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Items: 1 to 20 of 106

1.

Expanding the phenotypic spectrum of Caffey disease.

Suphapeetiporn K, Tongkobpetch S, Mahayosnond A, Shotelersuk V.

Clin Genet. 2007 Mar;71(3):280-4.

PMID:
17309652
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):947-9. doi: 10.1007/s10038-008-0328-5. Epub 2008 Aug 13.

PMID:
18704262
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.

4.

Caffey disease: an unlikely collagenopathy.

Glorieux FH.

J Clin Invest. 2005 May;115(5):1142-4.

5.

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
6.

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. doi: 10.1007/s00431-013-2252-8. Epub 2014 Jan 4. Review.

PMID:
24390061
7.

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. doi: 10.1007/s12098-010-0339-z. Epub 2011 Jan 20.

PMID:
21249479
8.

Hyperostosis in siblings.

Spranger JW, Lausch E.

S Afr Med J. 2016 May 25;106(6 Suppl 1):S98-9. doi: 10.7196/SAMJ.2016.v106i6.11007.

PMID:
27245539
9.

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.

10.

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. doi: 10.1097/BPO.0b013e318277d3a2. Review.

PMID:
23389580
11.

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
12.

[Caffey disease (infantile cortical hyperostosis)].

Benomar S, Najdi T.

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

PMID:
10223109
13.

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. doi: 10.1007/s00431-011-1463-0. Epub 2011 May 13.

14.

Infantile cortical hyperostosis (Caffey disease): a review.

Kamoun-Goldrat A, le Merrer M.

J Oral Maxillofac Surg. 2008 Oct;66(10):2145-50. doi: 10.1016/j.joms.2007.09.007. Review.

PMID:
18848116
15.

Caffey disease: new perspectives on old questions.

Nistala H, Mäkitie O, Jüppner H.

Bone. 2014 Mar;60:246-51. doi: 10.1016/j.bone.2013.12.030. Epub 2013 Dec 31. Review.

16.

Infantile cortical hyperostosis.

Frána L, Sekanina M.

Arch Dis Child. 1976 Aug;51(8):589-95.

17.

[Infantile cortical hyperostosis (Caffey's disease)].

Pohl A, Orha L, Drăgoi AM.

Rev Pediatr Obstet Ginecol Pediatr. 1989 Oct-Dec;38(4):369-73. Romanian.

PMID:
2518583
18.

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
19.

Familial infantile cortical hyperostosis.

Emmery L, Timmermans J, Christens J, Fryns JP.

Eur J Pediatr. 1983 Oct;141(1):56-8.

PMID:
6357801
20.

[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. French. No abstract available.

PMID:
3883874

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