Human Genome Epidemiology Literature Finder
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Records 1 - 26 (of 26 Records) |
| Query Trace: Adenoma and MEN1[original query] |
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| Pituitary disease in MEN type 1 (MEN1): data from the France-Belgium MEN1 multicenter study. The Journal of clinical endocrinology and metabolism 2002 Feb 87 (2): 457-65. Vergès Bruno, Boureille Françoise, Goudet Pierre, Murat Arnaud, Beckers Albert, Sassolas Geneviève, Cougard Patrick, Chambe Béatrice, Montvernay Corinne, Calender Ala |
| Clinical and genetic features of patients with multiple endocrine tumors who have neither family history nor MEN1 germline mutations. Endocrine 2004 Feb 23 (1): 45-9. Sakurai Akihiro, Katai Miyuki, Yumita Wataru, Minemura Kesami, Hashizume Kiyos |
| 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 |
| Germline CDKN1B/p27Kip1 mutation in multiple endocrine neoplasia. The Journal of clinical endocrinology and metabolism 2007 Aug 92 (8): 3321-5. Georgitsi Marianthi, Raitila Anniina, Karhu Auli, van der Luijt Rob B, Aalfs Cora M, Sane Timo, Vierimaa Outi, Mäkinen Markus J, Tuppurainen Karoliina, Paschke Ralph, Gimm Oliver, Koch Christian A, Gündogdu Sadi, Lucassen Anneke, Tischkowitz Marc, Izatt Louise, Aylwin Simon, Bano Gul, Hodgson Shirley, De Menis Ernesto, Launonen Virpi, Vahteristo Pia, Aaltonen Lauri |
| 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 |
| Multiple endocrine neoplasia type 1 (MEN1): its manifestations and effect of genetic screening on clinical outcome. Clinical endocrinology 2009 Apr 70 (4): 575-81. Pieterman C R C, Schreinemakers J M J, Koppeschaar H P F, Vriens M R, Rinkes I H M Borel, Zonnenberg B A, van der Luijt R B, Valk G |
| Mutation analysis of MEN1, HRPT2, CASR, CDKN1B, and AIP genes in primary hyperparathyroidism patients with features of genetic predisposition. Journal of endocrinological investigation 2009 Jun 32 (6): 512-8. Vierimaa O, Villablanca A, Alimov A, Georgitsi M, Raitila A, Vahteristo P, Larsson C, Ruokonen A, Eloranta E, Ebeling T M L, Ignatius J, Aaltonen L A, Leisti J, Salmela P |
| Prevalence of AIP mutations in a large series of sporadic Italian acromegalic patients and evaluation of CDKN1B status in acromegalic patients with multiple endocrine neoplasia. European journal of endocrinology / European Federation of Endocrine Societies 2010 Sep 163 (3): 369-76. Occhi G, Trivellin G, Ceccato F, De Lazzari P, Giorgi G, Demattè S, Grimaldi F, Castello R, Davì M V, Arnaldi G, Salviati L, Opocher G, Mantero F, Scaroni |
| Aryl hydrocarbon receptor interacting protein (AIP) mutations occur rarely in sporadic parathyroid adenomas. The Journal of clinical endocrinology and metabolism 2013 Jul 98 (7): 2800-10. Pardi Elena, Marcocci Claudio, Borsari Simona, Saponaro Federica, Torregrossa Liborio, Tancredi Mariella, Raspini Benedetta, Basolo Fulvio, Cetani Filome |
| LRRC4 haplotypes are associated with pituitary adenoma in a Chinese population. Medical oncology (Northwood, London, England) 2014 Apr 31 (4): 888. Xiao Lan, Tu Chaofeng, Chen Shuai, Yu Zhibin, Lei Qianqian, Wang Zeyou, Xu Gang, Wu Minghua, Li Guiyu |
| Polymorphisms in MEN1 and DRD2 genes are associated with the occurrence and characteristics of pituitary adenomas. European journal of endocrinology / European Federation of Endocrine Societies 2016 May . Peculis Raitis, Balcere Inga, Rovite Vita, Megnis Kaspars, Valtere Andra, Stukens Janis, Arnicane Ligita, Nikitina-Zake Liene, Lejnieks Aivars, Pirags Valdis, Klovins Jan |
| EZH2 and ZFX oncogenes in malignant behaviour of parathyroid neoplasms. Endocrine 2016 Feb . Sanpaolo E, Miroballo M, Corbetta S, Verdelli C, Baorda F, Balsamo T, Graziano P, Fabrizio F P, Cinque L, Scillitani A, Muscarella L A, Guarnieri Vi |
| MAJOR MOLECULAR GENETIC DRIVERS IN SPORADIC PRIMARY HYPERPARATHYROIDISM. Transactions of the American Clinical and Climatological Association 2017 1 127 235-244. Arnold Andr |
