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Journal Abstract Search

241 related items for PubMed ID: 6822598

  • 1. Osteogenesis imperfecta with dominant inheritance and normal sclerae.
    Paterson CR, McAllion S, Miller R.
    J Bone Joint Surg Br; 1983 Jan; 65(1):35-9. PubMed ID: 6822598
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  • 4. Osteogenesis imperfecta. Review of the literature with presentation of 29 cases.
    Shoenfeld Y.
    Am J Dis Child; 1975 Jun; 129(6):679-87. PubMed ID: 1098447
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  • 8. Osteogenesis imperfecta. A clinical and biochemical study of a generalized connective tissue disorder.
    Smith R, Francis MJ, Bauze RJ.
    Q J Med; 1975 Oct; 44(176):555-73. PubMed ID: 1202551
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  • 9. Four patients with Sillence type I osteogenesis imperfecta and mild bone fragility, complicated by left ventricular cardiac valvular disease and cardiac tissue fragility caused by type I collagen mutations.
    Vandersteen AM, Lund AM, Ferguson DJ, Sawle P, Pollitt RC, Holder SE, Wakeling E, Moat N, Pope FM.
    Am J Med Genet A; 2014 Feb; 164A(2):386-91. PubMed ID: 24311407
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  • 13. [A contribution to the recording and study of the disease pattern of osteogenesis imperfecta tarda (author's transl)].
    Matzen KA, Werner KC.
    Z Orthop Ihre Grenzgeb; 1979 Feb; 117(1):21-30. PubMed ID: 425623
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  • 14. Osteogenesis imperfecta and hyperplastic callus formation in a family: a report of three cases and a review of the literature.
    Ramírez N, Vilella FE, Colón M, Flynn JM.
    J Pediatr Orthop B; 2003 Mar; 12(2):88-96. PubMed ID: 12584490
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  • 15. Type V osteogenesis imperfecta: a new form of brittle bone disease.
    Glorieux FH, Rauch F, Plotkin H, Ward L, Travers R, Roughley P, Lalic L, Glorieux DF, Fassier F, Bishop NJ.
    J Bone Miner Res; 2000 Sep; 15(9):1650-8. PubMed ID: 10976985
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  • 16. [Pronounced osteoporosis, shrunken stature and blue coloration of sclerae in a 47-year old patient].
    Lang NK, Schalhorn A, Hiddemann W.
    Internist (Berl); 2001 Aug; 42(8):1151-5. PubMed ID: 11556110
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  • 17. Type I osteogenesis imperfecta and multiple osteochondromas in the same child.
    Calonge WM, Matos G, Pessoa DL, Sanches MC, Garcia H, Tercier S.
    J Pediatr Orthop B; 2009 Mar; 18(2):106-9. PubMed ID: 19238096
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  • 18. [Genetic heterogeneity of osteogenesis imperfecta. Study of 6 cases].
    Olivares JL, Hernández MC, Bueno M.
    An Esp Pediatr; 1986 Sep; 25(3):154-60. PubMed ID: 3789548
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  • 19. Osteogenesis imperfecta/lobstein syndrome associated with dentinogenesis imperfecta.
    Lingaraju N, Nagarathna PJ, Vijayalakshmi R, Sheshadri P.
    J Contemp Dent Pract; 2013 Jan 01; 14(1):140-2. PubMed ID: 23579912
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