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Journal Abstract Search

113 related items for PubMed ID: 5888657

  • 1. Inborn errors of iodine metabolism in Greece.
    Malamos B, Koutras DA, Sfontouris J, Rigopoulos G.
    Nucl Med (Stuttg); 1964 Apr 01; 4(1):45-55. PubMed ID: 5888657
    [No Abstract] [Full Text] [Related]

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  • 5. [Thyroid hormonosynthesis disorders due to iodotyrosine-dehalogenase deficiency. Value of the D.I.T. test for the detection of heterozygotes].
    Rochiccioli P, Dutau G.
    Arch Fr Pediatr; 1974 Jan 01; 31(1):25-36. PubMed ID: 4135480
    [No Abstract] [Full Text] [Related]

  • 6. Endemic goiter with hypothyroidism in three generations.
    Stanbury JB, Fierro-Benitez R, Estrella E, Milutinovic PS, Tellez MU, Refetoff S.
    J Clin Endocrinol Metab; 1969 Dec 01; 29(12):1596-600. PubMed ID: 5347689
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  • 8. Iodine kinetics in organification defect.
    Negri M, De Luca F, Cramarossa L, Benedetti GA.
    Folia Endocrinol; 1967 Apr 01; 20(2):205-13. PubMed ID: 4169478
    [No Abstract] [Full Text] [Related]

  • 9. Familial agoitrous cretinism accompanied by musclar hypertrophy.
    Cross HE, Hollander CS, Rimoin DL, McKusick VA.
    Pediatrics; 1968 Feb 01; 41(2):413-20. PubMed ID: 5637792
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  • 10. [Study of a family with goiter caused by an iodine organification defect].
    Limbert E, Botelho L, Sobrinho L.
    Arq Patol; 1972 Aug 01; 44(2):139-46. PubMed ID: 4641690
    [No Abstract] [Full Text] [Related]

  • 11. [Congenital absence of idothyronine deiodase].
    Codaccioni JL, Vague J.
    Cesk Pediatr; 1968 Sep 01; 23(9):827-30. PubMed ID: 5685542
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  • 13. [Clinical and chromosomal studies in a congenital hypothyroidism caused by thyroxin synthesis disorders and middle ear hearing disorders (Pendred- or goiter-deafness syndrome)].
    Kitlak W, Gebert P.
    Arch Kinderheilkd; 1968 Sep 01; 177(2):170-83. PubMed ID: 5723894
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  • 14. Biochemical and clinical studies in familial goitre caused by an iodotyrosine deiodinase defect.
    Niall HD, Wellby ML, Hetzel BS, Hudson B, Chenoweth RA.
    Australas Ann Med; 1968 May 01; 17(2):89-95. PubMed ID: 4299848
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  • 15. [Congenital hypothyroidism with goiter caused by altered structure of thyroid iodoproteins].
    Tangheroni W, Cao A.
    Folia Endocrinol; 1967 Jun 01; 20(3):261-75. PubMed ID: 5630798
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  • 16. [Physiological significance of iodotyrosine-deiodinases].
    Voss C, Hartmann N.
    Z Gesamte Inn Med; 1972 Mar 01; 27(5):193-7. PubMed ID: 4558910
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  • 17. Defective iodide organification in "cryptothyroidism".
    Smith JD, Cagas CR, Seely JR, Neeman J.
    J Okla State Med Assoc; 1970 May 01; 63(5):195-9. PubMed ID: 5511591
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  • 18. [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 01; 74(2):53-74. PubMed ID: 4190511
    [No Abstract] [Full Text] [Related]

  • 19. Familial isolated thyrotropin deficiency with cretinism.
    Miyai K, Azukizawa M, Kumahara Y.
    N Engl J Med; 1971 Nov 04; 285(19):1043-8. PubMed ID: 4106196
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  • 20. [Radioiodine diagnosis of hypothyroidism in childhood].
    Struwe FE, Kempe H.
    Monatsschr Kinderheilkd (1902); 1970 Jun 04; 118(6):217-20. PubMed ID: 5523639
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