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Items: 1 to 20 of 159

1.

Radiological aspects of prenatal-onset cortical hyperostosis [Caffey Dysplasia].

Nemec SF, Rimoin DL, Lachman RS.

Eur J Radiol. 2012 Apr;81(4):e565-72. doi: 10.1016/j.ejrad.2011.06.049. Epub 2011 Jul 2.

PMID:
21726971
2.

Antenatal onset of cortical hyperostosis (Caffey disease): case report and review.

Schweiger S, Chaoui R, Tennstedt C, Lehmann K, Mundlos S, Tinschert S.

Am J Med Genet A. 2003 Aug 1;120A(4):547-52. Review.

PMID:
12884437
3.

Familial occurrence of Caffey-Silverman syndrome.

Szwed A, Kołban M, Romanowska H, Baryła-Pankiewicz E.

Ortop Traumatol Rehabil. 2012 Jan-Feb;14(1):75-83. English, Polish.

PMID:
22408114
4.

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 15;146A(14):1820-4. doi: 10.1002/ajmg.a.32351.

PMID:
18553566
5.

Case report 363: Infantile cortical hyperostosis (Caffey disease ICH) iliac bones, femora, tibiae and left fibula.

Langer R, Kaufmann HJ.

Skeletal Radiol. 1986;15(5):377-82. No abstract available.

PMID:
3526563
6.

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.

8.

Infantile cortical hyperostosis of the ribs (Caffey's disease) without mandibular involvement.

Gentry RR, Rust RS, Lohr JA, Alford BA.

Pediatr Radiol. 1983;13(4):236-8.

PMID:
6351005
9.

Perinatal death in two sibs with infantile cortical hyperostosis (Caffey disease).

de Jong G, Muller LM.

Am J Med Genet. 1995 Nov 6;59(2):134-8.

PMID:
8588573
10.

Idiopathic cortical hyperostosis.

Jones ET, Hensinger RN, Holt JF.

Clin Orthop Relat Res. 1982 Mar;(163):210-3.

PMID:
7039916
11.

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):947-9. doi: 10.1007/s10038-008-0328-5. Epub 2008 Aug 13.

PMID:
18704262
12.

Lethal prenatal onset infantile cortical hyperostosis (Caffey disease).

Dahlstrom JE, Arbuckle SM, Kozlowski K, Peek MJ, Thomson M, Reynolds GJ, Sillence DO.

Pathology. 2001 Nov;33(4):521-5.

PMID:
11827425
13.

Swelling over the face: infantile cortical hyperostosis.

Jakubíková J, Macek M, Halasova E.

Int J Pediatr Otorhinolaryngol. 1994 Apr;29(2):147-50.

PMID:
8056497
14.

[Familial infantile cortical hyperostosis (Caffey's disease) with osteolytic lesions of the skull].

Lachaux A, Le Gall C, Loras Duclaux I, Hermier M.

Arch Fr Pediatr. 1992 Jun-Jul;49(6):525-8. French.

PMID:
1449354
15.

[Caffey disease (infantile cortical hyperostosis)].

Benomar S, Najdi T.

Arch Pediatr. 1998 Jan;5(1):31-4. French.

PMID:
10223109
16.

Autosomal dominant inheritance of Caffey-Silverman disease. Hyperostosis corticalis infantum.

Rogóyski A, Jakubowska K, Tronowska TD.

Padiatr Padol. 1984;19(4):401-8.

PMID:
6390299
17.

Infantile cortical hyperostosis associated with the Wiskott-Aldrich syndrome.

Abinun M, Mikuska M, Filipović B.

Eur J Pediatr. 1988 Jun;147(5):518-9.

PMID:
3044797
18.

[Infantile cortical hyperostosis (the Caffey-Silvermann syndrome)].

Ciharová K, Horák J, Bláhová K, Spicáková V, Janda J.

Cesk Pediatr. 1991 Feb;46(2):94-7. Czech.

PMID:
1769089
19.

Infantile cortical hyperostosis (Caffey's disease). Two case reports.

Rethmeier JW.

Radiol Clin (Basel). 1976;45(2-4):251-7.

PMID:
781725
20.

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.

PMID:
9267903
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