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 *

84 related articles for article (PubMed ID: 8576624)

  • 1. [Prenatal diagnosis of Hunter syndrome in a carrier and her twin sisters].
    Sakai N; Saito T; Hayashi Y; Hiroi M
    Nihon Sanka Fujinka Gakkai Zasshi; 1996 Jan; 48(1):65-8. PubMed ID: 8576624
    [No Abstract]   [Full Text] [Related]  

  • 2. Letter: Question raised regarding diagnosis of Hunter syndrome.
    Kelly TE
    Pediatrics; 1974 Oct; 54(4):522-3. PubMed ID: 4213222
    [No Abstract]   [Full Text] [Related]  

  • 3. Female twin with Hunter disease due to nonrandom inactivation of the X-chromosome: a consequence of twinning.
    Winchester B; Young E; Geddes S; Genet S; Hurst J; Middleton-Price H; Williams N; Webb M; Habel A; Malcolm S
    Am J Med Genet; 1992 Dec; 44(6):834-8. PubMed ID: 1481858
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal monitoring for the Hunter syndrome: the heterozygous female fetus.
    Kleijer WJ; Moody PD; Liebaers I; van de Kamp JJ; Niermeijer MF
    Clin Genet; 1979 Feb; 15(2):113-7. PubMed ID: 153809
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Hunter syndrome: prenatal diagnosis in maternal serum.
    Zlotogora J; Bach G
    Am J Hum Genet; 1986 Feb; 38(2):253-60. PubMed ID: 3080875
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome).
    Martin R; Beck M; Eng C; Giugliani R; Harmatz P; Muñoz V; Muenzer J
    Pediatrics; 2008 Feb; 121(2):e377-86. PubMed ID: 18245410
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Heterozygote detection in Hunter syndrome.
    Zlotogora J; Bach G
    Am J Med Genet; 1984 Mar; 17(3):661-5. PubMed ID: 6424473
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Detection of Hunter syndrome (mucopolysaccharidosis type II) in Taiwanese: biochemical and linkage studies of the iduronate-2-sulfatase gene defects in MPS II patients and carriers.
    Lin SP; Chang JH; Lee-Chen GJ; Lin DS; Lin HY; Chuang CK
    Clin Chim Acta; 2006 Jul; 369(1):29-34. PubMed ID: 16480701
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Combined enzymatic and linkage analysis for heterozygote detection in Hunter syndrome: identification of an apparent case of germinal mosaicism.
    Ben Simon-Schiff E; Bach G; Zlotogora J; Abeliovich D
    Am J Med Genet; 1993 Nov; 47(6):837-42. PubMed ID: 7904121
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The reliability of death certification in patients dying with mucopolysaccharidosis type II (Hunter syndrome).
    Seshadri D; Jones S; Burt K; Lavery L; Wraith JE
    Clin Genet; 2011 Jun; 79(6):599-600. PubMed ID: 21542835
    [No Abstract]   [Full Text] [Related]  

  • 12. First-trimester diagnosis of Hunter syndrome: very low iduronate sulphatase activity in chorionic villi from a heterozygous female fetus.
    Cooper A; Thornley M; Wraith JE
    Prenat Diagn; 1991 Sep; 11(9):731-5. PubMed ID: 1820774
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical presentation and diagnosis of mucopolysaccharidosis type 2 (Hunter syndrome).
    Patil R; Wasekar N; Jadhav SG; Zore R; Sangoi P; Vishwanathan D
    J Assoc Physicians India; 2013 Aug; 61(8):574-6. PubMed ID: 24818348
    [No Abstract]   [Full Text] [Related]  

  • 14. Intrauterine diagnosis of the hurler and hunter syndromes.
    Fratantoni JC; Neufeld EF; Uhlendorf BW; Jacobson CB
    N Engl J Med; 1969 Mar; 280(13):686-8. PubMed ID: 4179670
    [No Abstract]   [Full Text] [Related]  

  • 15. Mutations of the iduronate-2-sulfatase (IDS) gene in patients with Hunter syndrome (mucopolysaccharidosis II).
    Schröder W; Wulff K; Wehnert M; Seidlitz G; Herrmann FH
    Hum Mutat; 1994; 4(2):128-31. PubMed ID: 7981716
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mucopolysaccharidosis type II in females: case report and review of literature.
    Tuschl K; Gal A; Paschke E; Kircher S; Bodamer OA
    Pediatr Neurol; 2005 Apr; 32(4):270-2. PubMed ID: 15797184
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Mucopolysaccharidosis II (Hunter syndrome): identification of the carrier state of the disease by means of mutation analysis].
    Balzano N; Villani GR; Coppa G; Di Natale P
    Pediatr Med Chir; 1996; 18(1):91-3. PubMed ID: 8685031
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Skin rash with the histological absence of metachromatic granules as the presenting feature of Hunter syndrome in a 6-year-old boy.
    Sakata S; Orchard D; Mason G
    Br J Dermatol; 2008 Jul; 159(1):249-50. PubMed ID: 18489604
    [No Abstract]   [Full Text] [Related]  

  • 19. Picture of the month. Hunter syndrome (mucopolysaccharidosis IIA).
    Knoell KA; Tunnessen WW
    Arch Pediatr Adolesc Med; 2000 Jan; 154(1):85-6. PubMed ID: 10632258
    [No Abstract]   [Full Text] [Related]  

  • 20. In vitro selection for the Hunter gene.
    Booth CW; Nadler HL
    N Engl J Med; 1973 Mar; 288(12):636. PubMed ID: 4631420
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.