These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

97 related items for PubMed ID: 3833432

  • 1. [Benign autosomal dominant hereditary optic atrophy].
    Verin P, Comte P.
    Bull Soc Ophtalmol Fr; 1985; 85(6-7):825-7. PubMed ID: 3833432
    [No Abstract] [Full Text] [Related]

  • 2. [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]

  • 3. 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]

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

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. [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]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. [Differential diagnosis of hereditary optic atrophy (author's transl)].
    Kunz E, Oppong MC, Kern R.
    Klin Monbl Augenheilkd; 1980 Nov; 177(5):572-6. PubMed ID: 7253509
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Autosomal dominant optic atrophy with unilateral facial palsy: a new hereditary condition?
    Thomson AP, Neugebauer M, Fryer A.
    J Med Genet; 1999 Mar; 36(3):251-2. PubMed ID: 10204856
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Types of acquired colour deficiencies caused by autosomal-dominant infantile optic atrophy.
    Jaeger W, Früh D, Lauer HJ.
    Mod Probl Ophthalmol; 1972 Mar; 11():145-7. PubMed ID: 4544952
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.