iodine and Syndrome
iodine has been researched along with Syndrome in 83 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..
Syndrome: A characteristic symptom complex.
Research Excerpts
| Excerpt | Relevance | Reference |
|---|---|---|
| "It is very important to diagnose correctly the etiology of thyrotoxicosis, because the course and treatment of thyrotoxicosis with low radioactive iodine uptake differ significantly from that of hyperthyroidism due to Graves' disease or toxic nodular goiter." | 8.80 | Syndromes of thyrotoxicosis with low radioactive iodine uptake. ( Ross, DS, 1998) |
| " The dose-response relationship between feed intake, liver hemorrhagic score and liver lipid content was again demonstrated." | 5.25 | Effect of inositol, lecithin, vitamins (B12 with choline and E), and iodinated casein on induced fatty liver-hemorrhagic syndrome in laying chickens. ( Polin, D; Wolford, JH, 1975) |
| "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) |
| "It is very important to diagnose correctly the etiology of thyrotoxicosis, because the course and treatment of thyrotoxicosis with low radioactive iodine uptake differ significantly from that of hyperthyroidism due to Graves' disease or toxic nodular goiter." | 4.80 | Syndromes of thyrotoxicosis with low radioactive iodine uptake. ( Ross, DS, 1998) |
| "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) |
| "Endemic cretinism is the most severe manifestation of dietary iodine deficiency." | 3.68 | The neurology of endemic cretinism. A study of two endemias. ( Boyages, SC; Collins, JK; Eastman, CJ; Halpern, JP; Maberly, GF; Morris, JG, 1991) |
| " This was not considered to be a factor in the present case since the discovery of a goitre in the patient in association with an iodine dysfunction uncovered a Pendred's syndrome as the cause for the patient's hearing loss." | 3.65 | [A medical-legal question of hearing impairment following vaccination (author's transl)]. ( von Deuster, C, 1976) |
| " The differentiation is easily made if a goiter is discernible, but if it is not, radioiodine uptake should be measured, for in this condition the uptake is normal or greater." | 3.64 | Sporadic goitrous cretinism. ( MOSIER, HD, 1959) |
| "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) |
| "Careful evaluation of the varieties of cluster headache and trigeminal neuralgia, and the reporting of similar new cases as they arise are necessary to establish the nosologic boundaries of this syndrome." | 1.28 | Short-lasting unilateral neuralgiform headache attacks with tearing and conjunctival injection: the first "symptomatic" case? ( Bussone, G; Dalla Volta, G; Di Monda, V; Gasparotti, R; Leone, M; Strada, L, 1991) |
| "It was also found that in patients with cerebrovascular insufficiency accompanied by thyroid gland dysfunctions the clinical picture becomes more aggravated." | 1.26 | [Role of thyroid gland dysfunction in the pathogenesis and course of cerebral circulatory disorders]. ( Buletsa, BA; Fabri, ZI; Litvinova, LA; Pashchenko, AE; Semenchuk, MM, 1978) |
