HuGE Literature Finder
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| The Importance of Periodical Screening for Primary Hyperparathyroidism in a Pituitary Tumor Cohort in Searching Patients with MEN1 and its Genetic Profile. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2022 Mar . Damianse Sabrina S P, Nascimento Gilvan C, Rocha Viviane C C, Nascimento Ana Gisélia P A C, Gaido Nadja C, Azulay Rossana S S, Dos Santos Wellyandra C, Rodrigues Vandilson P, Quidute Ana Rosa P, Magalhães Marcelo, Faria Manuel Dos |
| Two Distinct Classes of Thymic Tumors in Patients with MEN1 Show LOH at the MEN1 Locus. Endocrine-related cancer 2021 Sep . Mandl Adel, Welch James M, Kapoor Gayathri, Parekh Vaishali I, Schrump David S, Ripley R Taylor, Walter Mary F, Del Rivero Jaydira, Jha Smita, Simonds William F, Jensen Robert T, Weinstein Lee S, Blau Jenny E, Agarwal Sunita |
| True MEN1 or phenocopy? Evidence for geno-phenotypic correlations in MEN1 syndrome. Endocrine 2019 May . Kövesdi Annamária, Tóth Miklós, Butz Henriett, Szücs Nikolette, Sármán Beatrix, Pusztai Péter, Toke Judit, Reismann Péter, Fáklya Mónika, Tóth Géza, Somogyi Anikó, Borka Katalin, Erdei Annamária, Nagy Endre V, Deák Veronika, Valkusz Zsuzsanna, Igaz Péter, Patócs Attila, Grolmusz Vince Korn |
| 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 |
| Co-occurrence of MEN1 p.Gly111fs and AIP p.Arg16His Variants in Familial MEN1 Phenotype. Anticancer research 2018 Jun 38 (6): 3683-3687. DE Melo Flavia Marques, Bastos-Rodrigues Luciana, Sarquis Maria Marta, Friedman Eitan, DE Marco Lu |
| Clinical Features, Treatments, and Outcomes of Patients with Thymic Carcinoids and Multiple Endocrine Neoplasia Type 1 Syndrome at MD Anderson Cancer Center. Hormones & cancer 2016 Jun . Christakis Ioannis, Qiu Wei, Silva Figueroa Angelica M, Hyde Samuel, Cote Gilbert J, Busaidy Naifa L, Williams Michelle, Grubbs Elizabeth, Lee Jeffrey E, Perrier Nancy |
| Prognostic role of the CDNK1B V109G polymorphism in multiple endocrine neoplasia type 1. Journal of cellular and molecular medicine 2015 Jul 19 (7): 1735-41. Circelli Luisa, Ramundo Valeria, Marotta Vincenzo, Sciammarella Concetta, Marciello Francesca, Del Prete Michela, Sabatino Lina, Pasquali Daniela, Izzo Francesco, Scala Stefania, Colao Annamaria, Faggiano Antongiulio, Colantuoni Vittorio, |
| 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 |
| Higher risk of aggressive pancreatic neuroendocrine tumors in MEN1 patients with MEN1 mutations affecting the CHES1 interacting MENIN domain. The Journal of clinical endocrinology and metabolism 2014 Nov 99 (11): E2387-91. Bartsch Detlef K, Slater Emily P, Albers Max, Knoop Richard, Chaloupka Brunhilde, Lopez Caroline L, Fendrich Volker, Kann Peter H, Waldmann Je |
| Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations. European journal of endocrinology / European Federation of Endocrine Societies 2014 Sep 171 (3): 335-42. Longuini Viviane C, Lourenço Delmar M, Sekiya Tomoko, Meirelles Osorio, Goncalves Tatiana D, Coutinho Flavia L, Francisco Guilherme, Osaki Luciana H, Chammas Roger, Alves Venancio A F, Siqueira Sheila A C, Schlesinger David, Naslavsky Michel S, Zatz Mayana, Duarte Yeda A O, Lebrão Maria Lucia, Gama Patricia, Lee Misu, Molatore Sara, Pereira Maria Adelaide A, Jallad Raquel S, Bronstein Marcello D, Cunha-Neto Malebranche B, Liberman Bernardo, Fragoso Maria Candida B V, Toledo Sergio P A, Pellegata Natalia S, Toledo Rodrigo |
| 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, |
