Zobrazeno 1 - 10
of 370
pro vyhledávání: '"Stoupa A"'
Autor:
Stoupa, Athanasia, Franca, Monica Malheiros, Abdulhadi-Atwan, Maha, Fujisawa, Haruki, Korwutthikulrangsri, Manassawee, Marchand, Isis, Polak, Gabrielle, Beltrand, Jacques, Polak, Michel, Kariyawasam, Dulanjalee, Liao, Xiao-Hui, Raimondi, Chantalle, Steigerwald, Connolly, Abreu, Nicolas J., Bauer, Andrew J., Carré, Aurore, Taneja, Charit, Mekhoubad, Allison Bauman, Dumitrescu, Alexandra M.
Publikováno v:
In Genetics in Medicine December 2024 26(12)
Autor:
Stoupa Hadidi, Marina1 (AUTHOR) marinahadidi@gmail.com, Rasheed, Murad2 (AUTHOR) murad_rasheed@yahoo.com, Bisharat, Yanal M.3 (AUTHOR) yanal.bisharat@mspharma.com, Al Helou, Heba H.3 (AUTHOR) heba.alhelou@mspharma.com, El Aina, Hussam A.4 (AUTHOR) hussam.alaina@mspharma.com, Batayneh, Hala M.4 (AUTHOR) hala.batayneh@mspharma.com, Aljabali, Alaa A. A.5 (AUTHOR) alaaj@yu.edu.jo, Gammoh, Omar6 (AUTHOR) omar.gammoh@yu.edu.jo
Publikováno v:
Journal of Clinical Medicine. Sep2024, Vol. 13 Issue 17, p5156. 11p.
Autor:
Hortense Didier-Mathon, Athanasia Stoupa, Dulanjalee Kariyawasam, Sonny Yde, Beatrix Cochant-Priollet, Lionel Groussin, Frédéric Sébag, Nicolas Cagnard, Patrick Nitschke, Dominique Luton, Michel Polak, Aurore Carré
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundBOREALIN/CDCA8 mutations are associated with congenital hypothyroidism and thyroid dysgenesis. Borealin is involved in mitosis as part of the Chromosomal Passenger Complex. Although BOREALIN mutations decrease thyrocyte adhesion and migrati
Externí odkaz:
https://doaj.org/article/7d77cbf8d7e84287ad063228ed6c37d0
Autor:
Veronica Mericq, German Iñiguez, Graziella Pinto, Laura G. Gonzalez-Briceño, Dinane Samara-Boustani, Caroline Thalassinos, Isabelle Flechtner, Athanasia Stoupa, Jacques Beltrand, Alix Besançon, Séverine Brabant, Khaldoun Ghazal, Monique Leban, Philippe Touraine, Gabriel Cavada, Michel Polak, Dulanjalee Kariyawasam
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
ObjectiveIsolated childhood growth hormone deficiency (GHD) can persist into adulthood, and re-testing at the transition period is needed to determine whether continued growth hormone therapy is indicated. Here, our objective was to identify predicto
Externí odkaz:
https://doaj.org/article/a6b9d575ff7443c8b456833f27974b5f
Akademický článek
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Autor:
Coutant, Régis, Lugat, Alexandre, Mirallié, Éric, Oliver-Petit, Isabelle, Stoupa, Athanasia, Drui, Delphine
Publikováno v:
In Annales d'Endocrinologie December 2022 83(6):431-434
Autor:
Oliveira, Isabela de Castro, Vieira, Ítalo Stoupa, Freitas, Samuel Galvão, Campos, Artur Kanadani, Araújo, Jackson Victor
Publikováno v:
In Biological Control August 2022 171
Publikováno v:
Pediatric Investigation, Vol 6, Iss 2, Pp 123-134 (2022)
ABSTRACT Congenital hypothyroidism (CH) is the most common neonatal endocrine disorder and one of the most common preventable causes of intellectual disability in the world. CH may be due to developmental or functional thyroid defects (primary or per
Externí odkaz:
https://doaj.org/article/16ff4bccd5bb47d38adec55ce33beee4
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
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Autor:
Fausto, Guilherme Costa *, Fausto, Mariana Costa, Vieira, Ítalo Stoupa, Freitas, Samuel Galvão de, Carvalho, Lorendane Millena de, Oliveira, Isabela de Castro, Silva, Edir Nepomuceno, Campos, Artur Kanadani, Araújo, Jackson Victor de
Publikováno v:
In Veterinary Parasitology July 2021 295