iodine has been researched along with Abnormalities, Multiple in 15 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..
Abnormalities, Multiple: Congenital abnormalities that affect more than one organ or body structure.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Pendred syndrome (PS) is an autosomal recessive disease that is characterized by congenital sensorineural hearing loss, goiter, and a partial iodine organification defect." | 3.74 | Analysis of the SLC26A4 gene in patients with Pendred syndrome in Taiwan. ( Chiu, CY; Jap, TS; Lai, CC; Shiao, AS; Tso, YC; Tu, TY; Wu, YC, 2007) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 10 (66.67) | 18.7374 |
| 1990's | 2 (13.33) | 18.2507 |
| 2000's | 1 (6.67) | 29.6817 |
| 2010's | 1 (6.67) | 24.3611 |
| 2020's | 1 (6.67) | 2.80 |
| Authors | Studies |
|---|---|
| Asakura, Y | 1 |
| Narumi, S | 1 |
| Muroya, K | 1 |
| Fujita, K | 1 |
| Aida, N | 1 |
| Hasagawa, T | 1 |
| Adachi, M | 1 |
| STANBURY, JB | 1 |
| OHELA, K | 1 |
| PITT-RIVERS, R | 1 |
| GARDNER, JU | 1 |
| HAYLES, AB | 1 |
| WOOLNER, LB | 1 |
| OWEN, CA | 1 |
| REINWEIN, D | 1 |
| KLEIN, E | 1 |
| Lai, CC | 1 |
| Chiu, CY | 1 |
| Shiao, AS | 1 |
| Tso, YC | 1 |
| Wu, YC | 1 |
| Tu, TY | 1 |
| Jap, TS | 1 |
| Held, KR | 1 |
| Cruz, ME | 1 |
| Moncayo, F | 1 |
| Jones, WS | 1 |
| Man, EB | 1 |
| Konigsmark, BW | 1 |
| Fraser, GR | 1 |
| Lenz, W | 1 |
| Mentzel, J | 1 |
| Wetzig, T | 1 |
| Rütten, A | 1 |
| Hörtnagel, K | 1 |
| Tischkowitz, M | 1 |
| Ziemer, M | 1 |
| Dumur, V | 1 |
| Gervais, R | 1 |
| Rigot, JM | 1 |
| Delomel-Vinner, E | 1 |
| Lafitte, JJ | 1 |
| Roussel, P | 1 |
| Silverman, BL | 1 |
| Lloyd-Still, JD | 1 |
| Hazinski, TA | 1 |
| Hunt, CE | 1 |
| Cat, I | 1 |
| Costa, O | 1 |
| Freire-Maia, N | 1 |
| Pavone, L | 1 |
| Zellweger, H | 1 |
| Abbo, G | 1 |
| Gauchat, R | 1 |
| Knecht, B | 1 |
1 review available for iodine and Abnormalities, Multiple
| Article | Year |
|---|---|
Hereditary deafness in man.
Topics: Abnormalities, Multiple; Amyloidosis; Blood Proteins; Bone Diseases; Craniofacial Dysostosis; Deafne | 1969 |
14 other studies available for iodine and Abnormalities, Multiple
| Article | Year |
|---|---|
A patient with Pendred syndrome whose goiter progressed with normal serum thyrotropin and iodine organification.
Topics: Abnormalities, Multiple; Adolescent; Adult; Amino Acid Sequence; Base Sequence; Child; Child, Presch | 2010 |
The metabolism of iodine in 2 goitrous cretins compared with that in 2 patients receiving methimazole.
Topics: Abnormalities, Multiple; Antithyroid Agents; Congenital Hypothyroidism; Humans; Iodine; Iodine Radio | 1955 |
Iodine metabolism in goitrous cretins.
Topics: Abnormalities, Multiple; Congenital Hypothyroidism; Humans; Iodine; Minerals; Syndrome | 1959 |
[A SPECIAL FORM OF IODINE USE IN SPORADIC CRETINISM. CLINICAL AND BIOCHEMICAL STUDY RESULTS].
Topics: Abnormalities, Multiple; Congenital Hypothyroidism; Goiter; Humans; Iodides; Iodine; Syndrome | 1963 |
Analysis of the SLC26A4 gene in patients with Pendred syndrome in Taiwan.
Topics: Abnormalities, Multiple; Adolescent; Adult; Base Sequence; Case-Control Studies; Child; DNA Mutation | 2007 |
Clinical pattern and the genetics of the fetal iodine deficiency disorder (endemic cretinism): results of a field study in Highland Ecuador.
Topics: Abnormalities, Multiple; Anthropometry; Congenital Hypothyroidism; Deafness; Dermatoglyphics; Ecuado | 1990 |
Thyroid function in human pregnancy. VI. Premature deliveries and reproductive failures of pregnant women with low serum butanol-extractable iodines. Maternal serum TBG and TBPA capacities.
Topics: Abnormalities, Multiple; Adolescent; Adult; Birth Weight; Female; Fetal Death; Fetal Diseases; Goite | 1969 |
The causes of profound deafness in childhood. In: Sensorinerual hearing loss.
Topics: Abnormalities, Multiple; Audiometry; Birth Weight; Child; Child, Preschool; Chromosome Aberrations; | 1970 |
Phenocopy.
Topics: Abnormalities, Multiple; Anemia, Aplastic; Arm; Congenital Hypothyroidism; Deafness; Female; Feminiz | 1970 |
Sweat duct proliferation associated with aggregation of elastic tissue and atrophodermia vermiculata: a simulator of microcystic adnexal carcinoma - a family with MALTA-syndrome.
Topics: Abnormalities, Multiple; Cell Proliferation; Darier Disease; Elastic Tissue; Eyebrows; Humans; Malta | 2021 |
Congenital bilateral absence of vas deferens in absence of cystic fibrosis.
Topics: Abnormalities, Multiple; Adult; Chlorides; Cystic Fibrosis; Humans; Infertility, Male; Kidney; Male; | 1995 |
Increased sweat chloride levels associated with prostaglandin E1 infusion.
Topics: Abnormalities, Multiple; Alprostadil; Chlorides; Cystic Fibrosis; Humans; Infant, Newborn; Long-Term | 1985 |
Odontotrichomelic hypohidrotic dysplasia. A clinical reappraisal.
Topics: Abnormalities, Multiple; Arm; Breast; Child; Cleft Lip; Ear; Ectodermal Dysplasia; Face; Female; Hai | 1972 |
A case of trisomy 18 mosaicism with peculiar features.
Topics: Abnormalities, Multiple; Chlorides; Chromatids; Chromosome Aberrations; Chromosome Disorders; Female | 1970 |