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Journal Abstract Search

93 related items for PubMed ID: 5996509

  • 1. [Complicated optic atrophy of infancy (Behr's disease)].
    Hermans G, Szliwowski H.
    J Genet Hum; 1966; 15():Suppl:219-27. PubMed ID: 5996509
    [No Abstract] [Full Text] [Related]

  • 2. [The heredo-degenerations of the optic nerve and their associations with systemic neurologic diseases. Complicated infantile optic atrophy (Behr's disease)].
    Franceschetti A.
    J Genet Hum; 1966 Dec; 15(3):322-31. PubMed ID: 5987543
    [No Abstract] [Full Text] [Related]

  • 3. [A recent case of dominant infantile hereditary optic atrophy].
    Biais B, Bouvery P.
    Bull Soc Ophtalmol Fr; 1978 Mar; 78(3):221-2. PubMed ID: 747872
    [No Abstract] [Full Text] [Related]

  • 4. Colour vision in a pedigree with autosomal dominant optic atrophy.
    Ohba N, Imamura PM, Tanino T.
    Mod Probl Ophthalmol; 1976 Mar; 17():315-9. PubMed ID: 1085884
    [No Abstract] [Full Text] [Related]

  • 5. [Twenty years observation of a family suffering from Behr's disease (heredo-familial complicated infantile optical atrophy) (author's transl)].
    Klein D.
    Rev Otoneuroophtalmol; 1980 Mar; 52(2):179-85. PubMed ID: 7414171
    [No Abstract] [Full Text] [Related]

  • 6. [Hereditary optic atrophies].
    Francois J.
    J Genet Hum; 1976 Sep; 24(3):183-200. PubMed ID: 1003172
    [Abstract] [Full Text] [Related]

  • 7. [Juvenile optic atrophy with dominant inheritance].
    Werner W, Benedikt O.
    Klin Monbl Augenheilkd; 1971 Dec; 159(6):798-803. PubMed ID: 5316708
    [No Abstract] [Full Text] [Related]

  • 8. Two different alleles for deuteranomaly within a family with Leber's optic atrophy.
    Grützner P, Schrapp A.
    Mod Probl Ophthalmol; 1974 Dec; 13(0):258-61. PubMed ID: 4548141
    [No Abstract] [Full Text] [Related]

  • 9. Congenital tritanopia without neuroretinal disease.
    Smith DP, Cole BL, Isaacs A.
    Invest Ophthalmol; 1973 Aug; 12(8):608-17. PubMed ID: 4542649
    [No Abstract] [Full Text] [Related]

  • 10. Hereditary optic atrophies in childhood.
    Jaeger W.
    J Genet Hum; 1966 Dec; 15(3):312-21. PubMed ID: 5299590
    [No Abstract] [Full Text] [Related]

  • 11. [Dominant transmitted optic atrophy combined with red-green-blindness in the sense of an acquired deutero disorder].
    Früh D, Lauer HJ.
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1972 Dec; 71():517-22. PubMed ID: 4542560
    [No Abstract] [Full Text] [Related]

  • 12. Further studies supporting the identity of congenital tritanopia and hereditary dominant optic atrophy.
    Krill AE, Smith VC, Pokorny J.
    Invest Ophthalmol; 1971 Jun; 10(6):457-65. PubMed ID: 5314165
    [No Abstract] [Full Text] [Related]

  • 13. The genetics of Leber's optic atrophy and its neurological sequelae.
    Went LN, Bruyn GW.
    J Genet Hum; 1966 Dec; 15(3):332-7. PubMed ID: 5987544
    [No Abstract] [Full Text] [Related]

  • 14. [Hereditary optic atrophy of the Kjer's type].
    Szałanda-Hora L.
    Neurol Neurochir Pol; 1979 Dec; 13(1):107-10. PubMed ID: 424046
    [Abstract] [Full Text] [Related]

  • 15. [Dominant juvenile optic atrophy].
    Cornez A, Putteman A, Zanen A, Van Regemorter N, Verstappen A, Verstraeten-Gobin C.
    Bull Soc Belge Ophtalmol; 1986 Dec; 219():29-38. PubMed ID: 3440186
    [No Abstract] [Full Text] [Related]

  • 16. 3-Methylglutaconic aciduria in "optic atrophy plus".
    Costeff H, Elpeleg O, Apter N, Divry P, Gadoth N.
    Ann Neurol; 1993 Jan; 33(1):103-4. PubMed ID: 8494328
    [Abstract] [Full Text] [Related]

  • 17. [Problems of Leber's disease. Discussion of observations of 2 families].
    Bronner A, Gerhard JP, Flament J, Franck H.
    Rev Otoneuroophtalmol; 1973 Jan; 45(5):411-20. PubMed ID: 4793205
    [No Abstract] [Full Text] [Related]

  • 18. Tritan pedigree without optic-nerve atrophy.
    Higgins KE, Brooks DN, Gottschalk G.
    Am J Optom Physiol Opt; 1983 Dec; 60(12):964-9. PubMed ID: 6606981
    [Abstract] [Full Text] [Related]

  • 19. Complicated optic atrophy (Bher's disease) associated with epilepsy and amino acid imbalance.
    Monaco F, Pirisi A, Sechi GP, Mutani R.
    Eur Neurol; 1979 Dec; 18(2):101-5. PubMed ID: 456388
    [Abstract] [Full Text] [Related]

  • 20. Family with optic atrophy and neurological symptoms.
    Lundberg PO, Wranne I, Brun A.
    Acta Neurol Scand; 1967 Dec; 43(1):87-105. PubMed ID: 6040327
    [No Abstract] [Full Text] [Related]

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