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 *

156 related articles for article (PubMed ID: 2521770)

  • 1. Branching enzyme activity of cultured amniocytes and chorionic villi: prenatal testing for type IV glycogen storage disease.
    Brown BI; Brown DH
    Am J Hum Genet; 1989 Mar; 44(3):378-81. PubMed ID: 2521770
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of glycogen storage disease type IV.
    Akman HO; Karadimas C; Gyftodimou Y; Grigoriadou M; Kokotas H; Konstantinidou A; Anninos H; Patsouris E; Thaker HM; Kaplan JB; Besharat I; Hatzikonstantinou K; Fotopoulos S; Dimauro S; Petersen MB
    Prenat Diagn; 2006 Oct; 26(10):951-5. PubMed ID: 16874838
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Type IV glycogen-storage disease. Light-microscopic, electron-microscopic, and enzymatic study.
    Bannayan GA; Dean WJ; Howell RR
    Am J Clin Pathol; 1976 Oct; 66(4):702-9. PubMed ID: 1067751
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Studies of the residual glycogen branching enzyme activity present in human skin fibroblasts from patients with type IV glycogen storage disease.
    Brown DH; Brown BI
    Biochem Biophys Res Commun; 1983 Mar; 111(2):636-43. PubMed ID: 6220706
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Glycogen storage disease type IV diagnosed biochemically. A case report.
    Friedman DJ; Lane AB; Katz S; Jenkins T
    S Afr Med J; 1978 Aug; 54(7):289-91. PubMed ID: 280962
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Placental involvement in glycogen storage disease type IV.
    Konstantinidou AE; Anninos H; Dertinger S; Nonni A; Petersen M; Karadimas C; Havaki S; Marinos E; Akman HO; DiMauro S; Patsouris E
    Placenta; 2008 Apr; 29(4):378-81. PubMed ID: 18289670
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Debranching enzyme in fibroblasts, amniotic fluid cells and chorionic villi: pre- and postnatal diagnosis of glycogenosis type III.
    van Diggelen OP; Janse HC; Smit GP
    Clin Chim Acta; 1985 Jul; 149(2-3):129-34. PubMed ID: 3161667
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A new variant of type IV glycogenosis: deficiency of branching enzyme activity without apparent progressive liver disease.
    Greene HL; Brown BI; McClenathan DT; Agostini RM; Taylor SR
    Hepatology; 1988; 8(2):302-6. PubMed ID: 3162725
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Branching enzyme in erythrocytes. Detection of type IV glycogenosis homozygotes and heterozygotes.
    Shin YS; Steigüber H; Klemm P; Endres W; Schwab O; Wolff G
    J Inherit Metab Dis; 1988; 11 Suppl 2():252-4. PubMed ID: 2972882
    [No Abstract]   [Full Text] [Related]  

  • 11. Enzymatic activity of glycogen metabolism in chorionic villi.
    Chowers M; Abeliovich D; Potashnik R; Bashan N
    Placenta; 1986; 7(6):505-9. PubMed ID: 3025829
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chorionic villi ultrastructure in the prenatal diagnosis of glycogenosis type II.
    San Millan B; Teijeira S; Domínguez C; Vieitez I; Navarro C
    J Inherit Metab Dis; 2010 Dec; 33 Suppl 3():S105-11. PubMed ID: 20157781
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Glycogen storage disease type IV: inherited deficiency of branching enzyme activity in cats.
    Fyfe JC; Giger U; Van Winkle TJ; Haskins ME; Steinberg SA; Wang P; Patterson DF
    Pediatr Res; 1992 Dec; 32(6):719-25. PubMed ID: 1337588
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A juvenile variant of glycogenosis IV (Andersen disease).
    Guerra AS; van Diggelen OP; Carneiro F; Tsou RM; Simoes S; Santos NT
    Eur J Pediatr; 1986 Aug; 145(3):179-81. PubMed ID: 3464425
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Postnatal and prenatal diagnosis of mucopolysaccharidosis type II (Hunter syndrome)].
    Zhang WM; Shi HP; Li BT; Zhao SM; Qi QW; Sun NH; Huang SZ
    Zhonghua Er Ke Za Zhi; 2006 Sep; 44(9):644-7. PubMed ID: 17217652
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Prenatal diagnosis of succinyl-coenzyme A:3-ketoacid coenzyme A transferase deficiency.
    Fukao T; Song XQ; Watanabe H; Hirayama K; Sakazaki H; Shintaku H; Imanaka M; Orii T; Kondo N
    Prenat Diagn; 1996 May; 16(5):471-4. PubMed ID: 8844009
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Prenatal diagnosis of 3-hydroxy-3-methylglutaric aciduria via enzyme activity measurements in chorionic villi, chorionic villous fibroblasts or amniocytes using a simple spectrophotometric method.
    Wanders RJ; Schutgens RB; Zoeters BH
    J Inherit Metab Dis; 1988; 11(4):430. PubMed ID: 2468820
    [No Abstract]   [Full Text] [Related]  

  • 19. Prenatal diagnosis of Hurler disease by analysis of alpha-iduronidase in chorionic villi.
    Young EP
    J Inherit Metab Dis; 1992; 15(2):224-30. PubMed ID: 1527990
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Immunoblot analyses of glycogen debranching enzyme in different subtypes of glycogen storage disease type III.
    Ding JH; de Barsy T; Brown BI; Coleman RA; Chen YT
    J Pediatr; 1990 Jan; 116(1):95-100. PubMed ID: 2295969
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.