Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Alison M. Emslie-Smith"'
Publikováno v:
Neurology. 72:2036-2043
The patient first noticed elbow contractures in childhood, and had always had small biceps muscles. He was never able to run as fast as his peers, and described a sensation of muscle tightening if he tried to run or move quickly, but was unaware of o
Publikováno v:
Gastroenterology. 116:959-963
Autor:
Hemlata, Varsani, Susan C, Charman, Charles K, Li, Suely K N, Marie, Anthony A, Amato, Brenda, Banwell, Kevin E, Bove, Andrea M, Corse, Alison M, Emslie-Smith, Thomas S, Jacques, Ingrid E, Lundberg, Carlo, Minetti, Inger, Nennesmo, Elisabeth J, Rushing, Adriana M E, Sallum, Caroline, Sewry, Clarissa A, Pilkington, Janice L, Holton, Lucy R, Wedderburn, Linda, Suffiel
Publikováno v:
Annals of the Rheumatic Diseases
ObjectivesTo study muscle biopsy tissue from patients with juvenile dermatomyositis (JDM) in order to test the reliability of a score tool designed to quantify the severity of histological abnormalities when applied to biceps humeri in addition to qu
Publikováno v:
Journal of Neuropathology and Experimental Neurology. 55:549-562
A number of myopathies whose common denominator is abnormal foci of desmin positivity have been described under the rubrics of spheroid body myopathy, cytoplasmic body myopathy, Mallory body myopathy, myopathy with granulofilamentous inclusions, desm
Publikováno v:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 21(2)
We report a patient with colchicine-induced myoneuropathy. Myoneuropathy is an under-recognized complication of colchicine. The weakness seen in our patient improved fairly rapidly after discontinuation of colchicine.
Publikováno v:
Annals of Neurology. 29:524-528
Specimens of muscle and fascia from 13 patients fulfilling the Centers for Disease Control criteria for the eosinophilia myalgia syndrome (EMS) were studied by quantitative immunocytochemical analysis. The immunolocalization of CD3, CD4, CD8, CD22, a
Autor:
Suely Kazue Nagahashi Marie, Carlo Minetti, Elisabeth J. Rushing, Susan C. Charman, Andrea M. Corse, Lucy R. Wedderburn, Katy Newton, Clarissa Pilkington, Ingrid E. Lundberg, Anthony A. Amato, Janice L. Holton, Charles K. Li, Brian Harding, Jessica E. Hoogendijk, Alison M. Emslie-Smith, Brenda Banwell, Inger Nennesmo, Hemlata Varsani, Kevin E. Bove, Caroline Sewry
Objective To devise and test a system with which to evaluate abnormalities on muscle biopsy samples obtained from children diagnosed with juvenile dermatomyositis (DM). Methods We established an International Consensus Group on Juvenile DM Biopsy and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f3ad717ef020fd08a0e99d8e62834e5
http://hdl.handle.net/11567/222532
http://hdl.handle.net/11567/222532
Publikováno v:
Neurology. 44(12)
1,1'-Ethylidenebis[tryptophan] (EBT), a derivative of L-tryptophan (LT), is a trace contaminant in batches of LT implicated by epidemiologic evidence in the pathogenesis of the eosinophilia-myalgia syndrome (EMS). We treated female Lewis rats with EB
Publikováno v:
Annals of neurology. 27(4)
In adult dermatomyositis 10 muscle specimens with no or minimal histological alterations were compared with 7 that showed typical alterations. Five specimens from patients with inclusion body myositis, 5 from patients with polymyositis, and 8 from no
Publikováno v:
Neurology. 53:1233-1233
Autoantibodies specific for the nicotinic acetylcholine receptor (AChR) of skeletal muscle impair neuromuscular transmission in myasthenia gravis (MG). Autoantibodies specific for alpha3 neuronal AChRs or voltage-gated potassium channels have been re