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 *

103 related articles for article (PubMed ID: 8508132)

  • 1. Prenatal diagnosis of Sanfilippo syndrome type A by early amniocentesis.
    Thompson JN; Huffman P; McConkie-Rosell A; Hessling J
    Biochem Mol Biol Int; 1993 Apr; 29(5):793-7. PubMed ID: 8508132
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Prenatal diagnosis of Sanfilippo A syndrome: experience in 35 pregnancies at risk and the use of a new fluorogenic substrate for the heparin sulphamidase assay.
    Kleijer WJ; Karpova EA; Geilen GC; Keulemans JL; Huijmans JG; Tsvetkova IV; Voznyi YaV ; van Diggelen OP
    Prenat Diagn; 1996 Sep; 16(9):829-35. PubMed ID: 8905897
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Ruling out fetal Sanfilippo's syndrome (mucopolysaccharidosis IIIA) in the first trimester of pregnancy].
    Bolodár A; Török O; Szabó M; Váradi V; Papp Z
    Orv Hetil; 1989 Jan; 130(5):233-4. PubMed ID: 2492654
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Sanfilippo syndrome, type D: a spectrophotometric assay with prenatal diagnostic potential.
    Nowakowski RW; Thompson JN; Taylor KB
    Pediatr Res; 1989 Nov; 26(5):462-6. PubMed ID: 2510119
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prediction of Sanfilippo phenotype severity from immunoquantification of heparan-N-sulfamidase in cultured fibroblasts from mucopolysaccharidosis type IIIA patients.
    Perkins KJ; Muller V; Weber B; Hopwood JJ
    Mol Genet Metab; 2001 Aug; 73(4):306-12. PubMed ID: 11509012
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sanfilippo A syndrome: sulfamidase deficiency in cultured skin fibroblasts and liver.
    Matalon R; Dorfman A
    J Clin Invest; 1974 Oct; 54(4):907-12. PubMed ID: 4214836
    [TBL] [Abstract][Full Text] [Related]  

  • 7. First-trimester diagnosis of mucopolysaccharidosis IIIA (Sanfilippo A disease).
    Kleijer WJ; Janse HC; Vosters RP; Niermeijer MF; van de Kamp JJ
    N Engl J Med; 1986 Jan; 314(3):185-6. PubMed ID: 3079882
    [No Abstract]   [Full Text] [Related]  

  • 8. [Prenatal diagnosis of a case of metachromatic leucodystrophy (author's transl)].
    Harzer K; Zahn V; Stengel-Rutkowski S; Gley EO
    Dtsch Med Wochenschr; 1975 Apr; 100(17):951-3. PubMed ID: 1122864
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sanfilippo D syndrome: estimation of N-acetylglucosamine-6-sulfatase activity with a radiolabeled monosulfated disaccharide substrate.
    Freeman C; Hopwood JJ
    Anal Biochem; 1989 Feb; 176(2):244-8. PubMed ID: 2500866
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Sanfilippo A disease in the fetus--comparison with pre- and postnatal cases.
    Ceuterick C; Martin JJ; Libert J; Farriaux JP
    Neuropadiatrie; 1980 May; 11(2):176-85. PubMed ID: 6777713
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. First-trimester diagnosis of Morquio disease type A.
    Kleijer WJ; Geilen GC; Garritsen V; Huijmans JG; Los FJ; Voznyi YV; van Diggelen OP
    Prenat Diagn; 2000 Mar; 20(3):183-5. PubMed ID: 10719317
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A false-positive diagnosis of Turner syndrome by amniocentesis.
    Griffiths MJ; Miller PR; Stibbe HM
    Prenat Diagn; 1996 May; 16(5):463-6. PubMed ID: 8844007
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Prenatal diagnosis of Sanfilippo A disease (mucopolysaccharidosis IIIA)].
    Török O; Váradi V; Szondy M; Molnár M; Szabó M; Papp Z
    Orv Hetil; 1986 Sep; 127(39):2385-7. PubMed ID: 3095766
    [No Abstract]   [Full Text] [Related]  

  • 15. Detection of the Sanfilippo D syndrome by the use of a radiolabeled monosaccharide sulfate as the substrate for the estimation of N-acetylglucosamine-6-sulfate sulfatase.
    Elliott H; Hopwood JJ
    Anal Biochem; 1984 Apr; 138(1):205-9. PubMed ID: 6428270
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Oligosaccharide substrates for heparin sulfamidase.
    Thompson JN; Rodén L; Reynertson R
    Anal Biochem; 1986 Feb; 152(2):412-22. PubMed ID: 3083713
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Radiolabelled oligosaccharides as substrates for the estimation of sulfamidase and the detection of the Sanfilippo type A syndrome.
    Hopwood JJ; Elliott H
    Clin Chim Acta; 1981 Apr; 112(1):55-66. PubMed ID: 6786803
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prenatal diagnosis of Maroteaux-Lamy syndrome.
    Van Dyke DL; Fluharty AL; Schafer IA; Shapiro LJ; Kihara H; Weiss L
    Am J Med Genet; 1981; 8(2):235-42. PubMed ID: 6792921
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Amniocentesis in early pregnancy: prenatal detection of genetic disease.
    Schmickel R; Bloom A; Work B; Jaffe R
    Mich Med; 1971 Jul; 70(16):611-3. PubMed ID: 5106404
    [No Abstract]   [Full Text] [Related]  

  • 20. Prenatal diagnosis of the Hunter syndrome and the introduction of a new fluorimetric enzyme assay.
    Keulemans JL; Sinigerska I; Garritsen VH; Huijmans JG; Voznyi YV; van Diggelen OP; Kleijer WJ
    Prenat Diagn; 2002 Nov; 22(11):1016-21. PubMed ID: 12424767
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.