BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 4609117)

  • 21. [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]  

  • 22. [A case of de Toni-Caffey syndrome].
    Axmann K; Svagrová E
    Cesk Radiol; 1984 Jul; 38(4):264-71. PubMed ID: 6386196
    [No Abstract]   [Full Text] [Related]  

  • 23. [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]  

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

  • 25. 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]  

  • 26. Autosomal dominant osteosclerosis.
    Gelman MI
    Radiology; 1977 Nov; 125(2):289-96. PubMed ID: 198844
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. [New cases of familial generalized cortical hyperostosis with dominant transmission (Worth's type) (author's transl)].
    Vayssairat M; Prier A; Meisel C; Camus JP; Grellet J
    J Radiol Electrol Med Nucl; 1976 Oct; 10(57):719-24. PubMed ID: 794463
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [The genetic factor in infantile cortical hyperostosis (Toni-Caffey-Silverman syndrome)].
    Boer GE; Battistella P
    Minerva Pediatr; 1966 Aug; 18(24):1291-9. PubMed ID: 4865843
    [No Abstract]   [Full Text] [Related]  

  • 30. Generalized cortical hyperostosis (Van Buchem disease): nosologic considerations.
    Eastman JR; Bixler D
    Radiology; 1977 Nov; 125(2):297-304. PubMed ID: 198845
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Van Buchem's disease (hyperostosis corticalis generalisata).
    Owen RH
    Br J Radiol; 1976 Feb; 49(578):126-32. PubMed ID: 181111
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Generalized hyperostosis corticalis (dominant transmission) (Worth's type)].
    Maroteaux P; Fontaine G; Scharfman W; Farriaux JP
    Arch Fr Pediatr; 1971; 28(7):685-98. PubMed ID: 4942110
    [No Abstract]   [Full Text] [Related]  

  • 33. [Dominant generalized cortical hyperostosis with multiple involvement of the cranial nerves].
    Lapresle J; Maroteaux P; Kuffer R; Said G; Meyer O
    Nouv Presse Med; 1976 Nov; 5(40):2703-6. PubMed ID: 794825
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. [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]  

  • 36. [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]  

  • 37. 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]  

  • 38. 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]  

  • 39. [A case of Caffey-Silverman syndrome in a 3.5 month old infant].
    Soboczyński A; Chwirot-Głyda I; Bittner J
    Otolaryngol Pol; 1989; 43(1):78-81. PubMed ID: 2682466
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.