Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sharon Bratman Morag"'
Autor:
J. Daniel Freedman, Rostislav Novak, Sharon Bratman Morag, Emily Avitan-Hersh, David Nikomarov
Publikováno v:
Rambam Maimonides Medical Journal, Vol 12, Iss 3, p e0024 (2021)
Mutations in FGF23, KL, and GALNT3 have been identified as the cause for the development of hyperphosphatemic familial tumoral calcinosis (HFTC). Patients with HFTC typically present in childhood or adolescence with periarticular soft tissue deposits
Externí odkaz:
https://doaj.org/article/1bd202a7a8f349e4bd497fe224eb0d30
Autor:
David Nikomarov, Sharon Bratman Morag, Rostislav Novak, Emily Avitan-Hersh, J Daniel Freedman
Publikováno v:
Rambam Maimonides Medical Journal
Rambam Maimonides Medical Journal, Vol 12, Iss 3, p e0024 (2021)
Rambam Maimonides Medical Journal, Vol 12, Iss 3, p e0024 (2021)
Mutations in FGF23, KL, and GALNT3 have been identified as the cause for the development of hyperphosphatemic familial tumoral calcinosis (HFTC). Patients with HFTC typically present in childhood or adolescence with periarticular soft tissue deposits
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cb286bc14f09d65cb89dacf4b957ce2
https://pubmed.ncbi.nlm.nih.gov/34270404
https://pubmed.ncbi.nlm.nih.gov/34270404
Autor:
Roie Tzadok, Petachia Reissman, Moshe Giladi, Amir Dagan, Sharon Bratman Morag, Ayal Hassidim, Yael Dagan
Publikováno v:
Journal of Surgical Research. 220:293-299
Background Patients with psychiatric disorders have an increased risk for morbidity and mortality from other medical conditions. Methods Medical records of all the patients undergoing appendectomy (n = 2594) and laparoscopic cholecystectomy (n = 2874
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::257ed70de5be53cfcd76bf67888f551d
https://doi.org/10.1016/j.jss.2017.07.018
https://doi.org/10.1016/j.jss.2017.07.018
Autor:
Yarin Hadid, Rachel Bello, Karin Weiss, Adi Mory, Tamar Paperna, Ariel F. Martinez, Sharon Bratman-Morag, Hagit N. Baris, Liran I. Shlush, Lior Cohen, Alina Kurolap, Nina Ekhilevitch, Maximilian Muenke
Publikováno v:
European Journal of Medical Genetics. 63:103643
Majewski Osteodysplastic Primordial Dwarfism type II (MOPDII) is a form of dwarfism associated with severe microcephaly, characteristic skeletal findings, distinct dysmorphic features and increased risk for cerebral infarctions. The condition is caus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcada196d429e5847c29791d097b3cbc
https://doi.org/10.1016/j.ejmg.2019.03.007
https://doi.org/10.1016/j.ejmg.2019.03.007