| "Hypothyroidism was secondary to an isolated defect in TSH, and a TRH stimulation test did not induce an increase in plasma TSH." | 1.26 | [Albright's type II osteodystrophy and hypothyroidism due to TSH deficiency. Apropos of a case in a child]. ( David, M; Floret, D; Jeune, M; Madjar, JJ; Sann, L; Terrier, M, 1977) |
| " The dose-response relationship between feed intake, liver hemorrhagic score and liver lipid content was again demonstrated." | 1.25 | Effect of inositol, lecithin, vitamins (B12 with choline and E), and iodinated casein on induced fatty liver-hemorrhagic syndrome in laying chickens. ( Polin, D; Wolford, JH, 1975) |
| "Pendred's syndrome is reported in three siblings." | 1.25 | Pituitary-thyroid function in Pendred's syndrome. ( Evered, DC; Gomez-Pan, A; Hall, R, 1974) |
Research
Studies (83)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 50 (60.24) | 18.7374 |
| 1990's | 13 (15.66) | 18.2507 |
| 2000's | 15 (18.07) | 29.6817 |
| 2010's | 5 (6.02) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
Authors
| Authors | Studies |
|---|---|
| Wémeau, JL | 2 |
| Kopp, P | 3 |
| Macías, EM | 1 |
| Muñoz-Bellido, FJ | 1 |
| Velasco, A | 1 |
| Moreno, E | 1 |
| Dávila, I | 1 |
| Bizhanova, A | 1 |
| Asakura, Y | 1 |
| Narumi, S | 1 |
| Muroya, K | 1 |
| Fujita, K | 1 |
| Aida, N | 1 |
| Hasagawa, T | 1 |
| Adachi, M | 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 |
| ZARA, M | 1 |
| CHIMENES, H | 1 |
| GALI, P | 1 |
| STANBURY, JB | 2 |
| OHELA, K | 1 |
| PITT-RIVERS, R | 1 |
| ABALLI, AJ | 1 |
| COSTALES, F | 1 |
| PRENDES, Z | 1 |
| SCHULTZ, AL | 1 |
| FLINK, EB | 1 |
| KENNEDY, BJ | 1 |
| ZIEVE, L | 1 |
| CASSANO, C | 1 |
| BASCHIERI, L | 1 |
| ANDREANI, D | 1 |
| MOSIER, HD | 1 |
| GARDNER, JU | 1 |
| HAYLES, AB | 1 |
| WOOLNER, LB | 1 |
| OWEN, CA | 1 |
| CHAVARRIA, C | 1 |
| MUNOS-FERREIRA, G | 1 |
| GUEVARA, G | 1 |
| RUPP, JJ | 1 |
| PASCHKIS, KE | 1 |
| DEGROOT, LJ | 2 |
| von HARNACK, G | 1 |
| HORST, W | 1 |
| LENZ, W | 1 |
| REINWEIN, D | 1 |
| KLEIN, E | 1 |
| CURZON, G | 1 |
| WALD, I | 1 |
| KVICALA, V | 1 |
| KOLAR, M | 1 |
| Hiyoshi, M | 1 |
| Yamane, H | 1 |
| Glaser, B | 2 |
| 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 | 2 |
| Dominguez-Gerpe, L | 1 |
| Alvarez, CV | 1 |
| Lado-Abeal, J | 1 |
| Medeiros-Neto, G | 2 |
| McCoy, MA | 1 |
| Smyth, JA | 1 |
| Ellis, WA | 1 |
| Kennedy, DG | 1 |
| al-Jaberi, TM | 1 |
| Hussein, AD | 1 |
| Heis, HA | 1 |
| Sheffield, VC | 1 |
| Kraiem, Z | 1 |
| Beck, JC | 1 |
| Nishimura, D | 1 |
| Stone, EM | 1 |
| Salameh, M | 1 |
| Sadeh, O | 1 |
| Ross, DS | 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 |
| Gonzalez Trevino, O | 1 |
| Karamanoglu Arseven, O | 1 |
| Ceballos, CJ | 1 |
| Vives, VI | 1 |
| Ramirez, RC | 1 |
| Gomez, VV | 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 |
| Vlaeminck-Guillem, V | 1 |
| Dubrulle, F | 1 |
| Dumur, V | 1 |
| Vincent, C | 1 |
| von Deuster, C | 1 |
| Wolford, JH | 1 |
| Polin, D | 1 |
| Buletsa, BA | 1 |
| Pashchenko, AE | 1 |
| Fabri, ZI | 1 |
| Litvinova, LA | 1 |
| Semenchuk, MM | 1 |
| Niepomniszcze, H | 1 |
| Coleoni, AH | 1 |
| Degrossi, OJ | 1 |
| Scavini, LM | 1 |
| Curutchet, HP | 1 |
| David, M | 1 |
| Madjar, JJ | 1 |
| Floret, D | 1 |
| Sann, L | 1 |
| Terrier, M | 1 |
