perchlorate has been researched along with Cretinism in 5 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (20.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 4 (80.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Khan, A; Khan, AU; Khan, K; Khan, SU; Ullah, H | 1 |
Adalet, I; Bakir, B; Baş, F; Darendeliler, F; Kuyumcu, S; Sanli, Y; Tamam, M; Türkmen, C | 1 |
BASCHIERI, L; BENEDETTI, G; DELUCA, F; NEGRI, M | 1 |
Beccaria, L; Beck-Peccoz, P; Carletto, M; Cortinovis, F; Fugazzola, L; Longari, V; Mannavola, D; Persani, L; Vannucchi, G; Vigone, MC; Weber, G | 1 |
Chiesa, A; González-Sarmiento, R; Gruñeiro-Papendieck, L; Louis-Tisserand, M; Rivolta, CM; Targovnik, HM; Varela, V | 1 |
5 other study(ies) available for perchlorate and Cretinism
Article | Year |
---|---|
Thyroid dyshormonogenesis detected through a modified perchlorate discharge test using a gamma-camera.
Topics: Child; Child, Preschool; Congenital Hypothyroidism; Gamma Cameras; Humans; Male; Perchlorates; Radionuclide Imaging; Thyroid Diseases | 2009 |
Diagnostic spectrum of congenital hypothyroidism in Turkish children.
Topics: Child; Congenital Hypothyroidism; Diagnosis, Differential; Female; Humans; Male; Perchlorates; Radionuclide Imaging; Thyroid Gland; Thyrotropin; Turkey; Ultrasonography, Doppler, Color | 2009 |
EVALUATION AND LIMITATIONS OF THE PERCHLORATE TEST IN THE STUDY OF THYROID FUNCTION.
Topics: Congenital Hypothyroidism; Deafness; Down Syndrome; Goiter; Heart Defects, Congenital; Humans; Intellectual Disability; Iodine Isotopes; Laurence-Moon Syndrome; Perchlorates; Pharmacology; Thyroid Function Tests | 1963 |
Thyroid scintigraphy and perchlorate test after recombinant human TSH: a new tool for the differential diagnosis of congenital hypothyroidism during infancy.
Topics: Child; Child, Preschool; Congenital Hypothyroidism; Female; Humans; Infant; Iodides; Iodine Radioisotopes; Male; Perchlorates; Radionuclide Imaging; Recombinant Proteins; Thyroid Neoplasms; Thyrotropin; Thyroxine; Time Factors | 2007 |
Two compound heterozygous mutations (c.215delA/c.2422T-->C and c.387delC/c.1159G-->A) in the thyroid peroxidase gene responsible for congenital goitre and iodide organification defect.
Topics: Amino Acid Sequence; Animals; Base Sequence; Congenital Hypothyroidism; Female; Genes, Recessive; Heterozygote; Humans; Iodide Peroxidase; Iodides; Membrane Proteins; Molecular Sequence Data; Mutation; Pedigree; Perchlorates; Polymorphism, Single-Stranded Conformational; Protein Structure, Secondary; Protein Structure, Tertiary; Sequence Analysis, DNA; Sequence Homology | 2007 |