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PUBMED FOR HANDHELDS

Journal Abstract Search


128 related items for PubMed ID: 6265330

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. [Pendred's syndrome].
    Cremers CW.
    Ned Tijdschr Geneeskd; 1977 Jul 23; 121(30):1202-5. PubMed ID: 196228
    [No Abstract] [Full Text] [Related]

  • 23. Pendred's syndrome in a rural Zambian family.
    Siddorn JA.
    Med J Zambia; 1978 Jul 23; 12(2):56-8. PubMed ID: 726656
    [Abstract] [Full Text] [Related]

  • 24. [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
    [No Abstract] [Full Text] [Related]

  • 25. Abnormal metabolism of thiourea-S 35 in Pendred's syndrome.
    Ibrahim MS, Abdel-Wahab MF, Megahed YM.
    Endokrinologie; 1966 Dec 01; 50(5):286-90. PubMed ID: 5991064
    [No Abstract] [Full Text] [Related]

  • 26. 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
    [Abstract] [Full Text] [Related]

  • 27. Pendred's syndrome: report of two cases.
    Dillon MJ.
    Guys Hosp Rep; 1969 Oct 01; 118(4):523-32. PubMed ID: 5386635
    [No Abstract] [Full Text] [Related]

  • 28. [Pendred's syndrome. Review and report of a case].
    Sebastián M, De Castro S, Marañón A, Iglesias JL, Herreros V, Lara FL, Dávila A.
    Rev Clin Esp; 1968 Jun 15; 109(5):433-8. PubMed ID: 5738385
    [No Abstract] [Full Text] [Related]

  • 29. [Pendred's syndrome. Physiopathological and clinical considerations apropos of 2 cases].
    Biassoni P, Perroni GL, Bestagno M.
    Arch Maragliano Patol Clin; 1965 Dec 15; 21(6):777-88. PubMed ID: 5898819
    [No Abstract] [Full Text] [Related]

  • 30.
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  • 31.
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  • 32. [Pendred's syndrome in 4 cousins].
    Szathmáry G, Fazekas A.
    Orv Hetil; 1971 May 09; 112(19):1098+. PubMed ID: 5088630
    [No Abstract] [Full Text] [Related]

  • 33. 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 09; 44(4):441-6. PubMed ID: 8706311
    [Abstract] [Full Text] [Related]

  • 34.
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  • 35.
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  • 36. [Genetic characterization of Pendred's syndrome and study of thyroid function by double isotope labeling].
    Medeiros-Neto GA, Toledo SP.
    Rev Hosp Clin Fac Med Sao Paulo; 1972 Apr 09; 27(3):115-22. PubMed ID: 4114174
    [No Abstract] [Full Text] [Related]

  • 37.
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  • 38. [Familial hypothyroidism with deafness (Pendred's syndrome)].
    Dubiel A, Januś S, Kubień E, Rudziński A, Piatkowska E.
    Endokrynol Pol; 1973 Apr 09; 24(3):257-64. PubMed ID: 4726258
    [No Abstract] [Full Text] [Related]

  • 39. [Pendred's syndrome: a clinical and biochemical study of abnormal thyroid hormone synthesis associated with congenital deaf-mutism].
    de Medeiros-Netto GA, Nicolau W, Cintra AB.
    Rev Paul Med; 1969 Feb 09; 74(2):53-74. PubMed ID: 4190511
    [No Abstract] [Full Text] [Related]

  • 40. Goiter and deaf mutism.
    Thieme ET.
    Ann Surg; 1975 Aug 09; 182(2):173-6. PubMed ID: 1211996
    [Abstract] [Full Text] [Related]


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