BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

142 related articles for article (PubMed ID: 23085318)

  • 1. [Neonatal cortical hyperostosis (Caffey disease)].
    de Blas A; Martín-Frías M; Toledano M; Gomez M; Corbatón J; Yturriaga R
    An Pediatr (Barc); 2013 Sep; 79(3):189-90. PubMed ID: 23085318
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. Autosomal dominant inheritance of Caffey disease.
    Bull MJ; Feingold M
    Birth Defects Orig Artic Ser; 1974; 10(9):139-46. PubMed ID: 4609117
    [No Abstract]   [Full Text] [Related]  

  • 4. [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]  

  • 5. [Infantile cortical hyperostosis. Apropos of 8 cases].
    Arnal JM; Moneo MI; Baldellou A
    An Esp Pediatr; 1988 Feb; 28(2):149-51. PubMed ID: 3281536
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. [Genetic study of infantile cortical hyperostosis].
    Frána L; Sekanina M; Plod P
    Cesk Pediatr; 1972 Mar; 27(3):118-21. PubMed ID: 4554654
    [No Abstract]   [Full Text] [Related]  

  • 9. [Caffey's disease in a mother and her 2 children].
    Landthaler G; Loizeau A; Tron P; Mallet E; Le Dosseur P; De Menibus CH
    Arch Fr Pediatr; 1984 Apr; 41(4):275-8. PubMed ID: 6383253
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Familial occurrence of infantile cortical hyperostosis. (Caffey-de Toni-Silvermann syndrome)].
    Pelikán L; Doubravský J; Mikes K; Cerný M
    Acta Chir Orthop Traumatol Cech; 1967 Oct; 34(5):430-4. PubMed ID: 4874755
    [No Abstract]   [Full Text] [Related]  

  • 11. Idiopathic cortical hyperostosis.
    Jones ET; Hensinger RN; Holt JF
    Clin Orthop Relat Res; 1982 Mar; (163):210-3. PubMed ID: 7039916
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Considerations on a case of Caffey-de Toni-Silverman disease (infantile cortical hyperostosis)].
    Barbero S; Lorenzi L
    Minerva Pediatr; 1967 May; 19(19):946-9. PubMed ID: 4885882
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. Infantile cortical hyperostosis.
    Dutta S; Jain N; Bhattacharya A; Mukhopadhyay K
    Indian Pediatr; 2005 Jan; 42(1):64-6. PubMed ID: 15695863
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Infantile cortical hyperostosis.
    Ho KK
    P N G Med J; 1976 Sep; 18(3):183-5. PubMed ID: 779336
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Infantile cortical hyperostosis-the Caffey-Silverman syndrome].
    Parízková E; Hrdinová V; Pozler O
    Cesk Pediatr; 1979 Feb; 34(2):84-6. PubMed ID: 371834
    [No Abstract]   [Full Text] [Related]  

  • 17. Late manifestations of infantile cortical hyperostosis (Caffey's disease).
    Pajewski M; Vure E
    Br J Radiol; 1967 Feb; 40(470):90-5. PubMed ID: 5334797
    [No Abstract]   [Full Text] [Related]  

  • 18. [Infantile cortical hyperostosis (author's transl)].
    Hoskens C; van Herreweghe W
    J Belge Radiol; 1981; 64(6):511-4. PubMed ID: 7050075
    [No Abstract]   [Full Text] [Related]  

  • 19. [Infantile cortical hyperostosis in 2 siblings (with different onset and course)].
    Westermann P; Rossi MV; Masserini C
    Minerva Pediatr; 1975 Aug; 27(25):1409-23. PubMed ID: 1099436
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.