Zobrazeno 1 - 7
of 7
pro vyhledávání: '"33"'
Autor:
Micol Frassi, Rossella Reggia, Mara Taraborelli, Marco Taglietti, Angela Tincani, Francesca Dall'Ara, Franco Franceschini, Laura Andreoli
Publikováno v:
Lupus. 23:1255-1258
Objective To assess the prevalence of disease- and therapy-related complications and of the organ damage after a follow-up of 15 years or more in patients with primary antiphospholipid syndrome (PAPS). Methods Medical records of patients prospectivel
Autor:
Eloisa Bonfa, C. A. A. Silva, A C Medeiros Ribeiro, V dos Santos T Viana, J Freire de Carvalho, D Martins de Medeiros, C. Bueno
Publikováno v:
Lupus. 23:1412-1416
Objective The objective of this report is to conduct short- and long-term evaluation of a large panel of antiphospholipid (aPL) autoantibodies following pandemic influenza A/H1N1 non-adjuvant vaccine in primary antiphospholipid syndrome (PAPS) patien
Publikováno v:
Lupus. 14:129-136
The antiphospholipid syndrome (APS) is characterized by the presence of antiphospholipid antibodies (aPL) in patients with thromboembolic complications. In APS, most aPL are autoantibodies to β2-glycoprotein I and prothrombin, which play a major rol
Autor:
P. Yaffe, Asher Ornoy, Y Shoenfeld, Zivanit Ergaz, Gil Goldzweig, Michael B. Blank, N. Patlas, A. Cohen, Dror Mevorach
Publikováno v:
Lupus. 19(14)
We evaluated the embryolethality and embryotoxicity of sera from patients suffering from autoimmune diseases during remission on post-implantation rat embryos cultured on these sera and determined the association between the patients’ clinical hist
Publikováno v:
Lupus. 16(2)
Seventy-two patients with antiphospholipid antibodies (aPL), with or without antiphospholipid syndrome (APS), were studied for detection of heparin-PF4-induced antibodies (HPIA) using a commercial kit (Asserachrom® HPIA) PF4-dependant enzyme-linked
Autor:
A.J. Chamorro, Jordi Yagüe, J C Botero, Miguel Ingelmo, S Segura, Ricard Cervera, Manuel Ramos-Casals, Josep Font, G Salvador, M T Campoamor
Publikováno v:
Lupus. 13(10)
The objective of the study was to analyse the prevalence and clinical significance of hypocomplementemia in a large series of patients diagnosed either with systemic lupus erythematosus (SLE) or with primary antiphospholipid syndrome (APS) and its as
Autor:
A F Masri, Nora Pashayan, Thurayya Arayssi, S Shaar, Samir F. Atweh, Stella Major, Imad Uthman, R Chidiac-Tannoury
Publikováno v:
Lupus. 11(11)
The objective of the study was to describe the practice patterns of the antiphospholipid syndrome (APS) as compared with consensus guidelines for diagnosis and to determine whether practice patterns correlate with patient demographics and physician s