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Year Number of Results
1973 1
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1980 1
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1986 2
1987 5
1988 3
1989 1
1990 3
1991 4
1992 3
1993 7
1994 8
1995 10
1996 12
1997 14
1998 10
1999 19
2000 11
2001 8
2002 10
2003 5
2004 16
2005 9
2006 22
2007 20
2008 14
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2010 12
2011 8
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2013 11
2014 13
2015 13
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2022 6
2023 9

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371 results

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Page 1
The Clinical Spectrum of McCune-Albright Syndrome and Its Management.
Spencer T, Pan KS, Collins MT, Boyce AM. Spencer T, et al. Horm Res Paediatr. 2019;92(6):347-356. doi: 10.1159/000504802. Epub 2019 Dec 19. Horm Res Paediatr. 2019. PMID: 31865341 Free PMC article. Review.
McCune-Albright syndrome (MAS) is a rare, mosaic disorder presenting along a broad clinical spectrum. ...Patients pre-sent clinically with a variable combination of fibrous dysplasia of bone (FD), cafe-au-lait skin macules, and hyperfunctioning
McCune-Albright syndrome (MAS) is a rare, mosaic disorder presenting along a broad clinical spectrum. ...Patients pre-s
Fibrous Dysplasia of Bone and McCune-Albright Syndrome: A Bench to Bedside Review.
Hartley I, Zhadina M, Collins MT, Boyce AM. Hartley I, et al. Calcif Tissue Int. 2019 May;104(5):517-529. doi: 10.1007/s00223-019-00550-z. Epub 2019 Apr 29. Calcif Tissue Int. 2019. PMID: 31037426 Free PMC article. Review.
Fibrous dysplasia is an uncommon mosaic disorder in which bone is replaced by structurally unsound fibro-osseous tissue. ...This manifests on a broad clinical spectrum ranging from insignificant solitary lesions to severe disease with deformities, fractures, functio
Fibrous dysplasia is an uncommon mosaic disorder in which bone is replaced by structurally unsound fibro-osseous tissue. ...Th
Best practice management guidelines for fibrous dysplasia/McCune-Albright syndrome: a consensus statement from the FD/MAS international consortium.
Javaid MK, Boyce A, Appelman-Dijkstra N, Ong J, Defabianis P, Offiah A, Arundel P, Shaw N, Pos VD, Underhil A, Portero D, Heral L, Heegaard AM, Masi L, Monsell F, Stanton R, Dijkstra PDS, Brandi ML, Chapurlat R, Hamdy NAT, Collins MT. Javaid MK, et al. Orphanet J Rare Dis. 2019 Jun 13;14(1):139. doi: 10.1186/s13023-019-1102-9. Orphanet J Rare Dis. 2019. PMID: 31196103 Free PMC article. Review.
Fibrous Dysplasia / McCune Albright syndrome (FD/MAS) represents a wide spectrum of diseases due to somatic gain-of-function mutations of the GNAS gene. ...
Fibrous Dysplasia / McCune Albright syndrome (FD/MAS) represents a wide spectrum of diseases due to somat
Fibrous Dysplasia/McCune-Albright Syndrome: A Rare, Mosaic Disease of Gα s Activation.
Boyce AM, Collins MT. Boyce AM, et al. Endocr Rev. 2020 Apr 1;41(2):345-70. doi: 10.1210/endrev/bnz011. Endocr Rev. 2020. PMID: 31673695 Free PMC article. Review.
Fibrous dysplasia/McCune-Albright syndrome (FD/MAS) is a rare disorder of striking complexity. ...
Fibrous dysplasia/McCune-Albright syndrome (FD/MAS) is a rare disorder of striking complexity. ...
GNAS Spectrum of Disorders.
Turan S, Bastepe M. Turan S, et al. Curr Osteoporos Rep. 2015 Jun;13(3):146-58. doi: 10.1007/s11914-015-0268-x. Curr Osteoporos Rep. 2015. PMID: 25851935 Free PMC article. Review.