| Jeune, M | 1 |
| Chan, V | 1 |
| Wang, C | 1 |
| Yeung, RT | 1 |
| Harms, RH | 1 |
| Roland, DA | 1 |
| Simpson, CF | 1 |
| Mutiga, ER | 1 |
| Hornabrook, RW | 1 |
| Kapoor, A | 1 |
| Godbole, M | 1 |
| Chauhan, S | 1 |
| Ghosh, BK | 1 |
| Rao, B | 1 |
| Crisalli, M | 1 |
| Chiossi, FM | 1 |
| Monteverde, R | 1 |
| Scafidi, M | 1 |
| Cave, WT | 1 |
| Dunn, JT | 1 |
| Halpern, JP | 1 |
| Boyages, SC | 1 |
| Maberly, GF | 1 |
| Collins, JK | 1 |
| Eastman, CJ | 1 |
| Morris, JG | 1 |
| Herrero, C | 1 |
| Font, J | 1 |
| Bielsa, I | 1 |
| Coca, A | 1 |
| Lamberg, BA | 1 |
| Gomez-Pan, A | 1 |
| Evered, DC | 1 |
| Hall, R | 1 |
| Illum, P | 1 |
| Kiaer, HW | 1 |
| Hvidberg-Hansen, J | 1 |
| Sondergaard, G | 1 |
| Purves, RD | 1 |
| Desai, KB | 1 |
| Mehta, MN | 1 |
| Patel, MC | 1 |
| Ramanna, L | 1 |
| Ganatra, RD | 1 |
| Fielden, ED | 1 |
| Macmillan, KL | 1 |
| Watson, JD | 1 |
| Bastenie, PA | 1 |
| Ectors, M | 1 |
| Thys, JP | 1 |
| Vanhaelst, L | 1 |
| Muri, P | 1 |
| Benard, B | 1 |
| DeWind, LT | 1 |
| Leon, HA | 1 |
| Brooksby, GA | 1 |
| Chackerian, MJ | 1 |
| Staley, RW | 1 |
| Williams, SN | 1 |
| Nussbaum, E | 1 |
| Chin, TW | 1 |
| Do, PC | 1 |
| Singh, KE | 1 |
| Randhawa, I | 1 |
| Eisenhardt, S | 1 |
| Fleckenstein, J | 1 |
| Brown, SM | 1 |
| Buchdahl, R | 1 |
| FANCONI, A | 1 |
| PRADER, A | 1 |
| ISLER, W | 1 |
| LUETHY, F | 1 |
| SIEBENMANN, R | 1 |
| DAVIES, DF | 1 |
| CLARK, HE | 1 |
| Xiaoming, S | 1 |
| Du, Y | 1 |
| Shi, X | 1 |
| Hussain, W | 1 |
| Layton, A | 1 |
| Baral, V | 1 |
| Connett, G | 1 |
| DEGOS, R | 1 |
| Stern, RC | 1 |
| Boat, TF | 1 |
| Doershuk, CF | 1 |
| Hillemeier, AC | 1 |
| Hen, J | 1 |
| Riely, CA | 1 |
| Dolan, TF | 1 |
| Gryboski, JD | 1 |
| Rosenstein, BJ | 1 |
| Langbaum, TS | 1 |
| Feingold, M | 1 |
| Bartoshesky, L | 1 |
| Geis, N | 1 |
| Ruocco, V | 1 |
| Florio, M | 1 |
| Polack, FP | 1 |
| Transue, DJ | 1 |
| Belknap, WM | 1 |
| Freij, BJ | 1 |
| Aughton, DJ | 1 |
| Leonard, NJ | 1 |
| Hughes, HE | 1 |
| Main, KM | 1 |
| Price, DA | 1 |
| Savage, MO | 1 |
| Skakkebae, NE | 1 |
| Mitchell, SC | 2 |
| Zhang, A | 1 |
| Smith, RL | 1 |
| Kumar, SA | 1 |
| Lester, MR | 1 |
| Bratton, DL | 1 |
| Cesur, Y | 1 |
| Bereket, A | 1 |
| Anadol, D | 1 |
| Kiper, N | 1 |
| Gocmen, A | 1 |
| Yordam, N | 1 |
| Rosenfeld, R | 1 |
| Spigelblatt, L | 1 |
| Chicoine, R | 1 |
| Bussone, G | 1 |
| Leone, M | 1 |
| Dalla Volta, G | 1 |
| Strada, L | 1 |
| Gasparotti, R | 1 |
| Di Monda, V | 1 |
| Schanker, HM | 1 |
| Rajfer, J | 1 |
| Saxon, A | 1 |
| Hopkins, A | 1 |
| Neville, B | 1 |
| Bannister, R | 1 |
| Ostrzeński, A | 1 |
| Cat, I | 1 |
| Costa, O | 1 |
| Freire-Maia, N | 1 |
Clinical Trials (1)
Trial Overview
| Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
|---|---|---|---|---|---|---|---|
| Study on the Compensatory Mechanism of Iodine Nutrition and the Optimal Intake Level of Lactating Women[NCT04492657] | 600 participants (Anticipated) | Observational | 2020-01-01 | Recruiting | |||
| [information is prepared from clinicaltrials.gov, extracted Sep-2024] | |||||||
Reviews
11 reviews available for iodine and Syndrome
| Article | Year |
|---|---|
Pendred syndrome.
