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Journal Abstract Search

131 related items for PubMed ID: 3694034

  • 1. Pendred's syndrome. Acoustic, vestibular and radiological findings in 17 unrelated patients.
    Johnsen T, Larsen C, Friis J, Hougaard-Jensen F.
    J Laryngol Otol; 1987 Nov; 101(11):1187-92. PubMed ID: 3694034
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  • 2. Mondini cochlea in Pendred's syndrome. A histological study.
    Johnsen T, Jørgensen MB, Johnsen S.
    Acta Otolaryngol; 1986 Nov; 102(3-4):239-47. PubMed ID: 3776519
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  • 3. CT-scanning of the cochlea in Pendred's syndrome.
    Johnsen T, Videbaek H, Olesen KP.
    Clin Otolaryngol Allied Sci; 1989 Oct; 14(5):389-93. PubMed ID: 2582633
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  • 4. Pendred's syndrome: a study of patients and relatives.
    Jamal MN, Arnaout MA, Jarrar R.
    Ann Otol Rhinol Laryngol; 1995 Dec; 104(12):957-62. PubMed ID: 7492068
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  • 5. The variable intrafamiliar expressivity in Pendred's syndrome.
    Johnsen T, Sørensen MS, Feldt-Rasmussen U, Friis J.
    Clin Otolaryngol Allied Sci; 1989 Oct; 14(5):395-9. PubMed ID: 2582634
    [Abstract] [Full Text] [Related]

  • 6. Pendred's syndrome: identification of the genetic defect a century after its recognition.
    Kopp P.
    Thyroid; 1999 Jan; 9(1):65-9. PubMed ID: 10037079
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  • 7. Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene.
    Kopp P, Arseven OK, Sabacan L, Kotlar T, Dupuis J, Cavaliere H, Santos CL, Jameson JL, Medeiros-Neto G.
    J Clin Endocrinol Metab; 1999 Jan; 84(1):336-41. PubMed ID: 9920104
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  • 8. Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome.
    Gausden E, Armour JA, Coyle B, Coffey R, Hochberg Z, Pembrey M, Britton KE, Grossman A, Reardon W, Trembath R.
    Clin Endocrinol (Oxf); 1996 Apr; 44(4):441-6. PubMed ID: 8706311
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  • 10. Molecular analysis of the Pendred's syndrome gene and magnetic resonance imaging studies of the inner ear are essential for the diagnosis of true Pendred's syndrome.
    Fugazzola L, Mannavola D, Cerutti N, Maghnie M, Pagella F, Bianchi P, Weber G, Persani L, Beck-Peccoz P.
    J Clin Endocrinol Metab; 2000 Jul; 85(7):2469-75. PubMed ID: 10902795
    [Abstract] [Full Text] [Related]

  • 11. Clinical and molecular analysis of three Mexican families with Pendred's syndrome.
    Gonzalez Trevino O, Karamanoglu Arseven O, Ceballos CJ, Vives VI, Ramirez RC, Gomez VV, Medeiros-Neto G, Kopp P.
    Eur J Endocrinol; 2001 Jun; 144(6):585-93. PubMed ID: 11375792
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  • 13. Female siblings with Pendred's syndrome.
    Nakagawa O, Ito S, Hanyu O, Yamazaki M, Urushiyama M, Tani N, Shibata A.
    Intern Med; 1994 Jun; 33(6):369-72. PubMed ID: 7919627
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  • 15. [Combined goiter and deafness as a hereditary condition (Pendred's syndrome)].
    Sundsfjord JA, Schjoth A, Odegaard AE, Harbitz HF.
    Tidsskr Nor Laegeforen; 1968 Jan 01; 88(1):19-23. PubMed ID: 4174251
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  • 16. Two Chinese families with Pendred's syndrome--radiological imaging of the ear and molecular analysis of the pendrin gene.
    Yong AM, Goh SS, Zhao Y, Eng PH, Koh LK, Khoo DH.
    J Clin Endocrinol Metab; 2001 Aug 01; 86(8):3907-11. PubMed ID: 11502831
    [Abstract] [Full Text] [Related]

  • 17. Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.
    Blons H, Feldmann D, Duval V, Messaz O, Denoyelle F, Loundon N, Sergout-Allaoui A, Houang M, Duriez F, Lacombe D, Delobel B, Leman J, Catros H, Journel H, Drouin-Garraud V, Obstoy MF, Toutain A, Oden S, Toublanc JE, Couderc R, Petit C, Garabédian EN, Marlin S.
    Clin Genet; 2004 Oct 01; 66(4):333-40. PubMed ID: 15355436
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  • 19. [Pendred's syndrome: a cause of goiter associated with deafness].
    Vázquez AG, Montesinos IG, Jiménez AM, García JA, García JG, Hernández JA.
    Endocrinol Nutr; 2009 Oct 01; 56(8):428-30. PubMed ID: 19959154
    [Abstract] [Full Text] [Related]

  • 20. [On the histomorphology of the thyroid gland in Pendred's goiter-deafness syndrome].
    Wildner GP, Wittig G.
    Zentralbl Allg Pathol; 1966 Oct 01; 109(1):52-61. PubMed ID: 5230968
    [No Abstract] [Full Text] [Related]

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