BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

252 related articles for article (PubMed ID: 24170100)

  • 1. Hepatobiliary and Pancreatic neoplasms in patients with McCune-Albright syndrome.
    Gaujoux S; Salenave S; Ronot M; Rangheard AS; Cros J; Belghiti J; Sauvanet A; Ruszniewski P; Chanson P
    J Clin Endocrinol Metab; 2014 Jan; 99(1):E97-101. PubMed ID: 24170100
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Lessons from McCune-Albright syndrome-associated intraductal papillary mucinous neoplasms: : GNAS-activating mutations in pancreatic carcinogenesis.
    Parvanescu A; Cros J; Ronot M; Hentic O; Grybek V; Couvelard A; Levy P; Chanson P; Ruszniewski P; Sauvanet A; Gaujoux S
    JAMA Surg; 2014 Aug; 149(8):858-62. PubMed ID: 24898823
    [TBL] [Abstract][Full Text] [Related]  

  • 3. McCune Albright syndrome is a genetic predisposition to intraductal papillary and mucinous neoplasms of the pancreas associated pancreatic cancer in relation with GNAS somatic mutation - a case report.
    Gaujoux S; Pasmant E; Silve C; Mehsen-Cetre N; Coriat R; Rouquette A; Douset B; Prat F; Leroy K
    Medicine (Baltimore); 2019 Dec; 98(50):e18102. PubMed ID: 31852070
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical and Radiographic Gastrointestinal Abnormalities in McCune-Albright Syndrome.
    Robinson C; Estrada A; Zaheer A; Singh VK; Wolfgang CL; Goggins MG; Hruban RH; Wood LD; Noë M; Montgomery EA; Guthrie LC; Lennon AM; Boyce AM; Collins MT
    J Clin Endocrinol Metab; 2018 Nov; 103(11):4293-4303. PubMed ID: 30124968
    [TBL] [Abstract][Full Text] [Related]  

  • 5. GNAS mutation detection is related to disease severity in girls with McCune-Albright syndrome and precocious puberty.
    Wagoner HA; Steinmetz R; Bethin KE; Eugster EA; Pescovitz OH; Hannon TS
    Pediatr Endocrinol Rev; 2007 Aug; 4 Suppl 4():395-400. PubMed ID: 17982386
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinical and endocrine characteristics and genetic analysis of Korean children with McCune-Albright syndrome: a retrospective cohort study.
    Cho EK; Kim J; Yang A; Ki CS; Lee JE; Cho SY; Jin DK
    Orphanet J Rare Dis; 2016 Aug; 11(1):113. PubMed ID: 27506760
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [McCune-Albright syndrome revealed by Blaschko-linear café-au-lait spots on the back].
    Jung AJ; Soskin S; Paris F; Lipsker D
    Ann Dermatol Venereol; 2016 Jan; 143(1):21-6. PubMed ID: 26610360
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Patients with McCune-Albright syndrome have a broad spectrum of abnormalities in the gastrointestinal tract and pancreas.
    Wood LD; Noë M; Hackeng W; Brosens LA; Bhaijee F; Debeljak M; Yu J; Suenaga M; Singhi AD; Zaheer A; Boyce A; Robinson C; Eshleman JR; Goggins MG; Hruban RH; Collins MT; Lennon AM; Montgomery EA
    Virchows Arch; 2017 Apr; 470(4):391-400. PubMed ID: 28188442
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A highly sensitive polymerase chain reaction method detects activating mutations of the GNAS gene in peripheral blood cells in McCune-Albright syndrome or isolated fibrous dysplasia.
    Lietman SA; Ding C; Levine MA
    J Bone Joint Surg Am; 2005 Nov; 87(11):2489-94. PubMed ID: 16264125
    [TBL] [Abstract][Full Text] [Related]  