Gsalpha-coding GNAS mutations that lead to diminished Gsalpha expression and/or function result in Albright's hereditary osteodystrophy (AHO) with or without hormone resistance, i.e., pseudohypoparathyroidism type-Ia/Ic and pseudo-pseudohypoparathyroidism, respectively. .. …
Gsalpha-coding GNAS mutations that lead to diminished Gsalpha expression and/or function result in Albright's hereditary osteodystrop …
Fibrous dysplasia of bone: craniofacial and dental implications.
Burke AB, Collins MT, Boyce AM. Burke AB, et al. Oral Dis. 2017 Sep;23(6):697-708. doi: 10.1111/odi.12563. Epub 2016 Sep 1. Oral Dis. 2017. PMID: 27493082 Free PMC article. Review.
Fibrous dysplasia (FD) is a rare bone disease caused by postzygotic somatic activating mutations in the GNAS gene, which lead to constitutive activation of adenylyl cyclase and elevated levels of cyclic AMP, which act on downstream signaling pathways and cause norma
Fibrous dysplasia (FD) is a rare bone disease caused by postzygotic somatic activating mutations in the GNAS gene, which lead
Fibrous dysplasia. Pathophysiology, evaluation, and treatment.
DiCaprio MR, Enneking WF. DiCaprio MR, et al. J Bone Joint Surg Am. 2005 Aug;87(8):1848-64. doi: 10.2106/JBJS.D.02942. J Bone Joint Surg Am. 2005. PMID: 16085630 Review.
Fibrous dysplasia is a common benign skeletal lesion that may involve one bone (monostotic) or multiple bones (polyostotic) and occurs throughout the skeleton with a predilection for the long bones, ribs, and craniofacial bones. The etiology of fibrous
Fibrous dysplasia is a common benign skeletal lesion that may involve one bone (monostotic) or multiple bones (polyostotic
Acromegaly and McCune-Albright syndrome.
Salenave S, Boyce AM, Collins MT, Chanson P. Salenave S, et al. J Clin Endocrinol Metab. 2014 Jun;99(6):1955-69. doi: 10.1210/jc.2013-3826. Epub 2014 Feb 11. J Clin Endocrinol Metab. 2014. PMID: 24517150 Free PMC article. Review.
BACKGROUND: McCune-Albright syndrome (MAS) includes the triad of poly/monostotic fibrous dysplasia, cafe-au-lait spots, and hyperfunctioning endocrinopathies. ...GH/IGF-1 excess was suggested by accelerated growth in 85% of pediatric cases. Acro …
BACKGROUND: McCune-Albright syndrome (MAS) includes the triad of poly/monostotic fibrous dysplasia, cafe- …
Fibrous Dysplasia/McCune-Albright Syndrome: Clinical and Translational Perspectives.
Robinson C, Collins MT, Boyce AM. Robinson C, et al. Curr Osteoporos Rep. 2016 Oct;14(5):178-86. doi: 10.1007/s11914-016-0317-0. Curr Osteoporos Rep. 2016. PMID: 27492469 Free PMC article. Review.
Fibrous dysplasia (FD) is an uncommon and debilitating skeletal disorder resulting in fractures, deformity, functional impairment, and pain. ...FD may occur in isolation or in combination with extraskeletal manifestations, including hyperfunctioning endocrinopathies
Fibrous dysplasia (FD) is an uncommon and debilitating skeletal disorder resulting in fractures, deformity, functional impairm
Precocious Puberty.
Banerjee S, Bajpai A. Banerjee S, et al. Indian J Pediatr. 2023 Jun;90(6):582-589. doi: 10.1007/s12098-023-04554-4. Epub 2023 Apr 19. Indian J Pediatr. 2023. PMID: 37074536 Review.
The management of rarer forms of peripheral precocious puberty (McCune Albright syndrome, congenital adrenal hyperplasia, and testotoxicosis) involves using experimental drugs under the guidance of specialists....
The management of rarer forms of peripheral precocious puberty (McCune Albright syndrome, congenital adrenal hyperplasi …
371 results