138 related articles for article (PubMed ID: 15864344)
1. Caffey disease: an unlikely collagenopathy.
Glorieux FH
J Clin Invest; 2005 May; 115(5):1142-4. PubMed ID: 15864344
[TBL] [Abstract][Full Text] [Related]
2. A novel COL1A1 mutation in infantile cortical hyperostosis (Caffey disease) expands the spectrum of collagen-related disorders.
Gensure RC; Mäkitie O; Barclay C; Chan C; Depalma SR; Bastepe M; Abuzahra H; Couper R; Mundlos S; Sillence D; Ala Kokko L; Seidman JG; Cole WG; Jüppner H
J Clin Invest; 2005 May; 115(5):1250-7. PubMed ID: 15864348
[TBL] [Abstract][Full Text] [Related]
3. Expanding the phenotypic spectrum of Caffey disease.
Suphapeetiporn K; Tongkobpetch S; Mahayosnond A; Shotelersuk V
Clin Genet; 2007 Mar; 71(3):280-4. PubMed ID: 17309652
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
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. Infantile cortical hyperostosis (Caffey disease): a review.
Kamoun-Goldrat A; le Merrer M
J Oral Maxillofac Surg; 2008 Oct; 66(10):2145-50. PubMed ID: 18848116
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Caffey disease: new perspectives on old questions.
Nistala H; Mäkitie O; Jüppner H
Bone; 2014 Mar; 60():246-51. PubMed ID: 24389367
[TBL] [Abstract][Full Text] [Related]
11. Two Japanese familial cases of Caffey disease with and without the common COL1A1 mutation and normal bone density, and review of the literature.
Kitaoka T; Miyoshi Y; Namba N; Miura K; Kubota T; Ohata Y; Fujiwara M; Takagi M; Hasegawa T; Jüppner H; Ozono K
Eur J Pediatr; 2014 Jun; 173(6):799-804. PubMed ID: 24390061
[TBL] [Abstract][Full Text] [Related]
12. Autosomal dominant inheritance of Caffey-Silverman disease. Hyperostosis corticalis infantum.
Rogóyski A; Jakubowska K; Tronowska TD
Padiatr Padol; 1984; 19(4):401-8. PubMed ID: 6390299
[TBL] [Abstract][Full Text] [Related]
13. The IFITM5 Ser40Leu variant can manifest as prenatal Caffey disease.
Yap JYC; Lim JY; Bhatia A; Tan VKJ; Koo S; Nishimura G; Moosa S; Koh AL; Tan EC; Fong N; Jamuar SS
Am J Med Genet A; 2024 Feb; 194(2):358-362. PubMed ID: 37799085
[TBL] [Abstract][Full Text] [Related]
14. Infantile cortical hyperostosis and COL1A1 mutation in four generations.
Cerruti-Mainardi P; Venturi G; Spunton M; Favaron E; Zignani M; Provera S; Dallapiccola B
Eur J Pediatr; 2011 Nov; 170(11):1385-90. PubMed ID: 21567126
[TBL] [Abstract][Full Text] [Related]
15. Three arginine to cysteine substitutions in the pro-alpha (I)-collagen chain cause Ehlers-Danlos syndrome with a propensity to arterial rupture in early adulthood.
Malfait F; Symoens S; De Backer J; Hermanns-Lê T; Sakalihasan N; Lapière CM; Coucke P; De Paepe A
Hum Mutat; 2007 Apr; 28(4):387-95. PubMed ID: 17211858
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Normal periosteal reactions and associated soft-tissue findings. Relationship to infantile colic and to the Caffey syndrome.
Ditkowsky SP; Goldman A; Barnett H; Baker M; Sammett J
Clin Pediatr (Phila); 1970 Sep; 9(9):515-24. PubMed ID: 4916528
[No Abstract] [Full Text] [Related]
18. Infantile cortical hyperostosis (Caffey's disease). Two case reports.
Rethmeier JW
Radiol Clin (Basel); 1976; 45(2-4):251-7. PubMed ID: 781725
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. [Infantile cortical hyperostosis (Caffey's disease)].
Pohl A; Orha L; Drăgoi AM
Rev Pediatr Obstet Ginecol Pediatr; 1989; 38(4):369-73. PubMed ID: 2518583
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]