| 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 |
| Higher risk of death among MEN1 patients with mutations in the JunD interacting domain: a Groupe d'etude des Tumeurs Endocrines (GTE) cohort study. Human molecular genetics 2013 Jan . Thevenon J, Bourredjem A, Faivre L, Cardot-Bauters C, Calender A, Murat A, Giraud S, Niccoli P, Odou MF, Borson-Chazot F, Barlier A, Lombard-Bohas C, Clauser E, Tabarin A, Parfait B, Chabre O, Castermans E, Ruszniewski P, Le Bras M, Delemer B, Bouchard P, Beckers A, Guilhem I, Rohmer V, Goichot B, Caron P, Baudin E, Chanson P, Groussin L, Du Boullay H, Weryha G, Lecomte P, Penfornis A, Bihan H, Archambeaud F, Kerlan V, Duron F, Kuhn JM, Vergès B, Rodier M, Renard M, Sadoul JL, Binquet C, Goudet P |
| Increased prevalence of impaired fasting glucose in MEN1 gene mutation carriers. Clinical endocrinology 2012 Jan 76 (1): 67-71. van Wijk J P H, Dreijerink K M A, Pieterman C R C, Lips C J M, Zelissen P M J, Valk G |
| Somatic mutation and germline sequence abnormalities in CDKN1B, encoding p27Kip1, in sporadic parathyroid adenomas. The Journal of clinical endocrinology and metabolism 2011 Apr 96 (4): E701-6. Costa-Guda Jessica, Marinoni Ilaria, Molatore Sara, Pellegata Natalia S, Arnold Andr |
| 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 |
| Should routine analysis of the MEN1 gene be performed in all patients with primary hyperparathyroidism under 40 years of age? World journal of surgery 2010 Jun 34 (6): 1294-8. Skandarajah Anita, Barlier Anne, Morlet-Barlat Nathalie, Sebag Frederic, Enjalbert Alain, Conte-Devolx Bernard, Henry Jean-Franço |
| 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 |
| Rare germline mutations in cyclin-dependent kinase inhibitor genes in multiple endocrine neoplasia type 1 and related states. The Journal of clinical endocrinology and metabolism 2009 May 94 (5): 1826-34. Agarwal Sunita K, Mateo Carmen M, Marx Stephen |
| 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 |
| 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 |
| 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 |
| 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 |
| Developing effective screening strategies in multiple endocrine neoplasia type 1 (MEN 1) on the basis of clinical and sequencing data of German patients with MEN 1. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2007 Sep 115 (8): 509-17. Schaaf L, Pickel J, Zinner K, Hering U, Höfler M, Goretzki P E, Spelsberg F, Raue F, von zur Mühlen A, Gerl H, Hensen J, Bartsch D K, Rothmund M, Schneyer U, Dralle H, Engelbach M, Karges W, Stalla G K, Höppner |
| Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas. Clinical endocrinology 2007 Sep 67 (3): 370-6. Haven C J, van Puijenbroek M, Tan M H, Teh B T, Fleuren G J, van Wezel T, Morreau |
| 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 |
| The impact of clinical and genetic screenings on the management of the multiple endocrine neoplasia type 1. Clinics (São Paulo, Brazil) 2007 Aug 62 (4): 465-76. Lourenço Delmar Muniz, Toledo Rodrigo Almeida, Coutinho Flavia Lima, Margarido Leontina Conceição, Siqueira Sheila Aparecida Coelho, dos Santos Marcelo Augusto Cortina Gonçalves, Montenegro Fabio Luiz de Menezes, Machado Marcel Cerqueira Cesar, Toledo Sergio Pereira Almei |
| 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 |
| 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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- Page last updated:Jun 22, 2022
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