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

219 related items for PubMed ID: 6810572

  • 1. [Biochemical characteristics and diagnosis of lysosomal diseases related to hereditary glycosidase deficiency].
    Vidershaĭn GIa.
    Vestn Akad Med Nauk SSSR; 1982; (6):42-7. PubMed ID: 6810572
    [No Abstract] [Full Text] [Related]

  • 2. Chemical diagnosis of inborn lysosomal storage disorders involving the eye.
    Dawson G, Tsay GC.
    Birth Defects Orig Artic Ser; 1976; 12(3):1-13. PubMed ID: 821555
    [No Abstract] [Full Text] [Related]

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

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

  • 5. [Lysosomal storage diseases: possibilities of the clinical-biochemical diagnostics (author's transl)].
    Wiesmann UN, Spycher MA, Gitzelmann R.
    Verh Dtsch Ges Pathol; 1976; ():106-10. PubMed ID: 828813
    [No Abstract] [Full Text] [Related]

  • 6. [Rare inborn errors of lysosomal metabolism, implications for pediatric research (author's transl)].
    Wiesmann N, Herschkowitz N.
    Schweiz Rundsch Med Prax; 1975 Sep 02; 64(35):114-9. PubMed ID: 2909
    [No Abstract] [Full Text] [Related]

  • 7. The mucopolysaccharidoses and mucolipidoses as model systems for the investigation of genetic disorders.
    Shapiro LJ.
    Birth Defects Orig Artic Ser; 1981 Sep 02; 17(2):191-203. PubMed ID: 6461367
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 11. [Hereditary diseases related to a disorder in the breakdown of carbohydrate-containing compounds].
    Vidershaĭn GIa.
    Usp Sovrem Biol; 1974 Sep 02; 77(3):434-51. PubMed ID: 4278594
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. The mucopolysaccharidoses: inborn errors of glycosaminoglycan catabolism.
    Cantz M, Gehler J.
    Hum Genet; 1976 Jun 29; 32(3):233-55. PubMed ID: 820626
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. [Mucopolysaccharidoses--biochemical mechanisms of diseases and therapeutic possibilities].
    Kloska A, Tylki-Szymańska A, Wegrzyn G.
    Postepy Biochem; 2011 Jun 29; 57(2):133-47. PubMed ID: 21913414
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.