226 related articles for article (PubMed ID: 24517547)
1. 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
J Dermatol; 2014 Apr; 41(4):319-21. PubMed ID: 24517547
[TBL] [Abstract][Full Text] [Related]
2. Medulloblastoma in a child with osteoma cutis - a rare association due to loss of
Suntharesan J; Lyulcheva-Bennett E; Hart R; Pizer B; Hayden J; Ramakrishnan R
J Pediatr Endocrinol Metab; 2024 May; 37(5):467-471. PubMed ID: 38529810
[TBL] [Abstract][Full Text] [Related]
3. Neonatal osteoma cutis due to a mutation in GNAS.
Levy-Shraga Y; Barel O; Javasky E; Barzilai A; Greenberger S
Pediatr Dermatol; 2019 Sep; 36(5):732-734. PubMed ID: 31215057
[TBL] [Abstract][Full Text] [Related]
4. A Novel Spindle Cell Population in a Case of Primary Osteoma Cutis With GNAS Mutation.
Beatty C; Zinn Z; Schultz C; Lynch MC
Am J Dermatopathol; 2020 Jun; 42(6):e72-e75. PubMed ID: 31977320
[TBL] [Abstract][Full Text] [Related]
5. Progressive osseous heteroplasia is not a Mendelian trait but a type 2 segmental manifestation of GNAS inactivation disorders: A hypothesis.
Happle R
Eur J Med Genet; 2016 May; 59(5):290-4. PubMed ID: 27058263
[TBL] [Abstract][Full Text] [Related]
6. Infantile-onset osteoma cutis with pseudopseudohypoparathyroidism.
Stembridge N; Durack A; Gass JK; Firth HV; Park SM; McDonald S; Thankamony A; Burrows NP
Clin Exp Dermatol; 2021 Oct; 46(7):1384-1386. PubMed ID: 34418133
[No Abstract] [Full Text] [Related]
7. 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
J Eur Acad Dermatol Venereol; 2018 Jun; 32(6):e209-e211. PubMed ID: 29224258
[No Abstract] [Full Text] [Related]
8. 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
Bone; 2013 Oct; 56(2):276-80. PubMed ID: 23796510
[TBL] [Abstract][Full Text] [Related]
9. Infantile osteoma cutis as a presentation of a GNAS mutation.
Martin J; Tucker M; Browning JC
Pediatr Dermatol; 2012; 29(4):483-4. PubMed ID: 22612068
[TBL] [Abstract][Full Text] [Related]
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
J Eur Acad Dermatol Venereol; 2016 May; 30(5):905-7. PubMed ID: 25752801
[No Abstract] [Full Text] [Related]
11. Progressive osseous heteroplasia, as an isolated entity or overlapping with Albright hereditary osteodystrophy.
Lin MH; Numbenjapon N; Germain-Lee EL; Pitukcheewanont P
J Pediatr Endocrinol Metab; 2015 Jul; 28(7-8):911-8. PubMed ID: 25894639
[TBL] [Abstract][Full Text] [Related]
12. Evaluating the variety of GNAS inactivation disorders and their clinical manifestations in 11 Chinese children.
Chang G; Li Q; Li N; Li G; Li J; Ding Y; Huang X; Shen Y; Wang J; Wang X
BMC Endocr Disord; 2022 Mar; 22(1):70. PubMed ID: 35296306
[TBL] [Abstract][Full Text] [Related]
13. Progressive osseous heteroplasia caused by a mosaic GNAS mutation.
Pereda A; Martos-Tello JM; Garin I; Errea-Dorronsoro J; Perez de Nanclares G
Clin Endocrinol (Oxf); 2018 Jun; 88(6):993-995. PubMed ID: 29464731
[No Abstract] [Full Text] [Related]
14. Activation of Hedgehog signaling by loss of GNAS causes heterotopic ossification.
Regard JB; Malhotra D; Gvozdenovic-Jeremic J; Josey M; Chen M; Weinstein LS; Lu J; Shore EM; Kaplan FS; Yang Y
Nat Med; 2013 Nov; 19(11):1505-12. PubMed ID: 24076664
[TBL] [Abstract][Full Text] [Related]
15. Endochondral ossification in a case of progressive osseous heteroplasia in a young female child.
Schrander DE; Welting TJ; Caron MM; Schrander JJ; van Rhijn LW; Körver-Keularts I; Schrander-Stumpel CT
J Pediatr Orthop B; 2014 Sep; 23(5):477-84. PubMed ID: 24626099
[TBL] [Abstract][Full Text] [Related]
16. 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
Am J Med Genet A; 2008 Jul; 146A(14):1788-96. PubMed ID: 18553568
[TBL] [Abstract][Full Text] [Related]
17. GNAS-associated disorders of cutaneous ossification: two different clinical presentations.
Schimmel RJ; Pasmans SG; Xu M; Stadhouders-Keet SA; Shore EM; Kaplan FS; Wulffraat NM
Bone; 2010 Mar; 46(3):868-72. PubMed ID: 19900597
[TBL] [Abstract][Full Text] [Related]
18. Mild progressive osseous heteroplasia overlap syndrome with PTH and TSH resistance appearing during adolescence and not early childhood.
Ozaki K; Mituboshi A; Nagai M; Nishiyama A; Nishimura G; Morisada N; Iijima K
Endocrine; 2021 Dec; 74(3):685-689. PubMed ID: 34254228
[TBL] [Abstract][Full Text] [Related]
19. GNAS mutations in Pseudohypoparathyroidism type 1a and related disorders.
Lemos MC; Thakker RV
Hum Mutat; 2015 Jan; 36(1):11-9. PubMed ID: 25219572
[TBL] [Abstract][Full Text] [Related]
20. Acquired plate-like osteoma cutis.
Vashi N; Chu J; Patel R
Dermatol Online J; 2011 Oct; 17(10):1. PubMed ID: 22031627
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]