Literature DB >> 13127963

[Etiology of infantile cortical hyperostosis (Caffey syndrome)].

K VELLER, A LAUR.   

Abstract

Entities:  

Keywords:  BONES/diseases

Mesh：

Year:  1953        PMID： 13127963

Source DB:  PubMed          Journal:  Fortschr Geb Rontgenstr


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  6 in total

1.  INFANTILE CORTICAL HYPEROSTOSIS (CAFFEY-SMYTH SYNDROME).

Authors:  G C CYPRESS
Journal:  J Natl Med Assoc       Date:  1964-03       Impact factor: 1.798

Review 2.  Radiographic overlap of recurrent Caffey disease and chronic recurrent multifocal osteomyelitis (CRMO) with considerations of molecular origins.

Authors:  Teresa Chapman; Sarah J Menashe; Benjamin H Taragin
Journal:  Pediatr Radiol       Date:  2019-12-23

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

Authors:  R Langer; H J Kaufmann
Journal:  Skeletal Radiol       Date:  1986       Impact factor: 2.199

4.  Familial infantile cortical hyperostosis in a large Canadian family.

Authors:  A K Maclachlan; J W Gerrard; C S Houston; E J Ives
Journal:  Can Med Assoc J       Date:  1984-05-01       Impact factor: 8.262

5.  Infantile cortical hyperostosis.

Authors:  L Frána; M Sekanina
Journal:  Arch Dis Child       Date:  1976-08       Impact factor: 3.791

6.  Birth Order and Maternal Age for Reported Cases of Severe Prenatal Cortical Hyperostosis (Caffey–Silverman Disease)

Authors:  Rolf R Engel; Raul F Cifuentes
Journal:  AJP Rep       Date:  2017-09-11
  6 in total

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