Results 91 to 100 of about 12,302 (171)

Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. The European Consortium on MEN1.

, 1997
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterised by tumours of the parathyroids, pancreas and anterior pituitary that represents one of the familial cancer syndromes.
Quincey, D, Höppener, JW, Gaudray, P, Weber, G, Calender, A, Thakker, RV, Lenoir, G, Bassett, JHD, Zhang, CX, Teh, BT, Parente, F, Thakker, Rajesh, Van de Ven, WJ, Hayward, N, DeWitte, K, De Witte, K, De Wit, MJ, Giraud, S, Farnebo, F, Wautot, V, Khodaei, S, Phelan, C, Hoppener, JWM, Forbes, SA, Larsson, C, Lips, CJM, Buisson, N, Pugeat, M, Grant, AL, Lips, CJ, DeWit, MJ, Lemmens, I, Kytölä, S, Pannett, AAJ, Salandre, J, Kas, K, VandeVen, WJM   +36 more
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Aspects of MEN1 Tumorigenesis in Endocrine Pancreas and Adrenal Glands

, 2015
Multiple endocrine neoplasia syndrome type 1 (MEN1) is an autosomal dominantly inherited disease, which is described as an association of tumors mainly in endocrine organs, including pancreas and adrenal glands.
Chu, Xia
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MEN1 (multiple endocrine neoplasia I) [PDF]

, 1999
Review on MEN1 (multiple endocrine neoplasia I), with data on DNA, on the protein encoded, and where the gene is ...
Calender, A
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Clinical practice guidelines for multiple endocrine neoplasia type 1 (MEN1).

, 2012
OBJECTIVE: The aim was to provide guidelines for evaluation, treatment, and genetic testing for multiple endocrine neoplasia type 1 (MEN1). PARTICIPANTS: The group, which comprised 10 experts, including physicians, surgeons, and geneticists from ...
Thakker, Rajesh V., Dralle, Henning, Walls, GV, Bilezikian, John, Thakker, RV, Brandi, Maria Luisa, Ebeling, Peter R., Melmed, S, Newey, PJ, Walls, Gerard, Sakurai, A, Melmed, Shlomo, Tonelli, F, Thakker, Rajesh, Sakurai, Akihiro, Walls, Gerard V., Ebeling, PR, Dralle, H, Newey, Paul J., Tonelli, Francesco, Brandi, ML, Bilezikian, J   +21 more
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Whole genome sequencing of apparently mutation-negative MEN1 patients

, 2020
OBJECTIVE:Multiple Endocrine Neoplasia type 1 (MEN1) is an autosomal dominant syndrome usually caused by loss-of-function mutations in the MEN1-gene. However, a minority of patients who fulfill the criteria for MEN1 are not found to harbor MEN1-mutations.
Backman, Samuel,, Skogseid, Britt,, Stålberg, Peter,, Bajic, Duska,, Hellman, Per,, Crona, Joakim,   +5 more
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A novel germline mutation at exon 10 of MEN1 gene: a clinical survey and positive genotype-phenotype analysis of a MEN1 Italian family, including monozygotic twins

, 2018
ContextClinical phenotype variability in MEN1 syndrome exists and evidence for an established genotype-phenotype is lacking. However, a higher aggressiveness of MEN1-associated gastro-entero-pancreatic (GEP) (neuro)endocrine tumours (NETs) tumours has ...
Del Toro, Rossella, Maggi, Daria, Concolino, Paola, Coppola, Roberto, Raffaelli, Marco, Manfrini, Silvia, Pantano, Francesco, Pozzilli, Paolo, Palermo, Andrea, Capoluongo, Ettore, Falchetti, Alberto, Defeudis, Giuseppe, Di Matteo, Francesco Maria   +12 more
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Case Report: A novel likely pathogenetic variant of the MEN1 gene in multiple endocrine neoplasia type 1

Frontiers in Endocrinology
BackgroundMultiple endocrine neoplasia type 1 (MEN1) is a rare disease caused by mutations in the oncosuppressor gene MEN1 and characterized by co-occurrence of tumors of the parathyroid gland, pancreas, and pituitary gland.
Mengli Sun, Xinxia Chang, Xianen Huang, Liangmiao Chen, Mengmeng Peng, Xiqiang Zhong   +5 more
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Clinical studies of multiple endocrine neoplasia type 1 (MEN1)

, 1996
Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by the combined occurrence of parathyroid, pancreatic islet and anterior pituitary tumours.
Wooding, C, Pang, JT, O'Halloran, D, Thakker, RV, Wheeler, MH, Buchanan, KD, Edwards, CR, Lips, K, Farren, B, Jackson, CE, Thakker, Rajesh, Trump, D, Sampson, J, Heath, DA, Jansen, S, Zink, A, Besser, GM, Monson, JP, Shalet, SM   +18 more
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Expression analysis of menin protein and MEN1 mRNA.

, 2013
Panel A: Real time quantitative RT-PCR analysis of MEN1 mRNA in normal parathyroid tissue, in MEN1 parathyroid adenomas, and in non-MEN1 parathyroid adenomas.
Francesca Marini (12576), Francesca Giusti (310007), Ettore Luzi (318000), Loredana Cavalli (318003), Gianna Galli (318002), Maria Luisa Brandi (910)   +5 more
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Cushing's disease as first clinical manifestation of multiple endocrine neoplasia type 1(MEN1) associeted with R460X mutation of MEN1 gene

, 2003
OBJETIVO: A Neoplasia Endocrina Multipla do tipo 1 ( MEN1 ) e uma doenca autossomica dominante causada por mutacao no gene da MEN1. A MEN1 predispoe ao desenvolvimento de tumores em diversos tecidos, principalmente na hipofise, glandulas paratiroides e ...
Matsuzaki, Lisa Nozawa [UNIFESP]
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