diiodotyrosine has been researched along with Cretinism in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 9 (69.23) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (15.38) | 29.6817 |
| 2010's | 1 (7.69) | 24.3611 |
| 2020's | 1 (7.69) | 2.80 |
| Authors | Studies |
|---|---|
| Abdullah, MA; Bertolini, A; Borsò, M; Bruellman, R; Dumitresu, AM; Furman, A; Refetoff, S; Saba, A; Shareef, R; Watanabe, Y; Weiss, RE; Zucchi, R | 1 |
| Cocho de Juan, JA; García-Nimo, L; Iglesias, A; Moreno, JC | 1 |
| Afink, G; Craen, M; de Randamie, J; Kulik, W; Overmars, H; Ris-Stalpers, C; van Cruchten, A; Veenboer, T | 1 |
| BLOCK, RJ; KASSENAAR, AA; MANDL, RH; WERNER, SC | 1 |
| BASTENIE, PA; DUMONT, JE; ERMANS, AM | 1 |
| RICCABONA, G | 1 |
| LINDEBOOM, GA; WIENER, JD | 1 |
| Baudon, JJ; Lagardère, B; Léger, A; Raux, MC | 1 |
| Fukata, S; Hishinuma, A; Ieiri, T; Kiwaki, K; Nishi, Y | 1 |
| Jones, B; Jones, JE; Lizarralde, G; Seal, US | 1 |
| Stanbury, JB | 1 |
| Alexander, NM; Burrow, GN | 1 |
| Bechet, MM; Bismuth, J; Koutras, DA; Lissitzky, S; Malamos, B; Matsaniotis, N; Moschos, A; Papadopoulos, SN; Vagenakis, AG | 1 |
3 review(s) available for diiodotyrosine and Cretinism
| Article | Year |
|---|---|
Towards the pre-clinical diagnosis of hypothyroidism caused by iodotyrosine deiodinase (DEHAL1) defects.
Topics: Biomarkers; Congenital Hypothyroidism; Diiodotyrosine; Genotype; Humans; Hydrolases; Hypothyroidism; Infant, Newborn; Iodide Peroxidase; Iodides; Membrane Proteins; Monoiodotyrosine; Neonatal Screening; Phenotype; Prevalence | 2014 |
[Iodide organification defect].
Topics: Congenital Hypothyroidism; Diagnosis, Differential; Diiodotyrosine; Dual Oxidases; Flavoproteins; Humans; Infant, Newborn; Iodide Peroxidase; Iodine; Mutation; NADPH Oxidases; Neonatal Screening; Prognosis; Thyroid Hormones | 2006 |
Radioisotopes in the diagnosis of hypothyroid states, iodine deficiency, and thyroiditis.
Topics: Adolescent; Blood Protein Disorders; Child, Preschool; Chile; Congenital Hypothyroidism; Congo; Deficiency Diseases; Diiodotyrosine; Humans; Hypothyroidism; Iodides; Iodine; Iodine Radioisotopes; Male; Metabolic Diseases; Peroxidases; Radionuclide Imaging; Serum Albumin; Thyroid Function Tests; Thyroid Gland; Thyroiditis; Tyrosine; Venezuela | 1965 |
10 other study(ies) available for diiodotyrosine and Cretinism
| Article | Year |
|---|---|
Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C).
Topics: Congenital Hypothyroidism; Diiodotyrosine; Humans; Iodide Peroxidase; Monoiodotyrosine; Mutation | 2023 |
Molecular characterization of iodotyrosine dehalogenase deficiency in patients with hypothyroidism.
Topics: Adolescent; Adult; Amino Acid Sequence; Calibration; Cell Line; Chromatography, High Pressure Liquid; Congenital Hypothyroidism; Diiodotyrosine; DNA Mutational Analysis; Female; Goiter; Humans; Hydrolases; Male; Membrane Proteins; Molecular Sequence Data; Monoiodotyrosine; Mutation, Missense; Phenotype; Plasmids; Reference Standards; Reproducibility of Results; Thyroglobulin; Thyroid Hormones; Transfection; Young Adult | 2008 |
Pathogenesis of a case of congenital goiter with abnormally high levels of SPI and with mono- and diiodotyrosine in the serum.
Topics: Congenital Hypothyroidism; Diiodotyrosine; Goiter; Humans; Infant, Newborn; Infant, Newborn, Diseases; Iodine; Tyrosine | 1957 |
THYROID FUNCTION IN A GOITER ENDEMIC. V. MECHANISM OF THYROID FAILURE IN THE UELE ENDEMIC CRETINS.
Topics: Chromatography; Congenital Hypothyroidism; Congo; Diiodotyrosine; Goiter; Iodides; Iodine Isotopes; Metabolism; Saliva; Thiocyanates; Thyroid Function Tests; Thyrotropin; Thyroxine; Triiodothyronine; Tyrosine | 1963 |
[IOSINE-TYROSYL COUPLING DEFECT IN CONGENITAL HYPOTHYROIDISM WITH GOITER].
Topics: Child; Congenital Hypothyroidism; Diiodotyrosine; Goiter; Humans; Hypothyroidism; Iodine; Iodine Isotopes; Metabolism; Thyroglobulin; Thyronines; Tyrosine | 1964 |
THE POSSIBLE OCCURRENCE OF TWO INBORN ERRORS OF IODINE METABOLISM IN ONE PATIENT.
Topics: Adolescent; Child; Congenital Hypothyroidism; Diiodotyrosine; Electrophoresis; Goiter; Humans; Iodides; Iodine; Metabolism, Inborn Errors; Thyroglobulin; Thyroid Function Tests; Thyroxine; Triiodothyronine; Tyrosine; Urine | 1964 |
[Congenital disorder of thyroid hormonegenesis with abnormal synthesis of iodohistidines].
Topics: Congenital Hypothyroidism; Diiodotyrosine; Female; Goiter; Humans; Hypothyroidism; Infant; Infant, Newborn; Iodine Radioisotopes; Iodoproteins; Male; Metabolic Clearance Rate; Monoiodotyrosine; Radioimmunoassay; Thyroglobulin; Thyroid Function Tests; Thyrotropin; Triiodothyronine | 1976 |
Goitrous cretinism with chromosomal aberration and defect in thyroglobulin synthesis.
Topics: Adult; Amino Acid Metabolism, Inborn Errors; Chromatography, Gel; Chromosome Aberrations; Chromosome Disorders; Congenital Hypothyroidism; Diiodotyrosine; Goiter; Humans; Immunodiffusion; Iodine Radioisotopes; Male; Mosaicism; Thyroglobulin; Thyroid Function Tests; Thyroxine; Triiodothyronine; Tyrosine; Ultracentrifugation | 1966 |
Thyroxine biosynthesis in human goitrous cretinism.
Topics: Adult; Centrifugation, Density Gradient; Chromatography, DEAE-Cellulose; Congenital Hypothyroidism; Diiodotyrosine; Female; Goiter; Humans; Immunoelectrophoresis; Iodoproteins; Ketoglutaric Acids; Male; Middle Aged; Mitochondria; Monoiodotyrosine; Peptide Hydrolases; Peroxidases; Thyroglobulin; Thyroid Function Tests; Thyrotropin; Thyroxine; Thyroxine-Binding Proteins; Transaminases; Tyrosine Transaminase | 1970 |
A case of a partial defect of the iodide trapping mechanism.
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 |