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Results: 1 to 20 of 43

PubMed Links for Books (Select 2963966)

1.

Severe thrombocytosis as initial manifestation of Caffey disease in a 4 month old infant.

Krishnamurthy S, Srinivasan S.

Pediatr Blood Cancer. 2012 Aug;59(2):345-6. doi: 10.1002/pbc.24063. Epub 2011 Dec 27. No abstract available.

PMID:
22213629
2.

Tumoral calcinosis of the cervical spine and its association with Caffey disease in a 4-month-old boy: case report and review of the literature.

Issa El Khoury F, Kreichati G, Kharrat K, Ghanem I.

J Pediatr Orthop B. 2012 May;21(3):286-91. doi: 10.1097/BPB.0b013e32834de561.

PMID:
22080299
3.

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
4.

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.

5.

Prenatal Caffey disease.

Hochwald O, Osiovich H.

Isr Med Assoc J. 2011 Feb;13(2):113-4. No abstract available.

6.

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
7.

Caffey disease.

Parnell SE, Parisi MT.

Pediatr Radiol. 2010 Dec;40 Suppl 1:S39. doi: 10.1007/s00247-010-1869-2. Epub 2010 Oct 22. No abstract available.

PMID:
20967539
8.

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.

9.

Dysphagia and hypervitaminosis A: cervical hyperostosis.

Wendling D, Hafsaoui C, Laurain JM, Runge M, Magy-Bertrand N, Prati C.

Joint Bone Spine. 2009 Jul;76(4):409-11. doi: 10.1016/j.jbspin.2008.11.004. Epub 2009 Mar 16.

PMID:
19289294
11.

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
12.

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
13.

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
14.

A novel missense mutation in GALNT3 causing hyperostosis-hyperphosphataemia syndrome.

Olauson H, Krajisnik T, Larsson C, Lindberg B, Larsson TE.

Eur J Endocrinol. 2008 Jun;158(6):929-34. doi: 10.1530/EJE-08-0011. Epub 2008 Mar 5.

15.

Cortical hyperostosis secondary to prolonged use of prostaglandin E1.

de Almeida JF, Kimura H, Hercowitz LH, Korkes H, Troster EJ.

Clinics (Sao Paulo). 2007 Jun;62(3):363-6. No abstract available.

16.

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
17.

Three arginine to cysteine substitutions in the pro-alpha (I)-collagen chain cause Ehlers-Danlos syndrome with a propensity to arterial rupture in early adulthood.

Malfait F, Symoens S, De Backer J, Hermanns-Lê T, Sakalihasan N, Lapière CM, Coucke P, De Paepe A.

Hum Mutat. 2007 Apr;28(4):387-95.

PMID:
17211858
18.

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.

19.

Caffey disease: an unlikely collagenopathy.

Glorieux FH.

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

20.

Infantile cortical hyperostosis of the mandible.

Restrepo S, Sánchez AM, Palacios E.

Ear Nose Throat J. 2004 Jul;83(7):454-5. Review. No abstract available.

PMID:
15372912
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