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PUBMED FOR HANDHELDS

Journal Abstract Search


182 related items for PubMed ID: 5473464

  • 1. Spongy glio-neuronal dystrophy in infancy and childhood.
    Jellinger K, Seitelberger F.
    Acta Neuropathol; 1970; 16(2):125-40. PubMed ID: 5473464
    [No Abstract] [Full Text] [Related]

  • 2. Hereditary hyperammonaemia.
    Bruton CJ, Corsellis JA, Russell A.
    Brain; 1970; 93(2):423-34. PubMed ID: 5310321
    [No Abstract] [Full Text] [Related]

  • 3. Spongy degeneration of the central nervous system in infancy.
    Jellinger K, Seitelberger F.
    Curr Top Pathol; 1970; 53():90-160. PubMed ID: 4925656
    [No Abstract] [Full Text] [Related]

  • 4. Axonal dystrophy in a case of Canavan's spongy degeneration.
    Kamoshita S, Reed GB, Aguilar MJ.
    Neurology; 1967 Sep; 17(9):895-8. PubMed ID: 6069089
    [No Abstract] [Full Text] [Related]

  • 5. Neuropathologic changes in a case of sulfite oxidase deficiency.
    Rosenblum WI.
    Neurology; 1968 Dec; 18(12):1187-96. PubMed ID: 4178656
    [No Abstract] [Full Text] [Related]

  • 6. Histopathology of the nervous system in carnosinase enzyme deficiency with mental retardation.
    Terplan KL, Cares HL.
    Neurology; 1972 Jun; 22(6):644-55. PubMed ID: 4673339
    [No Abstract] [Full Text] [Related]

  • 7. Spongy glio-neuronal dystrophy: a degenerative disease of the nervous system.
    Hopkins IJ, Turner B.
    J Neurol Neurosurg Psychiatry; 1973 Feb; 36(1):50-6. PubMed ID: 4691690
    [Abstract] [Full Text] [Related]

  • 8. [MRI as an aid for diagnosis of infantile neuroaxonal dystrophy].
    Ishii M, Tanabe Y, Goto M, Sugita K.
    No To Hattatsu; 1992 Sep; 24(5):491-3. PubMed ID: 1389334
    [Abstract] [Full Text] [Related]

  • 9. Spongy degeneration of grey matter in 3 children. Neuropathological report.
    Janota I.
    Arch Dis Child; 1974 Jul; 49(7):571-5. PubMed ID: 4854373
    [Abstract] [Full Text] [Related]

  • 10. Cerebral spongy degeneration of infancy. A biochemical and ultrastructural study of affected twins.
    Adornato BT, O'Brien JS, Lampert PW, Roe TF, Neustein HB.
    Neurology; 1972 Feb; 22(2):202-10. PubMed ID: 4333033
    [No Abstract] [Full Text] [Related]

  • 11. Progressive degeneration of the cerebral cortex in infancy.
    Laurence KM, Cavanagh JB.
    Brain; 1968 Jun; 91(2):261-80. PubMed ID: 5721929
    [No Abstract] [Full Text] [Related]

  • 12. Neuropathology.
    Kaufman MA, Roizin L, Gold G.
    Prog Neurol Psychiatry; 1971 Jun; 26():97-121. PubMed ID: 4363629
    [No Abstract] [Full Text] [Related]

  • 13. [Brain damage in infants--brain lesions in several cases of inborn errors of metabolism].
    Kamoshita S.
    Shinkei Kenkyu No Shimpo; 1972 Jun; 16(3):438-46. PubMed ID: 5066186
    [No Abstract] [Full Text] [Related]

  • 14. Neonatal encephalopathy with neuronal vacuolar degeneration.
    Twiss JL, Baisch M, Horoupian DS.
    Acta Neuropathol; 1993 Jun; 86(5):536-41. PubMed ID: 8310807
    [Abstract] [Full Text] [Related]

  • 15. Infantile neuroaxonal dystrophy.
    Crome L, Weller SD.
    Arch Dis Child; 1965 Oct; 40(213):502-7. PubMed ID: 5829994
    [No Abstract] [Full Text] [Related]

  • 16. Peroxisomal abnormalities in metabolic diseases.
    Goldfischer S, Johnson AB, Essner E, Moore C, Ritch RH.
    J Histochem Cytochem; 1973 Nov; 21(11):972-7. PubMed ID: 4587530
    [No Abstract] [Full Text] [Related]

  • 17. The proteins of human myelin in inborn errors of metabolism and in chromosomal anomalies.
    Palo J, Savolainen H.
    Acta Neuropathol; 1973 Mar 30; 24(1):56-61. PubMed ID: 4267002
    [No Abstract] [Full Text] [Related]

  • 18. Electron microscopical study of neuroaxonal dystrophy. Case report.
    De Coster W, Roels H, Vander Eecken H.
    Eur Neurol; 1971 Mar 30; 5(2):65-83. PubMed ID: 4330096
    [No Abstract] [Full Text] [Related]

  • 19. [Spongious glioneuronal dystrophy with diffuse fatty degeneration of the liver].
    Werner M, Künnert B, Lehmann J.
    Zentralbl Pathol; 1991 Mar 30; 137(4):380-4. PubMed ID: 1768691
    [Abstract] [Full Text] [Related]

  • 20. Neuropathology of subacute myelo-optico-neuropathy, "SMON".
    Shiraki H.
    Jpn J Med Sci Biol; 1971 Aug 30; 24(4):217-43. PubMed ID: 5316312
    [No Abstract] [Full Text] [Related]


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