  • 10. GNAS-activating mutations define a rare subgroup of inflammatory liver tumors characterized by STAT3 activation.
    Nault JC; Fabre M; Couchy G; Pilati C; Jeannot E; Tran Van Nhieu J; Saint-Paul MC; De Muret A; Redon MJ; Buffet C; Salenave S; Balabaud C; Prevot S; Labrune P; Bioulac-Sage P; Scoazec JY; Chanson P; Zucman-Rossi J
    J Hepatol; 2012 Jan; 56(1):184-91. PubMed ID: 21835143
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Thyroid carcinoma in the McCune-Albright syndrome: contributory role of activating Gs alpha mutations.
    Collins MT; Sarlis NJ; Merino MJ; Monroe J; Crawford SE; Krakoff JA; Guthrie LC; Bonat S; Robey PG; Shenker A
    J Clin Endocrinol Metab; 2003 Sep; 88(9):4413-7. PubMed ID: 12970318
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic and molecular aspects of McCune-Albright syndrome.
    Lietman SA; Schwindinger WF; Levine MA
    Pediatr Endocrinol Rev; 2007 Aug; 4 Suppl 4():380-5. PubMed ID: 17982384
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Extent of Extraskeletal Manifestations of Fibrous Dysplasia/McCune-Albright Syndrome in Patients with Mazabraud's Syndrome.
    Hagelstein-Rotman M; Appelman-Dijkstra NM; Boyce AM; Chapurlat R; Dur NBJ; Gensburger D; Majoor BCJ; van de Sande MAJ; Dijkstra PDS
    Calcif Tissue Int; 2022 Mar; 110(3):334-340. PubMed ID: 34854944
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Detection of Rare Somatic GNAS Mutation in McCune-Albright Syndrome Using a Novel Peptide Nucleic Acid Probe in a Single Tube.
    Lo FS; Chen TL; Chiou CC
    Molecules; 2017 Nov; 22(11):. PubMed ID: 29104223
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Combining Real-Time COLD- and MAMA-PCR TaqMan Techniques to Detect and Quantify R201 GNAS Mutations in the McCune-Albright Syndrome
.
    de Sanctis L; Galliano I; Montanari P; Matarazzo P; Tessaris D; Bergallo M
    Horm Res Paediatr; 2017; 87(5):342-349. PubMed ID: 28334704
    [TBL] [Abstract][Full Text] [Related]  

  • 16. McCune-Albright syndrome: a detailed pathological and genetic analysis of disease effects in an adult patient.
    Vasilev V; Daly AF; Thiry A; Petrossians P; Fina F; Rostomyan L; Silvy M; Enjalbert A; Barlier A; Beckers A
    J Clin Endocrinol Metab; 2014 Oct; 99(10):E2029-38. PubMed ID: 25062453
    [TBL] [Abstract][Full Text] [Related]  

  • 17. McCune-Albright syndrome and disorders due to activating mutations of GNAS1.
    Diaz A; Danon M; Crawford J
    J Pediatr Endocrinol Metab; 2007 Aug; 20(8):853-80. PubMed ID: 17937059
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Virilizing sclerosing-stromal tumor of the ovary in a young woman with McCune Albright syndrome: clinical, pathological, and immunohistochemical studies.
    Boussaïd K; Meduri G; Maiza JC; Gennero I; Escourrou G; Bros A; Leguevaque P; Bennet A; Caron P
    J Clin Endocrinol Metab; 2013 Feb; 98(2):E314-20. PubMed ID: 23365131
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Fibrous Dysplasia/McCune-Albright Syndrome: Clinical and Translational Perspectives.
    Robinson C; Collins MT; Boyce AM
    Curr Osteoporos Rep; 2016 Oct; 14(5):178-86. PubMed ID: 27492469
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A Novel GNAS Mutation Causing Isolated Infantile Cushing's Syndrome.
    Dejkhamron P; Ittiwut C; TangNgam H; Sunkonkit K; Natesirinilkul R; Suphapeetiporn K; Shotelersuk V
    Horm Res Paediatr; 2019; 92(3):196-202. PubMed ID: 31362300
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.