iodine has been researched along with Cochlear Hearing Loss 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..
| Excerpt | Relevance | Reference |
|---|---|---|
| "Slc26a4 (-/-) and (+/+) mice were fed up to 6 months on a standard or low iodine diet and were evaluated for thyroid structural abnormalities or biochemical hypothyroidism." | 7.77 | Absence of primary hypothyroidism and goiter in Slc26a4 (-/-) mice fed on a low iodine diet. ( Bonomi, M; Bottà, G; Calebiro, D; De Nittis, D; Fugazzola, L; Grindati, A; Lisi, S; Marinò, M; Persani, L; Porazzi, P, 2011) |
| "Pendred Syndrome, first described in 1896, is phenotypically characterized as the coexistence of sensorineural deafness and enlarged goiter with elevated iodine discharge after perchlorate administration." | 4.82 | Pendred syndrome. ( Glaser, B, 2003) |
| "Slc26a4 (-/-) and (+/+) mice were fed up to 6 months on a standard or low iodine diet and were evaluated for thyroid structural abnormalities or biochemical hypothyroidism." | 3.77 | Absence of primary hypothyroidism and goiter in Slc26a4 (-/-) mice fed on a low iodine diet. ( Bonomi, M; Bottà, G; Calebiro, D; De Nittis, D; Fugazzola, L; Grindati, A; Lisi, S; Marinò, M; Persani, L; Porazzi, P, 2011) |
| "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) |
| "Pendred syndrome is an autosomal recessive inherited disorder characterized by profound hearing impairment and inappropriate iodine release by the thyroid on perchlorate challenge." | 3.72 | Neuro-otological findings in Pendred syndrome. ( Britton, KE; Coffey, RA; Cohen, M; Jan, H; Luxon, LM; Phelps, PD; Reardon, W; Trembath, RC, 2003) |
| "Pendred syndrome is an autosomal recessive disorder that is classically defined by the combination of sensorineural deafness/hearing impairment, goiter, and an abnormal organification of iodide with or without hypothyroidism." | 2.55 | Pendred syndrome. ( Kopp, P; Wémeau, JL, 2017) |
| "Pendred syndrome is often associated with inner ear malformations, especially enlarged vestibular aqueduct (EVA)." | 1.31 | Phenotypes associated with replacement of His by Arg in the Pendred syndrome gene. ( Furuhashi, A; Miura, Y; Mori, N; Murakami, H; Naganawa, S; Nakashima, T; Nakayama, A; Sato, E; Tadokoro, M, 2001) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (13.33) | 18.7374 |
| 1990's | 1 (6.67) | 18.2507 |
| 2000's | 10 (66.67) | 29.6817 |
| 2010's | 2 (13.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Wémeau, JL | 1 |
| Kopp, P | 2 |
| Calebiro, D | 1 |
| Porazzi, P | 1 |
| Bonomi, M | 1 |
| Lisi, S | 1 |
| Grindati, A | 1 |
| De Nittis, D | 1 |
| Fugazzola, L | 1 |
| Marinò, M | 1 |
| Bottà, G | 1 |
| Persani, L | 1 |
| Luxon, LM | 1 |
| Cohen, M | 1 |
| Coffey, RA | 1 |
| Phelps, PD | 1 |
| Britton, KE | 1 |
| Jan, H | 1 |
| Trembath, RC | 1 |
| Reardon, W | 1 |
| HENI, F | 1 |
| SIEBNER, H | 1 |
| Bogazzi, F | 1 |
| Russo, D | 1 |
| Raggi, F | 1 |
| Ultimieri, F | 1 |
| Berrettini, S | 1 |
| Forli, F | 1 |
| Grasso, L | 1 |
| Ceccarelli, C | 1 |
| Mariotti, S | 1 |
| Pinchera, A | 1 |
| Bartalena, L | 1 |
| Martino, E | 1 |
| Hiyoshi, M | 1 |
| Yamane, H | 1 |
| Glaser, B | 1 |
| Lai, CC | 1 |
| Chiu, CY | 1 |
| Shiao, AS | 1 |
| Tso, YC | 1 |
| Wu, YC | 1 |
| Tu, TY | 1 |
| Jap, TS | 1 |
| Palos, F | 1 |
| García-Rendueles, ME | 1 |
| Araujo-Vilar, D | 1 |
| Obregon, MJ | 1 |
| Calvo, RM | 1 |
| Cameselle-Teijeiro, J | 1 |
| Bravo, SB | 1 |
| Perez-Guerra, O | 1 |
| Loidi, L | 1 |
| Czarnocka, B | 1 |
| Alvarez, P | 1 |
| Refetoff, S | 1 |
| Dominguez-Gerpe, L | 1 |
| Alvarez, CV | 1 |
| Lado-Abeal, J | 1 |
| Scott, DA | 1 |
| Wang, R | 1 |
| Kreman, TM | 1 |
| Andrews, M | 1 |
| McDonald, JM | 1 |
| Bishop, JR | 1 |
| Smith, RJ | 1 |
| Karniski, LP | 1 |
| Sheffield, VC | 1 |
| Bidart, JM | 1 |
| Lacroix, L | 1 |
| Evain-Brion, D | 1 |
| Caillou, B | 1 |
| Lazar, V | 1 |
| Frydman, R | 1 |
| Bellet, D | 1 |
| Filetti, S | 1 |
| Schlumberger, M | 1 |
| Gao, H | 1 |
| Li, J | 1 |
| Wang, E | 1 |
| Gonzalez Trevino, O | 1 |
| Karamanoglu Arseven, O | 1 |
| Ceballos, CJ | 1 |
| Vives, VI | 1 |
| Ramirez, RC | 1 |
| Gomez, VV | 1 |
| Medeiros-Neto, G | 1 |
| Sato, E | 1 |
| Nakashima, T | 1 |
| Miura, Y | 1 |
| Furuhashi, A | 1 |
| Nakayama, A | 1 |
| Mori, N | 1 |
| Murakami, H | 1 |
| Naganawa, S | 1 |
| Tadokoro, M | 1 |
| Boyages, SC | 1 |
| Collins, JK | 1 |
| Maberly, GF | 1 |
| Jupp, JJ | 1 |
| Morris, J | 1 |
| Eastman, CJ | 1 |
2 reviews available for iodine and Cochlear Hearing Loss
| Article | Year |
|---|---|
Pendred syndrome.
