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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

88 related items for PubMed ID: 414238

  • 1. Genetic variants of hexosaminidase deficiency.
    Patrick AD.
    Prog Clin Biol Res; 1977; 18():147-59. PubMed ID: 414238
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Current concepts in genetics. Lysosomal storage diseases.
    Kolodny EH.
    N Engl J Med; 1976 May 27; 294(22):1217-20. PubMed ID: 817200
    [No Abstract] [Full Text] [Related]

  • 6. Studies on complementation of beta hexosaminidase deficiency in human GM2 gangliosidosis.
    Rattazzi MC, Brown JA, Davidson RG, Shows TB.
    Am J Hum Genet; 1976 Mar 27; 28(2):143-54. PubMed ID: 817596
    [Abstract] [Full Text] [Related]

  • 7. Editorial: The use of tears for heterozygote detection and genetic counseling.
    Goldberg MF.
    Invest Ophthalmol; 1974 Mar 27; 13(3):159-60. PubMed ID: 4205146
    [No Abstract] [Full Text] [Related]

  • 8. The lipidoses: morphologic changes in the nervous system in Gaucher's disease, GM2 gangliosidoses and Niemann-Pick disease.
    Arey JB.
    Ann Clin Lab Sci; 1975 Mar 27; 5(6):475-88. PubMed ID: 812418
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Apparent deficiency of hexosaminidase A in healthy members of a family with Tay-Sachs disease.
    Navon R, Padeh B, Adam A.
    Am J Hum Genet; 1973 May 27; 25(3):287-93. PubMed ID: 4704860
    [No Abstract] [Full Text] [Related]

  • 12. [Inborn error of glycolipid metabolism].
    Suzuki Y.
    Horumon To Rinsho; 1975 Sep 27; 23(9):885-91. PubMed ID: 166
    [No Abstract] [Full Text] [Related]

  • 13. Animal model of human disease: GM2 gangliosidosis.
    Pierce KR, Kosanke SD, Bay WW, Bridges CH.
    Am J Pathol; 1976 May 27; 83(2):419-22. PubMed ID: 817606
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. [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 27; 30(1):45-60. PubMed ID: 4721587
    [No Abstract] [Full Text] [Related]

  • 16. A study of hexosaminadases in interspecific hybrids and in GM2 gangliosidosis with a discussion on their genetic control.
    Van Cong N, Weil D, Rebourcet R, Frézal J, Richard-Mollard AM.
    Ann Hum Genet; 1975 Jul 27; 39(1):111-23. PubMed ID: 810068
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Ganglioside catabolism in hexosaminidase A-deficient adults.
    Tallman JF, Brady RO, Navon R, Padeh B.
    Nature; 1974 Nov 15; 252(5480):254-5. PubMed ID: 4421837
    [No Abstract] [Full Text] [Related]

  • 19. Carrier detection in Sandhoff disease.
    Lowden JA, Ives EJ, Keene DL, Burton AL, Skomorowski MA, Howard F.
    Am J Hum Genet; 1978 Jan 15; 30(1):38-45. PubMed ID: 414620
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.