Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Malgorzata Trofimiuk-Müldner"'
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:
Milou E. Noltes, Schelto Kruijff, Walter Noordzij, Eef D. Telenga, David Vállez García, Malgorzata Trofimiuk-Müldner, Marta Opalińska, Alicja Hubalewska-Dydejczyk, Gert Luurtsema, Rudi A. J. O. Dierckx, Mostafa El Moumni, Ronald Boellaard, Adrienne H. Brouwers
Publikováno v:
EJNMMI Research, Vol 9, Iss 1, Pp 1-10 (2019)
Abstract Purpose To evaluate the optimal tracer uptake time, the minimal amount of radioactivity and the inter-observer agreement for 11C-choline positron emission tomography/computed tomography (PET/CT) in patients with primary hyperparathyroidism (
Externí odkaz:
https://doaj.org/article/c02878311bc5447fb35f481a5cda2d22
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
Autor:
Milou E, Noltes, Schelto, Kruijff, Walter, Noordzij, Eef D, Telenga, David, Vállez García, Malgorzata, Trofimiuk-Müldner, Marta, Opalińska, Alicja, Hubalewska-Dydejczyk, Gert, Luurtsema, Rudi A J O, Dierckx, Mostafa, El Moumni, Ronald, Boellaard, Adrienne H, Brouwers
Publikováno v:
EJNMMI Research
Purpose To evaluate the optimal tracer uptake time, the minimal amount of radioactivity and the inter-observer agreement for 11C-choline positron emission tomography/computed tomography (PET/CT) in patients with primary hyperparathyroidism (pHPT). Me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::426ae7cf0e8786694c994ee3baa6357a
https://pubmed.ncbi.nlm.nih.gov/31367792
https://pubmed.ncbi.nlm.nih.gov/31367792
Autor:
Noltes, Milou, Schelto Kruijff, Noordzij, Walter, Telenga, Eef, García, David Vállez, Malgorzata Trofimiuk-Müldner, Opalińska, Marta, Hubalewska-Dydejczyk, Alicja, Luurtsema, Gert, Dierckx, Rudi, Moumni, Mostafa, Boellaard, Ronald, Brouwers, Adrienne
Inter-observer agreement (DOCX 15 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0524f7732b1221d14c660ff768fdaaf7
Autor:
Noltes, Milou, Schelto Kruijff, Noordzij, Walter, Telenga, Eef, García, David Vállez, Malgorzata Trofimiuk-Müldner, Opalińska, Marta, Hubalewska-Dydejczyk, Alicja, Luurtsema, Gert, Dierckx, Rudi, Moumni, Mostafa, Boellaard, Ronald, Brouwers, Adrienne
11C-choline PET/CT (DOCX 16 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ba52b789878e5d8b282aa6bae7b22a2
Autor:
Noltes, Milou, Schelto Kruijff, Noordzij, Walter, Telenga, Eef, García, David Vállez, Malgorzata Trofimiuk-Müldner, Opalińska, Marta, Hubalewska-Dydejczyk, Alicja, Luurtsema, Gert, Dierckx, Rudi, Moumni, Mostafa, Boellaard, Ronald, Brouwers, Adrienne
Results optimal uptake time of tracer (DOCX 125 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35e86ddad821ae6d42f28ea33e3de800
Autor:
Noltes, Milou, Schelto Kruijff, Noordzij, Walter, Telenga, Eef, García, David Vállez, Malgorzata Trofimiuk-Müldner, Opalińska, Marta, Hubalewska-Dydejczyk, Alicja, Luurtsema, Gert, Dierckx, Rudi, Moumni, Mostafa, Boellaard, Ronald, Brouwers, Adrienne
Corrected calcium (PDF 152 kb)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cda90b5301623a4122efabf4693f657
Autor:
Anna, Sowa-Staszczak, Agnieszka, Stefanska, Pawel, Chrapczynski, Malgorzata, Trofimiuk-Müldner, Miroslaw, Szura, Alicja, Hubalewska-Dydejczyk
Publikováno v:
Endocrine journal. 64(2)
A number of detected neuroendocrine neoplasms (NENs) has been on the increase due to our awareness of the NENs risk and the development of different imaging techniques. Therapy of NENs involves surgery, chemotherapy, "cold" somatostatin analogs (SSA)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d32367de20a891ece11849483a17b67a
https://pubmed.ncbi.nlm.nih.gov/27853048
https://pubmed.ncbi.nlm.nih.gov/27853048
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