Zobrazeno 1 - 10
of 750
pro vyhledávání: '"Müldner, A"'
Autor:
Małgorzata Kałużna, Bartłomiej Budny, Michał Rabijewski, Agnieszka Dubiel, Małgorzata Trofimiuk-Müldner, Kosma Szutkowski, Adam Piotrowski, Elżbieta Wrotkowska, Alicja Hubalewska-Dydejczyk, Marek Ruchała, Katarzyna Ziemnicka
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
IntroductionNormosmic isolated hypogonadotropic hypogonadism (nIHH) is a clinically and genetically heterogeneous disorder. Deleterious variants in over 50 genes have been implicated in the etiology of IHH, which also indicates a possible role of dig
Externí odkaz:
https://doaj.org/article/ea0d1d6aca6e4ca18d762c12b2f79e77
Publikováno v:
In Journal of Archaeological Science: Reports December 2023 52
Publikováno v:
In Journal of Archaeological Science: Reports June 2023 49
Autor:
Skalniak, Anna1 (AUTHOR) anna.skalniak@uj.edu.pl, Trofimiuk-Müldner, Małgorzata2 (AUTHOR) malgorzata.trofimiuk@uj.edu.pl, Surmiak, Marcin1 (AUTHOR) marcin.surmiak@uj.edu.pl, Totoń-Żurańska, Justyna3 (AUTHOR) justyna.toton-zuranska@uj.edu.pl, Jabrocka-Hybel, Agata2 (AUTHOR) agata.jabrocka-hybel@uj.edu.pl, Hubalewska-Dydejczyk, Alicja2 (AUTHOR) alicja.hubalewska-dydejczyk@uj.edu.pl
Publikováno v:
International Journal of Molecular Sciences. Jan2024, Vol. 25 Issue 2, p1065. 11p.
Akademický článek
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Autor:
Anna Skalniak, Małgorzata Trofimiuk-Müldner, Marcin Surmiak, Justyna Totoń-Żurańska, Agata Jabrocka-Hybel, Alicja Hubalewska-Dydejczyk
Publikováno v:
International Journal of Molecular Sciences, Vol 25, Iss 2, p 1065 (2024)
Multiple endocrine neoplasia type 1 (MEN1) is a syndrome characterized by tumors in multiple organs. Although being a dominantly inherited monogenic disease, disease phenotypes are unpredictable and differ even among members of the same family. There
Externí odkaz:
https://doaj.org/article/18f71a6491804d57a4b22e199538a751
Publikováno v:
In Journal of Archaeological Science August 2022 144
Autor:
Line Tang Møllehave, Marie Holm Eliasen, Ieva Strēle, Allan Linneberg, Rodrigo Moreno-Reyes, Ludmila B Ivanova, Zvonko Kusić, Iris Erlund, Till Ittermann, Endre V Nagy, Ingibjorg Gunnarsdottir, Jonathan Eli Arbelle, Aaron Milton Troen, Valdis Pīrāgs, Lisbeth Dahl, Alicja Hubalewska-Dydejczyk, Malgorzata Trofimiuk-Müldner, João Jacome de Castro, Mafalda Marcelino, Simona Gaberšček, Katja Zaltel, Manuel Puig-Domingo, Lluis Vila, Sofia Manousou, Helena Filipsson Nyström, Michael Bruce Zimmermann, Karen R Mullan, Jayne Valerie Woodside, Henry Völzke, Betina Heinsbæk Thuesen
Publikováno v:
Endocrine Connections, Vol 11, Iss 3, Pp 1-11 (2022)
Objective: Registers of diagnoses and treatments exist in different forms in the European countries and are potential sources to answer important research questions. Prevalence and incidence of thyroid diseases are highly dependent on iodine intake a
Externí odkaz:
https://doaj.org/article/4d441f444be943b78b23077c0e00a839
Autor:
Bielska-Brodziak, Agnieszka, Gawlik-Starzyk, Aneta, Jakubowski, Tomasz, Trofimiuk-Müldner, Małgorzata
Publikováno v:
Bialostockie Studia Prawnicze; Sep2024, Vol. 29 Issue 3, p105-130, 26p
AIP gene germline variants in adult Polish patients with apparently sporadic pituitary macroadenomas
Autor:
Małgorzata Trofimiuk-Müldner, Bartosz Domagała, Grzegorz Sokołowski, Anna Skalniak, Alicja Hubalewska-Dydejczyk
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
IntroductionUp to 5% of all pituitary tumors are hereditary e.g. due to MEN1 or aryl hydrocarbon receptor-interacting protein (AIP) genes mutations.ObjectivesThe study was aimed at the assessment of the frequency and characteristics of AIP-mutation r
Externí odkaz:
https://doaj.org/article/26f06a2d69ae4944b63e7930eaae99b7