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Journal Abstract Search

184 related items for PubMed ID: 2111903

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. [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
    [Abstract] [Full Text] [Related]

  • 3. [Prenatal diagnosis of mucopolysaccharidosis type II].
    Zhang XS, Zhang HW, Gu XF.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Oct 13; 28(5):536-8. PubMed ID: 21983729
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. [Possibilities of prenatal diagnosis in hemophilia A based on DNA analysis].
    Németi M, Bolodár A, Török O, Papp Z.
    Orv Hetil; 1990 Jul 29; 131(30):1635-8. PubMed ID: 2119490
    [Abstract] [Full Text] [Related]

  • 6.
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  • 7. [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
    [No Abstract] [Full Text] [Related]

  • 8. [Sex-related neurologic diseases. Hunter's disease. Lesch-Nyhan syndrome].
    Nieto Barrera M.
    An Esp Pediatr; 1984 Oct 20; 21 Suppl 20():47-50. PubMed ID: 6440462
    [No Abstract] [Full Text] [Related]

  • 9. Prenatal mucopolysaccharidosis II (Hunter): a pathogenetic study.
    Wiesmann UN, Spycher MA, Meier C, Liebaers I, Herschkowitz N.
    Pediatr Res; 1980 May 20; 14(5):749-56. PubMed ID: 6770331
    [Abstract] [Full Text] [Related]

  • 10. Prenatal diagnosis of heterozygosis in a pregnancy at risk for Wolman's disease at the 8th week of gestation.
    Bona G, Gallina MR, Dolfin G, Iavarone A, Perona A, Zaffaroni M.
    Panminerva Med; 1989 May 20; 31(4):180-2. PubMed ID: 2633108
    [Abstract] [Full Text] [Related]

  • 11. Prenatal diagnosis and fetal pathology in a Turkish family harboring a novel nonsense mutation in the lysosomal alpha-N-acetyl-neuraminidase (sialidase) gene.
    Sergi C, Penzel R, Uhl J, Zoubaa S, Dietrich H, Decker N, Rieger P, Kopitz J, Otto HF, Kiessling M, Cantz M.
    Hum Genet; 2001 Oct 20; 109(4):421-8. PubMed ID: 11702224
    [Abstract] [Full Text] [Related]

  • 12. Prenatal exclusion of Pompe disease by electron microscopy.
    Phupong V, Shotelersuk V.
    Southeast Asian J Trop Med Public Health; 2006 Sep 20; 37(5):1021-4. PubMed ID: 17333749
    [Abstract] [Full Text] [Related]

  • 13. Multivalvular thickening in a case of Hunter's syndrome.
    Wander GS, Sandha GS, Chawla AS, Khurana SB.
    J Assoc Physicians India; 1994 Feb 20; 42(2):161-2. PubMed ID: 7860484
    [No Abstract] [Full Text] [Related]

  • 14. [Life experiences of mothers in parenting children with Hunter's syndrome].
    Kang SY.
    J Korean Acad Nurs; 2012 Oct 20; 42(5):609-21. PubMed ID: 23221651
    [Abstract] [Full Text] [Related]

  • 15. [Unusual findings in 2 patients with Hunter's disease].
    Fiehring C, Schramm G, Würbach G, Meerbach W, Koskowski H, Hoffmann W, Hellinger J, Buttenberg H.
    Dtsch Gesundheitsw; 1970 Jan 16; 25(2):78-82. PubMed ID: 4245072
    [No Abstract] [Full Text] [Related]

  • 16. Mucopolysaccharidosis (Hunter's syndrome) in a black family.
    Seedat YK, Narrandes R, Maharaj IC.
    S Afr Med J; 1981 Mar 07; 59(10):342-3. PubMed ID: 6781075
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Difficult prenatal diagnosis in mild Smith-Lemli-Opitz syndrome.
    Nowaczyk MJ, Heshka T, Kratz LE, Kelley RE.
    Am J Med Genet; 2000 Dec 11; 95(4):396-8. PubMed ID: 11186897
    [Abstract] [Full Text] [Related]

  • 19. 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 Dec 11; 2(1):43-8. PubMed ID: 3939973
    [Abstract] [Full Text] [Related]

  • 20. 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
    [Abstract] [Full Text] [Related]

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