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Journal Abstract Search

102 related items for PubMed ID: 6148552

  • 1. Chorion biopsy for prenatal testing in Hunter's syndrome.
    Harper PS, Bamforth S, Rees D, Roberts A, Upadhyaya M.
    Lancet; 1984 Oct 06; 2(8406):812-3. PubMed ID: 6148552
    [No Abstract] [Full Text] [Related]

  • 2. Iduronate sulfatase in amniotic fluid: an aid in the prenatal diagnosis of the hunter syndrome.
    Liebaers I, Di Natale P, Neufeld EF.
    J Pediatr; 1977 Mar 06; 90(3):423-5. PubMed ID: 402458
    [No Abstract] [Full Text] [Related]

  • 3. [Diagnosis of Hunter's disease. Enzyme study].
    Schiavulli E, Loffredo L, Vecchio L, Giugliano R, Carfagnini N, Carlomagno S.
    Minerva Pediatr; 1977 Oct 20; 29(32):1937-46. PubMed ID: 413027
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  • 5. DNA and enzyme studies on chorionic villi for use in antenatal diagnosis.
    Upadhyaya M, Archer IM, Harper PS, Jasani B, Roberts A, Shaw DJ, Thomas NS, Williams H.
    Clin Chim Acta; 1984 Jun 27; 140(1):39-46. PubMed ID: 6430598
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  • 7. First trimester diagnosis of Hunter syndrome on chorionic villi.
    Kleijer WJ, van Diggelen OP, Janse HC, Galjaard H, Dumez Y, Boué J.
    Lancet; 1984 Aug 25; 2(8400):472. PubMed ID: 6147543
    [No Abstract] [Full Text] [Related]

  • 8. Hunter syndrome: prenatal diagnosis in maternal serum.
    Zlotogora J, Bach G.
    Am J Hum Genet; 1986 Feb 25; 38(2):253-60. PubMed ID: 3080875
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  • 9. [Prenatal diagnosis of Hunter's disease].
    Bolodár A, Török O, Horváth K, Németi M, Szabó M, Papp Z.
    Orv Hetil; 1990 May 13; 131(19):1025-7. PubMed ID: 2111903
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  • 10. Prenatal diagnosis of Hunter syndrome using chorionic villi.
    Pannone N, Gatti R, Lombardo C, Di Natale P.
    Prenat Diagn; 1986 May 13; 6(3):207-10. PubMed ID: 3088561
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  • 15. Detection of hunter heterozygotes by enzymatic analysis of hair roots.
    Nwokoro N, Neufeld EF.
    Am J Hum Genet; 1979 Jan 13; 31(1):42-9. PubMed ID: 107796
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  • 17. Mucopolysaccharidosis type II (Hunter's syndrome) in Taiwan.
    Su PH, Hwu WL, Chiang SC, Chiu PC, Lin SJ, Shu SG, Wang TR.
    J Formos Med Assoc; 1998 Mar 13; 97(3):186-90. PubMed ID: 9549269
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  • 18. Challenges in the Management of Mucopolysaccharidosis Type II (Hunter's Syndrome) in a Developing Country: a Case Report.
    Rasheeedah I, Patrick O, Abdullateef A, Mohammed A, Sherifat K, Gbadebo I.
    Ethiop J Health Sci; 2015 Jul 13; 25(3):279-82. PubMed ID: 26633932
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  • 19. 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 13; 22(11):1016-21. PubMed ID: 12424767
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  • 20. [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 13; 44(9):644-7. PubMed ID: 17217652
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