These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
215 related articles for article (PubMed ID: 15959620)
1. Camurati-Engelmann disease (progressive diaphyseal dysplasia) in a Moroccan family. Simsek S; Janssens K; Kwee ML; Van Hul W; Veenstra J; Netelenbos JC Osteoporos Int; 2005 Sep; 16(9):1167-70. PubMed ID: 15959620 [TBL] [Abstract][Full Text] [Related]
2. The first Korean case of Camurati-Engelmann disease (progressive diaphyseal dysplasia) confirmed by TGFB1 gene mutation analysis. Park SJ; Yoon CS; Park HW; Choi JR; Chung JS; Lee KA J Korean Med Sci; 2009 Aug; 24(4):737-40. PubMed ID: 19654961 [TBL] [Abstract][Full Text] [Related]
3. Marked phenotypic variability in progressive diaphyseal dysplasia (Camurati-Engelmann disease): report of a four-generation pedigree, identification of a mutation in TGFB1, and review. Wallace SE; Lachman RS; Mekikian PB; Bui KK; Wilcox WR Am J Med Genet A; 2004 Sep; 129A(3):235-47. PubMed ID: 15326622 [TBL] [Abstract][Full Text] [Related]
4. Domain-specific mutations in TGFB1 result in Camurati-Engelmann disease. Kinoshita A; Saito T; Tomita H; Makita Y; Yoshida K; Ghadami M; Yamada K; Kondo S; Ikegawa S; Nishimura G; Fukushima Y; Nakagomi T; Saito H; Sugimoto T; Kamegaya M; Hisa K; Murray JC; Taniguchi N; Niikawa N; Yoshiura K Nat Genet; 2000 Sep; 26(1):19-20. PubMed ID: 10973241 [TBL] [Abstract][Full Text] [Related]
5. Camurati-Engelmann disease type II: progressive diaphyseal dysplasia with striations of the bones. Nishimura G; Nishimura H; Tanaka Y; Makita Y; Ikegawa S; Ghadami M; Kinoshita A; Niikawa N Am J Med Genet; 2002 Jan; 107(1):5-11. PubMed ID: 11807860 [TBL] [Abstract][Full Text] [Related]
7. Camurati-Engelmann disease (progressive diaphyseal dysplasia): reports of an Indian kindred. Bhadada SK; Sridhar S; Steenackers E; Dhiman V; Mortier G; Bhansali A; Van Hul W Calcif Tissue Int; 2014 Feb; 94(2):240-7. PubMed ID: 24154985 [TBL] [Abstract][Full Text] [Related]
8. Orthopedic Manifestations of Type I Camurati-Engelmann Disease. Yuldashev AJ; Shin CH; Kim YS; Jang WY; Park MS; Chae JH; Yoo WJ; Choi IH; Kim OH; Cho TJ Clin Orthop Surg; 2017 Mar; 9(1):109-115. PubMed ID: 28261436 [TBL] [Abstract][Full Text] [Related]
9. Mild Camurati‑Engelamann disease presenting with exophthalmos as the first and only manifestation: A case report. Jiajue R; Wu B; Jiang Y; Wang O; Li M; Xing X; Xia W Mol Med Rep; 2016 Sep; 14(3):2710-6. PubMed ID: 27484238 [TBL] [Abstract][Full Text] [Related]
10. Camurati-Engelmann disease--a rare cause of bone pain. Mundra V; Taxel P Conn Med; 2012 Jan; 76(1):33-7. PubMed ID: 22372177 [TBL] [Abstract][Full Text] [Related]
11. Localisation of the gene causing diaphyseal dysplasia Camurati-Engelmann to chromosome 19q13. Janssens K; Gershoni-Baruch R; Van Hul E; Brik R; Guañabens N; Migone N; Verbruggen LA; Ralston SH; Bonduelle M; Van Maldergem L; Vanhoenacker F; Van Hul W J Med Genet; 2000 Apr; 37(4):245-9. PubMed ID: 10745041 [TBL] [Abstract][Full Text] [Related]
12. Unveiling the uncommon: diagnostic journey of camurati-engelmann disease in a pediatric patient. Alkaya A; Yıldız AE; Bağlan E; Özdel S Pediatr Rheumatol Online J; 2024 Oct; 22(1):89. PubMed ID: 39379987 [TBL] [Abstract][Full Text] [Related]
13. Phenotypic variability at the TGF-beta1 locus in Camurati-Engelmann disease. Campos-Xavier B; Saraiva JM; Savarirayan R; Verloes A; Feingold J; Faivre L; Munnich A; Le Merrer M; Cormier-Daire V Hum Genet; 2001 Dec; 109(6):653-8. PubMed ID: 11810278 [TBL] [Abstract][Full Text] [Related]
14. Camurati-Engelmann Disease. Van Hul W; Boudin E; Vanhoenacker FM; Mortier G Calcif Tissue Int; 2019 May; 104(5):554-560. PubMed ID: 30721323 [TBL] [Abstract][Full Text] [Related]
15. Camurati-Engelmann disease: review of the clinical, radiological, and molecular data of 24 families and implications for diagnosis and treatment. Janssens K; Vanhoenacker F; Bonduelle M; Verbruggen L; Van Maldergem L; Ralston S; Guañabens N; Migone N; Wientroub S; Divizia MT; Bergmann C; Bennett C; Simsek S; Melançon S; Cundy T; Van Hul W J Med Genet; 2006 Jan; 43(1):1-11. PubMed ID: 15894597 [TBL] [Abstract][Full Text] [Related]
16. Mutations in the gene encoding the latency-associated peptide of TGF-beta 1 cause Camurati-Engelmann disease. Janssens K; Gershoni-Baruch R; Guañabens N; Migone N; Ralston S; Bonduelle M; Lissens W; Van Maldergem L; Vanhoenacker F; Verbruggen L; Van Hul W Nat Genet; 2000 Nov; 26(3):273-5. PubMed ID: 11062463 [TBL] [Abstract][Full Text] [Related]