scholarly journals Caffey disease

2020 ◽  
Author(s):  
Keyword(s):  
Caffey Disease

Expanding the phenotypic spectrum of Caffey disease

2007 ◽  
Vol 71 (3) ◽  
pp. 280-284 ◽  
Author(s):  
K Suphapeetiporn ◽  
S Tongkobpetch ◽  
A Mahayosnond ◽  
V Shotelersuk
Keyword(s):  
Caffey Disease ◽  
Phenotypic Spectrum

Caffey disease responding to high-dose immunoglobulin

1988 ◽  
Vol 147 (4) ◽  
pp. 443-444 ◽  
Author(s):  
M. Berthier ◽  
D. Bonneau ◽  
J. L. Huret
Keyword(s):  
High Dose ◽  
Caffey Disease

Caffey Disease

2021 ◽  
Author(s):  
Hien Tran ◽  
Tiffany Le ◽  
Edward Kuoy, MD ◽  
Christopher V. Nguyen, MD
Keyword(s):  
Caffey Disease

Caffey Disease

2012 ◽  
Keyword(s):  
Caffey Disease

scholarly journals Fetuin-A deficiency is associated with infantile cortical hyperostosis (Caffey disease)

2019 ◽  
Vol 86 (5) ◽  
pp. 603-607 ◽  
Author(s):  
Rona Merdler-Rabinowicz ◽  
Anna Grinberg ◽  
Jeffrey M. Jacobson ◽  
Ido Somekh ◽  
Christoph Klein ◽  
...  
Keyword(s):  
Fetuin A ◽  
Caffey Disease ◽  
Infantile Cortical Hyperostosis ◽  
Cortical Hyperostosis

Unilateral Caffey disease (infantile cortical hyperostosis)

BMJ ◽  
2014 ◽  
Vol 349 (sep10 1) ◽  
pp. g5289-g5289
Author(s):  
P. Mishra ◽  
R. R. Das
Keyword(s):  
Caffey Disease ◽  
Infantile Cortical Hyperostosis ◽  
Cortical Hyperostosis

COL1A1 Mutation in an Indian Child with Caffey Disease

2011 ◽  
Vol 78 (7) ◽  
pp. 877-879 ◽  
Author(s):  
Prajnya Ranganath ◽  
Christine M. Laine ◽  
Divya Gupta ◽  
Outi Mäkitie ◽  
Shubha R. Phadke
Keyword(s):  
Indian Child ◽  
Caffey Disease

scholarly journals Familial mutation in caffey disease with reduced penetrance: a case report

2016 ◽  
Vol 58 (6) ◽  
pp. 650 ◽  
Author(s):  
Özmert M.A. Özdemir ◽  
Hazal Tancer-Elçi ◽  
Aziz Polat ◽  
İnci Güçtürk ◽  
Emre Tepeli ◽  
...  
Keyword(s):  
Case Report ◽  
Caffey Disease ◽  
Reduced Penetrance

Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagen

2021 ◽  
Author(s):  
Tibbe Dhooge ◽  
Delfien Syx ◽  
Trinh Hermanns-Lê ◽  
Ingrid Hausser ◽  
Geert Mortier ◽  
...  
Keyword(s):  
Type I ◽  
Caffey Disease ◽  
Type I Procollagen

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

2005 ◽  
Vol 115 (5) ◽  
pp. 1250-1257 ◽  
Author(s):  
Robert C. Gensure ◽  
Outi Mäkitie ◽  
Catherine Barclay ◽  
Catherine Chan ◽  
Steven R. DePalma ◽  
...  
Keyword(s):  
Caffey Disease ◽  
Infantile Cortical Hyperostosis ◽  
Cortical Hyperostosis
Sign in / Sign up

Export Citation Format

Share Document