Topics: Anoctamin-1; Goiter, Nodular; Hearing Loss, Sensorineural; Humans; Hypothyroidism; Iodides; Iodine; | 2017 |
Minireview: The sodium-iodide symporter NIS and pendrin in iodide homeostasis of the thyroid.
Topics: Animals; Gene Expression Regulation; Homeostasis; Humans; Iodine; Membrane Transport Proteins; Metab | 2009 |
Pendred syndrome.
Topics: Biological Transport; Goiter; Hearing Loss, Sensorineural; Humans; Iodine; Membrane Transport Protei | 2003 |
Unusual manifestations of thyrotoxicosis.
Topics: Adenocarcinoma; Dexamethasone; Female; Glycoprotein Hormones, alpha Subunit; Humans; Hyperthyroidism | 1983 |
Syndromes of thyrotoxicosis with low radioactive iodine uptake.
Topics: Humans; Hyperthyroidism; Iodine; Iodine Radioisotopes; Syndrome; Thyroiditis, Subacute; Thyrotoxicos | 1998 |
[Pendred's syndrome. Current features].
Topics: Carrier Proteins; Deafness; Goiter; Humans; Iodine; Membrane Transport Proteins; Sulfate Transporter | 2001 |
Endemic Cretinism.
Topics: Adolescent; Adult; Aged; Brain; Child; Child, Preschool; Congenital Hypothyroidism; Congo; Deafness; | 1975 |
[Spontaneous hypothyroidism after 50].
Topics: Aged; Aging; Cardiovascular Diseases; Cerebellar Ataxia; Coma; Female; Humans; Hyponatremia; Hypothy | 1973 |
Traditional Chinese medicine valuably augments therapeutic options in the treatment of climacteric syndrome.
Topics: Acupuncture Therapy; Climacteric; Depression; Drugs, Chinese Herbal; Female; Headache; Hot Flashes; | 2016 |
Transient elevation of sweat chloride concentration in a malnourished girl with the Mauriac syndrome.
Topics: Child; Chlorides; Diabetes Complications; Diabetes Mellitus; Diabetes Mellitus, Type 1; Dwarfism; Fe | 1995 |
The fish-odor syndrome.
Topics: Diet; Halitosis; Humans; Metabolism, Inborn Errors; Methylamines; Odorants; Sweat; Syndrome | 1996 |
Trials
1 trial available for iodine and Syndrome
| Article | Year |
|---|---|
Parenteral iodine and selenium supplementation in stillbirth/perinatal weak calf syndrome.
Topics: Animals; Animals, Newborn; Cattle; Cattle Diseases; Female; Fetal Death; Injections; Iodine; Pregnan | 1995 |
Other Studies
71 other studies available for iodine and Syndrome
| Article | Year |
|---|---|
DRESS syndrome involving 2 unrelated substances: imipenem and iodinated contrast media.
Topics: Aged, 80 and over; Biopsy; Contrast Media; Drug Hypersensitivity; Eosinophilia; Erythema; Female; Hu | 2013 |
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 |
Neuro-otological findings in Pendred syndrome.
Topics: Adolescent; Adult; Audiometry, Pure-Tone; Child; Ear, Inner; Female; Hearing Loss, Sensorineural; Hu | 2003 |
[Hypothyroid muscular syndromes of the adult I131 treatment of hyperthyroidism].
