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Unusual Presentation of Fibrous Dysplasia in an Elderly Patient.

Alkhaibary A, Alassiri AH, Alsalman M, Edrees S.

J Radiol Case Rep. 2019 Feb 28;13(2):26-33. doi: 10.3941/jrcr.v13i2.3379. eCollection 2019 Feb.


Neonatal McCune-Albright Syndrome: A Unique Syndromic Profile With an Unfavorable Outcome.

Corsi A, Cherman N, Donaldson DL, Robey PG, Collins MT, Riminucci M.

JBMR Plus. 2019 Jan 15;3(8):e10134. doi: 10.1002/jbm4.10134. eCollection 2019 Aug.


Fibrous Dysplasia/McCune-Albright Syndrome.

Boyce AM, Florenzano P, de Castro LF, Collins MT.

In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2019.
2015 Feb 26 [updated 2019 Jun 27].


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. doi: 10.1007/s00223-019-00550-z. Epub 2019 Apr 29. Review.


HDAC8, A Potential Therapeutic Target, Regulates Proliferation and Differentiation of Bone Marrow Stromal Cells in Fibrous Dysplasia.

Xiao T, Fu Y, Zhu W, Xu R, Xu L, Zhang P, Du Y, Cheng J, Jiang H.

Stem Cells Transl Med. 2019 Feb;8(2):148-161. doi: 10.1002/sctm.18-0057. Epub 2018 Nov 13.


Polyostotic Fibrous Dysplasia With and Without McCune-Albright Syndrome-Clinical Features in a Nordic Pediatric Cohort.

Utriainen P, Valta H, Björnsdottir S, Mäkitie O, Horemuzova E.

Front Endocrinol (Lausanne). 2018 Mar 15;9:96. doi: 10.3389/fendo.2018.00096. eCollection 2018.


Expression of an active Gαs mutant in skeletal stem cells is sufficient and necessary for fibrous dysplasia initiation and maintenance.

Zhao X, Deng P, Iglesias-Bartolome R, Amornphimoltham P, Steffen DJ, Jin Y, Molinolo AA, de Castro LF, Ovejero D, Yuan Q, Chen Q, Han X, Bai D, Taylor SS, Yang Y, Collins MT, Gutkind JS.

Proc Natl Acad Sci U S A. 2018 Jan 16;115(3):E428-E437. doi: 10.1073/pnas.1713710115. Epub 2017 Dec 27.


Analysis of the influence of the T393C polymorphism of the GNAS gene on the clinical expression of primary hyperparathyroidism.

Piedra M, Berja A, Ramos L, García-Unzueta MT, Morán JM, Ruiz D, Amado JA.

Endocrinol Diabetes Nutr. 2017 Dec;64(10):524-530. doi: 10.1016/j.endinu.2017.08.006. Epub 2017 Oct 18. English, Spanish.


Induced GnasR201H expression from the endogenous Gnas locus causes fibrous dysplasia by up-regulating Wnt/β-catenin signaling.

Khan SK, Yadav PS, Elliott G, Hu DZ, Xu R, Yang Y.

Proc Natl Acad Sci U S A. 2018 Jan 16;115(3):E418-E427. doi: 10.1073/pnas.1714313114. Epub 2017 Nov 20.


McCune-Albright Syndrome.

Dean L.

In: Pratt V, McLeod H, Rubinstein W, Dean L, Kattman B, Malheiro A, editors. Medical Genetics Summaries [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2012-.
2012 Mar 8 [updated 2017 Mar 6].


A Novel T55A Variant of Gs α Associated with Impaired cAMP Production, Bone Fragility, and Osteolysis.

Wentworth K, Hsing A, Urrutia A, Zhu Y, Horvai AE, Bastepe M, Hsiao EC.

Case Rep Endocrinol. 2016;2016:2691385. doi: 10.1155/2016/2691385. Epub 2016 Aug 7.


Fibrous Dysplasia/McCune-Albright Syndrome: Clinical and Translational Perspectives.

Robinson C, Collins MT, Boyce AM.

Curr Osteoporos Rep. 2016 Oct;14(5):178-86. doi: 10.1007/s11914-016-0317-0. Review.


McCune-Albright syndrome, natural history and multidisciplinary management in a series of 14 pediatric cases.

Agopiantz M, Journeau P, Lebon-Labich B, Sorlin A, Cuny T, Weryha G, Leheup B.

Ann Endocrinol (Paris). 2016 Feb;77(1):7-13. doi: 10.1016/j.ando.2016.01.002. Epub 2016 Feb 2.


Bone-Grafting in Polyostotic Fibrous Dysplasia.

Leet AI, Boyce AM, Ibrahim KA, Wientroub S, Kushner H, Collins MT.

J Bone Joint Surg Am. 2016 Feb 3;98(3):211-9. doi: 10.2106/JBJS.O.00547.


Fibrous Dysplasia.

Boyce AM.

In: Feingold KR, Anawalt B, Boyce A, Chrousos G, Dungan K, Grossman A, Hershman JM, Kaltsas G, Koch C, Kopp P, Korbonits M, McLachlan R, Morley JE, New M, Perreault L, Purnell J, Rebar R, Singer F, Trence DL, Vinik A, Wilson DP, editors. Endotext [Internet]. South Dartmouth (MA):, Inc.; 2000-.
2019 Mar 27.


Constitutive expression of Gsα(R201C) in mice produces a heritable, direct replica of human fibrous dysplasia bone pathology and demonstrates its natural history.

Saggio I, Remoli C, Spica E, Cersosimo S, Sacchetti B, Robey PG, Holmbeck K, Cumano A, Boyde A, Bianco P, Riminucci M.

J Bone Miner Res. 2014 Nov;29(11):2357-68. doi: 10.1002/jbmr.2267.


Panostotic expansile bone disease with massive jaw tumor formation and a novel mutation in the signal peptide of RANK.

Schafer AL, Mumm S, El-Sayed I, McAlister WH, Horvai AE, Tom AM, Hsiao EC, Schaefer FV, Collins MT, Anderson MS, Whyte MP, Shoback DM.

J Bone Miner Res. 2014 Apr;29(4):911-21. doi: 10.1002/jbmr.2094.


[Fibrous dysplasia].

Wirth T.

Orthopade. 2012 Dec;41(12):993-1006. doi: 10.1007/s00132-012-1996-6. German.


[Fibrous dysplasia and McCune-Albright syndrome: case-report and differential diagnose with Paget bone disease].

Silva I, Mateus M, Branco JC.

Acta Reumatol Port. 2010 Oct-Dec;35(5):497-503. Portuguese.


[Fibrous dysplasia of bone in a young male].

Alonso G, Muñoz-Torres M.

Endocrinol Nutr. 2009 Apr;56(4):195-200. doi: 10.1016/S1575-0922(09)70984-2. Epub 2009 Jun 11. Spanish.


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