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Journal Abstract Search

150 related items for PubMed ID: 8962852

  • 1. [Maculopathy in hereditary metabolic diseases].
    Stănescu-Segall B.
    Oftalmologia; 1996; 40(3):261-3. PubMed ID: 8962852
    [Abstract] [Full Text] [Related]

  • 2. Ophthalmologic findings in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency caused by the G1528C mutation: a new type of hereditary metabolic chorioretinopathy.
    Tyni T, Kivelä T, Lappi M, Summanen P, Nikoskelainen E, Pihko H.
    Ophthalmology; 1998 May; 105(5):810-24. PubMed ID: 9593380
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  • 4. [Normal fundus and abnormal electroretinogram: differential diagnosis].
    Niemeyer G, Schaefer A.
    Klin Monbl Augenheilkd; 2002 Apr; 219(4):259-63. PubMed ID: 12022013
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  • 6. [Optic disc pits and maculopathy (electroretinography study)].
    Svĕrák J, Rencová E, Kvasnicka J, Peregrin J.
    Cesk Slov Oftalmol; 2002 Sep; 58(5):287-91. PubMed ID: 12428404
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  • 7. Bull's-eye maculopathy in an infant with Leigh disease.
    Laird PW, Mohney BG, Renaud DL.
    Am J Ophthalmol; 2006 Jul; 142(1):186-7. PubMed ID: 16815282
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  • 8. [Electroretinographic problems in the diagnosis of diseases of the cones and macula].
    Hache JC, Defoort S, Puech B, Bale F, Mancel E.
    Ophtalmologie; 1989 Jul; 3(4):279-82. PubMed ID: 2641135
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  • 9. 'Cherry red spot' in a patient with Tay-Sachs disease: case report.
    Aragão RE, Ramos RM, Pereira FB, Bezerra AF, Fernandes DN.
    Arq Bras Oftalmol; 2009 Jul; 72(4):537-9. PubMed ID: 19820796
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  • 10. Full-field ERG in patients with Batten/Spielmeyer-Vogt disease caused by mutations in the CLN3 gene.
    Eksandh LB, Ponjavic VB, Munroe PB, Eiberg HE, Uvebrant PE, Ehinger BE, Mole SE, Andréasson S.
    Ophthalmic Genet; 2000 Jun; 21(2):69-77. PubMed ID: 10916181
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  • 11. [Prenatal diagnosis of hereditary lysosomal diseases].
    Mirenburg TV, Aronovich EL, Lebedeva TV, Akhunov VS, Krasnopol'skaia KD.
    Vopr Med Khim; 1988 Jun; 34(4):41-6. PubMed ID: 3143186
    [Abstract] [Full Text] [Related]

  • 12. Electroretinographic and clinicopathologic correlations of retinal dysfunction in infantile neuronal ceroid lipofuscinosis (infantile Batten disease).
    Weleber RG, Gupta N, Trzupek KM, Wepner MS, Kurz DE, Milam AH.
    Mol Genet Metab; 2004 Jun; 83(1-2):128-37. PubMed ID: 15464427
    [Abstract] [Full Text] [Related]

  • 13. Retinal dysfunction in combined methylmalonic aciduria and homocystinuria (Cblc) disease: a spectrum of disorders.
    Gaillard MC, Matthieu JM, Borruat FX.
    Klin Monbl Augenheilkd; 2008 May; 225(5):491-4. PubMed ID: 18454408
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  • 14. Occult maculopathy and the focal ERG.
    Slavin ML.
    J Neuroophthalmol; 1998 Mar; 18(1):15-6. PubMed ID: 9532532
    [No Abstract] [Full Text] [Related]

  • 15. [Changes in the macula lutea of myopic children invisible with usual ophthalmoscopy].
    Averbukh SL, Blagodatnaia GA, Sasova LA, Strogal AS.
    Oftalmol Zh; 1975 Mar; 30(4):295-9. PubMed ID: 1143750
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  • 16. Juvenile neuronal ceroid lipofuscinosis (Batten disease) CLN3 mutation (Chrom 16p11.2) with different phenotypes in a sibling pair and low intensity in vivo autofluorescence.
    Mantel I, Brantley MA, Bellmann C, Robson AG, Holder GE, Taylor A, Anderson G, Moore AT.
    Klin Monbl Augenheilkd; 2004 May; 221(5):427-30. PubMed ID: 15162299
    [Abstract] [Full Text] [Related]

  • 17. Maculopathy in an elderly sub-human primate.
    Stafford TJ.
    Mod Probl Ophthalmol; 1974 May; 12(0):214-9. PubMed ID: 4421892
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