaw CM ; Wilkinson J ; King A ; Swash M ; Leigh PN ; Powell JA | 1995

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Livre

Motor neuron disease : Biology and management.

Leigh PN ; Swash M | Londres : Springer Verlag | 1995

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Article

Muscle & Nerve CT muscle imaging and the clinical assessment of neuromuscular disease

Swash M ; Martin M ; Thakkar C | 1995

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Article

Nature medicine, 1, 2. Regional changes of ciliary neurotrophic factor and nerve growth factor levels in post mortem spinal cord and cerebral cortex from patients with motor disease

Anand P ; Parrett A ; Martin J ; Zeman S ; Foley P ; Swash M ; Leigh PN ; Cedarbaum JM ; Lindsay RM ; Williams-Chestnut RE ; Sinicropi DV | 1995

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Article

Muscle & Nerve Arterial hypertension, nifedipine, and myasthenia gravis

Noguès MA ; Rivero A ; Swash M | 1993

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Article

Muscle & Nerve, 15. Adverse effect of verapamil in myasthenia gravis

Swash M ; Ingram DA | 1992

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Article

Neuromuscular disorders : NMD, 2, 1. Criteria for diagnosis of familial amyotrophic lateral sclerosis

Swash M ; Leigh N | 1992

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Article

Gastroenterology, 100. Hereditary internal anal sphincter myopathy causing proctalgia fugax and constipation.

Kamm MA ; Hoyle CHV ; Burleigh DE ; Law PJ ; Swash M ; Martin JE | 1991

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Article

Neuropathology and applied neurobiology, 16. Annotation New insights in motor neuron disease

Martin JF ; Swash M ; Schwartz MS | 1990

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Article

Muscle & Nerve, 10. The pattern of involvement of adult-onset acid maltase deficiency at autopsy

van der Walt JD ; Swash M ; Leake J ; Cox EL | 04/1987

Accès au résumé PubMed / to PubMed abstract

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Article

Journal of the neurological sciences, 52, 1. Familial multicore disease with focal loss of cross-striations and ophthalmoplegia

Swash M ; Schwartz MS | 1981

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Article

Journal of neurology, neurosurgery and psychiatry, 40. Implications of longitudinal muscle fibre splitting in neurogenic and myopathic disorders

Swash M ; Schwartz MS | 1977

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Détail de l'auteur

Auteur Swash M

Documents disponibles écrits par cet auteur (25)

Handbook of clinical neurology, 195. Upper and lower motor neuron neurophysiology and motor control

Journal of neurology, neurosurgery and psychiatry, 88, 7. Six issues in muscle disease

Journal of neurology, neurosurgery and psychiatry, 87, 6. Brown-Vialetto-Van Laere syndrome: a 28-year follow-up

Neuromuscular disorders : NMD, 23, 2. Congenital myopathy with focal loss of cross-striations revisited

Neuromuscular disorders : NMD, 18, 9-10. Late-onset axial myopathy with cores due to a novel dominant mutation in the skeletal muscle ryanodine receptor (RYR1) gene (Poster)

Brain, 130, 8. Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies

Neurology, 68, 12. Homozygous mutation in MYH7 in myosin storage myopathy and cardiomyopathy

Amyotrophic lateral sclerosis and other motor neuron disorders, 6, 1. Neurophysiological measures in amyotrophic lateral sclerosis: markers of progression in clinical trials

Neurology, 65, 12. Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene

Muscle & Nerve, 28. Clinical and neurophysiological evaluation of progression in amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 68, 2. Quantitative measure of fatiguability in myasthenia gravis

Journal of neurology, neurosurgery and psychiatry, 64, 1. Faecal incontinence in myotonic dystrophy

Neuromuscular disorders : NMD, 6, 3. HTLV-1 polymyositis

Human molecular genetics, 4, 7. Two novel mutations in the gene for copper zinc superoxide dismutase in UK families with amyotrophic lateral sclerosis

Motor neuron disease : Biology and management.

Muscle & Nerve CT muscle imaging and the clinical assessment of neuromuscular disease

Nature medicine, 1, 2. Regional changes of ciliary neurotrophic factor and nerve growth factor levels in post mortem spinal cord and cerebral cortex from patients with motor disease

Muscle & Nerve Arterial hypertension, nifedipine, and myasthenia gravis

Muscle & Nerve, 15. Adverse effect of verapamil in myasthenia gravis

Neuromuscular disorders : NMD, 2, 1. Criteria for diagnosis of familial amyotrophic lateral sclerosis

Gastroenterology, 100. Hereditary internal anal sphincter myopathy causing proctalgia fugax and constipation.

Neuropathology and applied neurobiology, 16. Annotation New insights in motor neuron disease

Muscle & Nerve, 10. The pattern of involvement of adult-onset acid maltase deficiency at autopsy

Journal of the neurological sciences, 52, 1. Familial multicore disease with focal loss of cross-striations and ophthalmoplegia

Journal of neurology, neurosurgery and psychiatry, 40. Implications of longitudinal muscle fibre splitting in neurogenic and myopathic disorders