BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 3329254)

  • 1. 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]  

  • 2. Prenatal diagnosis of glycogenosis type II (Pompe's disease) using chorionic villi biopsy.
    Besançon AM; Castelnau L; Nicolesco H; Dumez Y; Poenaru L
    Clin Genet; 1985 May; 27(5):479-82. PubMed ID: 3891160
    [TBL] [Abstract][Full Text] [Related]  

  • 3. First trimester diagnosis of Pompe's disease (glycogenosis type II) with normal outcome: assay of acid alpha-glucosidase in chorionic villous biopsy using antibodies.
    Grubisic A; Shin YS; Meyer W; Endres W; Becker U; Wischerath H
    Clin Genet; 1986 Oct; 30(4):298-301. PubMed ID: 3098466
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Prenatal diagnosis of glycogenosis II.--Pompe's disease].
    Macek M; Tomásová H; Hug G; Reinsteinová H; Seemanová E; Salichová J
    Cesk Pediatr; 1977 Jul; 32(7):427-30. PubMed ID: 270392
    [No Abstract]   [Full Text] [Related]  

  • 5. 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]  

  • 6. [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]  

  • 7. Prenatal detection of Pompe's disease by induction of alkaline phosphatase in cultured amniotic fluid cells.
    Hähnel R; Stratton CJ; Wysocki SJ; Hockey A
    Aust N Z J Obstet Gynaecol; 1981 Feb; 21(1):43-6. PubMed ID: 7020685
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 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. 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]  

  • 11. Glycogen storage disease type II (Pompe's disease): the first biochemical evidence in Thailand.
    Rangdaeng S; Scollard DM; Srichairatanakol S; Sutthachit M; Phornphutkul C
    J Med Assoc Thai; 1987 Sep; 70(9):536-42. PubMed ID: 2960768
    [No Abstract]   [Full Text] [Related]  

  • 12. [Biochemical diagnosis of glycogenosis type II (acid maltase deficiency) (author's transl)].
    Pilz H; Goebel HH; Stefan H; Seidel D; Kohlschütter A
    J Clin Chem Clin Biochem; 1977 Dec; 15(12):705-8. PubMed ID: 342670
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 14. Ultrastructure of the eye in fetal type II glycogenosis (Pompe's disease).
    Pokorny KS; Ritch R; Friedman AH; Desnick RJ
    Invest Ophthalmol Vis Sci; 1982 Jan; 22(1):25-31. PubMed ID: 6948796
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Laboratory diagnosis of the neuromuscular glycogen storage diseases.
    Farmer PM
    Ann Clin Lab Sci; 1982; 12(6):431-8. PubMed ID: 6817693
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chorionic villus ultrastructure in type II glycogen storage disease (Pompe's disease).
    Hug G; Chuck G; Chen YT; Kay HH; Bossen EH
    N Engl J Med; 1991 Jan; 324(5):342-3. PubMed ID: 1986298
    [No Abstract]   [Full Text] [Related]  

  • 17. [Tests for the detection of inborn errors of metabolism--urinary alpha-glucosidase analysis for the detection of glycogen storage disease type II (author's transl)].
    Soyama K; Ono E
    Rinsho Byori; 1978 Dec; 26(12):1022-6. PubMed ID: 370427
    [No Abstract]   [Full Text] [Related]  

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

  • 19. Amniotic cell 4-methylumbelliferyl-alpha-glucosidase activity for prenatal diagnosis of Pompe's disease.
    Fensom AH; Benson PF; Blunt S; Brown SP; Coltart TM
    J Med Genet; 1976 Apr; 13(2):148-9. PubMed ID: 1064728
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prenatal diagnosis of Pompe's disease (type II glycogenosis) in chorionic villus biopsy using maltose as a substrate.
    Park HK; Kay HH; McConkie-Rosell A; Lanman J; Chen YT
    Prenat Diagn; 1992 Mar; 12(3):169-73. PubMed ID: 1589418
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.