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Journal Abstract Search

135 related items for PubMed ID: 4058877

  • 1. Dominant optic nerve atrophy with progressive hearing loss and chronic progressive external ophthalmoplegia (CPEO).
    Meire F, De Laey JJ, de Bie S, van Staey M, Matton MT.
    Ophthalmic Paediatr Genet; 1985 Feb; 5(1-2):91-7. PubMed ID: 4058877
    [Abstract] [Full Text] [Related]

  • 2. Dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy. A new syndrome.
    Treft RL, Sanborn GE, Carey J, Swartz M, Crisp D, Wester DC, Creel D.
    Ophthalmology; 1984 Aug; 91(8):908-15. PubMed ID: 6493699
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  • 3. Dominant optic atrophy, sensorineural hearing loss, ptosis, and ophthalmoplegia: a syndrome caused by a missense mutation in OPA1.
    Payne M, Yang Z, Katz BJ, Warner JE, Weight CJ, Zhao Y, Pearson ED, Treft RL, Hillman T, Kennedy RJ, Meire FM, Zhang K.
    Am J Ophthalmol; 2004 Nov; 138(5):749-55. PubMed ID: 15531309
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  • 4. Probable autosomal dominant optic atrophy with hearing loss.
    Mets MB, Mhoon E.
    Ophthalmic Paediatr Genet; 1985 Feb; 5(1-2):85-9. PubMed ID: 4058876
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  • 7. [Ophthalmoplegia plus with optic atrophy. Apropos of a case].
    Augustin P, Dujardin M, Daluzeau N, Denis P.
    Rev Otoneuroophtalmol; 1984 Feb; 56(2):183-9. PubMed ID: 6474024
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  • 8. Autosomal dominant optic atrophy. A spectrum of disability.
    Hoyt CS.
    Ophthalmology; 1980 Mar; 87(3):245-51. PubMed ID: 7422264
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  • 11. Nerve deafness: optic nerve atrophy, and dementia: a new X-linked recessive syndrome?
    Jensen PK.
    Am J Med Genet; 1981 Mar; 9(1):55-60. PubMed ID: 7195649
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  • 12. Progressive autosomal dominant optic atrophy and sensorineural hearing loss in a Turkish family.
    Ozden S, Düzcan F, Wollnik B, Cetin OG, Sahiner T, Bayramoğlu I, Yüksel-Apak M, Bağci H.
    Ophthalmic Genet; 2002 Mar; 23(1):29-36. PubMed ID: 11910556
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  • 14. The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'.
    Harding AE.
    Brain; 1982 Mar; 105(Pt 1):1-28. PubMed ID: 7066668
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  • 15. Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy?
    Boltshauser E, Lang W, Spillmann T, Hof E.
    J Med Genet; 1989 Feb; 26(2):105-8. PubMed ID: 2918537
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  • 16. Autosomal dominant palmoplantar hyperkeratosis and sensorineural deafness in three generations.
    Sharland M, Bleach NR, Goberdhan PD, Patton MA.
    J Med Genet; 1992 Jan; 29(1):50-2. PubMed ID: 1532426
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  • 19. Progressive visual loss, diabetes mellitus, and associated abnormalities (DIDMOAD syndrome).
    Kocher GA, Spoor TC, Ferguson JG.
    J Clin Neuroophthalmol; 1982 Dec; 2(4):241-4. PubMed ID: 6226706
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