Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Hagit Yonath"'
Autor:
Shiraz Halevy, Gill Smollan, Olga Feld-Simon, Amitai Segev, Tal Zilberman-Daniels, O. Feld-Simon, Dalit Shachar, Gili Regev-Yochay, Adi Brom, C. Cohen, Ronen Fluss, Amnah Jbarien, Sharon Beni, Naty Keller, Eyal Meltzer, Mayan Gilboa, M. Gilboa, I. Tal, Nani Pinas-Zade, Howard Amital, Natasha Blausov, Hagit Yonath, E. Houri-Levi, Amit Hupert, Leonid Maizels, Carmit Rubin, Shmuel Stienlauf, Eyal Zimlichman, G. Regev-Yochay, Ilan Ben-Zvi, G. Rahav, A. Brom, Ilana Tal, Marina Romiantsev, Galia Rahav, Shoshi Segal, Esther Houri Levi, Kassem Sharif, S. Segal, Carmit Cohen, Y. Eden-Friedman, Shir Raibman-Spector, Yehudit Eden-Friedman, Haim Mayan, Avshalom Leibowitz, Gadi Segal
Publikováno v:
Clinical Microbiology and Infection. 26:1052-1057
Objectives The aim was to compare the burden of environmental shedding of toxigenic Clostridioides difficile among asymptomatic carriers, C. difficile-infected (CDI) patients and non-carriers in an inpatient non-epidemic setting. Methods C. difficile
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0ac6be5182715054a087a6eb7be2f43
https://doi.org/10.1016/j.cmi.2019.12.011
https://doi.org/10.1016/j.cmi.2019.12.011
Autor:
Ruth Eliahou, Mark Andrew Hellmann, Lili Bazak, Hagit Yonath, Oded Shor, Lina Basel-Salmon, Elon Pras, Adi Wilf-Yarkoni, Avi Fellner, Lior Greenbaum, Yael Goldberg, Shiri Shkedi-Rafid, Felix Benninger, Hadas Stiebel-Kalish
Publikováno v:
Neurology: Genetics
article-version (Version of Record) 3
article-version (Version of Record) 3
ObjectiveTo describe the WFS1 c.1672C>T; p.R558C missense variant, found in 1.34% of Ashkenazi Jews, that has a relatively mild phenotype and to use computational normal mode analysis (NMA) to explain the genotype-phenotype relationship.MethodsThe cl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a71d2eb9091b49fc9abb72b7645208a2
http://europepmc.org/articles/PMC7983365
http://europepmc.org/articles/PMC7983365
Publikováno v:
Clinical Rheumatology. 37:1257-1263
Inflammatory myopathies are a clinically diverse group of diseases, in which the detection of particular autoantibodies may facilitate diagnosis, treatment, and prognosis. The aim of this report is to summarize our experience with specific autoantibo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aa6ce5d63722efa3c8342ffe4f86575
https://doi.org/10.1007/s10067-018-4032-3
https://doi.org/10.1007/s10067-018-4032-3
Autor:
Amihood Singer, Ehud Kaliner, Dorit Lev, Ayala Frumkin, Lena Sagi-Dain, Tzipora C. Falik-Zaccai, Shay Ben Shachar, Hagit Yonath, Michal Feingold-Zadok, Idit Maya
Publikováno v:
European journal of obstetrics, gynecology, and reproductive biology. 222
Objective To examine the risk for clinically significant chromosomal microarray analysis (CMA) among fetuses with apparently isolated horseshoe kidney. Methods Data from all CMA analyses performed due to isolated horseshoe kidney reported to the Isra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1165bb47a6613f62f560716af7c33b88
https://pubmed.ncbi.nlm.nih.gov/29367169
https://pubmed.ncbi.nlm.nih.gov/29367169
Autor:
Hana Poran, Haike Reznik-Wolf, Tomer Ziv-Baran, Ori Eyal, Hagit Yonath, Michal Berkenstadt, Lior Greenbaum, Elon Pras
Publikováno v:
Molecular Genetics & Genomic Medicine
Background This study summarizes the results of prenatal diagnosis due to a history of de novo mutation in a previous pregnancy, in a tertiary center in Israel, over a 10‐year period. Methods We sorted all cases of de novo mutations from a pool of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3778e2bbb892dda166e70862fa24fea3
https://doi.org/10.1002/mgg3.573
https://doi.org/10.1002/mgg3.573
Publikováno v:
Clinical rheumatology. 25(5)
Transverse myelitis is a rare manifestation of antiphospholipid syndrome, usually secondary to systemic lupus erythematosus (Rheum Dis Clin North Am 20:129–158, 1994). Only about 110 reports of this complication have been reported (Lupus 10:851–8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5c7544af3821a96d4da89a3568e191b
https://pubmed.ncbi.nlm.nih.gov/16234992
https://pubmed.ncbi.nlm.nih.gov/16234992