|1.||Jüppner, Harald: 3 articles (06/2014 - 05/2005)|
|2.||Mäkitie, Outi: 3 articles (03/2014 - 05/2005)|
|3.||Lachman, Ralph S: 2 articles (04/2012 - 09/2002)|
|4.||Rimoin, David L: 2 articles (04/2012 - 09/2002)|
|5.||Cormier-Daire, Valérie: 2 articles (09/2009 - 09/2002)|
|6.||Le Merrer, Martine: 2 articles (09/2009 - 07/2008)|
|7.||Kamoun-Goldrat, Agnès: 2 articles (10/2008 - 07/2008)|
|8.||Mundlos, Stefan: 2 articles (05/2005 - 08/2003)|
|9.||Combourieu, Danièle: 1 article (04/2015)|
|10.||Cordier, Marie-Pierre: 1 article (04/2015)|
04/01/2015 - "Prenatal Caffey disease (prenatal cortical hyperostosis): severe forms with favorable outcome."
09/01/2013 - "[Neonatal cortical hyperostosis (Caffey disease)]."
03/01/2013 - "Although very rare and poorly recognized, the diagnosis of recurrent cortical hyperostosis must be evoked in a patient who suffered from Caffey disease in infancy, and presents similar clinical characteristics in the adolescent period. "
03/01/2013 - "The literature confirms the possibility but also the rarity of a recurrence of cortical hyperostosis in an adolescent who was diagnosed with Caffey disease in infancy. "
08/01/2003 - "We report on a fetus of 27 weeks of gestation whose clinical, radiological, and histopathological findings are compatible with the prenatal form of Caffey disease (cortical hyperostosis). "
|2.||Congenital Cortical Hyperostosis (Infantile Cortical Hyperostosis)
07/01/2013 - "Infantile cortical hyperostosis (Caffey disease): a case report and review of the literature--where are we after 70 years?"
07/01/2011 - "Caffey disease or infantile cortical hyperostosis is a rare skeletal disorder with both sporadic and familial occurrence. "
10/01/2010 - "Infantile cortical hyperostosis (Caffey disease) is a rare self-limiting inflammatory bony disease of early infancy. "
10/01/2010 - "Infantile cortical hyperostosis (Caffey disease): a possible misdiagnosis as physical abuse."
04/01/2010 - "Caffey disease or Infantile Cortical Hyperostosis (ICH) is a rare and mostly self limiting condition affecting young infants. "
03/01/2014 - "The autosomal dominant form of Caffey disease is a largely self-limiting infantile bone disorder characterized by acute inflammation of soft tissues and localized thickening of the underlying bone cortex. "
05/01/2005 - "Infantile cortical hyperostosis (also known as Caffey disease) is characterized by hyperirritability, acute inflammation of soft tissues, and profound alterations of the shape and structure of the underlying bones, particularly the long bones, mandible, clavicles, or ribs. "
05/01/2005 - "The deleterious effect of the mutation on collagen fibril morphology is demonstrated; however, the precise functional link between the reported missense mutation and the localized inflammation and hyperostosis seen in Caffey disease awaits future studies."
06/01/2014 - "Caffey disease, also known as infantile cortical hyperostosis, is a rare bone disease characterized by acute inflammation with swelling of soft tissues and hyperostosis of the outer cortical surface in early infancy. "
|4.||Wounds and Injuries (Trauma)
01/01/2012 - "After exclusion of other conditions such as trauma, osteomyelitis and congenital syphilis, the involvement of the tibial diaphysis, sparing the epiphyses and the benign course of the disease in family history, were indicative of Caffey disease. "
08/01/1986 - "Lamellated cortical hyperostosis about the long bones of a premature infant is usually an indication of trauma, congenital infection or Caffey disease. "
08/01/2012 - "Severe thrombocytosis as initial manifestation of Caffey disease in a 4 month old infant."
02/01/2008 - "Caffey disease with raised immunoglobulin levels and thrombocytosis."
02/01/2008 - "We report a case of Caffey disease highlighting its presentation with thrombocytosis and high serum immunoglobulin level to alert physicians to use steroids cautiously in view of the known thrombocythemic effect of the drug. "
|3.||Prostaglandin Antagonists (Prostaglandin Antagonist)