These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

88 related articles for article (PubMed ID: 105384)

  • 1. Biochemical expression of degenerative disorders associated with cognitive dysfunction.
    Wolfe LS
    Res Publ Assoc Res Nerv Ment Dis; 1979; 57():125-43. PubMed ID: 105384
    [No Abstract]   [Full Text] [Related]  

  • 2. [The activity of various lysosomal acid hydrolases in the normal child. Premise to the biochemical study of cerebral lipidosis].
    Giovannini M; Perego O; Crollari P; Sacchi G; Riva E
    Minerva Pediatr; 1978 Feb; 30(4):339-48. PubMed ID: 25375
    [No Abstract]   [Full Text] [Related]  

  • 3. Cerebromacular degeneration: progress and prospects in the search for the elusive biochemical defect.
    Wolfe LS; Kin NY; Andermann F
    Brain Dev; 1979; 1(3):147-51. PubMed ID: 551741
    [No Abstract]   [Full Text] [Related]  

  • 4. Age-dependent variations of the human N-acetyl- -D-hexosaminidases.
    Harzer K; Sandhoff K
    J Neurochem; 1971 Nov; 18(11):2041-50. PubMed ID: 4256910
    [No Abstract]   [Full Text] [Related]  

  • 5. Hexosaminidase activities in a case of systemic GM2 gangliosidosis of late infantile type.
    Schneck L; Friedland J; Pourfar M; Saifer A; Volk BW
    Proc Soc Exp Biol Med; 1970 Mar; 133(3):997-8. PubMed ID: 5435594
    [No Abstract]   [Full Text] [Related]  

  • 6. Some aspects of the cellular biochemistry of lysosomal and related glycosidases.
    Touster O
    Mol Cell Biochem; 1973 Dec; 2(2):169-77. PubMed ID: 4594433
    [No Abstract]   [Full Text] [Related]  

  • 7. The adnormal biochemistry of inherited disorders of lipid metabolism.
    Brady RO
    Fed Proc; 1973 Jun; 32(6):1660-7. PubMed ID: 4351098
    [No Abstract]   [Full Text] [Related]  

  • 8. Disorders of ganglioside metabolism.
    Brady RO; Kolodny EH
    Prog Med Genet; 1972; 8():225-41. PubMed ID: 4336471
    [No Abstract]   [Full Text] [Related]  

  • 9. Requirement of an activator for the hydrolysis of sphingoglycolipids by glycosidases of human liver.
    Li SC; Wan CC; Mazzotta MY; Li YT
    Carbohydr Res; 1974 May; 34(1):189-93. PubMed ID: 4835697
    [No Abstract]   [Full Text] [Related]  

  • 10. Multiple forms of glycosidases in the normal and pathological states.
    Robinson D
    Enzyme; 1974; 18(1):114-35. PubMed ID: 4277585
    [No Abstract]   [Full Text] [Related]  

  • 11. [Gangliosidoses: primary disorders of ganglioside metabolism].
    Klibansky C
    Harefuah; 1971 Sep; 81(6):289-93. PubMed ID: 4946742
    [No Abstract]   [Full Text] [Related]  

  • 12. Enzymic differentiation between different types of Tay-Sachs disease of similar clinical appearance.
    Clausen J; Melchior JC; Paerregaard P
    Eur Neurol; 1972; 7(1):56-64. PubMed ID: 4336274
    [No Abstract]   [Full Text] [Related]  

  • 13. Ganglioside storage diseases.
    O'Brien JS; Okada S; Ho MW; Fillerup DL; Veath ML; Adams K
    Fed Proc; 1971; 30(3):956-69. PubMed ID: 4252532
    [No Abstract]   [Full Text] [Related]  

  • 14. Brain hexosaminidase and arylsulfatase isoenzymes in normal and vitamin E-deficient rats: an hypothesis for isoenzyme patterns in GM2 gangliosidoses and MLD.
    Koenig H; Patel A
    Trans Am Neurol Assoc; 1974; 99():140-3. PubMed ID: 4463525
    [No Abstract]   [Full Text] [Related]  

  • 15. Brain beta-galactosidase and gm1 gangliosidosis.
    Chou L; Kaye CI; Nadler HL
    Pediatr Res; 1974 Feb; 8(2):120-5. PubMed ID: 4810509
    [No Abstract]   [Full Text] [Related]  

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

  • 17. Tay-sachs disease.
    Brady RO
    N Engl J Med; 1969 Nov; 281(22):1243-4. PubMed ID: 5347842
    [No Abstract]   [Full Text] [Related]  

  • 18. Multiple human hexosaminidases.
    Sandhoff K
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):214-22. PubMed ID: 4611533
    [No Abstract]   [Full Text] [Related]  

  • 19. The N-acetyl- -D-hexosaminidases of calf and human brain.
    Robinson D; Jordan TW; Horsburgh T
    J Neurochem; 1972 Aug; 19(8):1975-85. PubMed ID: 5047858
    [No Abstract]   [Full Text] [Related]  

  • 20. The enzymology of Tay-Sachs disease and its variant forms.
    Tallman JF
    UCLA Forum Med Sci; 1975; (18):479-99. PubMed ID: 812231
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.