Similar articles for PMID: 21910239

Year	Number of Results
1908	1
1949	1
2001	1
2002	1
2003	1
2004	6
2005	5
2006	2
2007	5
2008	7
2009	4
2010	8
2011	6
2012	3
2013	4
2014	5
2015	14
2016	4
2017	7
2018	2
2019	2
2021	2
2022	1
2024	0

1

Madelung deformity in a girl with a novel and de novo mutation in the GNAS gene.

Rump P, Jongbloed JD, Sikkema-Raddatz B, Mundlos S, Klopocki E, van der Luijt RB. Rump P, et al. Am J Med Genet A. 2011 Oct;155A(10):2566-70. doi: 10.1002/ajmg.a.34218. Epub 2011 Sep 9. Am J Med Genet A. 2011. PMID: 21910239

2

A novel GNAS mutation in an infant boy with pseudohypoparathyroidism type Ia and normal serum calcium and phosphate levels.

Reis MT, Cattani A, Mendonca BB, Corrêa PH, Martin RM. Reis MT, et al. Arq Bras Endocrinol Metabol. 2010 Nov;54(8):728-31. doi: 10.1590/s0004-27302010000800011. Arq Bras Endocrinol Metabol. 2010. PMID: 21340160

3

Pseudohypoparathyroidism type IA (PHP-Ia): maternally inherited GNAS gene mutation.

Semiz S, Duzcan F, Candemir M, Caner V, Thiele S, Semiz E, Hiort O. Semiz S, et al. J Pediatr Endocrinol Metab. 2009 Feb;22(2):107-8. doi: 10.1515/jpem.2009.22.2.107. J Pediatr Endocrinol Metab. 2009. PMID: 19449667 No abstract available.

4

A maternal epimutation of GNAS leads to Albright osteodystrophy and parathyroid hormone resistance.

Mariot V, Maupetit-Méhouas S, Sinding C, Kottler ML, Linglart A. Mariot V, et al. J Clin Endocrinol Metab. 2008 Mar;93(3):661-5. doi: 10.1210/jc.2007-0927. Epub 2008 Jan 8. J Clin Endocrinol Metab. 2008. PMID: 18182455

5

A disruptive mutation in exon 3 of the GNAS gene with albright hereditary osteodystrophy, normocalcemic pseudohypoparathyroidism, and selective long transcript variant Gsalpha-L deficiency.

Thiele S, Werner R, Ahrens W, Hoppe U, Marschke C, Staedt P, Hiort O. Thiele S, et al. J Clin Endocrinol Metab. 2007 May;92(5):1764-8. doi: 10.1210/jc.2006-2122. Epub 2007 Feb 13. J Clin Endocrinol Metab. 2007. PMID: 17299070

6

Selective deficiency of Gsalpha and the possible role of alternative gene products of GNAS in Albright hereditary osteodystrophy and pseudohypoparathyroidism type Ia.

Thiele S, Werner R, Ahrens W, Hübner A, Hinkel KG, Höppner W, Igl B, Hiort O. Thiele S, et al. Exp Clin Endocrinol Diabetes. 2010 Feb;118(2):127-32. doi: 10.1055/s-0029-1215589. Epub 2009 Aug 5. Exp Clin Endocrinol Diabetes. 2010. PMID: 19658058

7

New mutation type in pseudohypoparathyroidism type Ia.

Fernandez-Rebollo E, Barrio R, Pérez-Nanclares G, Carcavilla A, Garin I, Castaño L, de Nanclares GP. Fernandez-Rebollo E, et al. Clin Endocrinol (Oxf). 2008 Nov;69(5):705-12. doi: 10.1111/j.1365-2265.2008.03255.x. Epub 2008 Apr 3. Clin Endocrinol (Oxf). 2008. PMID: 18394017

8

Acroscyphodysplasia as a phenotypic variation of pseudohypoparathyroidism and acrodysostosis type 2.

Mitsui T, Kim OH, Hall CM, Offiah A, Johnson D, Jin DK, Toh TH, Soneda S, Keino D, Matsubayashi S, Ishii T, Nishimura G, Hasegawa T. Mitsui T, et al. Am J Med Genet A. 2014 Oct;164A(10):2529-34. doi: 10.1002/ajmg.a.36669. Epub 2014 Jul 10. Am J Med Genet A. 2014. PMID: 25044890

9

Epigenetic defects of GNAS in patients with pseudohypoparathyroidism and mild features of Albright's hereditary osteodystrophy.

de Nanclares GP, Fernández-Rebollo E, Santin I, García-Cuartero B, Gaztambide S, Menéndez E, Morales MJ, Pombo M, Bilbao JR, Barros F, Zazo N, Ahrens W, Jüppner H, Hiort O, Castaño L, Bastepe M. de Nanclares GP, et al. J Clin Endocrinol Metab. 2007 Jun;92(6):2370-3. doi: 10.1210/jc.2006-2287. Epub 2007 Apr 3. J Clin Endocrinol Metab. 2007. PMID: 17405843

10

Follow-up Findings in a Turkish Girl with Pseudohypoparathyroidism Type Ia Caused by a Novel Heterozygous Mutation in the GNAS Gene.

Şahin S, Hiort O, Thiele S, Evliyaoğlu O, Tüysüz B. Şahin S, et al. J Clin Res Pediatr Endocrinol. 2017 Mar 1;9(1):74-79. doi: 10.4274/jcrpe.3191. Epub 2016 Jul 18. J Clin Res Pediatr Endocrinol. 2017. PMID: 27425121 Free PMC article.

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