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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 10 (of 10 Records)

Query Trace: Hyperplasia and MEN1[original query]
Novel somatic MEN1 gene alterations in sporadic primary hyperparathyroidism and correlation with clinical characteristics.
Journal of endocrinological investigation 2004 Dec 27 (11): 1015-21.
Scarpelli D, D'Aloiso L, Arturi F, Scillitani A, Presta I, Bisceglia M, Cristofaro C, Russo D, Filetti
Detection of an MEN1 gene mutation depends on clinical features and supports current referral criteria for diagnostic molecular genetic testing.
Clinical endocrinology 2005 Feb 62 (2): 169-75.
Ellard S, Hattersley A T, Brewer C M, Vaidya
Clinical testing for mutations in the MEN1 gene in Sweden: a report on 200 unrelated cases.
The Journal of clinical endocrinology and metabolism 2007 Sep 92 (9): 3389-95.
Tham Emma, Grandell Ulla, Lindgren Eva, Toss Göran, Skogseid Britt, Nordenskjöld Magn
Assessment of p27 (cyclin-dependent kinase inhibitor 1B) and aryl hydrocarbon receptor-interacting protein (AIP) genes in multiple endocrine neoplasia (MEN1) syndrome patients without any detectable MEN1 gene mutations.
Clinical endocrinology 2009 Feb 70 (2): 259-64.
Igreja Susana, Chahal Harvinder S, Akker Scott A, Gueorguiev Maria, Popovic Vera, Damjanovic Svetozar, Burman Pia, Wass John A, Quinton Richard, Grossman Ashley B, Korbonits Már
PRSS1_p.Leu81Met mutation results in autoimmune pancreatitis.
World journal of gastroenterology : WJG 2013 Jun 19 (21): 21.
Gao F, Li YM, Hong GL, Xu ZF, Liu QC, He QL, Lin LQ, Weng SH
Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features.
PloS one 2017 10 12 (10): e0186485.
Pardi Elena, Borsari Simona, Saponaro Federica, Bogazzi Fausto, Urbani Claudio, Mariotti Stefano, Pigliaru Francesca, Satta Chiara, Pani Fabiana, Materazzi Gabriele, Miccoli Paolo, Grantaliano Lorena, Marcocci Claudio, Cetani Filome
ARMC5 Alterations in Patients With Sporadic Neuroendocrine Tumors and Multiple Endocrine Neoplasia Type 1 (MEN1).
The Journal of clinical endocrinology and metabolism 2020 9 105 (12): e4531-42.
Damjanovic Svetozar S, Antic Jadranka A, Elezovic-Kovacevic Valentina I, Dundjerovic Dusko M, Milicevic Ivana T, Beleslin-Cokic Bojana B, Ilic Bojana B, Rodic Gordana S, Berthon Annabel, Maria Andrea Gutierrez, Faucz Fabio R, Stratakis Constantine
A Parathyroid-Gut Axis: Hypercalcemia and the Pathogenesis of Gastrinoma in Multiple Endocrine Neoplasia 1.
Molecular cancer research : MCR 2021 3 19 (6): 946-949.
Hackeng Wenzel M, Dreijerink Koen M A, Offerhaus G Johan A, Brosens Lodewijk A
Genetic and clinical screening for hereditary primary hyperparathyroidism in a large Chinese cohort: a single-center study.
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2023 7 .
An Song, Yi Yang, Yue Jiang, Min Nie, Yan Jiang, Mei Li, Weibo Xia, Xiaoping Xing, Ou Wa
Clinical profile and treatment outcomes among patients with sporadic and multiple endocrine neoplasia syndrome-related primary hyperparathyroidism.
Clinical endocrinology 2023 7 .
Uthara E Mathew, Alpesh Goyal, Ashish D Upadhyay, Devasenathipathy Kandasamy, Shipra Agarwal, Chitresh K Sharma, Arundhati Sharma, Chandrasekhar Bal, Nikhil Tandon, Viveka P Jyots
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