Topics: Adult; Disease; Humans; Hyperthyroidism; Hypothyroidism; Iodine; Iodine Radioisotopes; Muscles; Musc | 1954 |
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 |
[Sporadic cretinism with goiter].
Topics: Congenital Hypothyroidism; Goiter; Humans; Iodine; Iodine Radioisotopes; Radioisotopes; Syndrome; Th | 1955 |
The exchangeable character of accumulated I131 in the thyroid gland of a goitrous cretin.
Topics: Congenital Hypothyroidism; Humans; Iodine; Iodine Radioisotopes; Radioisotopes; Syndrome | 1957 |
[Research on the metabolism of iodine in goiters & hyperadrenalism syndromes].
Topics: Adrenal Gland Diseases; Adrenal Medulla; Adrenocortical Hyperfunction; Disease; Goiter; Humans; Iodi | 1957 |
Sporadic goitrous cretinism.
Topics: Congenital Hypothyroidism; Goiter; Humans; Hypothyroidism; Infant; Iodides; Iodine; Iodine Radioisot | 1959 |
Iodine metabolism in goitrous cretins.
Topics: Abnormalities, Multiple; Congenital Hypothyroidism; Humans; Iodine; Minerals; Syndrome | 1959 |
Butanol-insoluble iodinated compound in the plasma of a goitrous cretin.
Topics: 1-Butanol; Butanols; Congenital Hypothyroidism; Goiter; Humans; Iodine; Syndrome | 1960 |
The syndrome of congenital goiter with butanol-insoluble serum iodine.
Topics: Butanols; Goiter; Humans; Iodine; Syndrome | 1959 |
[The hereditary syndrome of inner ear deafness and faulty iodine utilization with goiter].
Topics: Ear, Inner; Goiter; Humans; Iodine; Syndrome | 1961 |
[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 |
A QUANTITATIVE SIMOLA TEST AND ITS APPLICATION TO THE INVESTIGATION OF EXTRAPYRAMIDAL SYNDROMES.
Topics: Catecholamines; Central Nervous System Diseases; Chorea; Extrapyramidal Tracts; Hepatolenticular Deg | 1963 |
[I-131 MUSCLE CLEARANCE IN RADICULAR LUMBOSACRAL SYNDROMES].
Topics: Humans; Intervertebral Disc Displacement; Iodine; Iodine Isotopes; Lumbosacral Region; Muscles; Poly | 1964 |
[Syndrome of local and general intolerance after intrabronchial lipiodol].
Topics: Bronchi; Ethiodized Oil; Iodides; Iodine; Iodine Isotopes; Syndrome | 1951 |
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 |
Management of goitre in Pendred's syndrome.
Topics: Adolescent; Adult; Deafness; Female; Goiter; Humans; Iodine; Male; Recurrence; Syndrome; Thyroid Gla | 1994 |
Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification.
Topics: Chromosome Mapping; Chromosomes, Human, Pair 7; Deafness; Female; Genetic Linkage; Genetic Markers; | 1996 |
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 |
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 |
[A medical-legal question of hearing impairment following vaccination (author's transl)].
Topics: Adolescent; Deafness; Diagnosis, Differential; Encephalomyelitis, Acute Disseminated; Female; German | 1976 |
Effect of inositol, lecithin, vitamins (B12 with choline and E), and iodinated casein on induced fatty liver-hemorrhagic syndrome in laying chickens.
Topics: Animal Feed; Animals; Caseins; Chickens; Choline; Eggs; Fatty Liver; Female; Hemorrhage; Inositol; I | 1975 |
[Role of thyroid gland dysfunction in the pathogenesis and course of cerebral circulatory disorders].
Topics: Cerebral Hemorrhage; Cerebral Infarction; Cerebrovascular Disorders; Humans; Hypertension; Iodine; I | 1978 |
Biochemical studies on the iodine organification defect of Pendred's syndrome.
Topics: Adolescent; Chromatography, Paper; Deafness; Electrophoresis, Polyacrylamide Gel; Female; Goiter; Hu | 1978 |
[Albright's type II osteodystrophy and hypothyroidism due to TSH deficiency. Apropos of a case in a child].
