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Journal Abstract Search

121 related items for PubMed ID: 413027

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  • 2. [Hunter's disease: genetic, clinical and biochemical study of a new family].
    D'Auria N, D'Amore I, Di Iorio G, Annunziata P, Puoti S, Federico A.
    Acta Neurol Quad (Napoli); 1979; 39():90-100. PubMed ID: 162337
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  • 5. 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
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  • 6. [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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  • 9. Enzyme replacement therapy by fibroblast transplantation: long-term biochemical study in three cases of Hunter's syndrome.
    Dean MF, Stevens RL, Muir H, Benson PF, Button LR, Anderson RL, Boylston A, Mowbray J.
    J Clin Invest; 1979 Jan 13; 63(1):138-46. PubMed ID: 105013
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  • 12. Transplantation of amniotic epithelial membranes in patients with mucopolysaccharidoses.
    Akle C, McColl I, Dean M, Adinolfi M, Brown S, Fensom AH, Marsh J, Welsh K.
    Exp Clin Immunogenet; 1985 Jan 13; 2(1):43-8. PubMed ID: 3939973
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  • 15. [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 Jan 13; 18(1):91-3. PubMed ID: 8685031
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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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  • 20. Mucopolysaccharidosis type II (Hunter disease): identification and characterization of eight point mutations in the iduronate-2-sulfatase gene in Japanese patients.
    Sukegawa K, Tomatsu S, Fukao T, Iwata H, Song XQ, Yamada Y, Fukuda S, Isogai K, Orii T.
    Hum Mutat; 1995 Mar 13; 6(2):136-43. PubMed ID: 7581397
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