Literature DB >> 20967539

Caffey disease.

Shawn E Parnell1, Marguerite T Parisi.   

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Year:  2010        PMID： 20967539     DOI： 10.1007/s00247-010-1869-2

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN： 0301-0449


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  2 in total

1.  The c.3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease).

Authors:  Tae-Joon Cho; Hyuk Ju Moon; Dae-Yeon Cho; Moon Seok Park; Dong Yeon Lee; Won Joon Yoo; Chin Youb Chung; In Ho Choi
Journal:  J Hum Genet       Date:  2008-08-13       Impact factor: 3.172

Review 2.  Infantile cortical hyperostosis (Caffey disease): a review.

Authors:  Agnès Kamoun-Goldrat; Martine le Merrer
Journal:  J Oral Maxillofac Surg       Date:  2008-10       Impact factor: 1.895
  2 in total
  2 in total

1.  Infantile cortical hyperostosis: two cases with varied presentations.

Authors:  Pravakar Mishra; Shasanka Shekhar Panda; Manoranjan Tripathy; Meely Panda; Rashmi Ranjan Das
Journal:  J Clin Diagn Res       Date:  2014-10-20

2.  Caffey Disease in Infancy: A diagnostic dilemma for primary care physicians.

Authors:  Shahid A Siddiqui; Gulnaz F Siddiqui; Manisha Maurya; Anubha Shrivastava; Mukesh V Singh
Journal:  Sultan Qaboos Univ Med J       Date:  2020-03-09
  2 in total

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