Topics: Calcinosis; Calcium; Child; Child, Preschool; Cyclic AMP; Female; Humans; Hypothyroidism; Infant; Io | 1977 |
Dissociated thyroxine, triiodothyronine and reverse triiodothyronine levels in patients with familial goitre due to iodide organification defects.
Topics: Adolescent; Adult; Congenital Hypothyroidism; Deafness; Female; Goiter; Humans; Iodine; Male; Pedigr | 1979 |
Experimentally induced "fatty liver syndrome" condition in laying hens.
Topics: Animals; Body Weight; Chickens; Cholesterol; Estradiol; Fatty Liver; Female; Iodine; Liver; Poultry | 1977 |
Treatment of the repeat breeder cow syndrome in Kenya.
Topics: Ampicillin; Animals; Breeding; Cattle; Cattle Diseases; Chloramphenicol; Estrus; Female; Fertilizati | 1978 |
Congenital goitrous hypothyroidism due to organification defect--(a case report).
Topics: Child; Congenital Hypothyroidism; Female; Goiter; Humans; Iodine; Syndrome | 1977 |
[Studies on our cases of central and peripheral hypothyroidism].
Topics: Adolescent; Age Factors; Binding Sites; Child; Child, Preschool; Deafness; Female; Goiter; Humans; H | 1976 |
Studies on the thyroidal defect in an atypical form of Pendred's syndrome.
Topics: Amino Acids; Deafness; Female; Goiter; Humans; In Vitro Techniques; Iodine; Male; Middle Aged; Syndr | 1975 |
The neurology of endemic cretinism. A study of two endemias.
Topics: Adult; Brain; China; Congenital Hypothyroidism; Gait; Geography; Goiter; Humans; Hypothyroidism; Ind | 1991 |
[Treatment of Sweet's syndrome using potassium iodate].
Topics: Adult; Female; Fever; Humans; Iodates; Iodine; Leukocytosis; Potassium; Potassium Compounds; Skin Di | 1985 |
Congenital euthyroid goitre and partial peripheral resistance to thyroid hormones.
Topics: Adult; Antibodies; Cholesterol; Female; Goiter; Humans; Hydroxyproline; Iodine; Perchlorates; Pituit | 1973 |
Pituitary-thyroid function in Pendred's syndrome.
Topics: Adult; Deafness; Female; Goiter; Humans; Iodine; Iodine Radioisotopes; Male; Pituitary Gland; Retina | 1974 |
Fifteen cases of Pendred's syndrome. Congenital deafness and sporadic goiter.
Topics: Adenoma; Adolescent; Adult; Age Factors; Aged; Audiometry; Cochlea; Deafness; Female; Goiter; Goiter | 1972 |
Goitre and deafness: Pendred's syndrome.
Topics: Adult; Deafness; Genes, Recessive; Goiter; Humans; Iodine; Male; Pedigree; Perchlorates; Syndrome; T | 1972 |
Thyroidal iodopriteins in Pendred's syndrome.
Topics: Adult; Albumins; Chromatography; Deafness; Female; Goiter; Humans; Iodine; Monoiodotyrosine; Syndrom | 1974 |
The anoestrous syndrome in New Zealand dairy cattle. 1. A preliminary investigation.
Topics: Age Factors; Animals; Cattle; Cattle Diseases; Estradiol; Estrus; Female; Infertility, Female; Iodin | 1973 |
Letter: Post-ingestion prevention of rumen overload syndrome in cattle.
Topics: Animal Feed; Animals; Cattle; Cattle Diseases; Iodine; Rumen; Stomach Diseases; Syndrome | 1974 |
Studies of a sibship with apparent hereditary resistance to the intracellular action of thyroid hormone.
Topics: Adolescent; Bone Diseases, Developmental; Child; Deafness; Erythrocytes; Female; Fibroblasts; Goiter | 1972 |
Nutritional and hormonal aspects of the oxygen toxicity syndrome.
