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 *

90 related articles for article (PubMed ID: 3281122)

  • 1. Enhanced enzyme activity after incubation with zinc can be used to distinguish heterozygotes of Pompe's disease.
    Lin CY
    Pediatr Res; 1988 Mar; 23(3):283-7. PubMed ID: 3281122
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Enzyme inhibitory assay using monoclonal antibody against acid alpha-D-glucosidase in prenatal diagnosis to identify homozygotes of Pompe's disease.
    Wei CY; Yeh GP; Chen HF; Wang LY; Lin CY
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1992; 33(2):104-11. PubMed ID: 1514400
    [TBL] [Abstract][Full Text] [Related]  

  • 3. alpha-Glucosidase in Pompe's disease.
    Broadhead DM; Butterworth J
    J Inherit Metab Dis; 1978; 1(4):153-4. PubMed ID: 41974
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Muscular form of glycogenosis type II (Pompe's disease).
    Tanaka K; Shimazu S; Oya N; Tomisawa M; Kusunoki T; Soyama K; Ono E
    Pediatrics; 1979 Jan; 63(1):124-9. PubMed ID: 375166
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Laboratory diagnosis of lysosomal storage disease (glycoproteinosis Pompe's disease and Gaucher disease)].
    Shi HP; Zhang GX; Guo YF; Fang BL; Zhang WM; Chen F; Luo HY
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1985 Dec; 7(6):475-7. PubMed ID: 2940012
    [No Abstract]   [Full Text] [Related]  

  • 6. alpha-glucosidase activity in human leucocytes: choice of lymphocytes for the diagnosis of Pompe's disease and the carrier state.
    Taniguchi N; Kato E; Yoshida H; Iwaki S; Ohki T; Koizumi S
    Clin Chim Acta; 1978 Oct; 89(2):293-9. PubMed ID: 361294
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Urinary alpha-glucosidase analysis for the detection of the adult form of Pompe's disease.
    Soyama K; Ono E; Shimada N; Tanaka K; Kusunoki T
    Clin Chim Acta; 1977 May; 77(1):61-7. PubMed ID: 17490
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The change in the pH 4 and pH 6 forms of alpha-glucosidase in cultured amniotic fluid cells and its implication in prenatal diagnosis of Pompe's disease.
    Fujimoto A; Fluharty AL
    Clin Chim Acta; 1978 Dec; 90(2):157-61. PubMed ID: 31251
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diagnosis of Pompe's disease using pyridylamino-maltooligosaccharides as substrates of alpha-1,4-glucosidase.
    Midorikawa M; Okada S; Kato T; Yutaka T; Yabuuchi H
    Clin Chim Acta; 1985 Apr; 147(2):97-102. PubMed ID: 3886206
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Zinc can activate cellular acidic alpha-D-glucosidase activity.
    Lin CY; Hwang BT
    Biochem Genet; 1988 Jun; 26(5-6):323-9. PubMed ID: 3145735
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Angiocardiographic and enzyme studies in a patient with type II glycogenosis (Pompe's disease). A case report.
    Bonnici F; Shapiro R; Joffe HS; Petersen EM
    S Afr Med J; 1980 Nov; 58(21):860-2. PubMed ID: 6777881
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diagnosis of Pompe's disease using leukocyte preparations. Kinetic and immunological studies of 1,4-alpha-glucosidase in human fetal and adult tissues and cultured cells.
    Shin YS; Endres W; Unterreithmeier J; Rieth M; Schaub J
    Clin Chim Acta; 1985 May; 148(1):9-19. PubMed ID: 3891151
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The first trimester prenatal diagnosis of Pompe's disease at risk.
    Ezaki M; Sugiyama K; Wada Y; Suzumori K
    Jinrui Idengaku Zasshi; 1987 Sep; 32(3):267-9. PubMed ID: 3329254
    [No Abstract]   [Full Text] [Related]  

  • 14. Late-onset Pompe's disease.
    Teener JW
    Semin Neurol; 2012 Nov; 32(5):506-11. PubMed ID: 23677658
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A sensitive semi-automated kinetic assay of alpha-D-glucosidase for the prenatal diagnosis of type 2 glycogenosis (Pompe's disease).
    Blau K
    J Inherit Metab Dis; 1978; 1(3):85-8. PubMed ID: 116083
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Pompe's disease in Chinese and prenatal diagnosis by determination of alpha-glucosidase activity.
    Lin CY; Hwang B; Hsiao KJ; Jin YR
    J Inherit Metab Dis; 1987; 10(1):11-7. PubMed ID: 3106710
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Heterozygote detection in a family of Lapland dogs with a recessively inherited metabolic disease: canine glycogen storage disease type II.
    Walvoort HC; Koster JF; Reuser AJ
    Res Vet Sci; 1985 Mar; 38(2):174-8. PubMed ID: 3923581
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Identification of heterozygotes for glycogenosis 2 (acid maltase deficiency).
    Loonen MC; Schram AW; Koster JF; Niermeijer MF; Busch HF; Martin JJ; Brouwer-Kelder B; Mekes W; Slee RG; Tager JM
    Clin Genet; 1981 Jan; 19(1):55-63. PubMed ID: 7006871
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Pompe's disease: diagnosis in kidney and leucocytes using 4-methylumbelliferyl-alpha-D-glucopyranoside.
    Broadhead DM; Butterworth J
    Clin Genet; 1978 Jun; 13(6):504-10. PubMed ID: 352582
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Gaucher disease: accurate identification of asymptomatic French-Canadian carrier using nonlabeled authentic sphingolipid substrate N-palmitoyl dihydroglucocerebroside.
    Choy FY; Bouillon L; Laurin CA
    Am J Med Genet; 1987 Aug; 27(4):895-905. PubMed ID: 3425599
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.