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263 related items for PubMed ID: 17878646
1. McCune-Albright syndrome with acromegaly and fibrous dysplasia associated with the GNAS gene mutation identified by sensitive PNA-clamping method. Imanaka M, Iida K, Nishizawa H, Fukuoka H, Takeno R, Takahashi K, Kaji H, Takahashi Y, Okimura Y, Kaji H, Imanishi Y, Chihara K. Intern Med; 2007; 46(18):1577-83. PubMed ID: 17878646 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
3. McCune-Albright syndrome and the extraskeletal manifestations of fibrous dysplasia. Collins MT, Singer FR, Eugster E. Orphanet J Rare Dis; 2012 May 24; 7 Suppl 1(Suppl 1):S4. PubMed ID: 22640971 [Abstract] [Full Text] [Related]
4. A case of McCune-Albright syndrome associated with Gs alpha mutation in the bone tissue. Sargin H, Gozu H, Bircan R, Sargin M, Avsar M, Ekinci G, Yayla A, Gulec I, Bozbuga M, Cirakoglu B, Tanakol R. Endocr J; 2006 Feb 24; 53(1):35-44. PubMed ID: 16543670 [Abstract] [Full Text] [Related]
5. The diagnostic utility of the GNAS mutation in patients with fibrous dysplasia: meta-analysis of 168 sporadic cases. Lee SE, Lee EH, Park H, Sung JY, Lee HW, Kang SY, Seo S, Kim BH, Lee H, Seo AN, Ahn G, Choi YL. Hum Pathol; 2012 Aug 24; 43(8):1234-42. PubMed ID: 22245114 [Abstract] [Full Text] [Related]
12. Identification of GNAS Variants in Circulating Cell-Free DNA from Patients with Fibrous Dysplasia/McCune Albright Syndrome. Roszko KL, Guthrie L, Li X, Collins MT, de Castro LF, Boyce AM. J Bone Miner Res; 2023 Mar 24; 38(3):443-450. PubMed ID: 36593655 [Abstract] [Full Text] [Related]
14. Genetic diagnosis of multiple affected tissues in a patient with McCune-Albright syndrome. Zhou J, Sun LH, Cui B, Song HD, Li XY, Ning G, Liu JM. Endocrine; 2007 Apr 24; 31(2):212-7. PubMed ID: 17873334 [Abstract] [Full Text] [Related]