Topics: Anoctamin-1; Goiter, Nodular; Hearing Loss, Sensorineural; Humans; Hypothyroidism; Iodides; Iodine; | 2017 |
Pendred syndrome.
Topics: Biological Transport; Goiter; Hearing Loss, Sensorineural; Humans; Iodine; Membrane Transport Protei | 2003 |
13 other studies available for iodine and Cochlear Hearing Loss
| Article | Year |
|---|---|
Absence of primary hypothyroidism and goiter in Slc26a4 (-/-) mice fed on a low iodine diet.
Topics: Animals; Anion Transport Proteins; Diet; Disease Models, Animal; Goiter; Goiter, Nodular; Hearing Lo | 2011 |
Neuro-otological findings in Pendred syndrome.
Topics: Adolescent; Adult; Audiometry, Pure-Tone; Child; Ear, Inner; Female; Hearing Loss, Sensorineural; Hu | 2003 |
[STRUCTURAL AND NUMERICAL CHROMOSOME PATTERN (GROUP A AND E) IN A GIRL WITH THE PENDRED SYNDROME].
Topics: Adolescent; Cell Division; Chromosome Aberrations; Chromosome Disorders; Chromosomes; Dwarfism; Fema | 1963 |
Mutations in the SLC26A4 (pendrin) gene in patients with sensorineural deafness and enlarged vestibular aqueduct.
Topics: Adolescent; Adult; Audiometry; Child; DNA; Female; Goiter; Hearing Loss, Sensorineural; Humans; Iodi | 2004 |
A pedigree with Pendred syndrome: case report and discussion on hereditary hearing loss.
Topics: Consanguinity; Female; Genes, Recessive; Goiter; Hearing Loss, Sensorineural; Humans; Iodine; Membra | 2004 |
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 |
Pendred syndrome in two Galician families: insights into clinical phenotypes through cellular, genetic, and molecular studies.
Topics: Adult; Amino Acid Sequence; Female; Goiter, Nodular; Haplotypes; Hearing Loss, Sensorineural; Humans | 2008 |
Functional differences of the PDS gene product are associated with phenotypic variation in patients with Pendred syndrome and non-syndromic hearing loss (DFNB4).
Topics: Alleles; Amino Acid Substitution; Animals; Carrier Proteins; Female; Genetic Variation; Goiter; Hear | 2000 |
Expression of Na+/I- symporter and Pendred syndrome genes in trophoblast cells.
Topics: Carrier Proteins; Cells, Cultured; Chorionic Gonadotropin; Female; Goiter; Hearing Loss, Bilateral; | 2000 |
[Iodine deficiency and perceptive nerve deafness].
Topics: Adolescent; Child; Child, Preschool; Female; Hair; Hearing Loss, Sensorineural; Humans; Iodine; Male | 1998 |
Clinical and molecular analysis of three Mexican families with Pendred's syndrome.
Topics: Adolescent; Child; Female; Goiter; Haplotypes; Hearing Loss, Sensorineural; Humans; Iodides; Iodine; | 2001 |
Phenotypes associated with replacement of His by Arg in the Pendred syndrome gene.
Topics: Adolescent; Adult; Alleles; Amino Acid Substitution; Arginine; Carrier Proteins; Child; Endolymphati | 2001 |
Iodine deficiency impairs intellectual and neuromotor development in apparently-normal persons. A study of rural inhabitants of north-central China.
Topics: Adolescent; Adult; Audiometry; Child; China; Cognition Disorders; Cohort Studies; Congenital Hypothy | 1989 |