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Journal Abstract Search

170 related items for PubMed ID: 4121459

  • 1. Infantile type of so-called neuronal ceroid-lipofuscinosis. 2. Morphological and biochemical studies.
    Haltia M, Rapola J, Santavuori P, Keränen A.
    J Neurol Sci; 1973 Mar; 18(3):269-85. PubMed ID: 4121459
    [No Abstract] [Full Text] [Related]

  • 2. Canine ceroid-lipofuscinosis-a model for human neuronal ceroid-lipofuscinosis and aging.
    Koppang N.
    Mech Ageing Dev; 1973 Mar; 2(6):421-45. PubMed ID: 4134804
    [No Abstract] [Full Text] [Related]

  • 3. Abnormal accumulation of sialoglycoproteins in a case of late infantile amaurotic idiocy.
    Adelman LS, Young E, Bass NH.
    Neurology; 1974 Nov; 24(11):1045-50. PubMed ID: 4371546
    [No Abstract] [Full Text] [Related]

  • 4. Tay-sachs disease. Demonstration of the stored ganglioside in cultured cells from brain biopsy.
    Batzdorf U, Sarlieve LL, Gold VA, Menkes JH.
    Arch Neurol; 1969 Jun; 20(6):650-2. PubMed ID: 4890200
    [No Abstract] [Full Text] [Related]

  • 5. [Ceroid lipofuscinosis. Review of amaurotic idiocy without metabolic gnaglioside disorders].
    Rosich Pla A.
    Rev Clin Esp; 1978 Feb 28; 148(4):331-4. PubMed ID: 653053
    [No Abstract] [Full Text] [Related]

  • 6. Neuronal ceroid-lipofuscinosis (Batten's disease): relationship to amaurotic family idiocy?
    Zeman W, Dyken P.
    Pediatrics; 1969 Oct 28; 44(4):570-83. PubMed ID: 5346636
    [No Abstract] [Full Text] [Related]

  • 7. Large alterations in ganglioside and neutral glycosphingolipid patterns in brains from cases with infantile neuronal ceroid lipofuscinosis/polyunsaturated fatty acid lipidosis.
    Svennerholm L, Fredman P, Jungbjer B, Månsson JE, Rynmark BM, Boström K, Hagberg B, Norén L, Santavuori P.
    J Neurochem; 1987 Dec 28; 49(6):1772-83. PubMed ID: 3681296
    [Abstract] [Full Text] [Related]

  • 8. Infantile GM1 gangliosidosis. Histochemical, ultrastructural and biochemical studies.
    Severi F, Magrini U, Tettamanti G, Bianchi E, Lanzi G.
    Helv Paediatr Acta; 1971 Jun 28; 26(2):192-209. PubMed ID: 4257921
    [No Abstract] [Full Text] [Related]

  • 9. Is neuronal ceroid lipofuscinosis a single disease entity?
    Pampiglione G, Harden A.
    Trans Am Neurol Assoc; 1975 Jun 28; 100():227-9. PubMed ID: 1226622
    [No Abstract] [Full Text] [Related]

  • 10. Biochemical studies on two cases of neuronal lipid storage disease.
    Landolt R.
    Pathol Eur; 1968 Jun 28; 3(2):440-9. PubMed ID: 5688475
    [No Abstract] [Full Text] [Related]

  • 11. Morphological, histochemical and biochemical studies on a case of systemic late infantile lipidosis (generalized gangliosidosis).
    Suzuki K, Chen GC.
    J Neuropathol Exp Neurol; 1968 Jan 28; 27(1):15-38. PubMed ID: 5656575
    [No Abstract] [Full Text] [Related]

  • 12. Late infantile systemic lipidosis. Major monosialogangliosidosis. Delineation of two types.
    Derry DM, Fawcett JS, Andermann F, Wolfe LS.
    Neurology; 1968 Apr 28; 18(4):340-8. PubMed ID: 4173446
    [No Abstract] [Full Text] [Related]

  • 13. Atypical neuronal ceroid-lipofuscinosis.
    Greenwood RS, Nelson JS.
    Neurology; 1978 Jul 28; 28(7):710-7. PubMed ID: 566870
    [Abstract] [Full Text] [Related]

  • 14. Electron histochemical demonstration of gangliosides in normal and Tay-Sachs brain tissue.
    Halaris A, Jatzkewitz H.
    Acta Neuropathol; 1969 Jul 28; 13(2):157-68. PubMed ID: 4185163
    [No Abstract] [Full Text] [Related]

  • 15. Gm1-gangliosidosis and juvenile cerebral lipidosis. Clinical, histochemical, and chemical study.
    Patton VM, Dekaban AS.
    Arch Neurol; 1971 Jun 28; 24(6):529-37. PubMed ID: 5089899
    [No Abstract] [Full Text] [Related]

  • 16. Infantile type of so-called neuronal ceroid-lipofuscinosis. 1. A clinical study of 15 patients.
    Santavuori P, Haltia M, Rapola J, Raitta C.
    J Neurol Sci; 1973 Mar 28; 18(3):257-67. PubMed ID: 4698309
    [No Abstract] [Full Text] [Related]

  • 17. Morphological and chemical studies on a form of late infantile amaurotic idiocy in two siblings.
    Lenn NJ, Dawson G, Schulman S.
    Neurology; 1970 Apr 28; 20(4):410. PubMed ID: 4104907
    [No Abstract] [Full Text] [Related]

  • 18. Feline GM 1 gangliosidosis: biochemical and ultrastructural comparisons with the disease in man.
    Farrell DF, Baker HJ, Herndon RM, Lindsey JR, McKhann GM.
    J Neuropathol Exp Neurol; 1973 Jan 28; 32(1):1-18. PubMed ID: 4119597
    [No Abstract] [Full Text] [Related]

  • 19. GM1-gangliosidosis (gneralized gangliosidosis). Morphology and chemical pathology.
    Suzuki K, Chen GC.
    Pathol Eur; 1968 Jan 28; 3(2):389-408. PubMed ID: 5688472
    [No Abstract] [Full Text] [Related]

  • 20. A type of juvenile cerebromacular degeneration characterized by granular osmiophilic deposits.
    Carpenter S, Karpati G, Wolfe LS, Andermann F.
    J Neurol Sci; 1973 Jan 28; 18(1):67-87. PubMed ID: 4120484
    [No Abstract] [Full Text] [Related]

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