BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 23778871)

  • 1. A MEN1 syndrome with a paraganglioma.
    Jamilloux Y; Favier J; Pertuit M; Delage-Corre M; Lopez S; Teissier MP; Mathonnet M; Galinat S; Barlier A; Archambeaud F
    Eur J Hum Genet; 2014 Feb; 22(2):283-5. PubMed ID: 23778871
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Primary Renal Paragangliomas and Renal Neoplasia Associated with Pheochromocytoma/Paraganglioma: Analysis of von Hippel-Lindau (VHL), Succinate Dehydrogenase (SDHX) and Transmembrane Protein 127 (TMEM127).
    Gupta S; Zhang J; Milosevic D; Mills JR; Grebe SK; Smith SC; Erickson LA
    Endocr Pathol; 2017 Sep; 28(3):253-268. PubMed ID: 28646318
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pediatric paraganglioma: an early manifestation of an adult disease secondary to germline mutations.
    Mora J; Cascón A; Robledo M; Catala A
    Pediatr Blood Cancer; 2006 Nov; 47(6):785-9. PubMed ID: 16304664
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Novel SDHB and TMEM127 Mutations in Patients with Pheochromocytoma/Paraganglioma Syndrome.
    Patócs A; Lendvai NK; Butz H; Liko I; Sapi Z; Szucs N; Toth G; Grolmusz VK; Igaz P; Toth M; Rácz K
    Pathol Oncol Res; 2016 Oct; 22(4):673-9. PubMed ID: 26960314
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Germline mutations of the MEN1 gene in Korean families with multiple endocrine neoplasia type 1 (MEN1) or MEN1-related disorders.
    Park JH; Kim IJ; Kang HC; Lee SH; Shin Y; Kim KH; Lim SB; Kang SB; Lee K; Kim SY; Lee MS; Lee MK; Park JH; Moon SD; Park JG
    Clin Genet; 2003 Jul; 64(1):48-53. PubMed ID: 12791038
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Clinical testing for multiple endocrine neoplasia type 1 in a DNA diagnostic laboratory.
    Klein RD; Salih S; Bessoni J; Bale AE
    Genet Med; 2005 Feb; 7(2):131-8. PubMed ID: 15714081
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. ARMC5 Alterations in Patients With Sporadic Neuroendocrine Tumors and Multiple Endocrine Neoplasia Type 1 (MEN1).
    Damjanovic SS; Antic JA; Elezovic-Kovacevic VI; Dundjerovic DM; Milicevic IT; Beleslin-Cokic BB; Ilic BB; Rodic GS; Berthon A; Maria AG; Faucz FR; Stratakis CA
    J Clin Endocrinol Metab; 2020 Dec; 105(12):e4531-42. PubMed ID: 32901291
    [TBL] [Abstract][Full Text] [Related]  

  • 10. LOH on chromosome 11q, but not SDHD and Men1 mutations was frequently detectable in Chinese patients with pheochromocytoma and paraganglioma.
    Sun HY; Cui B; Su DW; Jin XL; Sun FK; Zu Y; Jiang L; Wang WQ; Ning G
    Endocrine; 2006 Dec; 30(3):307-12. PubMed ID: 17526943
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Compound heterozygous mutation with a novel splice donor region DNA sequence variant in the succinate dehydrogenase subunit B gene in malignant paraganglioma.
    Majumdar S; Friedrich CA; Koch CA; Megason GC; Fratkin JD; Moll GW
    Pediatr Blood Cancer; 2010 Mar; 54(3):473-5. PubMed ID: 19927285
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Primary hyperparathyroidism associatiated with aldosterone-producing adrenocortical adenoma and breast cancer: relation to MEN1 gene.
    Honda M; Tsukada T; Horiuchi T; Tanaka R; Yamaguchi K; Obara T; Miyakawa H; Yamaji T; Ishibashi M
    Intern Med; 2004 Apr; 43(4):310-4. PubMed ID: 15168774
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Unusual presentation of multiple endocrine neoplasia type 1 in a young woman with a novel mutation of the MEN1 gene.
    Balogh K; Patócs A; Majnik J; Varga F; Illyés G; Hunyady L; Rácz K
    J Hum Genet; 2004; 49(7):380-386. PubMed ID: 15205994
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Multiple endocrine neoplasia type 1.
    Marini F; Falchetti A; Del Monte F; Carbonell Sala S; Gozzini A; Luzi E; Brandi ML
    Orphanet J Rare Dis; 2006 Oct; 1():38. PubMed ID: 17014705
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Two novel mutations in the MEN1 gene in subjects with multiple endocrine neoplasia-1.
    Ozturk M; Chiu CY; Akdeniz N; Jenq SF; Chang SC; Hsa CY; Jap TS
    J Endocrinol Invest; 2006 Jun; 29(6):523-7. PubMed ID: 16840830
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Bilateral adrenocortical carcinoma in a patient with multiple endocrine neoplasia type 1 (MEN1) and a novel mutation in the MEN1 gene.
    Griniatsos JE; Dimitriou N; Zilos A; Sakellariou S; Evangelou K; Kamakari S; Korkolopoulou P; Kaltsas G
    World J Surg Oncol; 2011 Jan; 9():6. PubMed ID: 21266030
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Screening for MEN1 mutations in patients with atypical endocrine neoplasia.
    Dackiw AP; Cote GJ; Fleming JB; Schultz PN; Stanford P; Vassilopoulou-Sellin R; Evans DB; Gagel RF; Lee JE
    Surgery; 1999 Dec; 126(6):1097-103; discussion 1103-4. PubMed ID: 10598193
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.