Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Gal Meidan"'
Autor:
Anat Shnaiderman-Torban, Amir Steinman, Gal Meidan, Yossi Paitan, Wiessam Abu Ahmad, Shiri Navon-Venezia
Publikováno v:
Frontiers in Microbiology, Vol 10 (2019)
Extended spectrum beta-lactamases and AmpC-producing Enterobacteriaceae (ESBL/AmpC-E) have become a great concern in both human and veterinary medicine. One setting in which this risk could be particularly prominent is petting zoos, in which humans,
Externí odkaz:
https://doaj.org/article/3d0481f6dc784d6ebfc404d9dd6f740d
Autor:
Tzipora C. Falik Zaccai, Limor Kalfon, Aharon Klar, Mordechai Ben Elisha, Haggit Hurvitz, Galina Weingarten, Emelia Chechik, Vered Fleisher Sheffer, Raid Haj Yahya, Gal Meidan, Eva Gross‐Kieselstein, Dvora Bauman, Sylvia Hershkovitz, Yuval Yaron, Avi Orr‐Urtreger, Efrat Wertheimer
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 2, Iss 1, Pp 64-72 (2014)
Abstract Donohue syndrome (DS) is a rare and lethal autosomal recessive disease caused by mutations in the insulin receptor (INSR) gene, manifesting marked insulin resistance, severe growth retardation, hypertrichosis, and characteristic dysmorphic f
Externí odkaz:
https://doaj.org/article/039df10551044c4eb1c6ec8e2471ca8a
Autor:
Dvora Bauman, Tzipora C. Falik Zaccai, Sylvia Hershkovitz, Raid Haj Yahya, Mordechai Ben Elisha, Haggit Hurvitz, Gal Meidan, Eva Gross-Kieselstein, Avi Orr-Urtreger, Aharon Klar, Vered Fleisher Sheffer, Emelia Chechik, Galina Weingarten, Limor Kalfon, Yuval Yaron, Efrat Wertheimer
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 2, Iss 1, Pp 64-72 (2014)
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine
Donohue syndrome (DS) is a rare and lethal autosomal recessive disease caused by mutations in the insulin receptor (INSR) gene, manifesting marked insulin resistance, severe growth retardation, hypertrichosis, and characteristic dysmorphic features.