BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 1099436)

  • 1. [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]  

  • 2. [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]  

  • 3. 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]  

  • 4. [Familial infantile cortical hyperostosis with prenatal beginning].
    Schärer K; Szabó J
    Fortschr Geb Rontgenstr Nuklearmed; 1966 Aug; 105(2):154-63. PubMed ID: 4891339
    [No Abstract]   [Full Text] [Related]  

  • 5. [Familial infantile cortical hyperostosis].
    Lund K
    Ugeskr Laeger; 1979 Sep; 141(38):2615-6. PubMed ID: 384634
    [No Abstract]   [Full Text] [Related]  

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

  • 7. 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]  

  • 8. [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]  

  • 9. [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]  

  • 10. [Familial infantile cortical hyperostosis (author's transl)].
    Baldellou Vázquez A; Gomá Brufau A; Carreras Calvete A; Used Aznar MD; Gómez Beltrán JL
    An Esp Pediatr; 1979 Feb; 12(2):155-8. PubMed ID: 371475
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 12. [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]  

  • 13. 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]  

  • 14. [A case of infantile cortical hyperostosis in 2 siblings].
    Snobl O; Neugebauerová L; Tůma S
    Cesk Radiol; 1968 Mar; 22(2):122-8. PubMed ID: 4874177
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. [Familial infantile cortical hyperostosis (Caffey's disease) with osteolytic lesions of the skull].
    Lachaux A; Le Gall C; Loras Duclaux I; Hermier M
    Arch Fr Pediatr; 1992; 49(6):525-8. PubMed ID: 1449354
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Familial aspects of Caffey's disease.
    Bernstein RM; Zaleske DJ
    Am J Orthop (Belle Mead NJ); 1995 Oct; 24(10):777-81. PubMed ID: 8593560
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.