203 related articles for article (PubMed ID: 20523775)
1. Osteoma cutis as the presenting feature of albright hereditary osteodystrophy associated with pseudopseudohypoparathyroidism.
Jeong KH; Lew BL; Sim WY
Ann Dermatol; 2009 May; 21(2):154-8. PubMed ID: 20523775
[TBL] [Abstract][Full Text] [Related]
2. Albright hereditary osteodystrophy with hypothyroidism, normocalcemia, and normal Gs protein activity: a family presenting with congenital osteoma cutis.
Izraeli S; Metzker A; Horev G; Karmi D; Merlob P; Farfel Z
Am J Med Genet; 1992 Jul; 43(4):764-7. PubMed ID: 1621772
[TBL] [Abstract][Full Text] [Related]
3. Multiple miliary osteoma cutis of the face associated with Albright hereditary osteodystrophy in the setting of acne vulgaris: a case report.
Caravaglio JV; Gupta R; Weinstein D
Dermatol Online J; 2017 Mar; 23(3):. PubMed ID: 28329522
[TBL] [Abstract][Full Text] [Related]
4. Osteoma cutis as a presenting sign of pseudohypoparathyroidism.
Prendiville JS; Lucky AW; Mallory SB; Mughal Z; Mimouni F; Langman CB
Pediatr Dermatol; 1992 Mar; 9(1):11-8. PubMed ID: 1574470
[TBL] [Abstract][Full Text] [Related]
5. Cognitive impairment is prevalent in pseudohypoparathyroidism type Ia, but not in pseudopseudohypoparathyroidism: possible cerebral imprinting of Gsalpha.
Mouallem M; Shaharabany M; Weintrob N; Shalitin S; Nagelberg N; Shapira H; Zadik Z; Farfel Z
Clin Endocrinol (Oxf); 2008 Feb; 68(2):233-9. PubMed ID: 17803690
[TBL] [Abstract][Full Text] [Related]
6. Skeletal Complications With GNAS Mutation: An Unusual Case With Osteoma Cutis, Gout, and Synovial Chondromatosis in a Patient With Pseudopseudohypoparathyroidism.
Rhyu J; Bhat SP
AACE Clin Case Rep; 2021; 7(3):180-183. PubMed ID: 34095483
[TBL] [Abstract][Full Text] [Related]
7. Three cases of osteoma cutis occurring in infancy. A brief overview of osteoma cutis and its association with pseudo-pseudohypoparathyroidism.
Ward S; Sugo E; Verge CF; Wargon O
Australas J Dermatol; 2011 May; 52(2):127-31. PubMed ID: 21605097
[TBL] [Abstract][Full Text] [Related]
8. Identification of novel pathogenic variants and features in patients with pseudohypoparathyroidism and acrodysostosis, subtypes of the newly classified inactivating PTH/PTHrP signaling disorders.
Truelove A; Mulay A; Prapa M; Casey RT; Adler AI; Offiah AC; Poole KES; Trotman J; Al Hasso N; Park SM
Am J Med Genet A; 2019 Jul; 179(7):1330-1337. PubMed ID: 31041856
[TBL] [Abstract][Full Text] [Related]
9. A novel mutation causing pseudohypoparathyroidism 1A with congenital hypothyroidism and osteoma cutis.
Lubell T; Garzon M; Anyane Yeboa K; Shah B
J Clin Res Pediatr Endocrinol; 2009; 1(5):244-7. PubMed ID: 21274302
[TBL] [Abstract][Full Text] [Related]
10. 2q37 Deletions in Patients With an Albright Hereditary Osteodystrophy Phenotype and PTH Resistance.
Elli FM; de Sanctis L; Madeo B; Maffini MA; Bordogna P; Pirelli A; Arosio M; Mantovani G
Front Endocrinol (Lausanne); 2019; 10():604. PubMed ID: 31555217
[TBL] [Abstract][Full Text] [Related]
11. Familial Albright's hereditary osteodystrophy with hypoparathyroidism: normal structural Gs alpha gene.
Shapira H; Friedman E; Mouallem M; Farfel Z
J Clin Endocrinol Metab; 1996 Apr; 81(4):1660-2. PubMed ID: 8636385
[TBL] [Abstract][Full Text] [Related]
12. Osteoma cutis in pseudohypoparathyroidism.
Sethuraman G; Malhotra AK; Khaitan BK; Kumar R; Sharma VK; Kabra M; Singh MK
Clin Exp Dermatol; 2006 Mar; 31(2):225-7. PubMed ID: 16487097
[TBL] [Abstract][Full Text] [Related]
13. Cutaneous ossification in Albright's hereditary osteodystrophy.
Trüeb RM; Panizzon RG; Burg G
Dermatology; 1993; 186(3):205-9. PubMed ID: 8453149
[TBL] [Abstract][Full Text] [Related]
14. Clinical characterization and identification of two novel mutations of the GNAS gene in patients with pseudohypoparathyroidism and pseudopseudohypoparathyroidism.
Jin HY; Lee BH; Choi JH; Kim GH; Kim JK; Lee JH; Yu J; Yoo JH; Ko CW; Lim HH; Chung HR; Yoo HW
Clin Endocrinol (Oxf); 2011 Aug; 75(2):207-13. PubMed ID: 21521295
[TBL] [Abstract][Full Text] [Related]
15. Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism.
De Sanctis L; Romagnolo D; Olivero M; Buzi F; Maghnie M; Scirè G; Crino A; Baroncelli GI; Salerno M; Di Maio S; Cappa M; Grosso S; Rigon F; Lala R; De Sanctis C; Dianzani I
Pediatr Res; 2003 May; 53(5):749-55. PubMed ID: 12621129
[TBL] [Abstract][Full Text] [Related]
16. Progressive osseous heteroplasia-like heterotopic ossification in a male infant with pseudohypoparathyroidism type Ia: a case report.
Gelfand IM; Hub RS; Shore EM; Kaplan FS; Dimeglio LA
Bone; 2007 May; 40(5):1425-8. PubMed ID: 17321228
[TBL] [Abstract][Full Text] [Related]
17. Albright hereditary osteodystrophy: a case report.
Hugar D; Sajjanshetty S; Hugar S; Kadani M
J Clin Diagn Res; 2014 Oct; 8(10):ZD28-30. PubMed ID: 25478468
[TBL] [Abstract][Full Text] [Related]
18. Identification of a novel mutation in a patient with pseudohypoparathyroidism type Ia.
Lee YS; Kim HK; Kim HR; Lee JY; Choi JW; Bae EJ; Oh PS; Park WI; Ki CS; Lee HJ
Korean J Pediatr; 2014 May; 57(5):240-4. PubMed ID: 25045367
[TBL] [Abstract][Full Text] [Related]
19. Identification of two novel deletion mutations within the Gs alpha gene (GNAS1) in Albright hereditary osteodystrophy.
Yu D; Yu S; Schuster V; Kruse K; Clericuzio CL; Weinstein LS
J Clin Endocrinol Metab; 1999 Sep; 84(9):3254-9. PubMed ID: 10487696
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
