Maladie de Behçet

N Filali-Ansary, S HANNAT, H AL HALOUI… - Maroc Médical, 2002 - revues.imist.ma
Résumé La maladie de Behçet est une vascularite à prédominance veineuse. Elle a été
décrite initialement comme une triade clinique associant aphtose buccale, aphtose génitale …

[PDF][PDF] BEHÇET HASTALARINDA KIR GEN POLİMORFİZMİNİN İNCELENMESİ

Z TOPKARCI, G AZİZLERLİ - nek.istanbul.edu.tr
Eğitimim boyunca beni destekleyen, her zaman yanımda olan canım anneme, babama, kız
kardeşime ve ağabeyim Uzm. Dr. Mehmet MELĐKOĞLU'na, sabır ve hoşgörü ile bana her …

[PDF][PDF] Intracardiac Thrombosis and Endomyocardial Fibrosis in Behcet's Disease

S El Bouhali, A Soufiani, Z Idrissi… - REVUE MAROCAINE …, 2019 - smcmaroc.org
Behçet's Disease (BD) is a rare multisystemic inflammatory disorder classified as a systemic
vasculitis of unknown aetiology. Cardiac involvement is rare in BD (6%) and considered a …

Hemoptysis, history of oral ulcers, and abnormal chest radiograph in a 64-year-old man

MI Schwarz - Chest, 2003 - journal.chestnet.org
A 64-year-old man presents with 2 months of intermittent blood-tinged sputum and cough.
He also noted mild dyspnea and subjective fevers. For the past 30 years, he has noted self …

Incomplete intestinal obstruction as the possible main complaint in Behcet's disease after surgery for recurrent abdominal aortic pseudoaneurysms: a case report and …

F Jiang, H Xiang, ZY Peng - BMC Cardiovascular Disorders, 2018 - Springer
Background Behcet's disease (BD) is a systemic vasculitis characterized by oral and genital
aphthosis, and ocular and skin lesions. The disease is involved in vascular, gastrointestinal …

Recurrent panuveitis. First manifestation of Behçet's syndrome in childhood: First manifestation of Behçet's syndrome in childhood

B Mock, S Richter, G Hein, U Wollina - Der Ophthalmologe, 1998 - Springer
Background: Behçet's disease is a rare systemic vasculitis of unknown etiology. The typical
symptoms includ recurrent oral and/or genital aphthous lesions, iridocyclitis (historically with …

HLA-B* 51 pozitif behçet hastalarında HLA-B* 51 allellerinin araştırılması

S Topçu - 2018 - search.proquest.com
Behçet hastalığı (BH), Türk Dermatoloji Profesörü Hulusi Behçet tarafından 1937 yılında
bulunmuştur. Tekrarlayan oral aft, genital yaralar ve üveit ile birlikte üç semptomlu anlatılan …

Ocular Manifestations of Pediatric Rheumatic Diseases

RC Walton, C Lin, RW Enzenauer - The Eye in Pediatric Systemic Disease, 2017 - Springer
Ocular manifestations are relatively common among children with rheumatic diseases. Many
of these disorders may lead to vision loss and life-long disability if not detected and treated …

[PDF][PDF] Enfermedad de Behçet

CG William, GA Javier, HE Jorge - Revista Cubana de Reumatología - researchgate.net
RESUMEN La Enfermedad de Behçet o Behcet es una enfermedad inflamatoria crónica,
recurrente, multisistémica, de etiología desconocida. Todas las manifestaciones son …

[PDF][PDF] Familial vs sporadic rheumatoid arthritis (RA). No differences in disease severity, course and prognosis detected

TRDJ Radstake, A Balsa, LCM Piet… - Elucidation of genetic … - repository.ubn.ru.nl
Rheumatoid arthritis (RA) is a chronic, inflammatory, autoimmune disease mainly affecting
the synovial joints with a preference for the small joints of the hands and feet RA has a …