Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Zufit Hexner-Erlichman"'
Autor:
Zufit Hexner-Erlichman, Maria Veiga-da-Cunha, Yoav Zehavi, Zahava Vadasz, Adi D. Sabag, Sameh Tatour, Ronen Spiegel
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
BackgroundGlycogen storage disease type 1b (GSD1b) is an ultra-rare autosomal recessive disorder, caused by mutations in SLC37A4 gene. Affected patients present with episodes of fasting hypoglycemia and lactic acidosis, hepatomegaly, growth retardati
Externí odkaz:
https://doaj.org/article/9ddd4db544c94b418be2850a58e52445
Autor:
Zufit Hexner-Erlichman, Boris Fichtman, Yoav Zehavi, Morad Khayat, Haneen Jabaly-Habib, Lee S. Izhaki-Tavor, Moshe Dessau, Orly Elpeleg, Ronen Spiegel
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Cleft lip and/or cleft palate are a common group of birth defects that further classify into syndromic and non-syndromic forms. The syndromic forms are usually accompanied by additional physical or cognitive abnormalities. Isolated cleft palate syndr
Externí odkaz:
https://doaj.org/article/087cf9bd0d9e459e85e1bb186eac1b0c
Autor:
Zufit Hexner‐Erlichman, Joanne Yacobovich, Philippe Trougouboff, Moran Avraham‐Kelbert, Harel Eitam, Ronen Spiegel, Shay Yeganeh, Carina Levin
Publikováno v:
eJHaem, Vol 1, Iss 1, Pp 304-308 (2020)
Abstract Autoimmune myelofibrosis (AIMF) is an uncommon cause of myelofibrosis associated with favorable outcome. Primary AIMF, AIMF without a known systemic autoimmune disorder, has been described in adults, but never in children. Here, we present,
Externí odkaz:
https://doaj.org/article/5b8248cb7e8b47b9b4a21f451d5ab2d7
Autor:
Waheeb Sakran, Zufit Hexner-Erlichman, Ronen Spiegel, Hamed Batheesh, Raphael Halevy, Ariel Koren
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-5 (2020)
Abstract Gastroenteritis is common among children. Campylobacter jejuni is one of the main causative bacterial pathogens, together with Shigella, Salmonella and invasive Escherichia coli. Campylobacteriosis is a zoonotic, usually self-limited disease
Externí odkaz:
https://doaj.org/article/de0204269cfc4168aeb31fac7797e528
Autor:
Harel Eitam, Moran Avraham-Kelbert, Ronen Spiegel, Joanne Yacobovich, Carina Levin, Philippe Trougouboff, Zufit Hexner-Erlichman, Shay Yeganeh
Publikováno v:
eJHaem. 1:304-308
Autor:
Zufit, Hexner-Erlichman, Maria, Veiga-da-Cunha, Yoav, Zehavi, Zahava, Vadasz, Adi D, Sabag, Sameh, Tatour, Ronen, Spiegel
Publikováno v:
Frontiers in pediatrics, Vol. 10, no.-, p. 1071464 (2022)
BackgroundGlycogen storage disease type 1b (GSD1b) is an ultra-rare autosomal recessive disorder, caused by mutations in SLC37A4 gene. Affected patients present with episodes of fasting hypoglycemia and lactic acidosis, hepatomegaly, growth retardati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da5d744dd6060518bd2c28546860b3ec
https://hdl.handle.net/2078.1/271398
https://hdl.handle.net/2078.1/271398
Autor:
Raphael Halevy, Ronen Spiegel, Hamed Batheesh, Waheeb Sakran, Ariel Koren, Zufit Hexner-Erlichman
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-5 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-5 (2020)
Gastroenteritis is common among children. Campylobacter jejuni is one of the main causative bacterial pathogens, together with Shigella, Salmonella and invasive Escherichia coli. Campylobacteriosis is a zoonotic, usually self-limited disease that doe