BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

550 related articles for article (PubMed ID: 19953642)

  • 21. Multiple endocrine neoplasia type 1 (MEN1): its manifestations and effect of genetic screening on clinical outcome.
    Pieterman CR; Schreinemakers JM; Koppeschaar HP; Vriens MR; Rinkes IH; Zonnenberg BA; van der Luijt RB; Valk GD
    Clin Endocrinol (Oxf); 2009 Apr; 70(4):575-81. PubMed ID: 18616711
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Diagnosis and treatment of multiple endocrine neoplasia type 1 (MEN1).
    Gaztambide S; Vazquez F; Castaño L
    Minerva Endocrinol; 2013 Mar; 38(1):17-28. PubMed ID: 23435440
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Concepts for screening and diagnostic follow-up in multiple endocrine neoplasia type 1 (MEN1).
    Karges W; Schaaf L; Dralle H; Boehm BO
    Exp Clin Endocrinol Diabetes; 2000; 108(5):334-40. PubMed ID: 10989951
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Identification of MEN1 and HRPT2 somatic mutations in paraffin-embedded (sporadic) parathyroid carcinomas.
    Haven CJ; van Puijenbroek M; Tan MH; Teh BT; Fleuren GJ; van Wezel T; Morreau H
    Clin Endocrinol (Oxf); 2007 Sep; 67(3):370-6. PubMed ID: 17555500
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Screening of the Men1 gene and discovery of germ-line and somatic mutations in apparently sporadic parathyroid tumors.
    Uchino S; Noguchi S; Sato M; Yamashita H; Yamashita H; Watanabe S; Murakami T; Toda M; Ohshima A; Futata T; Mizukoshi T; Koike E; Takatsu K; Terao K; Wakiya S; Nagatomo M; Adachi M
    Cancer Res; 2000 Oct; 60(19):5553-7. PubMed ID: 11034102
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic testing in multiple endocrine neoplasia and related syndromes.
    Calender A
    Forum (Genova); 1998; 8(2):146-59. PubMed ID: 9666051
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Clinical symptoms, diagnosis and treatment of multiple endocrine neoplasia type 1. Results of genetic screening in Hungarian patients].
    Balogh K; Hunyady L; Patócs A; Valkusz Z; Bertalan R; Gergics P; Majnik J; Toke J; Tóth M; Szucs N; Gláz E; Futo L; Horányi J; Rácz K; Tulassay Z
    Orv Hetil; 2005 Oct; 146(43):2191-7. PubMed ID: 16323565
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genetic analysis of the MEN1 gene and HPRT2 locus in two Italian kindreds with familial isolated hyperparathyroidism.
    Cetani F; Pardi E; Giovannetti A; Vignali E; Borsari S; Golia F; Cianferotti L; Viacava P; Miccoli P; Gasperi M; Pinchera A; Marcocci C
    Clin Endocrinol (Oxf); 2002 Apr; 56(4):457-64. PubMed ID: 11966738
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Correlation of mutant menin stability with clinical expression of multiple endocrine neoplasia type 1 and its incomplete forms.
    Shimazu S; Nagamura Y; Yaguchi H; Ohkura N; Tsukada T
    Cancer Sci; 2011 Nov; 102(11):2097-102. PubMed ID: 21819486
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A mouse model of multiple endocrine neoplasia, type 1, develops multiple endocrine tumors.
    Crabtree JS; Scacheri PC; Ward JM; Garrett-Beal L; Emmert-Buck MR; Edgemon KA; Lorang D; Libutti SK; Chandrasekharappa SC; Marx SJ; Spiegel AM; Collins FS
    Proc Natl Acad Sci U S A; 2001 Jan; 98(3):1118-23. PubMed ID: 11158604
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Cutaneous lesions associated to multiple endocrine neoplasia syndrome type 1.
    Vidal A; Iglesias MJ; Fernández B; Fonseca E; Cordido F
    J Eur Acad Dermatol Venereol; 2008 Jul; 22(7):835-8. PubMed ID: 18435740
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Mutation analysis in a Chinese family with multiple endocrine neoplasia type 1.
    Zha BB; Liang W; Liu J; Cheng J; Hong XW; Liu J; Li YM; Ma D
    Chin Med J (Engl); 2010 Mar; 123(5):569-73. PubMed ID: 20367983
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Genetic screening for MEN1 mutations in families presenting with familial primary hyperparathyroidism.
    Perrier ND; Villablanca A; Larsson C; Wong M; Ituarte P; Teh BT; Clark OH
    World J Surg; 2002 Aug; 26(8):907-13. PubMed ID: 12016470
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Germline mutation profile of MEN1 in multiple endocrine neoplasia type 1: search for correlation between phenotype and the functional domains of the MEN1 protein.
    Wautot V; Vercherat C; Lespinasse J; Chambe B; Lenoir GM; Zhang CX; Porchet N; Cordier M; Béroud C; Calender A
    Hum Mutat; 2002 Jul; 20(1):35-47. PubMed ID: 12112656
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Analysis of gross deletions in the MEN1 gene in patients with multiple endocrine neoplasia type 1.
    Owens M; Ellard S; Vaidya B
    Clin Endocrinol (Oxf); 2008 Mar; 68(3):350-4. PubMed ID: 17854391
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular genetics of primary and secondary hyperparathyroidism.
    Dotzenrath C; Goretzki PE; Farnebo F; Teh BT; Weber G; Röher HD; Larsson C
    Exp Clin Endocrinol Diabetes; 1996; 104 Suppl 4():105-7. PubMed ID: 8981014
    [TBL] [Abstract][Full Text] [Related]  

  • 38. MEN1 gene and its mutations: basic and clinical implications.
    Tsukada T; Nagamura Y; Ohkura N
    Cancer Sci; 2009 Feb; 100(2):209-15. PubMed ID: 19068082
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A novel deletion of the MEN1 gene in a large family of multiple endocrine neoplasia type 1 (MEN1) with aggressive phenotype.
    Raef H; Zou M; Baitei EY; Al-Rijjal RA; Kaya N; Al-Hamed M; Monies D; Abu-Dheim NN; Al-Hindi H; Al-Ghamdi MH; Meyer BF; Shi Y
    Clin Endocrinol (Oxf); 2011 Dec; 75(6):791-800. PubMed ID: 21627674
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Novel mutations in MEN1, CDKN1B and AIP genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain.
    Belar O; De La Hoz C; Pérez-Nanclares G; Castaño L; Gaztambide S;
    Clin Endocrinol (Oxf); 2012 May; 76(5):719-24. PubMed ID: 22026581
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 28.