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Journal Abstract Search

184 related items for PubMed ID: 2111903

  • 21. [Hunter's disease: study of a family from the plain of Paestum].
    Carlomagno S, Federico A, Pinto L, Balbi R, Vitolo G, Guazzi GC.
    Acta Neurol (Napoli); 1973; 28(3):323-49. PubMed ID: 4270001
    [No Abstract] [Full Text] [Related]

  • 22. Diagnosis of Hunter's syndrome carriers; radioactive sulphate incorporation into fibroblasts in the presence or fructose 1-phosphate.
    Tønnesen T, Lykkelund C, Güttler F.
    Hum Genet; 1982; 60(2):167-71. PubMed ID: 6210620
    [Abstract] [Full Text] [Related]

  • 23. 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; 97(3):186-90. PubMed ID: 9549269
    [Abstract] [Full Text] [Related]

  • 24. [Hunter's syndrome (type II) in a 4-year-old child].
    Zoch-Zwierz W, Zadrozna B, Kilczewska D.
    Wiad Lek; 1976 Apr 01; 29(7):641-4. PubMed ID: 131419
    [No Abstract] [Full Text] [Related]

  • 25. [Case of mucopolysaccharidosis II--Hunter's syndrome].
    Walczak M, Pawlaczyk B, Sioda T, Piontek E.
    Pediatr Pol; 1976 Jan 01; 51(1):77-80. PubMed ID: 813178
    [No Abstract] [Full Text] [Related]

  • 26. Hunter's syndrome: a study in airway obstruction.
    Sasaki CT, Ruiz R, Gaito R, Kirchner JA, Seshi B.
    Laryngoscope; 1987 Mar 01; 97(3 Pt 1):280-5. PubMed ID: 3102869
    [Abstract] [Full Text] [Related]

  • 27. 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 01; 25(3):279-82. PubMed ID: 26633932
    [Abstract] [Full Text] [Related]

  • 28. [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 Jul 01; 39():90-100. PubMed ID: 162337
    [No Abstract] [Full Text] [Related]

  • 29. 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 01; 11(9):731-5. PubMed ID: 1820774
    [Abstract] [Full Text] [Related]

  • 30. Prenatal diagnosis of methylmalonic aciduria by analysis of organic acids and total homocysteine in amniotic fluid.
    Zhang Y, Yang YL, Hasegawa Y, Yamaguchi S, Shi CY, Song JQ, Sayami S, Liu P, Yan R, Dong JH, Qin J.
    Chin Med J (Engl); 2008 Feb 05; 121(3):216-9. PubMed ID: 18298912
    [Abstract] [Full Text] [Related]

  • 31. Mitral valve replacement for mitral stenosis secondary to Hunter's syndrome.
    Bhattacharya K, Gibson SC, Pathi VL.
    Ann Thorac Surg; 2005 Nov 05; 80(5):1911-2. PubMed ID: 16242483
    [Abstract] [Full Text] [Related]

  • 32. Hunter's syndrome: activity of iduronate sulfate sulfatase in the serum of pregnant heterozygotes.
    Zlotogora J, Bach G.
    N Engl J Med; 1984 Aug 02; 311(5):331-2. PubMed ID: 6429538
    [No Abstract] [Full Text] [Related]

  • 33. [Two differentiated types of gargoylism--Hurler's and Hunter's].
    Likavcan M, Vajda P.
    Cesk Pediatr; 1972 Aug 02; 27(8):391-3. PubMed ID: 4626309
    [No Abstract] [Full Text] [Related]

  • 34. [Mucolipidosis II (I cell disease). First case report in the Czech Republic and prenatal diagnosis in a family].
    Elleder M, Poupĕtová H, Zeman J, Hrebícek M, Ledvinová J, Baxová A, Podhola M.
    Cas Lek Cesk; 1997 Nov 19; 136(22):702-6. PubMed ID: 9476383
    [Abstract] [Full Text] [Related]

  • 35. Hunter's syndrome: a case report.
    Savitha NS, Saurabh G, Krishnamoorthy SH, Nandan S, Ambili A.
    J Indian Soc Pedod Prev Dent; 2015 Nov 19; 33(1):66-8. PubMed ID: 25572378
    [Abstract] [Full Text] [Related]

  • 36. Prenatal diagnosis of X-linked hypohidrotic ectodermal dysplasia by linkage analysis.
    Zonana J, Schinzel A, Upadhyaya M, Thomas NS, Anton-Lamprecht I, Harper PS.
    Am J Med Genet; 1990 Jan 19; 35(1):132-5. PubMed ID: 2301463
    [Abstract] [Full Text] [Related]

  • 37. 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 Jan 19; 4(2):128-31. PubMed ID: 7981716
    [Abstract] [Full Text] [Related]

  • 38. 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 19; 32(4):270-2. PubMed ID: 15797184
    [Abstract] [Full Text] [Related]

  • 39. Prenatal diagnosis of DMD in a female foetus affected by Turner syndrome.
    Satre V, Monnier N, Devillard F, Amblard F, Lunardi J.
    Prenat Diagn; 2004 Nov 19; 24(11):913-7. PubMed ID: 15565644
    [Abstract] [Full Text] [Related]

  • 40. Lumbar kyphosis in Hunter's disease (MPS ii).
    Benson PF, Button LR, Fensom AH, Dean MF.
    Clin Genet; 1979 Nov 19; 16(5):317-22. PubMed ID: 117962
    [Abstract] [Full Text] [Related]

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