BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

194 related articles for article (PubMed ID: 34889280)

  • 41. A novel mutation of the MEN1 gene in a patient with multiple endocrine neoplasia type 1 and recurrent fibromyxoid sarcoma - a case report.
    Radman M; Milicevic T
    BMC Med Genet; 2020 Sep; 21(1):190. PubMed ID: 32993530
    [TBL] [Abstract][Full Text] [Related]  

  • 42. [Clinicogenetic study of MEN1: recent physiopathological data and clinical applications. Study Group of Multiple Endocrine Neoplasia (GENEM)].
    Calender A; Giraud S; Porchet N; Gaudray P; Cadiot G; Mignon M
    Ann Endocrinol (Paris); 1998; 59(6):444-51. PubMed ID: 10189986
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A Novel Germline c.1267T>A
    Gierlikowski W; Skwarek-Szewczyk A; Popow M
    Genes (Basel); 2020 Nov; 11(11):. PubMed ID: 33233395
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Safety and efficacy of percutaneous parathyroid ethanol ablation in patients with recurrent primary hyperparathyroidism and multiple endocrine neoplasia type 1.
    Singh Ospina N; Thompson GB; Lee RA; Reading CC; Young WF
    J Clin Endocrinol Metab; 2015 Jan; 100(1):E87-90. PubMed ID: 25337928
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Novel Germline p.Gly42Val
    Koehler VF; Jungheim K; Groß U; Iacovazzo D; Mann A; Korbonits M
    Ann Clin Lab Sci; 2017 Sep; 47(5):606-610. PubMed ID: 29066490
    [TBL] [Abstract][Full Text] [Related]  

  • 46. A novel mutation of the MEN1 gene in a Japanese kindred with familial isolated primary hyperparathyroidism.
    Honda M; Tsukada T; Tanaka H; Maruyama K; Yamaguchi K; Obara T; Yamaji T; Ishibashi M
    Eur J Endocrinol; 2000 Feb; 142(2):138-43. PubMed ID: 10664521
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4).
    Thakker RV
    Mol Cell Endocrinol; 2014 Apr; 386(1-2):2-15. PubMed ID: 23933118
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Germ-line mutation analysis in patients with multiple endocrine neoplasia type 1 and related disorders.
    Giraud S; Zhang CX; Serova-Sinilnikova O; Wautot V; Salandre J; Buisson N; Waterlot C; Bauters C; Porchet N; Aubert JP; Emy P; Cadiot G; Delemer B; Chabre O; Niccoli P; Leprat F; Duron F; Emperauger B; Cougard P; Goudet P; Sarfati E; Riou JP; Guichard S; Rodier M; Meyrier A; Caron P; Vantyghem MC; Assayag M; Peix JL; Pugeat M; Rohmer V; Vallotton M; Lenoir G; Gaudray P; Proye C; Conte-Devolx B; Chanson P; Shugart YY; Goldgar D; Murat A; Calender A
    Am J Hum Genet; 1998 Aug; 63(2):455-67. PubMed ID: 9683585
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Analysis of genotype-phenotype correlations and survival outcomes in patients with primary hyperparathyroidism caused by multiple endocrine neoplasia type 1: the experience at a single institution.
    Horiuchi K; Okamoto T; Iihara M; Tsukada T
    Surg Today; 2013 Aug; 43(8):894-9. PubMed ID: 23052745
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Multiple endocrine neoplasia type 1.
    Agarwal SK
    Front Horm Res; 2013; 41():1-15. PubMed ID: 23652667
    [TBL] [Abstract][Full Text] [Related]  

  • 51. A novel menin gene deletional mutation in a little series of Italian patients affected by apparently sporadic multiple endocrine neoplasia type 1 syndrome.
    Giacché M; Panarotto A; Mori L; Daffini L; Tacchetti MC; Pirola I; Agabiti Rosei E; Castellano M
    J Endocrinol Invest; 2012 Feb; 35(2):124-8. PubMed ID: 22490989
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Asymptomatic children with multiple endocrine neoplasia type 1 mutations may harbor nonfunctioning pancreatic neuroendocrine tumors.
    Newey PJ; Jeyabalan J; Walls GV; Christie PT; Gleeson FV; Gould S; Johnson PR; Phillips RR; Ryan FJ; Shine B; Bowl MR; Thakker RV
    J Clin Endocrinol Metab; 2009 Oct; 94(10):3640-6. PubMed ID: 19622622
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Genetic analysis of parathyroid and pancreatic tumors in a patient with multiple endocrine neoplasia type 1 using whole-exome sequencing.
    Kim BY; Park MH; Woo HM; Jo HY; Kim JH; Choi HJ; Koo SK
    BMC Med Genet; 2017 Oct; 18(1):106. PubMed ID: 28969599
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Multiple endocrine neoplasia type 1 (MEN1): analysis of 1336 mutations reported in the first decade following identification of the gene.
    Lemos MC; Thakker RV
    Hum Mutat; 2008 Jan; 29(1):22-32. PubMed ID: 17879353
    [TBL] [Abstract][Full Text] [Related]  

  • 55. A puzzling case of phospho-soda-induced hypocalcemia in a patient with multiple endocrine neoplasia type 1-associated primary hyperparathyroidism.
    Ozveren A; Akinci B; Makay O; Sarsik B; Simsir IY; Berdeli A; Akyildiz M
    Intern Med; 2012; 51(22):3145-9. PubMed ID: 23154721
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Hyperparathyroidism in hereditary syndromes: special expressions and special managements.
    Marx SJ; Simonds WF; Agarwal SK; Burns AL; Weinstein LS; Cochran C; Skarulis MC; Spiegel AM; Libutti SK; Alexander HR; Chen CC; Chang R; Chandrasekharappa SC; Collins FS
    J Bone Miner Res; 2002 Nov; 17 Suppl 2():N37-43. PubMed ID: 12412776
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Clinical aspects of multiple endocrine neoplasia type 1.
    Al-Salameh A; Cadiot G; Calender A; Goudet P; Chanson P
    Nat Rev Endocrinol; 2021 Apr; 17(4):207-224. PubMed ID: 33564173
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Growth hormone-releasing hormone-producing pancreatic neuroendocrine tumor in a multiple endocrine neoplasia type 1 family with an uncommon phenotype.
    Sala E; Ferrante E; Verrua E; Malchiodi E; Mantovani G; Filopanti M; Ferrero S; Pietrabissa A; Vanoli A; La Rosa S; Zatelli MC; Beck-Peccoz P; Verga U
    Eur J Gastroenterol Hepatol; 2013 Jul; 25(7):858-62. PubMed ID: 23542451
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Expression and functional analysis of menin in a multiple endocrine neoplasia type 1 (MEN1) patient with somatic loss of heterozygosity in chromosome 11q13 and unidentified germline mutation of the MEN1 gene.
    Naito J; Kaji H; Sowa H; Kitazawa R; Kitazawa S; Tsukada T; Hendy GN; Sugimoto T; Chihara K
    Endocrine; 2006 Jun; 29(3):485-90. PubMed ID: 16943588
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A new mutation in the menin gene causes the multiple endocrine neoplasia type 1 syndrome with adrenocortical carcinoma.
    Haase M; Anlauf M; Schott M; Schinner S; Kaminsky E; Scherbaum WA; Willenberg HS
    Endocrine; 2011 Apr; 39(2):153-9. PubMed ID: 21069576
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.