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 *

120 related articles for article (PubMed ID: 4835758)

  • 1. Cardiac involvement in Sandhoff's disease. Inborn error of glycosphingolipid metabolism.
    Blieden LC; Desnick RJ; Carter JB; Krivit W; Moller JH; Sharp HL
    Am J Cardiol; 1974 Jul; 34(1):83-8. PubMed ID: 4835758
    [No Abstract]   [Full Text] [Related]  

  • 2. Studies in Tay-Sachs and Sandhoff's diseases. Immunologic and structural properties of hexosaminidase A and hexosaminidase B.
    Beutler E; Srivastava SK
    Isr J Med Sci; 1973; 9(9):1335-7. PubMed ID: 4798071
    [No Abstract]   [Full Text] [Related]  

  • 3. [GM2 gangliosidosis with total beta-N-acetyl-hexosaminidase deficit or Sandhoff's disease].
    Juif JG; Luckel JC; Nussbaum JL; Stoebner R; Kapps R
    Arch Fr Pediatr; 1973 Jan; 30(1):29-43. PubMed ID: 4721586
    [No Abstract]   [Full Text] [Related]  

  • 4. Ganglioside catabolism in hexosaminidase A-deficient adults.
    Tallman JF; Brady RO; Navon R; Padeh B
    Nature; 1974 Nov; 252(5480):254-5. PubMed ID: 4421837
    [No Abstract]   [Full Text] [Related]  

  • 5. [Amaurotic familial idiocy within the scope of GM2-gangliosidosis. Apropos of a case of Sandhoff's disease studied on the clinical, neuropathological, enzymatic, and genetic levels].
    Mounoud RL
    J Genet Hum; 1974 Jun; 22(2):139-83. PubMed ID: 4609324
    [No Abstract]   [Full Text] [Related]  

  • 6. Gm2-gangliosidosis: studies in cultured fibroblasts.
    Kolodny EH; Milunsky A; Sheng GS
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):130-5. PubMed ID: 4611525
    [No Abstract]   [Full Text] [Related]  

  • 7. [Sandhoff's disease (GM2 gangliosidosis, type 2). Clinical, biochemical and anatomo-clinical study].
    Vidailhet M; Neimann N; Grignon G; Hartemann P; Philippart M; Paysant P; Nabet P; Floquet J
    Arch Fr Pediatr; 1973 Jan; 30(1):45-60. PubMed ID: 4721587
    [No Abstract]   [Full Text] [Related]  

  • 8. Sandhoff's disease (GM 2 gangliosidosis type 2): clinical, chemical, and enzyme studies in five patients.
    Okada S; McCrea M; O'Brien JS
    Pediatr Res; 1972 Jul; 6(7):606-15. PubMed ID: 5057290
    [No Abstract]   [Full Text] [Related]  

  • 9. On the molecular basis of Sandhoff's disease.
    Ropers HH; Schwantes U
    Humangenetik; 1973; 20(2):167-70. PubMed ID: 4785164
    [No Abstract]   [Full Text] [Related]  

  • 10. Inheritance of the enzyme deficiency in three neurolipidoses: variant 0 of Tay-Sachs disease (Sandhoff's disease), classic Tay-Sachs disease, and metachromatic leukodystrophy. Identification of the heterozygous carriers.
    Harzer K
    Humangenetik; 1973; 20(1):9-24. PubMed ID: 4776531
    [No Abstract]   [Full Text] [Related]  

  • 11. NN'-diacetylchitobiase activity in Tay-Sachs disease and Sandhoff's disease.
    Stirling JL
    Biochem J; 1974 Aug; 141(2):597-9. PubMed ID: 4455225
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diagnosis of homozygotes and heterozygotes of GM2 gangliosidosis by hexoaminidases assay.
    Harteman P; Paternotte P; Vagner F; Nabet P; Paysant P
    Biomedicine; 1974 May; 20(3):242-8. PubMed ID: 4433658
    [No Abstract]   [Full Text] [Related]  

  • 13. [Sandhoff's disease: clinical and genetic study of a French-Canadian child].
    Melançon SB; Potier M; Geoffroy G; Dallaire L
    Union Med Can; 1974 Jul; 103(7):1218-22. PubMed ID: 4210450
    [No Abstract]   [Full Text] [Related]  

  • 14. GM2 Type 2--gangliosidosis (Sandhoff's disease)--ocular and pathological manifestations.
    Tremblay M; Szots F
    Can J Ophthalmol; 1974 Jul; 9(3):338-46. PubMed ID: 4276769
    [No Abstract]   [Full Text] [Related]  

  • 15. Hexosaminidase-A and hexosaminidase-B: studies in Tay-Sachs' and Sandhoff's disease.
    Srivastava SK; Beutler E
    Nature; 1973 Feb; 241(5390):463. PubMed ID: 4122341
    [No Abstract]   [Full Text] [Related]  

  • 16. Myocardial sarcoidosis presenting as acute mitral insufficiency.
    Zoneraich S; Gupta MP; Mehta J; Zoneraich O; Wessely Z
    Chest; 1974 Oct; 66(4):452-4. PubMed ID: 4137859
    [No Abstract]   [Full Text] [Related]  

  • 17. Sandhoff's disease (GM2gangliosidosis, type 2) in a Scottish family.
    Bain AD; Tateson R; Anderson JM; Cumings JN
    J Ment Defic Res; 1972 Jun; 16(2):119-27. PubMed ID: 4671982
    [No Abstract]   [Full Text] [Related]  

  • 18. A review of cardiac amyloidosis. Report of a case presenting as constrictive pericarditis.
    Crockett LK; Thompson M; Dekker A
    Am J Med Sci; 1972 Aug; 264(2):149-56. PubMed ID: 4653119
    [No Abstract]   [Full Text] [Related]  

  • 19. Absence of -N-acetyl-D-hexosaminidase A activity in a healthy woman.
    Vidgoff J; Buist NR; O'Brien JS
    Am J Hum Genet; 1973 Jul; 25(4):372-81. PubMed ID: 4716656
    [No Abstract]   [Full Text] [Related]  

  • 20. An autopsy case of Sandhoff's disease.
    Takahashi A; Saito K; Koizumi Y
    Beitr Pathol; 1974 Sep; 152(4):418-28. PubMed ID: 4138910
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.