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1.
Rev Med Inst Mex Seguro Soc ; 55(3): 380-381, 2017.
Artigo em Espanhol | MEDLINE | ID: mdl-28440995

RESUMO

Before 1950, cases of necrotizing vasculitis were commonly published in journals of pathology. Most of these cases were designated as polyarteritis nodosa. In 1952, the pathologist Pearl Zeek critically reviewed and summarized the literature dealing with polyarteritis nodosa and first grouped the different types of necrotizing vasculitis. But she omitted some types of not well-characterized vasculitis, among them granulomatosis with polyangiitis (Wegener's granulomatosis).


Antes de 1950, los casos de vasculitis necrosantes comúnmente se publicaban en revistas de patología. La mayoría de los casos se designaban poliarteritis nodosa. En 1952, la patóloga Pearl Zeek revisó críticamente la literatura sobre poliarteritis nodosa y por primera vez agrupó los diferentes tipos de vasculitis necrosantes. Sin embargo, omitió algunos tipos de vasculitis, hasta entonces no bien caracterizadas, entre las cuales estaba la granulomatosis con poliangeítis (antes granulomatosis de Wegener).


Assuntos
Granulomatose com Poliangiite/história , Alemanha , Granulomatose com Poliangiite/diagnóstico , História do Século XX , Humanos , New York
2.
Nephrol Dial Transplant ; 30 Suppl 1: i8-13, 2015 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-25805749

RESUMO

In this essay we describe a number of the known and not so known experiences of the early anti-neutrophil cytoplasmic antibodies (ANCAs) days, explaining why and how we reached consensus on the standard indirect immunofluorescence (IIF) techniques, the naming of the two principal C- and P-ANCA patterns, why we chose to use IIF as the standard technique, how the solid phase assays have developed and where we stand today, the use of ANCA for diagnosis and the importance of using several techniques for that purpose, how ANCA titres are related to disease activity and the clinical impact of this, and finally the implications of ANCA being a natural, polyclonal antibody response against various epitopes in relation to diagnostics and disease patterns.


Assuntos
Anticorpos Anticitoplasma de Neutrófilos/história , Biomarcadores , Técnica Indireta de Fluorescência para Anticorpo/história , Granulomatose com Poliangiite/história , Anticorpos Anticitoplasma de Neutrófilos/sangue , Autoantígenos/história , Autoantígenos/imunologia , Técnica Indireta de Fluorescência para Anticorpo/normas , Granulomatose com Poliangiite/imunologia , História do Século XX , História do Século XXI , Humanos
7.
Ned Tijdschr Geneeskd ; 156(34): A4557, 2012.
Artigo em Holandês | MEDLINE | ID: mdl-22914056

RESUMO

This article describes the history and significance of the eponym 'Wegener'. After the American College of Chest Physicians awarded Wegener with the Master Clinician Award, discussion about his Nazi past arose. Should the eponym 'Wegener' be maintained?


Assuntos
Granulomatose com Poliangiite/história , Socialismo Nacional/história , Alemanha , História do Século XX
8.
Oral Dis ; 18(2): 214-6, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22247971

RESUMO

The use of eponyms has long been contentious, but many remain in common use, as discussed elsewhere (Editorial: Oral Diseases. 2009: 15; 185). The use of eponyms in diseases of the head and neck is found mainly in specialties dealing with medically compromised individuals (paediatric dentistry, special care dentistry, oral and maxillofacial medicine, oral and maxillofacial pathology and oral, oral and maxillofacial radiology and maxillofacial surgery) and particularly by hospital-centred practitioners. This series has selected some of the more recognized relevant eponymous conditions and presents them alphabetically. The information is based largely on data available from MEDLINE and a number of internet websites as noted below: the authors would welcome any corrections. This document summarizes data about Wegener granulomatosis.


Assuntos
Epônimos , Granulomatose com Poliangiite/história , Anticorpos Anticitoplasma de Neutrófilos/imunologia , Alemanha , Granulomatose com Poliangiite/patologia , História do Século XIX , História do Século XX , Humanos
13.
Lupus ; 19(7): 781-2, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20305047
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