monoiodotyrosine and Metabolism--Inborn-Errors

monoiodotyrosine has been researched along with Metabolism--Inborn-Errors* in 7 studies

Reviews

1 review(s) available for monoiodotyrosine and Metabolism--Inborn-Errors

ArticleYear
[Physiological significance of iodotyrosine-deiodinases].
    Zeitschrift fur die gesamte innere Medizin und ihre Grenzgebiete, 1972, Mar-01, Volume: 27, Issue:5

    Topics: Biopsy; Chemical Phenomena; Chemistry; Chromosomes; Congenital Hypothyroidism; Culture Techniques; Decarboxylation; Female; Genes, Dominant; Genes, Recessive; Goiter; Humans; Hypothyroidism; Iodine; Iodine Isotopes; Male; Metabolism, Inborn Errors; Monoiodotyrosine; Oxidoreductases; Thyroid Gland; Thyroxine; Triiodothyronine

1972

Other Studies

6 other study(ies) available for monoiodotyrosine and Metabolism--Inborn-Errors

ArticleYear
Congenital iodide organification defect accompanied by a large nodular goiter: a case report.
    Endocrinologia japonica, 1985, Volume: 32, Issue:3

    A girl who had a nontoxic diffuse goiter with a congenital organification defect of iodide was first seen at the age of 8 years, and since then she has been followed up for a long period. The nodularity of the thyroid gland had gradually progressed, because of intermittent failure of ingestion of thyroid hormone preparation which was followed by excess TSH secretion. 18 years later, a nodular goiter developed and the patient underwent subtotal thyroidectomy. In order to prevent the development of nodular change in the thyroid gland in this disorder, supplemental thyroid hormone medication should be started as soon as the diagnosis is confirmed, and the therapy should be carried out regularly.

    Topics: Adult; Diiodotyrosine; Female; Goiter, Nodular; Humans; Iodides; Metabolism, Inborn Errors; Monoiodotyrosine; Pedigree

1985
[Thyroid peroxidase insufficiency as factor in the etiopathogenesis of endemic and sporadic goiter].
    Endokrinologie, 1971, Volume: 57, Issue:3

    Topics: Diiodotyrosine; Goiter; Goiter, Endemic; Goiter, Nodular; Humans; Iodides; Metabolism, Inborn Errors; Monoiodotyrosine; Perchlorates; Peroxidases; Thyroid Gland; Thyroid Hormones

1971
A case of a partial defect of the iodide trapping mechanism.
    The Journal of clinical endocrinology and metabolism, 1970, Volume: 30, Issue:3

    Topics: Age Determination by Skeleton; Child; Congenital Hypothyroidism; Diiodotyrosine; Goiter; Humans; Iodides; Iodine Radioisotopes; Male; Metabolism, Inborn Errors; Microscopy, Electron; Monoiodotyrosine; Thyroglobulin; Thyroid Gland; Thyroxine

1970
[Hypothyroidism caused by congenital familial defect of iodotyrosine deiodation].
    Acta paediatrica Belgica, 1970, Volume: 24, Issue:2

    Topics: Female; Humans; Hypothyroidism; Male; Metabolism, Inborn Errors; Molecular Biology; Monoiodotyrosine; Thyroid Hormones; Tyrosine

1970
Defective deiodinase activity and abnormal thyroidal iodoproteins.
    The Journal of clinical endocrinology and metabolism, 1969, Volume: 29, Issue:9

    Topics: Autoradiography; Centrifugation, Density Gradient; Diiodotyrosine; Goiter; Humans; Hyperplasia; Hypothyroidism; In Vitro Techniques; Iodine; Iodine Isotopes; Iodoproteins; Metabolism, Inborn Errors; Monoiodotyrosine; Proteins; Thyroid Gland

1969
ABSENT AND DEFECTIVE IODOTYROSINE DEIODINATION IN A FAMILY SOME OF WHOSE MEMBERS ARE GOITROUS CRETINS.
    Lancet (London, England), 1965, Jan-23, Volume: 1, Issue:7378

    Topics: Adolescent; Congenital Hypothyroidism; Enzymes; Fluids and Secretions; Genetics, Medical; Goiter; Humans; Iodine Isotopes; Metabolism, Inborn Errors; Monoiodotyrosine; Thyroid Hormones; Thyroxine; Urine

1965