Resultats de la cerca - David Hilton‐Jones
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The myotonic dystrophies: diagnosis and management per C Turner, David Hilton‐Jones
Publicat 2010Artigo -
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Diagnostic criteria for inclusion body myositis per David Hilton‐Jones, Stefen Brady
Publicat 2016Revisão -
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Spontaneous intracranial hypotension. per Shelley Renowden, Ralph Gregory, N. Hyman, David Hilton‐Jones
Publicat 1995Artigo -
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Motor neuron disease in England and Wales, 1959-1979. per Jonathan Buckley, C Warlow, Peter G. Smith, David Hilton‐Jones, S Irvine, John Tew
Publicat 1983Artigo -
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Amyloid deposits and inflammatory infiltrates in sporadic inclusion body myositis: the inflammatory egg comes before the degenerative chicken per Olivier Benvéniste, Werner Stenzel, David Hilton‐Jones, Marco Sandri, Olivier Boyer, Baziel G.M. van Engelen
Publicat 2015Revisão -
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The need for biochemical testing in beta‐enolase deficiency in the genomic era per Ralph Wigley, R. Scalco, A. Gardiner, Richard Godfrey, Suzanne Booth, Richard Kirk, David Hilton‐Jones, Henry Houlden, Simon Heales, Rosaline C. M. Quinlivan
Publicat 2019Artigo -
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Guidelines for treatment of autoimmune neuromuscular transmission disorders per Geir Skeie, Slobodan Apostolski, Amelia Evoli, Nils Erik Gilhus, Isabel Illa, Lutz Harms, David Hilton‐Jones, Arthur Melms, Jan J.G.M. Verschuuren, H. W. Horge
Publicat 2010Artigo -
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Long-term observational study of sporadic inclusion body myositis per Olivier Benvéniste, Marguerite Guiguet, John Freebody, O. Dubourg, Waney Squier, Thierry Maisonobe, Tanya Stojkovic, Maria Isabel Leite, Yves Allenbach, S. Herson, Stefen Brady, B. Eymard, David Hilton‐Jones
Publicat 2011Artigo -
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Guidelines for the treatment of autoimmune neuromuscular transmission disorders per Geir Skeie, Slobodan Apostolski, Amelia Evoli, Nils Erik Gilhus, I. K. Hart, Lutz Harms, David Hilton‐Jones, Arthur Melms, Jan J.G.M. Verschuuren, H. W. Horge
Publicat 2006Artigo -
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Clinical Features and Diagnostic Usefulness of Antibodies to Clustered Acetylcholine Receptors in the Diagnosis of Seronegative Myasthenia Gravis per Pedro M. Rodríguez Cruz, Michal Al-Hajjar, Saif Huda, Leslie Jacobson, Mark Woodhall, Sandeep Jayawant, Camilla Buckley, David Hilton‐Jones, David Beeson, Angela Vincent, Maria Isabel Leite, Jacqueline Palace
Publicat 2015Artigo -
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IgG-specific cell-based assay detects potentially pathogenic MuSK-Abs in seronegative MG per Saif Huda, Patrick Waters, Mark Woodhall, Maria Isabel Leite, Leslie Jacobson, Anna De Rosa, Michelangelo Maestri, Roberta Ricciardi, Jeannine M. Heckmann, Angelina Maniaol, Amelia Evoli, Judy Cossins, David Hilton‐Jones, Angela Vincent
Publicat 2017Artigo -
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Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland per Boglárka Bánsági, Thalia Antoniadi, Sarah Burton‐Jones, Sinéad M. Murphy, John C. McHugh, Michael Alexander, Richard A. Wells, Joanna P. Davies, David Hilton‐Jones, Hanns Lochmüller, Patrick F. Chinnery, Rita Horváth
Publicat 2015Artigo -
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Chronic pain has a strong impact on quality of life in facioscapulohumeral muscular dystrophy per Germán Morís, Libby Wood, Roberto Fernández‐Torrón, José Andrés González Coraspe, Chris Turner, David Hilton‐Jones, Fiona Norwood, Tracey Willis, Matt Parton, Mark Rogers, Simon Hammans, Mark Roberts, Elizabeth Househam, Maggie Williams, Hanns Lochmüller, Teresinha Evangelista
Publicat 2017Artigo -
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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 USA per Mark Price, Victoria Barghout, Olivier Benvéniste, Lisa Christopher‐Stine, Alastair Corbett, Marjolein Visser, David Hilton‐Jones, John T. Kissel, Thomas E. Lloyd, Ingrid E. Lundberg, Francis Mastaglia, Tahseen Mozaffar, Merrilee Needham, Jens Schmidt, Kumaraswamy Sivakumar, Carla DeMuro, Brian S. Tseng
Publicat 2016Artigo
Eines de cerca:
Matèries relacionades
Medicine
Internal medicine
Biology
Genetics
Gene
Mutation
Pathology
Immunology
Myasthenia gravis
Myopathy
Disease
Inclusion body myositis
Antibody
Myositis
Pediatrics
Environmental health
Gastroenterology
Missense mutation
Phenotype
Population
Anatomy
Lambert-Eaton myasthenic syndrome
Molecular biology
Pathological
Polymyositis
Receptor
Surgery
Acetylcholine receptor
Biochemistry
Cell biology