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PUBMED FOR HANDHELDS

Journal Abstract Search


226 related items for PubMed ID: 7239850

  • 1. Low ocular rigidity in patients with osteogenesis imperfecta.
    Kaiser-Kupfer MI, McCain L, Shapiro JR, Podgor MJ, Kupfer C, Rowe D.
    Invest Ophthalmol Vis Sci; 1981 Jun; 20(6):807-9. PubMed ID: 7239850
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  • 2. Correlation of ocular rigidity and blue sclerae in osteogenesis imperfecta.
    Kaiser-Kupfer MI, Podgor MJ, McCain L, Kupfer C, Shapiro JR.
    Trans Ophthalmol Soc U K (1962); 1985 Jun; 104 ( Pt 2)():191-5. PubMed ID: 3857778
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  • 4. Natural history of blue sclerae in osteogenesis imperfecta.
    Sillence D, Butler B, Latham M, Barlow K.
    Am J Med Genet; 1993 Jan 15; 45(2):183-6. PubMed ID: 8456800
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  • 5. Evidence that abnormal high bone mineralization in growing children with osteogenesis imperfecta is not associated with specific collagen mutations.
    Roschger P, Fratzl-Zelman N, Misof BM, Glorieux FH, Klaushofer K, Rauch F.
    Calcif Tissue Int; 2008 Apr 15; 82(4):263-70. PubMed ID: 18311573
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  • 7. Central corneal thickness is lower in osteogenesis imperfecta and negatively correlates with the presence of blue sclera.
    Evereklioglu C, Madenci E, Bayazit YA, Yilmaz K, Balat A, Bekir NA.
    Ophthalmic Physiol Opt; 2002 Nov 15; 22(6):511-5. PubMed ID: 12477015
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  • 8. Ocular characteristics and complications in patients with osteogenesis imperfecta: a systematic review.
    Treurniet S, Burger P, Ghyczy EAE, Verbraak FD, Curro-Tafili KR, Micha D, Bravenboer N, Ralston SH, de Vries R, Moll AC, Eekhoff EMW.
    Acta Ophthalmol; 2022 Feb 15; 100(1):e16-e28. PubMed ID: 34009739
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  • 9. [Multiple osteogenesis imperfecta in one family].
    Nakajima H, Tada S.
    Seikei Geka; 1971 Feb 15; 22(9):733-8. PubMed ID: 5106824
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  • 10. A standardized tool to measure and describe scleral colour in osteogenesis imperfecta.
    Zack P, Zack LR, Surtees R, Neville BG.
    Ophthalmic Physiol Opt; 2007 Mar 15; 27(2):174-8. PubMed ID: 17324207
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  • 15. Osteogenesis imperfecta and hearing loss.
    Verstreken M, Claes J, Van de Heyning PH.
    Acta Otorhinolaryngol Belg; 1996 Mar 15; 50(2):91-8. PubMed ID: 8767251
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  • 16. COL1A1 mutation analysis in Lithuanian patients with osteogenesis imperfecta.
    Benusiené E, Kucinskas V.
    J Appl Genet; 2003 Mar 15; 44(1):95-102. PubMed ID: 12590186
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  • 17. [On a case of osteogenesis imperfecta of the Lobstein type, associated with the Ehlers-Danlos syndrome, hydrocephaly and club feet].
    Bolletti M, Disertori A.
    Pediatria (Napoli); 1967 Mar 15; 75(2):310-30. PubMed ID: 5615137
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  • 18. Rieger's anomaly and other ocular abnormalities in association with osteogenesis imperfecta and a COL1A1 mutation.
    Nwosu BU, Raygada M, Tsilou ET, Rennert OM, Stratakis CA.
    Ophthalmic Genet; 2005 Sep 15; 26(3):135-8. PubMed ID: 16272059
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  • 20. [Familial occurrence of Ekman-Lebstein-van der Hoeve syndrome].
    Pecoldowa K, Warchalewska-Pykalowa U.
    Klin Oczna; 1970 Sep 15; 40(2):227-32. PubMed ID: 5446659
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