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7. The Clinical Spectrum of McCune-Albright Syndrome and Its Management. Spencer T; Pan KS; Collins MT; Boyce AM Horm Res Paediatr; 2019; 92(6):347-356. PubMed ID: 31865341 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. [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]
11. 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]
12. Brain and eye involvement in McCune-Albright Syndrome: clinical and translational insights. Mascioli I; Iapadre G; Ingrosso D; Donato GD; Giannini C; Salpietro V; Chiarelli F; Farello G Front Endocrinol (Lausanne); 2023; 14():1092252. PubMed ID: 37274327 [TBL] [Abstract][Full Text] [Related]
13. Fibrous Dysplasia of Bone and McCune-Albright Syndrome: A Bench to Bedside Review. Hartley I; Zhadina M; Collins MT; Boyce AM Calcif Tissue Int; 2019 May; 104(5):517-529. PubMed ID: 31037426 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. McCune-Albright syndrome associated with pituitary adenoma: a clinicopathological study of ten cases and literature review. Li Z; Liu R; Liu P Br J Neurosurg; 2024 Aug; 38(4):867-876. PubMed ID: 34632888 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. The role of type 1 and type 2 5'-deiodinase in the pathophysiology of the 3,5,3'-triiodothyronine toxicosis of McCune-Albright syndrome. Celi FS; Coppotelli G; Chidakel A; Kelly M; Brillante BA; Shawker T; Cherman N; Feuillan PP; Collins MT J Clin Endocrinol Metab; 2008 Jun; 93(6):2383-9. PubMed ID: 18349068 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. McCune-Albright syndrome and the extraskeletal manifestations of fibrous dysplasia. Collins MT; Singer FR; Eugster E Orphanet J Rare Dis; 2012 May; 7 Suppl 1(Suppl 1):S4. PubMed ID: 22640971 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]