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Journal Abstract Search

136 related items for PubMed ID: 4135480

  • 1. [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; 31(1):25-36. PubMed ID: 4135480
    [No Abstract] [Full Text] [Related]

  • 2. [Infantile hypothyroidism caused by iodotyrosine-dehalogenase deficiency. I. 4 new cases].
    Codaccioni JL, Pierron H, Rouault R, Bismuth J, Aquaron R.
    Ann Endocrinol (Paris); 1970 Jan; 31(6):1161-73. PubMed ID: 4101669
    [No Abstract] [Full Text] [Related]

  • 3. 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; 17(2):89-95. PubMed ID: 4299848
    [No Abstract] [Full Text] [Related]

  • 4. Familial goiter due to an organification defect in euthyroid siblings.
    Furth ED, Carvalho M, Vianna B.
    J Clin Endocrinol Metab; 1967 Aug; 27(8):1137-40. PubMed ID: 4166581
    [No Abstract] [Full Text] [Related]

  • 5. [Hypothyroidism due to congenital abnormality of thyroglobulin synthesis. Apropos of 3 cases].
    Sultan C, Bismuth J, CASTAY M, Dumas R, Michel-Bechet M, Lissitzky S, Jean R.
    Arch Fr Pediatr; 1974 Jan; 31(1):11-23. PubMed ID: 4135555
    [No Abstract] [Full Text] [Related]

  • 6. [Congenital hypothyroisis with goiter caused by a genetic defect of thyroid hormone synthesis in 2 brothers].
    Zhukovskiĭ MA, Sherbacheva LN.
    Pediatriia; 1970 Jul; 49(7):81-2. PubMed ID: 5479971
    [No Abstract] [Full Text] [Related]

  • 7. [Goiter and hypothyroidism due to a familial defect o deiodation of iodotyrosine].
    Bigozzi U, Bigazzi M, Guazzelli R, Melani F.
    Acta Genet Med Gemellol (Roma); 1967 Oct; 16(4):410-6. PubMed ID: 4173309
    [No Abstract] [Full Text] [Related]

  • 8. [Congenital absence of idothyronine deiodase].
    Codaccioni JL, Vague J.
    Cesk Pediatr; 1968 Sep; 23(9):827-30. PubMed ID: 5685542
    [No Abstract] [Full Text] [Related]

  • 9. [Quantitative study of iodine metabolism in a case of hypothyroidism with goiter due to a defect of iodotyrosine deshalogenase].
    Lissitzky S, Comar D, Rivière R, Codaccioni JL.
    Rev Fr Etud Clin Biol; 1965 Sep; 10(6):631-9. PubMed ID: 4158342
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. [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; 177(2):170-83. PubMed ID: 5723894
    [No Abstract] [Full Text] [Related]

  • 12. [Histopathologic aspects of goiter with disorders of hormonsynthesis. Apropos of 7 anatomoclinical cases].
    Vilde F, Nezelof C.
    Ann Anat Pathol (Paris); 1966 Sep; 11(4):397-414. PubMed ID: 5972272
    [No Abstract] [Full Text] [Related]

  • 13. Clinical consequences of heterozygosity for autosomal-recessive diseases.
    Vogel F.
    Clin Genet; 1984 May; 25(5):381-415. PubMed ID: 6373070
    [Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
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  • 15. [Diagnosis of iodotyrosine-dehalogenase deficiency after 3 normal pregnancies].
    Elewaut A, Baele G, Schelstraete K, Vermeulen A.
    Ann Endocrinol (Paris); 1972 May; 33(6):599-605. PubMed ID: 4665419
    [No Abstract] [Full Text] [Related]

  • 16. [Late sporadic goiter in adults, with dehalogenase enzyme deficiency. Clinical, biochemical, isotope study].
    Jaffiol C, Khalil R, Pastorello R, Baldet L, Mirouze J.
    Rev Fr Endocrinol Clin; 1969 May; 10(1):67-71. PubMed ID: 5802745
    [No Abstract] [Full Text] [Related]

  • 17. Genetic intrathyroidal hormone defects.
    Ibrahim MS, Khalifa AS, Abdel-Wahab MF.
    J Egypt Med Assoc; 1970 May; 53(1):1-12. PubMed ID: 5507465
    [No Abstract] [Full Text] [Related]

  • 18. Congenital hypothyroidism. Aetiological and clinical aspects.
    Mäenpää J.
    Arch Dis Child; 1972 Dec; 47(256):914-23. PubMed ID: 4119068
    [Abstract] [Full Text] [Related]

  • 19. [INBORN ERRORS IN THE SYNTHESIS OF THYROID HORMONES. REPORT ON 3 CASES].
    ROOTWELT K, STEEN-JOHNSEN J.
    Tidsskr Nor Laegeforen; 1964 Oct 15; 84():1420-5. PubMed ID: 14226935
    [No Abstract] [Full Text] [Related]

  • 20. Goitrous cretinism with chromosomal aberration and defect in thyroglobulin synthesis.
    Lizarralde G, Jones B, Seal US, Jones JE.
    J Clin Endocrinol Metab; 1966 Nov 15; 26(11):1227-31. PubMed ID: 4162599
    [No Abstract] [Full Text] [Related]

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