Similar articles for PMID: 31977320

Year	Number of Results
1948	1
1949	1
1951	1
1954	1
1962	2
1963	2
1964	1
1993	1
1994	1
1996	1
1997	1
1998	1
1999	1
2000	3
2002	3
2004	1
2006	3
2007	2
2008	3
2009	5
2010	2
2011	6
2012	3
2013	8
2014	8
2015	9
2016	5
2017	7
2018	8
2019	10
2020	5
2021	6
2022	9
2023	11
2024	2

1

A Novel Spindle Cell Population in a Case of Primary Osteoma Cutis With GNAS Mutation.

Beatty C, Zinn Z, Schultz C, Lynch MC. Beatty C, et al. Am J Dermatopathol. 2020 Jun;42(6):e72-e75. doi: 10.1097/DAD.0000000000001611. Am J Dermatopathol. 2020. PMID: 31977320 Free PMC article.

2

Neonatal osteoma cutis due to a mutation in GNAS.

Levy-Shraga Y, Barel O, Javasky E, Barzilai A, Greenberger S. Levy-Shraga Y, et al. Pediatr Dermatol. 2019 Sep;36(5):732-734. doi: 10.1111/pde.13879. Epub 2019 Jun 18. Pediatr Dermatol. 2019. PMID: 31215057

3

Progressive osseous heteroplasia is not a Mendelian trait but a type 2 segmental manifestation of GNAS inactivation disorders: A hypothesis.

Happle R. Happle R. Eur J Med Genet. 2016 May;59(5):290-4. doi: 10.1016/j.ejmg.2016.04.001. Epub 2016 Apr 4. Eur J Med Genet. 2016. PMID: 27058263 Review.

4

Novel nonsense GNAS mutation in a 14-month-old boy with plate-like osteoma cutis and medulloblastoma.

Huh JY, Kwon MJ, Seo KY, Kim MK, Chae KY, Kim SH, Ki CS, Yoon MS, Kim DH. Huh JY, et al. J Dermatol. 2014 Apr;41(4):319-21. doi: 10.1111/1346-8138.12284. Epub 2014 Feb 11. J Dermatol. 2014. PMID: 24517547

5

Progressive osseous heteroplasia in a Chinese infant and a novel mutation in the GNAS gene.

Zhang SD, Xie ZL, Zhang KQ, Nh-Tseung K, Zhao JJ. Zhang SD, et al. J Eur Acad Dermatol Venereol. 2018 Jun;32(6):e209-e211. doi: 10.1111/jdv.14743. Epub 2017 Dec 26. J Eur Acad Dermatol Venereol. 2018. PMID: 29224258 No abstract available.

6

Infantile-onset osteoma cutis with pseudopseudohypoparathyroidism.

Stembridge N, Durack A, Gass JK, Firth HV, Park SM, McDonald S, Thankamony A, Burrows NP. Stembridge N, et al. Clin Exp Dermatol. 2021 Oct;46(7):1384-1386. doi: 10.1111/ced.14700. Epub 2021 Aug 21. Clin Exp Dermatol. 2021. PMID: 34418133 No abstract available.

7

Progressive osseous heteroplasia, as an isolated entity or overlapping with Albright hereditary osteodystrophy.

Lin MH, Numbenjapon N, Germain-Lee EL, Pitukcheewanont P. Lin MH, et al. J Pediatr Endocrinol Metab. 2015 Jul;28(7-8):911-8. doi: 10.1515/jpem-2014-0435. J Pediatr Endocrinol Metab. 2015. PMID: 25894639

8

Diagnostic and mutational spectrum of progressive osseous heteroplasia (POH) and other forms of GNAS-based heterotopic ossification.

Adegbite NS, Xu M, Kaplan FS, Shore EM, Pignolo RJ. Adegbite NS, et al. Am J Med Genet A. 2008 Jul 15;146A(14):1788-96. doi: 10.1002/ajmg.a.32346. Am J Med Genet A. 2008. PMID: 18553568 Free PMC article.

9

Screening for GNAS genetic and epigenetic alterations in progressive osseous heteroplasia: first Italian series.

Elli FM, Barbieri AM, Bordogna P, Ferrari P, Bufo R, Ferrante E, Giardino E, Beck-Peccoz P, Spada A, Mantovani G. Elli FM, et al. Bone. 2013 Oct;56(2):276-80. doi: 10.1016/j.bone.2013.06.015. Epub 2013 Jun 21. Bone. 2013. PMID: 23796510 Free article.

10

Progressive osseous heteroplasia in a 7-year-old girl with osteoma cutis and autoimmune thyroiditis: the importance of investigating GNAS mutations.

Mariani M, Rigante D, Guerriero C, Ricci F, Sani I, Rossodivita A. Mariani M, et al. J Eur Acad Dermatol Venereol. 2016 May;30(5):905-7. doi: 10.1111/jdv.13075. Epub 2015 Mar 6. J Eur Acad Dermatol Venereol. 2016. PMID: 25752801 No abstract available.

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