Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Elias, Assad"'
Autor:
Tal Almagor, Shlomo Almashanu, Ghadir Elias-Assad, Osnat Admoni, Hanna Ludar, Shira London, Shoshana Rath, Alina German, Naama Shwartz, Yardena Tenenbaum-Rakover
Publikováno v:
Endocrine Connections, Vol 13, Iss 12, Pp 1-9 (2024)
Objectives: The incidence of congenital hypothyroidism (CH) has increased worldwide over the last decades, mainly due to the lowering of screening thresholds, resulting in the increased identification of newborns with transient CH. Several studies ha
Externí odkaz:
https://doaj.org/article/f3b3e128fce541b3b9e8414d678cc926
Autor:
Elias-Assad, Ghadir, Saab, Raunak, Molnes, Janne, Hess, Ora, Abu-Ras, Rasmi, Darawshi, Hussein, Rasmus Njølstad, Pal, Tenenbaum-Rakover, Yardena
Publikováno v:
In Diabetes Research and Clinical Practice May 2021 175
Autor:
Yardena Tenenbaum-Rakover, Osnat Admoni, Ghadir Elias-Assad, Shira London, Marie Noufi-Barhoum, Hanna Ludar, Tal Almagor, Yoav Zehavi, Charles Sultan, Rita Bertalan, Anu Bashamboo, Kenneth McElreavey
Publikováno v:
Endocrine Connections, Vol 10, Iss 6, Pp 620-629 (2021)
Objective: Disorders of sex development (DSD) are defined as congenital co nditions in which the development of chromosomal, gonadal and anatomical sex is atypical. Despite wide laboratory and imaging investigations, the etiology of DSD is unknown in
Externí odkaz:
https://doaj.org/article/8e62f22b0df84f8b8d68bd427b01a1df
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Inbal Halabi, Marie Noufi Barohom, Sarit Peleg, Phillippe Trougouboff, Ghadir Elias-Assad, Rhania Agbaria, Yardena Tenenbaum-Rakover
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) is a rare monogenic disorder, associated with endocrine deficiencies and non-endocrine involvement. Gastrointestinal (GI) manifestations appear in approximately 25% of patients a
Externí odkaz:
https://doaj.org/article/ee36ead201fa4fbcadc6d218d37db75b
Autor:
Shira London, Elisa De Franco, Ghadir Elias-Assad, Marie Noufi Barhoum, Clari Felszer, Marina Paniakov, Scott A. Weiner, Yardena Tenenbaum-Rakover
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
BackgroundMutations in GLIS3 cause a rare syndrome characterized by neonatal diabetes mellitus (NDM), congenital hypothyroidism, congenital glaucoma and cystic kidneys. To date, 14 mutations in GLIS3 have been reported, inherited in an autosomal rece
Externí odkaz:
https://doaj.org/article/f1de03af23094f3ca5070d38763dcafb
Publikováno v:
Frontiers in Endocrinology, Vol 11 (2020)
Background: Autoimmune thyroiditis (AIT) is the most common cause of acquired hypothyroidism in children. The natural outcome of AIT in childhood has been reported previously however follow-up duration is generally short and results variable.Objectiv
Externí odkaz:
https://doaj.org/article/7379beb283784afa8e3b4f741dc4a21b
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Ludar, Hanna, Levy-Shraga, Yael, Admoni, Osnat, Majdoub, Hussein, Aronovitch, Kineret Mazor, Koren, Ilana, Rath, Shoshana, Elias-assad, Ghadir, Almashanu, Shlomo, Mantovani, Giovanna, Hamiel, Orit Pinhas, Tenenbaum-Rakover, Yardena
Publikováno v:
Journal of Clinical Endocrinology & Metabolism; Feb2024, Vol. 109 Issue 2, p424-438, 15p
Autor:
Ghadir Elias-Assad, Osnat Admoni, Shira London, Tal Almagor, Ken McElreavey, Marie Noufi-Barhoum, Rita Bertalan, Anu Bashamboo, Yoav Zehavi, Yardena Tenenbaum-Rakover, Hanna Ludar, Charles Sultan
Publikováno v:
Endocrine Connections, Vol 10, Iss 6, Pp 620-629 (2021)
Endocrine Connections
Endocrine Connections, 2021, 10 (6), pp.620-629. ⟨10.1530/EC-21-0019⟩
Endocrine Connections
Endocrine Connections, 2021, 10 (6), pp.620-629. ⟨10.1530/EC-21-0019⟩
Objective Disorders of sex development (DSD) are defined as congenital conditions in which the development of chromosomal, gonadal and anatomical sex is atypical. Despite wide laboratory and imaging investigations, the etiology of DSD is unknown in o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db7305618fab5137b7c654a8e83834a2
https://ec.bioscientifica.com/view/journals/ec/10/6/EC-21-0019.xml
https://ec.bioscientifica.com/view/journals/ec/10/6/EC-21-0019.xml