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 *

132 related articles for article (PubMed ID: 4264156)

  • 21. Acid -glucosidase in amniotic fluid.
    Fluharty AL; Scott ML; Porter MT; Kihara H; Wilson MG; Towner JW
    Biochem Med; 1973 Feb; 7(1):39-51. PubMed ID: 4265155
    [No Abstract]   [Full Text] [Related]  

  • 22. Metachromasia in cultured fibroblasts of subjects with glycogenosis type II.
    Tenconi R; Baccichetti C; Zacchello F; Sartori E
    Experientia; 1970 Nov; 26(11):1238-9. PubMed ID: 4098624
    [No Abstract]   [Full Text] [Related]  

  • 23. 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]  

  • 24. Qualitative characteristics of the beta-glucosidase isozymes.
    Choy FY; Davidson RG
    Prog Clin Biol Res; 1982; 95():415-41. PubMed ID: 6812079
    [No Abstract]   [Full Text] [Related]  

  • 25. Demonstration of acid maltase protein in Pompe disease by use of immunohistochemical and enzyme immunoassay methods.
    Ninomiya N; Iwamasa T; Matsuda I; Nonaka I
    J Inherit Metab Dis; 1983; 6(3):131-2. PubMed ID: 6422147
    [No Abstract]   [Full Text] [Related]  

  • 26. Deficiency of acid alpha glucosidase in the urine of patients with Pompe's disease.
    Salafsky IS; Nadler HL
    J Pediatr; 1973 Feb; 82(2):294-7. PubMed ID: 4265199
    [No Abstract]   [Full Text] [Related]  

  • 27. Amylo-1,6-glucosidase in human fibroblasts: studies 3 glycogen storage disease.
    Justice P; Ryan C; Hsia DY; Krmpotik E
    Biochem Biophys Res Commun; 1970 May; 39(3):301-6. PubMed ID: 5270292
    [No Abstract]   [Full Text] [Related]  

  • 28. Zonal differences of alpha-glucosidases in human kidney: studies in controls and in patients with glycogenosis type II.
    Pfister K; Gitzelmann R; Steinmann B
    Clin Chim Acta; 1983 Nov; 134(3):307-15. PubMed ID: 6357553
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Deficiency of glucosylsphingosine: beta-glucosidase in Gaucher disease.
    Raghavan SS; Mumford RA; Kanfer JN
    Biochem Biophys Res Commun; 1973 Sep; 54(1):256-63. PubMed ID: 4741565
    [No Abstract]   [Full Text] [Related]  

  • 30. Immunological studies on glycogen storage diseases type 3 and V. Demonstration of the presence of an immunoreactive protein in one case of muscle phosphorylase deficiency.
    Dreyfus JC; Alexandre Y
    Biochem Biophys Res Commun; 1971 Sep; 44(6):1364-70. PubMed ID: 5003690
    [No Abstract]   [Full Text] [Related]  

  • 31. A method for rapid prenatal diagnosis of glycogenosis II (Pompe's disease).
    Galjaard H; Mekes M; Josselin de Jong JE DE; Niermeijer MF
    Clin Chim Acta; 1973 Dec; 49(3):361-75. PubMed ID: 4272965
    [No Abstract]   [Full Text] [Related]  

  • 32. Enzymes of glycogen metabolism in human skin with particular reference to differential diagnosis of the glycogen storage diseases.
    Leathwood PD; Ryman BE
    Clin Sci; 1971 Mar; 40(3):261-9. PubMed ID: 4323870
    [No Abstract]   [Full Text] [Related]  

  • 33. The molecular heterogeneity of purified human liver lysosomal alpha-glucosidase (acid alpha-glucosidase).
    Murray AK; Brown BI; Brown DH
    Arch Biochem Biophys; 1978 Jan; 185(2):511-24. PubMed ID: 24417
    [No Abstract]   [Full Text] [Related]  

  • 34. Multiple neutral maltase activities in normal and acid maltase-deficient human muscle.
    Shanske S; Bresolin N; DiMauro S
    Exp Neurol; 1984 Jun; 84(3):565-78. PubMed ID: 6426997
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Soluble and membranous neutral beta-glucosidases.
    Ben-Yoseph Y; Nadler HL
    Prog Clin Biol Res; 1982; 95():465-80. PubMed ID: 6812082
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Acid maltase deficiency of adult life.
    Engel AG
    Trans Am Neurol Assoc; 1969; 94():250-2. PubMed ID: 4244774
    [No Abstract]   [Full Text] [Related]  

  • 38. Electrophoretic heterogeneity of human -mannosidase.
    Poenaru L; Dreyfus JC
    Biochim Biophys Acta; 1973 Mar; 303(1):171-4. PubMed ID: 4702001
    [No Abstract]   [Full Text] [Related]  

  • 39. Comparative study of acid maltase deficiency. Biochemical differences between infantile, childhood, and adult types.
    Angelini C; Engel AG
    Arch Neurol; 1972 Apr; 26(4):344-9. PubMed ID: 4501990
    [No Abstract]   [Full Text] [Related]  

  • 40. [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]  

    [Previous]   [Next]    [New Search]
    of 7.