Literature DB >> 13898040

Familial infantile cortical hyperostosis.

J W GERRARD, G H HOLMAN, A A GORMAN, I H MORROW.   

Abstract

Entities:  

Keywords:  BONE DISEASES/genetics

Mesh:

Year:  1961        PMID: 13898040     DOI: 10.1016/s0022-3476(61)80238-2

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


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  9 in total

Review 1.  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

2.  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

3.  A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.

Authors:  Robert C Gensure; Outi Mäkitie; Catherine Barclay; Catherine Chan; Steven R Depalma; Murat Bastepe; Hilal Abuzahra; Richard Couper; Stefan Mundlos; David Sillence; Leena Ala Kokko; Jonathan G Seidman; William G Cole; Harald Jüppner
Journal:  J Clin Invest       Date:  2005-05       Impact factor: 14.808

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.  Wiskott-Aldrich syndrome associated with idiopathic infantile cortical hyperostosis (Caffey's disease).

Authors:  G McEnery; F W Nash
Journal:  Arch Dis Child       Date:  1973-10       Impact factor: 3.791

6.  Infantile cortical hyperostosis.

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

7.  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

8.  Familial infantile cortical hyperostosis.

Authors:  L Emmery; J Timmermans; J Christens; J P Fryns
Journal:  Eur J Pediatr       Date:  1983-10       Impact factor: 3.183

9.  Infantile cortical hyperostosis and COL1A1 mutation in four generations.

Authors:  Paola Cerruti-Mainardi; Giacomo Venturi; Marianna Spunton; Elena Favaron; Michela Zignani; Sandro Provera; Bruno Dallapiccola
Journal:  Eur J Pediatr       Date:  2011-05-13       Impact factor: 3.183

  9 in total

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