Infantile cortical hyperostosis (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Infantile cortical hyperostosis" in English language version.

refsWebsite

Global rank English rank

2^nd place

4^th place

11^th place

8^th place

doi.org

Kamoun-Goldrat A, Martinovic J, Saada J, Sonigo-Cohen P, Razavi F, Munnich A, et al. (July 2008). "Prenatal cortical hyperostosis with COL1A1 gene mutation". American Journal of Medical Genetics. Part A. 146A (14): 1820–1824. doi:10.1002/ajmg.a.32351. PMID 18553566. S2CID 205309510.
Yap JY, Lim JY, Bhatia A, Tan VK, Koo S, Nishimura G, et al. (February 2024). "The IFITM5 Ser40Leu variant can manifest as prenatal Caffey disease". American Journal of Medical Genetics. Part A. 194 (2): 358–362. doi:10.1002/ajmg.a.63420. PMID 37799085.
Lewis AB, Freed MD, Heymann MA, Roehl SL, Kensey RC (November 1981). "Side effects of therapy with prostaglandin E1 in infants with critical congenital heart disease". Circulation. 64 (5): 893–898. doi:10.1161/01.cir.64.5.893. PMID 7285304.
Caffey J (November 1946). "Infantile cortical hyperostoses". The Journal of Pediatrics. 29 (5): 541–559. doi:10.1016/S0022-3476(46)80122-7. PMID 21002859.

Kamoun-Goldrat A, Martinovic J, Saada J, Sonigo-Cohen P, Razavi F, Munnich A, et al. (July 2008). "Prenatal cortical hyperostosis with COL1A1 gene mutation". American Journal of Medical Genetics. Part A. 146A (14): 1820–1824. doi:10.1002/ajmg.a.32351. PMID 18553566. S2CID 205309510.
Yap JY, Lim JY, Bhatia A, Tan VK, Koo S, Nishimura G, et al. (February 2024). "The IFITM5 Ser40Leu variant can manifest as prenatal Caffey disease". American Journal of Medical Genetics. Part A. 194 (2): 358–362. doi:10.1002/ajmg.a.63420. PMID 37799085.
Lewis AB, Freed MD, Heymann MA, Roehl SL, Kensey RC (November 1981). "Side effects of therapy with prostaglandin E1 in infants with critical congenital heart disease". Circulation. 64 (5): 893–898. doi:10.1161/01.cir.64.5.893. PMID 7285304.
Caffey J (November 1946). "Infantile cortical hyperostoses". The Journal of Pediatrics. 29 (5): 541–559. doi:10.1016/S0022-3476(46)80122-7. PMID 21002859.

Kamoun-Goldrat A, Martinovic J, Saada J, Sonigo-Cohen P, Razavi F, Munnich A, et al. (July 2008). "Prenatal cortical hyperostosis with COL1A1 gene mutation". American Journal of Medical Genetics. Part A. 146A (14): 1820–1824. doi:10.1002/ajmg.a.32351. PMID 18553566. S2CID 205309510.