| Novel Mutations in Serbian MEN1 Patients: Genotype-phenotype Correlation. Journal of medical biochemistry 2019 Mar 38 (1): 38-44. Isailovic Tatjana, Milicevic Ivana, Macut Djuro, Petakov Milan, Ognjanovic Sanja, Popovic Bojana, Antic Ivana Bozic, Bogavac Tamara, Kovacevic Valentina Elezovic, Ilic Dusan, Damjanovic Svetoz |
| Three Novel MEN1 Variants in AIP-Negative Familial Isolated Pituitary Adenoma Patients. Pathobiology : journal of immunopathology, molecular and cellular biology 2019 Jan 1-7. Yarman Sema, Tuncer Feyza Nur, Serbest Es |
| Analysis of Activating GCM2 Sequence Variants in Sporadic Parathyroid Adenomas. The Journal of clinical endocrinology and metabolism 2019 1 104 (6): 1948-1952. Riccardi Aaliyah, Aspir Tori, Shen Lilia, Kuo Chia-Ling, Brown Taylor C, Korah Reju, Murtha Timothy D, Bellizzi Justin, Parham Kourosh, Carling Tobias, Costa-Guda Jessica, Arnold Andr |
| Differentiated thyroid carcinoma in sporadic and familial presentations of acromegaly: A case series. Annales d'endocrinologie 2020 8 81 (5): 482-486. Rogozinski Amelia, Daly Adrian F, Reyes Adriana, Furioso Alejandra, Beckers Albert, Lowenstein Alic |
| The recurrent p.(Pro540Ser) MEN1 genetic variant should be considered nonpathogenic: A case report. American journal of medical genetics. Part A 2021 7 185 (12): 3872-3876. Villabona Carles, Oriola Josep, Serrano Teresa, Guerrero-Pérez Fernando, Valdés Nuria, Chiara Mariló, Robledo Merced |
| Achalasia and acromegaly: Co-incidence of these diseases or a new syndrome? Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia 2021 7 166 (2): 228-235. Dolina Jiri, Kunovsky Lumir, Kroupa Radek, Stary Karel, Jabandziev Petr, Nesporova Tereza, Maca Karel, Andrasina Tomas, Marek Filip, Kala Zdenek, Vaculova Jitka, Said David, Zapletalova Martina, Lochman Jan, Palova Noskova Hana, Slaby Ondrej, Izakovicova Holla Lydie, Borilova Linhartova Pet |
| Integrated Whole-Exome and Transcriptome Sequencing of Sporadic Parathyroid Adenoma. Frontiers in endocrinology 2021 5 12 631680. Hu Ya, Zhang Xiang, Wang Ou, Cui Ming, Li Xiaobin, Wang Mengyi, Hua Surong, Liao Qu |
| Clinical Profile and Mutations Associated with Multiple Endocrine Neoplasia-Type1 (MEN1) and Their First-Degree Relatives at Risk of Developing MEN1: A Prospective Study. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2021 4 53 (4): 245-256. Shyamasunder Asha Hesarghatta, Pai Rekha, Ramamoorthy Hemalatha, Sakhti Dhananjayan, Manipadam Marie Therese, Kapoor Nitin, Paul Thomas Vizhalil, Jebasingh Felix, Thomas Nihal, Abraham Deepak Thomas, Paul Mazhuvanchary Jacob, Chacko Ari George, Prabhu Krishna, Rajaratnam Sim |
| [MEN for multiple endocrin neoplasms: When evokate MEN? Update 2022]. La Revue de medecine interne 2022 10 44 (1): 12-18. Duval M, Haissaguerre |
| Germline CDKN1B variant type and site are associated with phenotype in MEN4. Endocrine-related cancer 2022 10 30 (1): . Halperin Reut, Arnon Liat, Nasirov Sapir, Friedensohn Limor, Gershinsky Michal, Telerman Alona, Friedman Eitan, Bernstein-Molho Rinat, Tirosh Am |
| The clinical and therapeutic profiles of prolactinomas associated with germline pathogenic variants in the aryl hydrocarbon receptor interacting protein (AIP) gene. Frontiers in endocrinology 2023 9 14 1242588. Laurent Vroonen, Albert Beckers, Severine Camby, Thomas Cuny, Pablo Beckers, Marie-Lise Jaffrain-Rea, Muriel Cogne, Luciana Naves, Amandine Ferriere, Pauline Romanet, Atanaska Elenkova, Auli Karhu, Thierry Brue, Anne Barlier, Patrick Pétrossians, Adrian F Da |
| Genomic profiling reveals the variant landscape of sporadic parathyroid adenomas in Chinese population. The Journal of clinical endocrinology and metabolism 2023 1 . Tao Xiaohui, Xu Tian, Lin Xiaoyun, Xu Shuqin, Fan Youben, Guo Bomin, Deng Xianzhao, Jiao Qiong, Chen Lihui, Wei Zhe, Chen Chengkun, Yang Wendi, Zhang Zhenlin, Yu Xiangtian, Yue H |
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