Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Multiple endocrine neoplasia, type 1 (MEN 1)"'
Autor:
Maria Rossing, Ulrich Knigge, Åse Krogh Rasmussen, Ulla Feldt-Rasmussen, Grigoris Effraimidis, Peter Oturai
Publikováno v:
Seminars in Cancer Biology. 79:141-162
Neuroendocrine neoplasms (NENs) are relatively rare neoplasms with 6.4-times increasing age-adjusted annual incidence during the last four decades. NENs arise from neuroendocrine cells, which release hormones in response to neuronal stimuli and they
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 105:e1106-e1114
Context Information regarding the impact of parental multiple endocrine neoplasia type 1 (MEN 1) on neonatal outcomes is limited to case reports. Objective To determine the impact of parental MEN 1 on neonatal outcomes. Methods Retrospective cohort a
Akademický článek
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Autor:
Al-Mrayat Maen, Sing Yang Sim
Publikováno v:
Endocrine Abstracts.
Autor:
Francesca Giusti, Laura Masi, Francesca Marini, Maria Luisa Brandi, Federica Cioppi, Caterina Fossi, Francesco Tonelli
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background MEN1 is a complex, rare, syndrome inherited in an autosomal dominant tract and characterized by the development of multiple neuroendocrine tumors, requiring lifelong surveillance and multiple medical and surgical therapies throughout the p
Introduction: Multiple endocrine neoplasia type 1 (MEN 1) is a rare disorder that is inherited autosomally dominantly and is characterized by a predisposition to the tumor of the parathyroid glands, anterior pituitary gland, and pancreas. It is cause
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::741a696439f55c661c1c96e4b4fb9cef
https://www.bib.irb.hr/1120046
https://www.bib.irb.hr/1120046
Publikováno v:
Endocrine Abstracts.
Publikováno v:
Endocrine Abstracts.
Autor:
Giselle Mumbach, Wenxiu Zhao, Laura E. Dichtel, Francisco J Guarda, Lisa B. Nachtigall, Xun Zhang, Nicholas A. Tritos, Alireza Ghajar, Brooke Swearingen, Karen K. Miller, Rajesh V. Thakker, Kate E Lines
Publikováno v:
The Journal of Clinical Endocrinology and Metabolism
Context Clinical multiple endocrine neoplasia type 1 (MEN-1) is diagnosed by the presence of at least 2 MEN-1–associated tumors. Many patients with acromegaly and clinical MEN-1 yield negative testing for MEN1 mutations. While cases of acromegaly a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9bf574492f4b0479082b4dd01eaf9b7
https://ora.ox.ac.uk/objects/uuid:71ad8f1f-94f9-48e0-aa61-fce145a61c65
https://ora.ox.ac.uk/objects/uuid:71ad8f1f-94f9-48e0-aa61-fce145a61c65
Autor:
Sing Yang Sim, Ma'en Al-Mrayat
Publikováno v:
Endocrine Abstracts.