Zobrazeno 1 - 10
of 39
pro vyhledávání: '"D, Sean Riminton"'
Publikováno v:
BMJ Neurology Open, Vol 4, Iss 1 (2022)
Case A 39-year-old man with thymoma-associated acetylcholine receptor antibody myasthenia gravis (MG) presented with fevers, night sweats, abdominal pain and weight loss. Marked splenomegaly and intra-abdominal lymphadenopathy were found. Biopsies co
Externí odkaz:
https://doaj.org/article/437740eac3a6475c91745ad97441b311
Publikováno v:
BMJ neurology open. 4(1)
A 39-year-old man with thymoma-associated acetylcholine receptor antibody myasthenia gravis (MG) presented with fevers, night sweats, abdominal pain and weight loss. Marked splenomegaly and intra-abdominal lymphadenopathy were found. Biopsies confirm
Publikováno v:
Journal of neuroimmunology. 369
Neurosarcoidosis is an important diagnosis to exclude in the work-up for suspected multiple sclerosis (MS). The distinction between the two conditions is usually possible due to characteristic clinical manifestations, magnetic resonance imaging (MRI)
Autor:
Adrian P. Grech, D. Sean Riminton, Melinda J. Gabor, Charles L. Hardy, Jonathon D. Sedgwick, Dale I. Godfrey
Publikováno v:
Clinical and Developmental Immunology, Vol 8, Iss 1, Pp 61-74 (2000)
Externí odkaz:
https://doaj.org/article/8455f4a48fe04933857eb7660b9d0d8a
Publikováno v:
BMJ Neurology Open. 4:e000285
CaseA 39-year-old man with thymoma-associated acetylcholine receptor antibody myasthenia gravis (MG) presented with fevers, night sweats, abdominal pain and weight loss. Marked splenomegaly and intra-abdominal lymphadenopathy were found. Biopsies con
Publikováno v:
Multiple sclerosis and related disorders. 45
Autor:
Umaimainthan Palendira, Carol Low, Anna Chan, Andrew D Hislop, Edwin Ho, Tri Giang Phan, Elissa Deenick, Matthew C Cook, D Sean Riminton, Sharon Choo, Richard Loh, Frank Alvaro, Claire Booth, H Bobby Gaspar, Alessandro Moretta, Rajiv Khanna, Alan B Rickinson, Stuart G Tangye
Publikováno v:
PLoS Biology, Vol 9, Iss 11, p e1001187 (2011)
X-linked lymphoproliferative disease (XLP) is a primary immunodeficiency caused by mutations in SH2D1A which encodes SAP. SAP functions in signalling pathways elicited by the SLAM family of leukocyte receptors. A defining feature of XLP is exquisite
Externí odkaz:
https://doaj.org/article/2f8dac67c92b469bb76a09f459caef5b
Publikováno v:
Musclenerve. 60(3)
Introduction Muscle-specific tyrosine kinase (MuSK) autoantibody related myasthenia gravis is characterized by bulbar and respiratory manifestations, a poor response to anticholinergics, and a generally good response to plasma exchange and rituximab.
Publikováno v:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 67
A case of progressive multifocal leukoencephalopathy (PML) occurring on low dose immunosuppression for systemic lupus erythematosus (SLE) and Sjogren's syndrome (SS) is presented. Neurologic changes in patients with SLE or SS should not be assumed to
Autor:
Stephen W. Reddel, MaiAnh Nguyen, Todd A. Hardy, Michael Barnett, Lai Yin Law, D. Sean Riminton
Publikováno v:
Neurology. 93(9)
The presentation of a patient with brainstem symptoms and signs invokes a number of common and less common differential diagnoses, and accurate diagnosis can be challenging. We review the major immune-mediated and inflammatory syndromes that can affe