HuGE Literature Finder
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Records 1-22
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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 |
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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 |
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Whole-Exome Sequencing Identifies Novel Recurrent Somatic Mutations in Sporadic Parathyroid Adenomas.
Endocrinology 2018 Jul . Wei Zhe, Sun Bin, Wang Zong-Ping, He Jin-Wei, Fu Wen-Zhen, Fan You-Ben, Zhang Zhen-L |
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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 |
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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 |
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Histologic and Molecular Profile of Pediatric Insulinomas: Evidence of a Paternal Parent-of-Origin Effect.
The Journal of clinical endocrinology and metabolism 2016 Jan jc20152914. Bhatti Tricia R, Ganapathy Karthik, Huppmann Alison R, Conlin Laura, Boodhansingh Kara E, MacMullen Courtney, Becker Susan, Ernst Linda M, Adzick N Scott, Ruchelli Eduardo D, Ganguly Arupa, Stanley Charles |
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Novel MEN 1 gene findings in rare sporadic insulinoma-a case control study.
BMC endocrine disorders 2015 15 (1): 44. Jyotsna Viveka P, Malik Ekta, Birla Shweta, Sharma Arundha |
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p.Ala541Thr variant of MEN1 gene: a non deleterious polymorphism or a pathogenic mutation?
Annales d'endocrinologie 2014 Jul 75 (3): 133-40. Nozières Cecile, Zhang Chang-Xian, Buffet Alexandre, Dupasquier Stéphanie, Vargas-Poussou Rosa, Guillaud-Bataille Marine, Cordier-Bussat Martine, Ruszniewski Philippe, Christin-Maitre Sophie, Murat Arnaud, Groussin Lionel, Vezzosi Delphine, Cardot-Bauters Catherine, Hervieu Valérie, Joly Marie-Odile, Giraud Sophie, Odou Marie-Françoise, Gimenez-Roqueplo Anne-Paule, Goudet Pierre, Borson-Chazot Françoise, Calender Alain, |
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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 |
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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 |
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Genetic analysis in young patients with sporadic pituitary macroadenomas: besides AIP don't forget MEN1 genetic analysis.
European journal of endocrinology / European Federation of Endocrine Societies 2013 Apr 168 (4): 533-41. Cuny Thomas, Pertuit Morgane, Sahnoun-Fathallah Mona, Daly Adrian, Occhi Gianluca, Odou Marie Françoise, Tabarin Antoine, Nunes Marie Laure, Delemer Brigitte, Rohmer Vincent, Desailloud Rachel, Kerlan Véronique, Chabre Olivier, Sadoul Jean-Louis, Cogne Muriel, Caron Philippe, Cortet-Rudelli Christine, Lienhardt Anne, Raingeard Isabelle, Guedj Anne-Marie, Brue Thierry, Beckers Albert, Weryha Georges, Enjalbert Alain, Barlier An |
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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 |
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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 |
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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 |
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Insulinomatosis: a multicentric insulinoma disease that frequently causes early recurrent hyperinsulinemic hypoglycemia.
The American journal of surgical pathology 2009 Mar 33 (3): 339-46. Anlauf Martin, Bauersfeld Juliane, Raffel Andreas, Koch Christian A, Henopp Tobias, Alkatout Ibrahim, Schmitt Anja, Weber Achim, Kruse Marie L, Braunstein Stefan, Kaserer Klaus, Brauckhoff Michael, Dralle Henning, Moch Holger, Heitz Philipp U, Komminoth Paul, Knoefel Wolfram T, Perren Aurel, Klöppel Günt |
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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 |
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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 |
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Mutations in the aryl hydrocarbon receptor interacting protein gene are not highly prevalent among subjects with sporadic pituitary adenomas.
The Journal of clinical endocrinology and metabolism 2007 May 92 (5): 1952-5. Barlier Anne, Vanbellinghen Jean-François, Daly Adrian F, Silvy Monique, Jaffrain-Rea Marie-Lise, Trouillas Jacqueline, Tamagno Gianluca, Cazabat Laure, Bours Vincent, Brue Thierry, Enjalbert Alain, Beckers Albe |
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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 |
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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 |
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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 |
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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 |
- Page last reviewed:Jul 30, 2019
- Page last updated:Oct 10, 2019
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