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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]
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]
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] Page: [Next] [New Search]