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PUBMED FOR HANDHELDS

Journal Abstract Search


112 related items for PubMed ID: 476845

  • 41.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 42.
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  • 43. [Leber's disease associated with myelinated fibers].
    Czechowicz-Janicka K, Iwaszkiewicz E.
    Klin Oczna; 1974 Feb; 44(2):173-7. PubMed ID: 4453100
    [No Abstract] [Full Text] [Related]

  • 44. [Leber's disease and nervous-system-degeneration syndromes].
    Bronner A, Gerhard JP, Collard M, Malamet S.
    Rev Otoneuroophtalmol; 1979 Feb; 51(1):19-24. PubMed ID: 472584
    [No Abstract] [Full Text] [Related]

  • 45. [Hereditary optic atrophy].
    Wisnia K.
    Arch Ophtalmol Rev Gen Ophtalmol; 1974 Oct; 34(10):681-90. PubMed ID: 4282227
    [No Abstract] [Full Text] [Related]

  • 46. [2 familial cases of Leber's disease].
    Bigorgne J, Corlay, Sourdille P, Hermann P.
    Bull Soc Ophtalmol Fr; 1974 Mar; 74(3):353-7. PubMed ID: 4468130
    [No Abstract] [Full Text] [Related]

  • 47.
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  • 48. [Familial form of Leber's miliary retinal angiomatosis].
    Renard G, Bernard JA, Pouliquen YM, Bons G, Dureuil J, Lebuisson DA.
    Bull Soc Ophtalmol Fr; 1974 Dec; 74(12):1163-7. PubMed ID: 4468833
    [No Abstract] [Full Text] [Related]

  • 49. 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]

  • 50. [Leber's retinal disease].
    Bijedić M.
    Med Arh; 1963 Dec; 17(2):55-8. PubMed ID: 5196677
    [No Abstract] [Full Text] [Related]

  • 51.
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  • 52. [Problems of Leber's disease].
    Kurozumi I.
    Ganka; 1970 Nov; 12(11):930-3. PubMed ID: 5530890
    [No Abstract] [Full Text] [Related]

  • 53. Fundus findings in Leber's hereditary optic neuroretinopathy.
    Nikoskelainen E, Hoyt WF, Nummelin K.
    Ophthalmic Paediatr Genet; 1985 Feb; 5(1-2):125-30. PubMed ID: 4058865
    [Abstract] [Full Text] [Related]

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

  • 55. [Leber's disease. Anomalies of the cerebrospinal fluid circulation in the course of cases with late manifestations].
    Truelle JL, Bigorgne J, Pouplard F, Berthelot J, Larget-Piet L, Emile J.
    Rev Otoneuroophtalmol; 1975 Feb; 47(4):275-83. PubMed ID: 1215731
    [No Abstract] [Full Text] [Related]

  • 56. White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation.
    Lev D, Yanoov-Sharav M, Watemberg N, Leshinsky-Silver E, Lerman-Sagie T.
    Eur J Paediatr Neurol; 2002 Feb; 6(2):121-3. PubMed ID: 11995959
    [Abstract] [Full Text] [Related]

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

  • 58. Leber's disease.
    Rayudu GB, Pal D.
    Indian Pediatr; 1974 Apr; 11(4):327-9. PubMed ID: 4423530
    [No Abstract] [Full Text] [Related]

  • 59. Leber's disease. 3.
    Seedorff T.
    Acta Ophthalmol (Copenh); 1969 Apr; 47(1):23-9. PubMed ID: 5819833
    [No Abstract] [Full Text] [Related]

  • 60. [The importance of electroretinography in hereditary optic atrophies].
    Stanescu B, David M, Wawernia E.
    Arch Ophtalmol Rev Gen Ophtalmol; 1972 Mar; 32(3):203-8. PubMed ID: 4263262
    [No Abstract] [Full Text] [Related]


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