Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Liron Talmi"'
Autor:
Jorik M. van Rijn, Lael Werner, Yusuf Aydemir, Joey M.A. Spronck, Ben Pode-Shakked, Marliek van Hoesel, Elee Shimshoni, Sylvie Polak-Charcon, Liron Talmi, Makbule Eren, Batia Weiss, Roderick H.J. Houwen, Iris Barshack, Raz Somech, Edward E.S. Nieuwenhuis, Irit Sagi, Annick Raas-Rothschild, Sabine Middendorp, Dror S. Shouval
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 21, p 8200 (2020)
Hyaline fibromatosis syndrome (HFS), resulting from ANTXR2 mutations, is an ultra-rare disease that causes intestinal lymphangiectasia and protein-losing enteropathy (PLE). The mechanisms leading to the gastrointestinal phenotype in these patients ar
Externí odkaz:
https://doaj.org/article/807faf00ac10468ebb777592b46fbbb6
Autor:
Yaniv Lustig, Or Kriger, Carmit Cohen, Galia Barkai, Asaf Biber, Liron Talmi, Gili Regev-Yochay, Sharon Amit, Shiraz Gefen-Halevi, Bella Mechnik
Publikováno v:
Clinical Microbiology and Infection
Objective The role of school closure in mitigating coronavirus disease 2019 (COVID-19) transmission has been questioned. In our medical centre, during a 9-week national lockdown, an alternative school was opened for health-care workers' (HCW) childre
Autor:
Marliek van Hoesel, Jorik M. van Rijn, Batia Weiss, Makbule Eren, Iris Barshack, Roderick H. J. Houwen, Dror S. Shouval, Joey M A Spronck, Liron Talmi, Annick Raas-Rothschild, Raz Somech, Sabine Middendorp, Edward E. S. Nieuwenhuis, Elee Shimshoni, Sylvie Polak-Charcon, Ben Pode-Shakked, Irit Sagi, Yusuf Aydemir, Lael Werner
Publikováno v:
International Journal of Molecular Sciences
Volume 21
Issue 21
International Journal of Molecular Sciences, Vol 21, Iss 8200, p 8200 (2020)
Volume 21
Issue 21
International Journal of Molecular Sciences, Vol 21, Iss 8200, p 8200 (2020)
Hyaline fibromatosis syndrome (HFS), resulting from ANTXR2 mutations, is an ultra-rare disease that causes intestinal lymphangiectasia and protein-losing enteropathy (PLE). The mechanisms leading to the gastrointestinal phenotype in these patients ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0666c4b30100251874f673eacb2849e6
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-427181
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-427181
Publikováno v:
The Israel Medical Association journal : IMAJ. 20(7)