149 related articles for article (PubMed ID: 21567126)
1. Infantile cortical hyperostosis and COL1A1 mutation in four generations.
Cerruti-Mainardi P; Venturi G; Spunton M; Favaron E; Zignani M; Provera S; Dallapiccola B
Eur J Pediatr; 2011 Nov; 170(11):1385-90. PubMed ID: 21567126
[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. 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]
4. Caffey disease: an unlikely collagenopathy.
Glorieux FH
J Clin Invest; 2005 May; 115(5):1142-4. PubMed ID: 15864344
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. 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]
8. Mutation of PFN1 Gene in an Early Onset, Polyostotic Paget-like Disease.
Merlotti D; Materozzi M; Bianciardi S; Guarnieri V; Rendina D; Volterrani L; Bellan C; Mingiano C; Picchioni T; Frosali A; Orfanelli U; Cenci S; Gennari L
J Clin Endocrinol Metab; 2020 Aug; 105(8):. PubMed ID: 32392277
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. Familial infantile cortical hyperostosis: an update.
Newberg AH; Tampas JP
AJR Am J Roentgenol; 1981 Jul; 137(1):93-6. PubMed ID: 6787897
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Autosomal dominant inheritance of Caffey-Silverman disease. Hyperostosis corticalis infantum.
Rogóyski A; Jakubowska K; Tronowska TD
Padiatr Padol; 1984; 19(4):401-8. PubMed ID: 6390299
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. COL1A1 C-propeptide cleavage site mutation causes high bone mass, bone fragility and jaw lesions: a new cause of gnathodiaphyseal dysplasia?
McInerney-Leo AM; Duncan EL; Leo PJ; Gardiner B; Bradbury LA; Harris JE; Clark GR; Brown MA; Zankl A
Clin Genet; 2015 Jul; 88(1):49-55. PubMed ID: 24891183
[TBL] [Abstract][Full Text] [Related]
16. Autosomal dominant hyperostosis/osteosclerosis with high serum alkaline phosphatase activity.
Hernandez-Cassis C; Vogel CK; Hernandez TP; Econs MJ; Iglesias M; Iglesias A; Levis S; Roos BA; Howard GA; Iglesias Gamarra A
J Clin Endocrinol Metab; 2003 Jun; 88(6):2650-5. PubMed ID: 12788869
[TBL] [Abstract][Full Text] [Related]
17. Infantile cortical hyperostosis.
Frána L; Sekanina M
Arch Dis Child; 1976 Aug; 51(8):589-95. PubMed ID: 786183
[TBL] [Abstract][Full Text] [Related]
18. Segregation of a M404V mutation of the p62/sequestosome 1 (p62/SQSTM1) gene with polyostotic Paget's disease of bone in an Italian family.
Falchetti A; Di Stefano M; Marini F; Del Monte F; Gozzini A; Masi L; Tanini A; Amedei A; Carossino A; Isaia G; Brandi ML
Arthritis Res Ther; 2005; 7(6):R1289-95. PubMed ID: 16277682
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
