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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 - 8 (of 8 Records)

Query Trace: Multiple Endocrine Neoplasia Type 1 and AIP[original query]
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
Anterior pituitary adenomas: inherited syndromes, novel genes and molecular pathways.
Expert review of endocrinology & metabolism 2011 1 5 (5): 697-709.
Xekouki Paraskevi, Azevedo Monalisa, Stratakis Constantine
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
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
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
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
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, Dos S Faria Manu
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