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[PDF] Behçet's disease: familial clustering and immunogenetics


P Fietta - Clinical and experimental rheumatology, 2005 - clinexprheumatol.org
ABSTRACT Behçet's disease (BD) is a relapsing, multisystemic inflammatory
disorder, characterized by major symptoms con- sisting of recurrent orogenital
ulcera- tions, eye and skin lesions. Other clini- cal features may include ...
Cited by 10 - Related articles - View as HTML - BL Direct - All 4 versions

IL-10 genotype analysis in patients with Behcet's disease


GR Wallace, E Kondeatis, RW Vaughan, DH … - Human immunology, 2007 - Elsevier
Behçet's disease (BD) is a multisystem inflammatory disease characterized by
recurrent orogenital ulceration, ocular inflammation, and skin lesions. The
etiology of the disease is currently unknown but evidence suggests that ...
Cited by 5 - Related articles - All 4 versions

Neuro-Behçet's disease: epidemiology, clinical characteristics, and management


A Al-Araji, DP Kidd - Lancet Neurology, 2009 - Elsevier
Behçet's disease (BD) is a multisystem relapsing inflammatory disorder of
unknown cause. In neuro-BD (NBD), the CNS can be involved in one or both of two
ways: first, and most commonly, through the development of an ...
Cited by 4 - Related articles - All 16 versions

[PDF] Behçet Hastal›¤› nda Sistemik Tutulum ve Faktör V Leiden Gen Mutasyonu Aras› ndaki‹ liflki


F Cebeci, E Topçu, N Onsun, Ö Su - journalagent.com
Yaz›flflma Adresi/Address for Correspondence: Dr. Filiz Cebeci, Vak›f Gureba
E¤itim ve Araflt›rma Hastanesi, Dermatoloji ve Veneroloji Klini¤i,
‹stanbul, Türkiye E-posta: cebecifiliz@hotmail.com Geliflfl ...
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