Page last updated: 2024-10-18

iodine and Genetic Diseases

iodine has been researched along with Genetic Diseases in 3 studies

Iodine: A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
diiodine : Molecule comprising two covalently bonded iodine atoms with overall zero charge..

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Brent, RL1
Langer, P1
Tajtakova, M1
Kocan, A1
Drobna, B1
Kostalova, L1
Fodor, G1
Klimes, I1
Beckmann, G1

Other Studies

3 other studies available for iodine and Genetic Diseases

ArticleYear
The role of the pediatrician in preventing congenital malformations.
    Pediatrics in review, 2011, Volume: 32, Issue:10

    Topics: Abnormalities, Drug-Induced; Congenital Abnormalities; Down Syndrome; Environmental Exposure; Female

2011
Thyroid volume, iodine intake, autoimmune thyroid disorders, inborn factors, and endocrine disruptors: twenty-year studies of multiple effects puzzle in Slovakia.
    Endocrine regulations, 2012, Volume: 46, Issue:4

    Topics: Adolescent; Adult; Aged; Autoimmune Diseases; Child; Deficiency Diseases; Eating; Endocrine Disrupto

2012
[Etiologic problems of hearing disorders in "risk children"].
    HNO, 1969, Volume: 17, Issue:8

    Topics: Abnormalities, Drug-Induced; Chromosome Aberrations; Chromosome Disorders; Consanguinity; Deafness;

1969