Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Hanan Gur"'
Publikováno v:
Clinical Biochemistry. 42:1628-1634
Patients with acute decompensated heart failure (ADHF) are frequently treated with unnecessary antibiotics since they are confused with pneumonia patients.To study the efficacy of measuring C-reactive protein (CRP) levels on admission and CRP velocit
Autor:
Itamar Goldstein, Michael Ehrenfeld, Esther Rosenthal, Ilan Bank, Alexander Koltakov, Pnina Langevitz, Hanan Gur, Shomron Ben-Horin
Publikováno v:
Journal of Clinical Immunology. 27:580-588
The alpha1beta1 integrin, very late antigen (VLA)-1, characterizes collagen adherent interferon (IFN) gamma producing memory T cells in inflamed synovium. We now report that the mean percentage of VLA-1+ T cells is significantly lower among periphera
Publikováno v:
Seminars in Arthritis and Rheumatism. 32:189-195
Objective: To define characteristics of sternoclavicular infection (SCI) in previously healthy patients. Methods: SCI in a previously healthy man is reported along with 4 similar cases found by surveying the hospital's database; 22 previously reporte
Publikováno v:
Seminars in Arthritis and Rheumatism. 30:403-410
Background and Objective: Renal failure, pulmonary hypertension, and interstitial lung disease are major causes of morbidity and mortality in systemic sclerosis (SSc). However, the concomitant occurrence of pulmonary hemorrhage associated with acute
Autor:
Tinaztepe K, Nesrin Besbas, Hanan Gur, Eldad Ben-Chetrit, Meral Calguneri, Tekin Akpolat, Seza Ozen, Aydin Turkmen, Ilkser Akpolat, Aysin Bakkaloglu, Cetin Turgan, Murat Danaci
Publikováno v:
Seminars in Arthritis and Rheumatism. 30:281-287
Background: Familial Mediterranean Fever (FMF) is caused by mutations in the gene encoding pyrin and is characterized by self-limited, recurrent attacks of fever and serositis. Vasculitis has been increasingly reported in FMF. A study evaluating the
Publikováno v:
Journal of Autoimmunity. 13:3-10
The bm12 mutation in the class II I-A(b)molecule can profoundly influence experimental autoimmune disease, enhancing the development of systemic lupus erythematosus-like syndromes in NZB.H-2(bm12)mice or, conversely, abolishing the susceptibility of
Publikováno v:
Scopus-Elsevier
Background The clinical manifestations and outcome of all adult patients with polyarteritis nodosa (PAN), allocated during a 15- year period in the largest medical center in Israel, were examined. Methods A retrospective analysis of patients with PAN
Publikováno v:
Journal of Neuroimmunology. 96:9-20
The effect of the bm12 mutation on susceptibility to MOG-induced EAE, TCR repertoire and fine epitope specificity of the encephalitogenic T-cells, was assessed. prMOG35-55 was encephalitogenic for H-2 bm12 and H-2 b mice. Despite only minor differenc
Autor:
Yoav Goor, Marina Anouk, Ori Elkayam, Hanan Gur, Jonathan Wollman, Doron Boltin, Jacob N. Ablin, Dan Caspi
Publikováno v:
Rheumatology International. 27:985-987
The diagnosis of Takayasu arteritis requires a high degree of clinical suspicion. We herein present two cases of Takayasu arteritis that demonstrate two important aspects of the disease, which leaded to a significant delay in the diagnosis. The first
Autor:
Ilan Bark, Michael Ehrenfeld, Carrait Rachima Maoz, Pnina Langevitz, Avi Livneh, Menachemem Sadeh, Zvia Blumstein, Hanan Gur
Publikováno v:
Seminars in Arthritis and Rheumatism. 27:319-324
Objectives: Dermatomyositis and polymyositis (DM/PM) are associated with neoplasms. The aim of the present study is to compare our experience in Israel with other published data. Methods: Thirty-five adult patients with DM/PM, admitted to Sheba Medic