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Journal Abstract Search

68 related items for PubMed ID: 5860349

  • 21. Marcus Gunn phenomenon (a report of five cases).
    Naidu A, Khandelwal MK.
    J All India Ophthalmol Soc; 1966 Oct; 14(5):217-22. PubMed ID: 5982334
    [No Abstract] [Full Text] [Related]

  • 22. [Stilling-Duane syndrome: a family case].
    Calmettes L, Déodati F, Delfour G, Béchac G.
    Bull Soc Ophtalmol Fr; 1968 Mar; 68(3):364-8. PubMed ID: 5746420
    [No Abstract] [Full Text] [Related]

  • 23. [Familial hematuria and inner ear deafness (Alport's syndrome)].
    Goetz O, Karl HJ, Dattenberg T.
    Z Kinderheilkd; 1965 Oct 01; 94(1):63-79. PubMed ID: 5888333
    [No Abstract] [Full Text] [Related]

  • 24. [On some cases of familial congenital nephropathy with internal type deafness and lenticonus. (Clinical, anatomopathologic, pathogenetic and genealogic considerations)].
    Gambaro GC, Ravera M, Ciurlo G.
    Arch Maragliano Patol Clin; 1966 Feb 01; 22(1):41-79. PubMed ID: 5952262
    [No Abstract] [Full Text] [Related]

  • 25. 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 01; 138(5):749-55. PubMed ID: 15531309
    [Abstract] [Full Text] [Related]

  • 26. [On the Marcus-Gunn phenomenon].
    Domke H, Krüger KE, Tost M.
    Klin Monbl Augenheilkd; 1965 Nov 01; 147(6):885-93. PubMed ID: 5882577
    [No Abstract] [Full Text] [Related]

  • 27. [Etiology of Marcus Gunn phenomenon].
    Shimono M, Soejima N, Shibazaki H, Shida K, Kuroiwa Y.
    Rinsho Shinkeigaku; 1975 Jun 01; 15(6):347-54. PubMed ID: 1171752
    [No Abstract] [Full Text] [Related]

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  • 30. [Myasthenic internuclear pseudo-ophthalmoplegia].
    Pierrot-Deseilligny C, Michelin T.
    Rev Neurol (Paris); 1983 Jun 01; 139(8-9):527-8. PubMed ID: 6648206
    [Abstract] [Full Text] [Related]

  • 31. [A case of familial muscular atrophy mainly due to neurogenic origin with external ophthalmoplegia, baldness, cataract and myxovirus-like inclusion bodies (author's transl)].
    Nakano Y, Katagiri H, Kita K, Hirayama K, Tomonaga M.
    Rinsho Shinkeigaku; 1982 Feb 01; 22(2):120-7. PubMed ID: 7094488
    [No Abstract] [Full Text] [Related]

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  • 34. [Familial cases of oculopharyngeal muscular dystrophy. A case].
    Friol-Vercelletto M, Mussini JM, Dumas-Guillemot A, Denis G, Lavenant-Oger F, Feve JR.
    Rev Otoneuroophtalmol; 1983 Feb 01; 55(4):329-36. PubMed ID: 6669860
    [No Abstract] [Full Text] [Related]

  • 35. [Familial congenital horizontal gaze paralysis].
    Steffen H, Thomsen M, Kolling GH.
    Ophthalmologe; 1996 Aug 01; 93(4):380-2. PubMed ID: 8963135
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  • 38. [Marfan syndrome].
    Liska V.
    Cesk Slov Oftalmol; 1997 Feb 01; 53(1):40-5. PubMed ID: 9213523
    [Abstract] [Full Text] [Related]

  • 39. [Genetic counseling in eye diseases].
    Hammerstein W.
    Buch Augenarzt; 1980 Feb 01; (81):1-89. PubMed ID: 7192591
    [No Abstract] [Full Text] [Related]

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