Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ofra Goldzweig"'
Autor:
Maskit Bar-Meir, Alex Guri, Max E. Godfrey, Avram R. Shack, Philip J. Hashkes, Ofra Goldzweig, Orli Megged
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-5 (2021)
Abstract To characterize the new SARS-Co-V-2 related multisystem inflammatory syndrome in children (MIS-C) among Israeli children and to compare it with Kawasaki disease (KD). We compared, in two medical centers, the clinical and laboratory character
Externí odkaz:
https://doaj.org/article/e83219188fd34f9cae257c35046eb677
Autor:
Yonatan Butbul Aviel, Philip J. Hashkes, Yotam Dizitzer, Kanteman Inbar, Yackov Berkun, Eli M. Eisenstein, Mohamad Hamad Saied, Ofra Goldzweig, Merav Heshin-Bekenstein, Eduard Ling, Michal Feldon, Rotem Tal, Shiran Pinchevski-Kadir, Irit Tirosh, Liora Harel, Gil Amarilyo, Kfir Kaidar
Publikováno v:
Vaccines, Vol 10, Iss 8, p 1207 (2022)
Introduction: Since the development of COVID-19 vaccines, more than 4.8 billion people have been immunized worldwide. Soon after vaccinations were initiated, reports on cases of myocarditis following the second vaccine dose emerged. This study aimed
Externí odkaz:
https://doaj.org/article/a9352207246046e789d64cfb7d957169
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Juvenile dermatomyositis (JDM) is a multisystem vasculopathy that infrequently presents with acute complications (1). We report here the case of a 12-year-old girl with JDM who developed Thrombotic Thrombocytopenic purpura (TTP) and Purtscher's retin
Externí odkaz:
https://doaj.org/article/8897d1c470544c7f8dca330d0828660c
Abatacept in the treatment of polyarticular JIA: development, clinical utility, and place in therapy
Autor:
Ofra Goldzweig, Philip J Hashkes
Publikováno v:
Drug Design, Development and Therapy, Vol 2011, Iss default, Pp 61-70 (2011)
Ofra Goldzweig1, Philip J Hashkes2,31Rainbow Babies and Children's Hospital, Cleveland, OH, USA; 2Pediatric Rheumatology Unit, Shaare Zedek Medical Center, Jerusalem, Israel; 3Cleveland Clinic Lerner Medical School of Case Western Reserve University,
Externí odkaz:
https://doaj.org/article/b7c20d283c1d4ad894488f564de8b3af
Autor:
Kfir Kaidar, Yotam Dizitzer, Philip J Hashkes, Linda Wagner-Weiner, Melissa Tesher, Yonatan Butbul Aviel, Kanteman Inbar, Yackov Berkun, Eli M Eisenstein, Mohamad Hamad Saied, Ofra Goldzweig, Merav Heshin-Bekenstein, Eduard Ling, Michal Feldon, Yoel Levinsky, Rotem Tal, Liora Harel, Gil Amarilyo
Publikováno v:
Rheumatology.
Objectives To identify predictors of a severe clinical course of multisystem inflammatory syndrome in children (MIS-C), as defined by the need for inotropic support. Methods This retrospective study included patients diagnosed with MIS-C (according t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89112ca8f361d387c420e3d3bc04c2f2
https://doi.org/10.1093/rheumatology/keac692
https://doi.org/10.1093/rheumatology/keac692
Autor:
Ofra Goldzweig, Maskit Bar-Meir, Avram R. Shack, Alex Guri, Philip J. Hashkes, Orli Megged, Max Godfrey
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-5 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-5 (2021)
To characterize the new SARS-Co-V-2 related multisystem inflammatory syndrome in children (MIS-C) among Israeli children and to compare it with Kawasaki disease (KD). We compared, in two medical centers, the clinical and laboratory characteristics of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::227f4c1f0594801b2efbdbcead954b83
http://europepmc.org/articles/PMC8257717
http://europepmc.org/articles/PMC8257717
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2020)
Frontiers in Pediatrics
Frontiers in Pediatrics
Juvenile dermatomyositis (JDM) is a multisystem vasculopathy that infrequently presents with acute complications (1). We report here the case of a 12-year-old girl with JDM who developed Thrombotic Thrombocytopenic purpura (TTP) and Purtscher's retin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe9ebd7646550b494bdf54e24182681d
https://www.frontiersin.org/article/10.3389/fped.2020.00436/full
https://www.frontiersin.org/article/10.3389/fped.2020.00436/full
Autor:
Merav, Lidar, Yael, Brantz, Yael, Shinar, Haike, Reznik-Wolf, Avi, Livneh, Ilan, Ben Zvi, Rinat, Cohen, Yaakov, Berkun, Philip J, Hashkes, Hagit, Peleg, Aharon, Kessel, Gleb, Slobodin, Michael, Rozenbaum, Ofra, Goldzweig, Elon, Pras
Publikováno v:
Clinical and experimental rheumatology. 35(6)
Cryopyrin associated periodic syndromes (CAPS) comprise a spectrum of autoinflammatory disorders of varying severity caused by mutations in the NLRP3 gene. The NLRP3-Q703K allele has been reported both as a functional polymorphism and as a low penetr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e2bb5931ba6c2b2a98bd9822aad7c219
https://pubmed.ncbi.nlm.nih.gov/29148409
https://pubmed.ncbi.nlm.nih.gov/29148409
Publikováno v:
Seminars in arthritis and rheumatism. 43(1)
Objectives Intraarticular corticosteroid injections are an important part of the treatment for juvenile idiopathic arthritis due to the ability to achieve high concentration of the medication in the affected joint, while minimizing potential systemic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2d816964bd97c7dc6edb3cbdced36d5
https://pubmed.ncbi.nlm.nih.gov/23332901
https://pubmed.ncbi.nlm.nih.gov/23332901
Autor:
Judith Barash, Ofra Goldzweig
Publikováno v:
Arthritis and rheumatism. 57(5)
Introduction Juvenile idiopathic arthritis (JIA) is defined as onset of disease at 16 years of age, with arthritis persisting in 1 joint for at least 6 weeks and with active exclusion of other well-defined diseases such as systemic lupus erythematosu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::195b182d6e53b7e48bb1d72d244acd6b
https://pubmed.ncbi.nlm.nih.gov/17530690
https://pubmed.ncbi.nlm.nih.gov/17530690