Zobrazeno 1 - 8
of 8
pro vyhledávání: '"GNAS gene mutation"'
Autor:
Mohammad Haddadi, Elahe Lal Kheirkhah, Mojgan Ansari, Samieh Ahmadzade, Zeinab Taraz, Saeid Yazdi
Publikováno v:
Clinical Case Reports, Vol 10, Iss 7, Pp n/a-n/a (2022)
Abstract McCune–Albright syndrome is a non‐hereditary disease characterized by café‐au‐lait skin spots, fibrous dysplasia of bone, and endocrinopathies. We report a boy with a history of repeated hospitalizations from birth due to severe jau
Externí odkaz:
https://doaj.org/article/c5f77143cb7a40ea83280b18b96be4e1
Autor:
Agnieszka Walczyk, Grzegorz Chmielewski, Kajetan Zgubieński, Artur Kowalik, Aldona Kowalska, Kinga Hińcza-Nowak
Publikováno v:
Polish archives of internal medicine. 132(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11fbbf218986a5ff532c24f84e7380ad
https://pubmed.ncbi.nlm.nih.gov/34851063
https://pubmed.ncbi.nlm.nih.gov/34851063
Publikováno v:
Journal of Pediatric Gastroenterology & Nutrition. 68:e54-e57
McCune-Albright syndrome (MAS) results from a GNAS gene mutation. It is associated with café au lait macules, fibrous dysplasia, and several endocrinopathies to include gonadotropin-independent precocious puberty, growth hormone excess, Cushing synd
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f1e3b36ae6541744637e9586305c7dc
https://doi.org/10.1097/mpg.0000000000002266
https://doi.org/10.1097/mpg.0000000000002266
Autor:
Lania AG, Ferrero S, Mantovani G, Peverelli E, Beck Peccoz P, Spada A, PIVONELLO, ROSARIO, DI SARNO, ANTONELLA, COLAO, ANNAMARIA
CONTEXT: Mixed PRL- and GH-secreting pituitary adenomas are relatively common because somatotrophs and lactotrophs share the common somato-mammotroph progenitor lineage. Conversely, the occurrence of a prolactinoma evolving into clinically and bioche
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::264cd66ccc01367070fe58631de11253
http://hdl.handle.net/11588/378205
http://hdl.handle.net/11588/378205
Autor:
Ender Semiz, Maşallah Candemir, Füsun Düzcan, Vildan Caner, Olaf Hiort, Serap Semiz, Susanne Thiele
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 22
Not Available
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::117375f03f50eaaff7bbd8d5eaac2bd7
https://doi.org/10.1515/jpem.2009.22.2.107
https://doi.org/10.1515/jpem.2009.22.2.107
Akademický článek
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Akademický článek
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Autor:
Haddadi M; Department of Nursing Tabas Branch Islamic Azad University Tabas Iran., Lal Kheirkhah E; Department of Nursing Esfarayen University of Medical Sciences Esfarayen Iran., Ansari M; Department of Nursing, Nursing & Midwifery School Sabzevar University of Medical Sciences Sabzevar Iran., Ahmadzade S; Imam Khomeini Hospital Esfarayen Faculty of Medical Sciences Esfarayen Iran., Taraz Z; Payambar Azam Hospital Kerman Faculty of Medical Sciences Kerman Iran., Yazdi S; Imam Khomeini Hospital Esfarayen Faculty of Medical Sciences Esfarayen Iran.
Publikováno v:
Clinical case reports [Clin Case Rep] 2022 Jul 19; Vol. 10 (7), pp. e6077. Date of Electronic Publication: 2022 Jul 19 (Print Publication: 2022).