142 related articles for article (PubMed ID: 11385236)
1. Syndactyly/brachyphalangy and nail dysplasias as marker lesions for sclerosteosis.
Itin PH; Keserü B; Hauser V
Dermatology; 2001; 202(3):259-60. PubMed ID: 11385236
[TBL] [Abstract][Full Text] [Related]
2. Sclerosteosis (craniotubular hyperostosis-syndactyly) with complex hyperphalangy of the index finger.
Yagi H; Takagi M; Hasegawa Y; Kayserili H; Nishimura G
Pediatr Radiol; 2015 Jul; 45(8):1239-43. PubMed ID: 25835322
[TBL] [Abstract][Full Text] [Related]
3. A known SOST gene mutation causes sclerosteosis in a familial and an isolated case from Brazilian origin.
Kim CA; Honjo R; Bertola D; Albano L; Oliveira L; Jales S; Siqueira J; Castilho A; Balemans W; Piters E; Jennes K; Van Hul W
Genet Test; 2008 Dec; 12(4):475-9. PubMed ID: 19072561
[TBL] [Abstract][Full Text] [Related]
4. Localization of the gene for sclerosteosis to the van Buchem disease-gene region on chromosome 17q12-q21.
Balemans W; Van Den Ende J; Freire Paes-Alves A; Dikkers FG; Willems PJ; Vanhoenacker F; de Almeida-Melo N; Alves CF; Stratakis CA; Hill SC; Van Hul W
Am J Hum Genet; 1999 Jun; 64(6):1661-9. PubMed ID: 10330353
[TBL] [Abstract][Full Text] [Related]
5. Sclerosteosis. A case report.
Sugiura Y; Yasuhara T
J Bone Joint Surg Am; 1975 Mar; 57(2):273-7. PubMed ID: 163261
[No Abstract] [Full Text] [Related]
6. Genetics of Sost/SOST in sclerosteosis and van Buchem disease animal models.
Sebastian A; Loots GG
Metabolism; 2018 Mar; 80():38-47. PubMed ID: 29080811
[TBL] [Abstract][Full Text] [Related]
7. The syndromic status of sclerosteosis and van Buchem disease.
Beighton P; Barnard A; Hamersma H; van der Wouden A
Clin Genet; 1984 Feb; 25(2):175-81. PubMed ID: 6323069
[TBL] [Abstract][Full Text] [Related]
8. Prevalence and new phenotypic and radiologic findings in congenital onychodysplasia of the index finger.
Prais D; Horev G; Merlob P
Pediatr Dermatol; 1999; 16(3):201-4. PubMed ID: 10383775
[TBL] [Abstract][Full Text] [Related]
9. Sclerosteosis: Report of type 1 or 2 in three Indian Tamil families and literature review.
Whyte MP; Deepak Amalnath S; McAlister WH; Pedapati R; Muthupillai V; Duan S; Huskey M; Bijanki VN; Mumm S
Bone; 2018 Nov; 116():321-332. PubMed ID: 30077757
[TBL] [Abstract][Full Text] [Related]
10. Increased bone density in sclerosteosis is due to the deficiency of a novel secreted protein (SOST).
Balemans W; Ebeling M; Patel N; Van Hul E; Olson P; Dioszegi M; Lacza C; Wuyts W; Van Den Ende J; Willems P; Paes-Alves AF; Hill S; Bueno M; Ramos FJ; Tacconi P; Dikkers FG; Stratakis C; Lindpaintner K; Vickery B; Foernzler D; Van Hul W
Hum Mol Genet; 2001 Mar; 10(5):537-43. PubMed ID: 11181578
[TBL] [Abstract][Full Text] [Related]
11. Sclerosteosis involving the temporal bone: clinical and radiologic aspects.
Nager GT; Stein SA; Dorst JP; Holliday MJ; Kennedy DW; Diehn KW; Jabs EW
Am J Otolaryngol; 1983; 4(1):1-17. PubMed ID: 6673595
[TBL] [Abstract][Full Text] [Related]
12. Limb anomalies in the CHARGE association.
Meinecke P; Polke A; Schmiegelow P
J Med Genet; 1989 Mar; 26(3):202-3. PubMed ID: 2468773
[TBL] [Abstract][Full Text] [Related]
13. Sclerosteosis in South Africa.
Beighton P; Hamersma H
S Afr Med J; 1979 May; 55(20):783-8. PubMed ID: 223247
[TBL] [Abstract][Full Text] [Related]
14. Sclerostin deficiency in humans.
van Lierop AH; Appelman-Dijkstra NM; Papapoulos SE
Bone; 2017 Mar; 96():51-62. PubMed ID: 27742500
[TBL] [Abstract][Full Text] [Related]
15. Novel SOST gene mutation in a sclerosteosis patient from Morocco: a case report.
Belkhribchia MR; Collet C; Laplanche JL; Hassani R
Eur J Med Genet; 2014 Mar; 57(4):133-7. PubMed ID: 24594238
[TBL] [Abstract][Full Text] [Related]
16. The natural history of sclerosteosis.
Hamersma H; Gardner J; Beighton P
Clin Genet; 2003 Mar; 63(3):192-7. PubMed ID: 12694228
[TBL] [Abstract][Full Text] [Related]
17. Unusual manifestations of ectodermal dysplasia-syndactyly syndrome type I in two Yemeni siblings.
Mohammad A
Dermatol Online J; 2015 Jan; 21(1):. PubMed ID: 25612123
[TBL] [Abstract][Full Text] [Related]
18. A Novel Mutation in a Gene Causes Sclerosteosis in a Family of Mediterranean Origin.
Ekhzaimy AA; Alyusuf EY; Alswailem M; Alzahrani AS
Medicina (Kaunas); 2022 Jan; 58(2):. PubMed ID: 35208525
[No Abstract] [Full Text] [Related]
19. Nail dystrophy mystery.
Neville SA; O'Grady MJ
J Pediatr; 2014 Jun; 164(6):1496. PubMed ID: 24681181
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
