Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Nizar Jiries"'
Publikováno v:
Brain Sciences, Vol 14, Iss 9, p 862 (2024)
Delirium is often the first symptom of incipient acute illness or complications and must therefore be detected promptly. Nevertheless, routine screening for delirium in acute care hospital wards is often inadequate. We recently implemented a simple,
Externí odkaz:
https://doaj.org/article/618619ad6a8b49f5b39a8ee1dd52c3f5
Autor:
Ilana Levy, Aharon Kessel, Alona Paz, Anna Solopov, Boaz Weller, Doron Rimar, Idit Dobrecky-Mery, Liliana Schliamser, Milian Croitoru, Nizar Jiries, Shira Ginsberg, Tamar Tadmor
Publikováno v:
Journal of Clinical and Medical Case Reports. :1-4
Hypereosinophilic syndrome (HES) is a rare and potentially life-threatening disorder. While many conditions can cause eosinophilia, it can also be provoked by rarer diseases such as vasculitis or myeloproliferative disorders. Here we present an almos
Autor:
Shira Ginsberg, Michael Rozenbaum, Doron Rimar, Itzhak Rosner, Gleb Slobodin, Abid Awisat, Nizar Jiries, Haya Hussein, Nina Boulman, Lisa Kaly, Amal Silawy
Publikováno v:
Clinical Rheumatology. 39:571-574
Crowned dens syndrome (CDS) is defined as acute cervical or occipital pain due to a local inflammatory reaction related to calcifications in the ligaments surrounding the odontoid process. Virtually, all previous descriptions of CDS have related to c
Autor:
Zahava Vadasz, Abid Awisat, Michael Rozenbaum, Marc Humbert, Lisa Kaly, Nizar Jiries, Michael Lurie, Christophe Guignabert, Doron Rimar, Alexandra Balbir Gurman, Shira Ginsberg, Yair Goldberg, Karina Zilber, Francesca Ingegnoli, Gleb Slobodin, Dominique Farge, Pier Luigi Meroni, Itzhak Rosner, Maria-Rosa Ghigna, Yair Levi, Nina Boulman, Yolada Braun-Moscovici
Publikováno v:
Rheumatology. 58:1547-1555
Objective Lysyl oxidase (LOX) is an extracellular enzyme that cross-links collagen fibrils. LOX was found to be increased in serum of SSc patients and was suggested to be related to skin fibrosis, yet a vascular source of LOX has been demonstrated in
Publikováno v:
Rheumatology (Oxford, England). 60(3)
Publikováno v:
Acta Haematologica. 139:7-11
Acquired amegakaryocytic thrombocytopenia (AAT), a rare entity characterized by severe thrombocytopenia and the absence of megakaryocytes in the bone marrow, may mimic or precede the diagnosis of aplastic anemia (AA). Here, we describe a patient who
Autor:
Doron Rimar, Karina Zilber, Ofrat Beyar-Katz, Nizar Jiries, Abid Awisat, Gleb Slobodin, Lisa Kaly, Itzhak Rosner, Michel Rozenbaum, Nina Boulman, Shira Ginsberg
Publikováno v:
Seminars in Arthritis and Rheumatism. 46:367-371
Autoinflammatory diseases are characterized by recurrent episodes of fever and localized or systemic inflammation and are caused by monogenic defects of innate immunity. The skin is commonly involved with various manifestations including erysipelas l
Autor:
Amal Silawy, Doron Rimar, Michael Rosenbaum, Nizar Jiries, Gleb Slobodin, Lisa Kaly, Shira Ginsberg, Haya Husseuin, Nina Boulman, Itzhak Rosner, Irina Novofastovski, Abid Awisat
Publikováno v:
Saturday, 15 June 2019.
Background Polyarteritis Nodosa (PAN) is a necrotizing vasculitis predominantly affecting medium and small size arteries (1). Cyclophosphamide, a drug with narrow therapeutic range and poor safety profile, constitutes the treatment of choice for PAN
Autor:
Amal Silawy, Michael Rosenbaum, Elias Toubi, Itzhak Rosner, Merav Lidar, Shira Ginsberg, Doron Rimar, Lisa Kaly, Zahava Vadasz, Abid Awisat, Nizar Jiries, Nina Boulman, Gleb Slobodin, Nasrin Eiza
Publikováno v:
Abstracts Accepted for Publication.
Background Semaphorins are a family of proteins, involved in axon-guidance, malignancy spread and angiogenesis. Semaphorin 3A (sema3A) is recognized also as “immune semaphorin”, it is expressed on regulatory T cells and has been shown to enhance
Autor:
Irina Novofastovski, Abid Awisat, Haya Hussein, Doron Rimar, Lisa Kaly, Gleb Slobodin, Michael Rozenbaum, Shira Ginsberg, Itzhak Rosner, Nina Boulman, Nizar Jiries, Amal Silawy
Publikováno v:
Clinical rheumatology. 38(10)
Polyarteritis nodosa (PAN) is a necrotizing vasculitis predominantly affecting medium and small size arteries. Cyclophosphamide, a drug with narrow therapeutic range and poor safety profile, constitutes the treatment of choice for PAN vasculitis with