157 related articles for article (PubMed ID: 9267903)
1. Recurrent severe infantile cortical hyperostosis (Caffey disease) in siblings.
Drinkwater BM; Crino JP; Garcia J; Ogburn J; Hecht JT
Prenat Diagn; 1997 Aug; 17(8):773-6. PubMed ID: 9267903
[TBL] [Abstract][Full Text] [Related]
2. Antenatal onset of cortical hyperostosis (Caffey disease): case report and review.
Schweiger S; Chaoui R; Tennstedt C; Lehmann K; Mundlos S; Tinschert S
Am J Med Genet A; 2003 Aug; 120A(4):547-52. PubMed ID: 12884437
[TBL] [Abstract][Full Text] [Related]
3. Perinatal death in two sibs with infantile cortical hyperostosis (Caffey disease).
de Jong G; Muller LM
Am J Med Genet; 1995 Nov; 59(2):134-8. PubMed ID: 8588573
[TBL] [Abstract][Full Text] [Related]
4. Hyperostosis in siblings.
Spranger JW; Lausch E
S Afr Med J; 2016 May; 106(6 Suppl 1):S98-9. PubMed ID: 27245539
[TBL] [Abstract][Full Text] [Related]
5. Familial occurrence of Caffey-Silverman syndrome.
Szwed A; Kołban M; Romanowska H; Baryła-Pankiewicz E
Ortop Traumatol Rehabil; 2012; 14(1):75-83. PubMed ID: 22408114
[TBL] [Abstract][Full Text] [Related]
6. Prenatal Caffey disease (prenatal cortical hyperostosis): severe forms with favorable outcome.
Hoen N; Cagneaux M; Combourieu D; Cordier MP; Massardier J; Lacalm A; Gaucherand P; Guibaud L; Massoud M
Prenat Diagn; 2015 Apr; 35(4):409-11. PubMed ID: 25630842
[No Abstract] [Full Text] [Related]
7. Recurrence of infantile cortical hyperostosis: a case report and review of the literature.
Navarre P; Pehlivanov I; Morin B
J Pediatr Orthop; 2013 Mar; 33(2):e10-7. PubMed ID: 23389580
[TBL] [Abstract][Full Text] [Related]
8. COL1A1 mutation in an Indian child with Caffey disease.
Ranganath P; Laine CM; Gupta D; Mäkitie O; Phadke SR
Indian J Pediatr; 2011 Jul; 78(7):877-9. PubMed ID: 21249479
[TBL] [Abstract][Full Text] [Related]
9. Lethal prenatal onset infantile cortical hyperostosis (Caffey disease).
Dahlstrom JE; Arbuckle SM; Kozlowski K; Peek MJ; Thomson M; Reynolds GJ; Sillence DO
Pathology; 2001 Nov; 33(4):521-5. PubMed ID: 11827425
[TBL] [Abstract][Full Text] [Related]
10. Autosomal dominant inheritance with incomplete penetrance of Caffey disease (infantile cortical hyperostosis).
Fried K; Manor A; Pajewski M; Starinsky R; Vure E
Clin Genet; 1981 Apr; 19(4):271-4. PubMed ID: 7023758
[No Abstract] [Full Text] [Related]
11. Familial infantile cortical hyperostosis.
Emmery L; Timmermans J; Christens J; Fryns JP
Eur J Pediatr; 1983 Oct; 141(1):56-8. PubMed ID: 6357801
[TBL] [Abstract][Full Text] [Related]
12. [Caffey disease (infantile cortical hyperostosis). Apropos of a familial form].
Castel Y; Toudic L; Crenn P; Le Fur JM
Ann Pediatr (Paris); 1985 Feb; 32(2):143-7. PubMed ID: 3883874
[No Abstract] [Full Text] [Related]
13. Prenatal cortical hyperostosis with COL1A1 gene mutation.
Kamoun-Goldrat A; Martinovic J; Saada J; Sonigo-Cohen P; Razavi F; Munnich A; Le Merrer M
Am J Med Genet A; 2008 Jul; 146A(14):1820-4. PubMed ID: 18553566
[TBL] [Abstract][Full Text] [Related]
14. [Prenatal diagnosis of Caffey's disease (infantile cortical hyperostosis)].
Langer R; Kaufmann HJ
Klin Padiatr; 1985; 197(6):473-6. PubMed ID: 3910953
[TBL] [Abstract][Full Text] [Related]
15. Radiological aspects of prenatal-onset cortical hyperostosis [Caffey Dysplasia].
Nemec SF; Rimoin DL; Lachman RS
Eur J Radiol; 2012 Apr; 81(4):e565-72. PubMed ID: 21726971
[TBL] [Abstract][Full Text] [Related]
16. The c.3040C > T mutation in COL1A1 is recurrent in Korean patients with infantile cortical hyperostosis (Caffey disease).
Cho TJ; Moon HJ; Cho DY; Park MS; Lee DY; Yoo WJ; Chung CY; Choi IH
J Hum Genet; 2008; 53(10):947. PubMed ID: 18704262
[TBL] [Abstract][Full Text] [Related]
17. Severe prenatal infantile cortical hyperostosis (Caffey's disease).
Turnpenny PD; Davidson R; Stockdale EJ; Tolmie JL; Sutton AM
Clin Dysmorphol; 1993 Jan; 2(1):81-6. PubMed ID: 8298744
[TBL] [Abstract][Full Text] [Related]
18. [The difficulty of diagnosing Caffey's disease in utero. Apropos of a case simulating lethal osteogenesis imperfecta].
Bercau G; Gonzalez M; Afriat R; Lecolier B; de Kermadec S
Ann Pediatr (Paris); 1991 Jan; 38(1):15-8. PubMed ID: 2006827
[TBL] [Abstract][Full Text] [Related]
19. Familial infantile cortical hyperostosis: an update.
Newberg AH; Tampas JP
AJR Am J Roentgenol; 1981 Jul; 137(1):93-6. PubMed ID: 6787897
[TBL] [Abstract][Full Text] [Related]
20. Prenatal infantile cortical hyperostosis (Caffey's disease): a 'hepatic myeloid hyperplasia-pulmonary hypoplasia sequence' can explain the lethality of early onset cases.
Wright JR; Van den Hof MC; Macken MB
Prenat Diagn; 2005 Oct; 25(10):939-44. PubMed ID: 16193456
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
