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 *

134 related articles for article (PubMed ID: 6424473)

  • 1. 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]  

  • 2. Iduronate sulfatase activity in serum, lymphocytes, and fibroblasts--simplified diagnosis of the Hunter syndrome.
    Liebaers I; Neufeld E
    Pediatr Res; 1976 Aug; 10(8):733-6. PubMed ID: 821034
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hunter's syndrome: activity of iduronate sulfate sulfatase in the serum of pregnant heterozygotes.
    Zlotogora J; Bach G
    N Engl J Med; 1984 Aug; 311(5):331-2. PubMed ID: 6429538
    [No Abstract]   [Full Text] [Related]  

  • 4. Carrier detection in Hunter syndrome.
    Archer IM; Young ID; Rees DW; Oladimeji A; Wusteman FS; Harper PS
    Am J Med Genet; 1983 Sep; 16(1):61-9. PubMed ID: 6227239
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Iduronate sulfatase determination for the diagnosis of the Hunter syndrome and the detection of the carrier state.
    Neufeld EF; Liebaers I; Lim TW
    Adv Exp Med Biol; 1976; 68():253-60. PubMed ID: 820168
    [No 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. Iduronate sulfatase analysis of hair roots for identification of Hunter syndrome heterozygotes.
    Yutaka T; Fluharty AL; Stevens RL; Kihara H
    Am J Hum Genet; 1978 Nov; 30(6):575-82. PubMed ID: 106723
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 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. Mutations of the iduronate-2-sulfatase gene in 12 Polish patients with mucopolysaccharidosis type II (Hunter syndrome).
    Popowska E; Rathmann M; Tylki-Szymanska A; Bunge S; Steglich C; Schwinger E; Gal A
    Hum Mutat; 1995; 5(1):97-100. PubMed ID: 7728156
    [No Abstract]   [Full Text] [Related]  

  • 11. Detection of hunter heterozygotes by enzymatic analysis of hair roots.
    Nwokoro N; Neufeld EF
    Am J Hum Genet; 1979 Jan; 31(1):42-9. PubMed ID: 107796
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. [A new mutation of iduronate-2-sulfatase gene from the patient with Hunter syndrome].
    Guo YB; Lin QD; Du CS
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Feb; 23(1):67-9. PubMed ID: 16456790
    [TBL] [Abstract][Full Text] [Related]  

  • 14. An improved assay for iduronate 2-sulphate sulphatase in serum and its use in the detection of carriers of the Hunter syndrome.
    Archer IM; Harper PS; Wusteman FS
    Clin Chim Acta; 1981 Apr; 112(1):107-12. PubMed ID: 6786801
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hunter syndrome: presence of material cross-reacting with antibodies against iduronate sulfatase.
    Daniele A; Di Natale P
    Hum Genet; 1987 Mar; 75(3):234-8. PubMed ID: 3104200
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mucopolysaccharidoses type II: enzymatic activity and quantitative and qualitative studies of urinary glycosaminoglycans in five patients.
    Gallegos-Arreola MP; González-Noriega A; Zúñiga-González GM; Flores-Martínez SE; Morán Moguel MC; Figuera LE; Sánchez-Corona J
    Arch Med Res; 1997; 28(1):91-4. PubMed ID: 9078594
    [TBL] [Abstract][Full Text] [Related]  

  • 17. X-linked Hunter syndrome: the heterozygous phenotype in cell culture.
    Migeon BR; Sprenkle JA; Liebaers I; Scott JF; Neufeld EF
    Am J Hum Genet; 1977 Sep; 29(5):448-54. PubMed ID: 409283
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Administration of iduronate sulfatase by plasma exchange to patients with the Hunter syndrome: a clinical study.
    Brown FR; Hall CW; Neufeld EF; Munoz LL; Braine H; Andrzejewski S; Camargo EE; Mark SA; Richard JM; Moser HW
    Am J Med Genet; 1982 Nov; 13(3):309-18. PubMed ID: 6817638
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutational spectrum of the iduronate 2 sulfatase gene in 25 unrelated Korean Hunter syndrome patients: identification of 13 novel mutations.
    Kim CH; Hwang HZ; Song SM; Paik KH; Kwon EK; Moon KB; Yoon JH; Han CK; Jin DK
    Hum Mutat; 2003 Apr; 21(4):449-50. PubMed ID: 12655569
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hunter disease in a girl caused by R468Q mutation in the iduronate-2-sulfatase gene and skewed inactivation of the X chromosome carrying the normal allele.
    Sukegawa K; Song XQ; Masuno M; Fukao T; Shimozawa N; Fukuda S; Isogai K; Nishio H; Matsuo M; Tomatsu S; Kondo N; Orii T
    Hum Mutat; 1997; 10(5):361-7. PubMed ID: 9375851
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.