BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 4611528)

  • 1. Enzyme replacement in Pompe disease: an attempt with purified human acid alpha-glucosidase.
    de Barsy T; Jacquemin P; Van Hoof F; Hers HG
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):184-90. PubMed ID: 4611528
    [No Abstract]   [Full Text] [Related]  

  • 2. Alpha-glucosidase administration: experiences in two patients with glycogen storage disease compared with animal experiments.
    Huijing F; Waltuck BL; Whelan WJ
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):191-4. PubMed ID: 4611530
    [No Abstract]   [Full Text] [Related]  

  • 3. Enzyme replacement in Pompe disease with an alpha-glucosidase-low density lipoprotein complex.
    Williams JC; Murray AK
    Birth Defects Orig Artic Ser; 1980; 16(1):415-23. PubMed ID: 7004520
    [No Abstract]   [Full Text] [Related]  

  • 4. Electrophoretic characterization of acidic and neutral amylo 1-4-glucosidase (acid maltase) in human tissues and evidence for two electrophoretic variants in acid maltase deficiency.
    Dreyfus JC; Alexandre Y
    Biochem Biophys Res Commun; 1972 Aug; 48(4):914-20. PubMed ID: 4264156
    [No Abstract]   [Full Text] [Related]  

  • 5. Administration of a mixture of fungal glucosidases to a patient with type II glycogenosis (Pompe's disease).
    Lauer RM; Mascarinas T; Racela AS; Diehl AM; Brown BI
    Pediatrics; 1968 Oct; 42(4):672-6. PubMed ID: 5245517
    [No Abstract]   [Full Text] [Related]  

  • 6. Alpha-glucosidases (gamma-amylases) in human and animal organisms.
    Rosenfeld EL
    Pathol Biol (Paris); 1975 Jan; 23(1):71-84. PubMed ID: 1105329
    [No Abstract]   [Full Text] [Related]  

  • 7. Adult acid maltase deficiency. Abnormalities in fibroblasts cultured from patients.
    Angelini C; Engel AG; Titus JL
    N Engl J Med; 1972 Nov; 287(19):948-51. PubMed ID: 4507329
    [No Abstract]   [Full Text] [Related]  

  • 8. Treatment related observations in solid tissues, fibroblast cultured and amniotic fluid cells of type II glycogenosis, Hurler disease and metachromatic leukodystrophy.
    Hug G; Schubert WK; Soukup S
    Birth Defects Orig Artic Ser; 1973 Mar; 9(2):160-83. PubMed ID: 4215475
    [No Abstract]   [Full Text] [Related]  

  • 9. [Prenatal diagnosis of glycogenosis type II (Pompe) and subsequent therapeutic abortion (author's transl)].
    Schaub J; Osang M; von Bassewitz DB; Grote W; Terinde R; Lombeck I; Bremer HJ
    Dtsch Med Wochenschr; 1974 Nov; 99(44):2219-22, 27. PubMed ID: 4529697
    [No Abstract]   [Full Text] [Related]  

  • 10. Simultaneous absence of alpha-1,4-glucosidase and alpha-1,6-glucosidase activities (pH 4) in tissues of children with type II glycogen storage disease.
    Brown BI; Brown DH; Jeffrey PL
    Biochemistry; 1970 Mar; 9(6):1423-8. PubMed ID: 5264799
    [No Abstract]   [Full Text] [Related]  

  • 11. Incorporation of [14C]glucose into alpha-1,4 bonds of glycogen by leukocytes and fibroblasts of patients with type III glycogen storage disease.
    Gutman A; Barash V; Schramm H; Deckelbaum RJ; Granot E; Aker M; Kohn G
    Pediatr Res; 1985 Jan; 19(1):28-32. PubMed ID: 3918291
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The use of leucocytes as an aid in the diagnosis of glycogen storage disease type II (Pompe's disease).
    Koster JF; Slee RG; Hülsmann WC
    Clin Chim Acta; 1974 Mar; 51(3):319-25. PubMed ID: 4524047
    [No Abstract]   [Full Text] [Related]  

  • 13. [Enzyme study of 21 cases of glycogenosis].
    Mathieu M; Cotte J
    Rev Eur Etud Clin Biol; 1970; 15(7):800-6. PubMed ID: 4320573
    [No Abstract]   [Full Text] [Related]  

  • 14. [Characterization of alpha-glucosidase in skin fibroblasts in the diagnosis of glycogenosis type 2 (Pompe disease)].
    Braulke T; Sandig KR
    Kinderarztl Prax; 1984 Aug; 52(8):377-82. PubMed ID: 6384623
    [No Abstract]   [Full Text] [Related]  

  • 15. [Glycogenosis Type 3. Forbes' disease].
    Vuust J
    Ugeskr Laeger; 1970 Jul; 132(28):1305-10. PubMed ID: 5271188
    [No Abstract]   [Full Text] [Related]  

  • 16. The muscular variant of Pompe's disease.
    Roth JC; Williams HE
    J Pediatr; 1967 Oct; 71(4):567-73. PubMed ID: 5233049
    [No Abstract]   [Full Text] [Related]  

  • 17. [Histochemical and ultrastructural study of a case of type 3 glycogenosis].
    Chamlian A; Mariani R; Lafon J; Adechy-Benkoel L; Mounition L
    Ann Anat Pathol (Paris); 1971; 16(1):85-92. PubMed ID: 4327013
    [No Abstract]   [Full Text] [Related]  

  • 18. Lysosomal alpha-glucosidase in type II glycogenosis; activity in leukocytes and cell cultures in relation to genotype.
    Nitowsky HM; Grunfeld A
    J Lab Clin Med; 1967 Mar; 69(3):472-84. PubMed ID: 5226931
    [No Abstract]   [Full Text] [Related]  

  • 19. Nosology of lysosomal glycogen storage diseases without in vitro acid maltase deficiency. Delineation of a neonatal form.
    Verloes A; Massin M; Lombet J; Grattagliano B; Soyeur D; Rigo J; Koulischer L; Van Hoof F
    Am J Med Genet; 1997 Oct; 72(2):135-42. PubMed ID: 9382133
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A micro-radiochemical assay for alpha-1,4-glucosidase and its use in the assessment of type II glycogenosis (Pompe's disease).
    Nelson PV; Carey WF; Pollard AC
    Clin Chim Acta; 1977 Jun; 77(3):337-42. PubMed ID: 17494
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.