Immunosuppressant and immunomodulatory treatment for dermatomyositis and polymyositis

PA Gordon, JB Winer, JE Hoogendijk… - Cochrane Database …, 2012 - cochranelibrary.com
Background Idiopathic inflammatory myopathies are chronic diseases with significant
mortality and morbidity. Whilst immunosuppressive and immunomodulatory therapies are …

[HTML][HTML] Guillain Barré syndrome

JB Winer - Molecular pathology, 2001 - ncbi.nlm.nih.gov
Guillain Barré syndrome is one of the best examples of a post infectious immune disease
and offers insights into the mechanism of tissue damage in other more common autoimmune …

The American College of Rheumatology nomenclature and case definitions for neuropsychiatric lupus syndromes

MH Liang, M Corzillius, SC Bae, RA Lew… - Arthritis and …, 1999 - pure.johnshopkins.edu
Objective. To develop a standardized nomenclature system for the neuropsychiatric
syndromes of systemic lupus erythematosus (NPSLE). Methods. An international …

[HTML][HTML] An update in guillain-barré syndrome

JB Winer - Autoimmune diseases, 2014 - hindawi.com
Guillain-Barré syndrome (GBS) was first described in 1916 (Guillain G, 1916) and is
approaching its 100th anniversary. Our knowledge of the syndrome has hugely expanded …

A prospective study of acute idiopathic neuropathy. II. Antecedent events.

JB Winer, RA Hughes, MJ Anderson… - Journal of Neurology …, 1988 - jnnp.bmj.com
The incidence of antecedent events and serological evidence of preceding infection were
studied in 100 patients with acute idiopathic neuropathy and age and sex matched control …

A prospective study of acute idiopathic neuropathy. I. Clinical features and their prognostic value.

JB Winer, RA Hughes, C Osmond - Journal of Neurology …, 1988 - jnnp.bmj.com
A prospective study in South-East England during 15 months in 1983-1984 recruited 100
patients with acute idiopathic neuropathy. After 12 months 67% had recovered completely …

Coexistent hereditary and inflammatory neuropathy

L Ginsberg, O Malik, AR Kenton, D Sharp, JR Muddle… - Brain, 2004 - academic.oup.com
Classically, the course of Charcot–Marie–Tooth (CMT) disease is gradually progressive. We
describe eight atypical patients who developed acute or subacute deterioration. Seven of …

Serum kynurenine-to-tryptophan ratio increases with progressive disease in HIV-infected patients

M Huengsberg, JB Winer, M Gompels… - Clinical …, 1998 - academic.oup.com
An alternative pathway of Trp metabolism involves the conversion of Trp to kynurenine by
indoleamine-2, 3-dioxygenase, which leads to synthesis of the neurotoxin, quinolinic acid …

Titin founder mutation is a common cause of myofibrillar myopathy with early respiratory failure

G Pfeffer, R Barresi, IJ Wilson, SA Hardy… - Journal of Neurology …, 2014 - jnnp.bmj.com
Objective Titin gene (TTN) mutations have been described in eight families with hereditary
myopathy with early respiratory failure (HMERF). Some of the original patients had features …

A clinicopathological study of the Guillain-Barré syndrome: nine cases and literature review

M HONAVAR, JKJ Tharakan, RAC Hughes… - Brain, 1991 - academic.oup.com
The postmortem findings are reported from 9 cases of the Guillain-Barré syndrome with
survival between 10 days and 1 yr. In 8 cases there was multifocal loss of myelin throughout …