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Journal Abstract Search

123 related items for PubMed ID: 4784677

  • 21. 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
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  • 25. 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
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  • 26. Thyroidal iodoproteins in Pendred's syndrome.
    Medeiros-Neto GA, Nicolau W, Kieffer J, Cintra AB.
    J Clin Endocrinol Metab; 1968 Aug; 28(8):1205-13. PubMed ID: 4970955
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  • 27. [Pendred's syndrome. Current features].
    Wémeau JL, Vlaeminck-Guillem V, Dubrulle F, Dumur V, Vincent C.
    Presse Med; 2001 Nov 17; 30(34):1689-94. PubMed ID: 11760600
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  • 28. Pendred's syndrome.
    Hashmi MI, Khan MJ, Abbasi N, Cheema IA, Qasim G.
    J Coll Physicians Surg Pak; 2003 Aug 17; 13(8):463-4. PubMed ID: 12921687
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  • 29. Pendred's syndrome. A historical note.
    Smith RE.
    Guys Hosp Rep; 1969 Aug 17; 118(4):519-21. PubMed ID: 4917343
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  • 30. Pendred's syndrome in Mombasa.
    Rahim MS.
    East Afr Med J; 1977 Jun 17; 54(6):338-40. PubMed ID: 923487
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  • 31. Pituitary-thyroid function in Pendred's syndrome.
    Gomez-Pan A, Evered DC, Hall R.
    Br Med J; 1974 Apr 20; 2(5911):152-3. PubMed ID: 4132986
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  • 34. A novel mutation in the pendrin gene associated with Pendred's syndrome.
    Bogazzi F, Raggi F, Ultimieri F, Campomori A, Cosci C, Berrettini S, Neri E, La Rocca R, Ronca G, Martino E, Bartalena L.
    Clin Endocrinol (Oxf); 2000 Mar 20; 52(3):279-85. PubMed ID: 10718825
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  • 35. The causes of profound deafness in childhood. In: Sensorinerual hearing loss.
    Fraser GR.
    Ciba Found Symp; 1970 Mar 20; ():5-40. PubMed ID: 5210930
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  • 36. [Pendred's syndrome].
    Cremers CW.
    Ned Tijdschr Geneeskd; 1977 Jul 23; 121(30):1202-5. PubMed ID: 196228
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  • 37. [Pendred's syndrome. Report on 2 cases in a family].
    Nuño de la Rosa Pozuelo JA, Claver Valderas MA, Sanz García D.
    Rev Clin Esp; 1977 Dec 15; 147(5):523-6. PubMed ID: 605261
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  • 38. [Two families with Pendred's syndrome].
    Etzioni A, Benderly, Levy J.
    Harefuah; 1980 Dec 15; 99(12):425-6. PubMed ID: 6265330
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  • 39. Management of goitre in Pendred's syndrome.
    al-Jaberi TM, Hussein AD, Heis HA.
    Br J Surg; 1994 Oct 15; 81(10):1511. PubMed ID: 7820488
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  • 40. Pendred's syndrome and non-syndromic DFNB4 deafness associated with the homozygous T410M mutation in the SLC26A4 gene in siblings.
    Arellano B, Pera A, Ramírez-Camacho R, Villamar M, Trinidad A, García JR, Moreno F, Hernández-Chico C.
    Clin Genet; 2005 May 15; 67(5):438-40. PubMed ID: 15811013
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