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Journal Abstract Search

322 related items for PubMed ID: 4202279

  • 21. [Possibilities of serum heterozygote tests in genetic mucopolysaccharidoses].
    Gehler J, Cantz M, Spranger J.
    Monatsschr Kinderheilkd (1902); 1974 Jul; 122(7):578-9. PubMed ID: 4212748
    [No Abstract] [Full Text] [Related]

  • 22. Lysosomal enzyme variations in thirteen cell strains cultured from one amniotic fluid.
    Sutherland GR, Butterworth J, Broadhead DM, Bain AD.
    Clin Chim Acta; 1974 Apr; 52(2):211-7. PubMed ID: 4828230
    [No Abstract] [Full Text] [Related]

  • 23. Various sulfatase activities in leukocytes and cultured skin fibroblasts from heterozygotes for the multiple sulfatase deficiency (mukosulfatidosis).
    Eto Y, Tahara T, Tokoro T, Maekawa K.
    Pediatr Res; 1983 Feb; 17(2):97-100. PubMed ID: 6572356
    [Abstract] [Full Text] [Related]

  • 24.
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  • 25. Intrauterine diagnosis: comparative enzymology of cells cultivated from maternal skin, fetal skin, and amniotic fluid cells.
    Kaback MM, Leonard CO, Parmley TH.
    Pediatr Res; 1971 Aug; 5(8):366-71. PubMed ID: 5146085
    [No Abstract] [Full Text] [Related]

  • 26.
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  • 27. Elevated activity of lysosomal enzymes in amniotic fluid of a fetus with mucolipidosis II (I-cell disease).
    Huijing F, Warren RJ, McLeod AG.
    Clin Chim Acta; 1973 Mar 30; 44(3):453-5. PubMed ID: 4694487
    [No Abstract] [Full Text] [Related]

  • 28. Mannosidosis: detection of the disease and of heterozygotes using serum and leucocytes.
    Masson PK, Lundblad A.
    Biochem Biophys Res Commun; 1974 Jan 23; 56(2):296-303. PubMed ID: 4207355
    [No Abstract] [Full Text] [Related]

  • 29. Prenatal diagnosis of a heterozygote for mucopolysaccharidosis type VII (beta-glucuronidase deficiency).
    Poenaru L, Castelnau L, Mossman J, Boué J, Dreyfus JC.
    Prenat Diagn; 1982 Oct 23; 2(4):251-6. PubMed ID: 6818536
    [Abstract] [Full Text] [Related]

  • 30.
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  • 31. Arylsulfatase B deficiency in Maroteaux-Lamy syndrome: Cellular studies and carrier identification.
    Beratis NG, Turner BM, Weiss R, Hirschhorn K.
    Pediatr Res; 1975 May 23; 9(5):475-80. PubMed ID: 806052
    [Abstract] [Full Text] [Related]

  • 32. Enzyme patterns in tissues and body fluids in mucopolysaccharidoses.
    Ockerman PA, Hultberg B, Eriksson O.
    Clin Chim Acta; 1969 Jul 23; 25(1):97-102. PubMed ID: 4240390
    [No Abstract] [Full Text] [Related]

  • 33. Influence of age and sex on plasma acid hydrolases.
    Eriksson O, Ginsburg BE, Hultberg B, Ockerman PA.
    Clin Chim Acta; 1972 Aug 23; 40(1):181-5. PubMed ID: 5056627
    [No Abstract] [Full Text] [Related]

  • 34. Glycosidases in normal human leukocytes and abnormalities in G M1 -gangliosidosis.
    Hindman J, Cotlier E.
    Clin Chem; 1972 Sep 23; 18(9):971-5. PubMed ID: 5052099
    [No Abstract] [Full Text] [Related]

  • 35. Plasma activities of acid hydrolases after hepatic dearterialization in the pig.
    Fredlund PE, Ockerman PA, Vang JO.
    Eur Surg Res; 1972 Sep 23; 4(3):175-85. PubMed ID: 5071270
    [No Abstract] [Full Text] [Related]

  • 36. Lysosomal enzymes of amniotic fluid in relation to gestational age.
    Butterworth J, Broadhead DM, Sutherland GR, Bain AD.
    Am J Obstet Gynecol; 1974 Jul 15; 119(6):821-8. PubMed ID: 4841183
    [No Abstract] [Full Text] [Related]

  • 37. Letter: Intestinal biopsy in lysosomal storage disease.
    Den Tandt WR, Vio PM, Eggermont E.
    Lancet; 1974 Nov 09; 2(7889):1149. PubMed ID: 4139453
    [No Abstract] [Full Text] [Related]

  • 38. Ganglioside storage diseases.
    O'Brien JS, Okada S, Ho MW, Fillerup DL, Veath ML, Adams K.
    Fed Proc; 1971 Nov 09; 30(3):956-69. PubMed ID: 4252532
    [No Abstract] [Full Text] [Related]

  • 39. Enzyme defects of glycosaminoglycan degradation in the mucopolysaccharidoses.
    Benson PF.
    Dev Med Child Neurol; 1974 Aug 09; 16(4):534-9. PubMed ID: 4277471
    [No Abstract] [Full Text] [Related]

  • 40.
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