150 related articles for article (PubMed ID: 21249479)
1. COL1A1 mutation in an Indian child with Caffey disease.
Ranganath P; Laine CM; Gupta D; Mäkitie O; Phadke SR
Indian J Pediatr; 2011 Jul; 78(7):877-9. PubMed ID: 21249479
[TBL] [Abstract][Full Text] [Related]
2. The c.3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease).
Cho TJ; Moon HJ; Cho DY; Park MS; Lee DY; Yoo WJ; Chung CY; Choi IH
J Hum Genet; 2008; 53(10):947. PubMed ID: 18704262
[TBL] [Abstract][Full Text] [Related]
3. Prenatal cortical hyperostosis with COL1A1 gene mutation.
Kamoun-Goldrat A; Martinovic J; Saada J; Sonigo-Cohen P; Razavi F; Munnich A; Le Merrer M
Am J Med Genet A; 2008 Jul; 146A(14):1820-4. PubMed ID: 18553566
[TBL] [Abstract][Full Text] [Related]
4. Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature.
Kitaoka T; Miyoshi Y; Namba N; Miura K; Kubota T; Ohata Y; Fujiwara M; Takagi M; Hasegawa T; Jüppner H; Ozono K
Eur J Pediatr; 2014 Jun; 173(6):799-804. PubMed ID: 24390061
[TBL] [Abstract][Full Text] [Related]
5. Hyperostosis in siblings.
Spranger JW; Lausch E
S Afr Med J; 2016 May; 106(6 Suppl 1):S98-9. PubMed ID: 27245539
[TBL] [Abstract][Full Text] [Related]
6. Recurrence of infantile cortical hyperostosis: a case report and review of the literature.
Navarre P; Pehlivanov I; Morin B
J Pediatr Orthop; 2013 Mar; 33(2):e10-7. PubMed ID: 23389580
[TBL] [Abstract][Full Text] [Related]
7. Caffey disease: an unlikely collagenopathy.
Glorieux FH
J Clin Invest; 2005 May; 115(5):1142-4. PubMed ID: 15864344
[TBL] [Abstract][Full Text] [Related]
8. A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.
Gensure RC; Mäkitie O; Barclay C; Chan C; Depalma SR; Bastepe M; Abuzahra H; Couper R; Mundlos S; Sillence D; Ala Kokko L; Seidman JG; Cole WG; Jüppner H
J Clin Invest; 2005 May; 115(5):1250-7. PubMed ID: 15864348
[TBL] [Abstract][Full Text] [Related]
9. Expanding the phenotypic spectrum of Caffey disease.
Suphapeetiporn K; Tongkobpetch S; Mahayosnond A; Shotelersuk V
Clin Genet; 2007 Mar; 71(3):280-4. PubMed ID: 17309652
[TBL] [Abstract][Full Text] [Related]
10. [Caffey disease (infantile cortical hyperostosis). Apropos of a familial form].
Castel Y; Toudic L; Crenn P; Le Fur JM
Ann Pediatr (Paris); 1985 Feb; 32(2):143-7. PubMed ID: 3883874
[No Abstract] [Full Text] [Related]
11. Recurrent severe infantile cortical hyperostosis (Caffey disease) in siblings.
Drinkwater BM; Crino JP; Garcia J; Ogburn J; Hecht JT
Prenat Diagn; 1997 Aug; 17(8):773-6. PubMed ID: 9267903
[TBL] [Abstract][Full Text] [Related]
12. Familial occurrence of Caffey-Silverman syndrome.
Szwed A; Kołban M; Romanowska H; Baryła-Pankiewicz E
Ortop Traumatol Rehabil; 2012; 14(1):75-83. PubMed ID: 22408114
[TBL] [Abstract][Full Text] [Related]
13. The IFITM5 Ser40Leu variant can manifest as prenatal Caffey disease.
Yap JYC; Lim JY; Bhatia A; Tan VKJ; Koo S; Nishimura G; Moosa S; Koh AL; Tan EC; Fong N; Jamuar SS
Am J Med Genet A; 2024 Feb; 194(2):358-362. PubMed ID: 37799085
[TBL] [Abstract][Full Text] [Related]
14. Infantile cortical hyperostosis (Caffey disease): a review.
Kamoun-Goldrat A; le Merrer M
J Oral Maxillofac Surg; 2008 Oct; 66(10):2145-50. PubMed ID: 18848116
[TBL] [Abstract][Full Text] [Related]
15. Infantile cortical hyperostosis (Caffey disease): a possible misdiagnosis as physical abuse.
Lo HP; Lau HY; Li CH; So KT
Hong Kong Med J; 2010 Oct; 16(5):397-9. PubMed ID: 20890006
[TBL] [Abstract][Full Text] [Related]
16. Familial infantile cortical hyperostosis.
Emmery L; Timmermans J; Christens J; Fryns JP
Eur J Pediatr; 1983 Oct; 141(1):56-8. PubMed ID: 6357801
[TBL] [Abstract][Full Text] [Related]
17. Fetuin-A deficiency is associated with infantile cortical hyperostosis (Caffey disease).
Merdler-Rabinowicz R; Grinberg A; Jacobson JM; Somekh I; Klein C; Lev A; Ihsan S; Habib A; Somech R; Simon AJ
Pediatr Res; 2019 Nov; 86(5):603-607. PubMed ID: 31288248
[TBL] [Abstract][Full Text] [Related]
18. [Familial occurrence of infantile cortical hyperostosis. (Caffey-de Toni-Silvermann syndrome)].
Pelikán L; Doubravský J; Mikes K; Cerný M
Acta Chir Orthop Traumatol Cech; 1967 Oct; 34(5):430-4. PubMed ID: 4874755
[No Abstract] [Full Text] [Related]
19. Autosomal dominant inheritance with incomplete penetrance of Caffey disease (infantile cortical hyperostosis).
Fried K; Manor A; Pajewski M; Starinsky R; Vure E
Clin Genet; 1981 Apr; 19(4):271-4. PubMed ID: 7023758
[No Abstract] [Full Text] [Related]
20. Caffey disease: new perspectives on old questions.
Nistala H; Mäkitie O; Jüppner H
Bone; 2014 Mar; 60():246-51. PubMed ID: 24389367
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
