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8. 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]
9. 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]
10. Activating GNAS mutations in parosteal osteosarcoma. Carter JM; Inwards CY; Jin L; Evers B; Wenger DE; Oliveira AM; Fritchie KJ Am J Surg Pathol; 2014 Mar; 38(3):402-9. PubMed ID: 24525511 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. 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]
17. Minireview: GNAS: normal and abnormal functions. Weinstein LS; Liu J; Sakamoto A; Xie T; Chen M Endocrinology; 2004 Dec; 145(12):5459-64. PubMed ID: 15331575 [TBL] [Abstract][Full Text] [Related]
18. Quantitative and sensitive detection of GNAS mutations causing mccune-albright syndrome with next generation sequencing. Narumi S; Matsuo K; Ishii T; Tanahashi Y; Hasegawa T PLoS One; 2013; 8(3):e60525. PubMed ID: 23536913 [TBL] [Abstract][Full Text] [Related]
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20. Using Digital Droplet Polymerase Chain Reaction to Detect the Mosaic GNAS Mutations in Whole Blood DNA or Circulating Cell-Free DNA in Fibrous Dysplasia and McCune-Albright Syndrome. Romanet P; Philibert P; Fina F; Cuny T; Roche C; Ouafik L; Paris F; Reynaud R; Barlier A J Pediatr; 2019 Feb; 205():281-285.e4. PubMed ID: 30442414 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]