Topics: Aerospace Medicine; Amino Acids; Animals; Atmospheric Pressure; Blood Glucose; Blood Proteins; Carbo | 1971 |
Diagnosis of cystic fibrosis in the kindred of an infant with CFTR-related metabolic syndrome: importance of follow-up that includes monitoring sweat chloride concentrations over time.
Topics: Adolescent; Child; Child, Preschool; Chlorides; Cystic Fibrosis; Cystic Fibrosis Transmembrane Condu | 2014 |
Shwachman-Diamond syndrome in a child presenting with cystic fibrosis-type symptoms and a false-positive sweat test.
Topics: Bone Marrow Diseases; Chronic Disease; Cystic Fibrosis; Diagnosis, Differential; False Positive Reac | 2008 |
[ADDISON'S DISEASE WITH CEREBRAL SCLEROSIS IN CHILDHOOD. A HEREDITARY SYNDROME TRANSMITTED THROUGH CHROMOSOME X?].
Topics: 17-Ketosteroids; Addison Disease; Adolescent; Adrenal Insufficiency; Adrenocorticotropic Hormone; Ch | 1963 |
A hypertensive syndrome with relative adrenal cortical overactivity.
Topics: Adrenal Cortex; Blood Pressure; Blood Pressure Determination; Humans; Hypertension; Sweat; Syndrome | 1950 |
The pathogenesis of climacteric syndrome and principle of acupuncture treatment based on TCM theory about brain.
Topics: Acupuncture Therapy; Brain; Brain Diseases; Climacteric; Diagnosis, Differential; Dizziness; Female; | 2005 |
'Blue sheet syndrome'.
Topics: Acne Vulgaris; Adult; Anti-Bacterial Agents; Bedding and Linens; Female; Humans; Minocycline; Skin P | 2006 |
Acute intestinal obstruction as a presentation of cystic fibrosis in infancy.
Topics: Cystic Fibrosis; Diseases in Twins; Female; Humans; Infant; Intestinal Obstruction; Sweat; Syndrome; | 2008 |
[New avitaminosis C cutaneo-mucous syndromes; depapillating glossitis, diminishing salivary and sweat secretions; onyxis].
Topics: Ascorbic Acid; Ascorbic Acid Deficiency; Avitaminosis; Glossitis; Humans; Sweat; Syndrome | 1948 |
Obstructive azoospermia as a diagnostic criterion for the cystic fibrosis syndrome.
Topics: Adolescent; Adult; Child; Chlorides; Cystic Fibrosis; Diagnosis, Differential; Humans; Lung Diseases | 1982 |
Meconium peritonitis and increasing sweat chloride determinations in a case of familial progressive intrahepatic cholestasis.
Topics: Child; Chlorides; Cholestasis, Intrahepatic; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mal | 1982 |
Incidence of meconium abnormalities in newborn infants with cystic fibrosis.
Topics: Child, Preschool; Cystic Fibrosis; Humans; Infant; Infant, Newborn; Intestinal Diseases; Intestinal | 1980 |
TAR syndrome: Dorsal pedal edema and excessive perspiration.
Topics: Edema; Eosinophilia; Foot Diseases; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Lymp | 1980 |
Fish-odor syndrome: an olfactory diagnosis.
Topics: Diet; Humans; Metabolism, Inborn Errors; Methylamines; Odorants; Sweat; Syndrome | 1995 |
An unknown spondyloepimetaphyseal dysplasia with a positive sweat chloride test, sparse hair and mild facial dysmorphism.
Topics: Child, Preschool; Chlorides; Facial Bones; Female; Hair Diseases; Humans; Osteochondrodysplasias; Ra | 1994 |
Decreased sweating in seven patients with Laron syndrome.
Topics: Adolescent; Adult; Child; Female; Growth Hormone; Humans; Male; Potassium; Reference Values; Sodium; | 1993 |
Fish-odour syndrome and impaired N-oxidation.
Topics: Diet; Female; Genetic Carrier Screening; Homozygote; Humans; Male; Metal Metabolism, Inborn Errors; | 1996 |
KID syndrome associated with elevated sweat chloride.
Topics: Child, Preschool; Chlorides; Deafness; Humans; Ichthyosis; Keratitis; Male; Sweat; Syndrome | 1996 |
Triple A syndrome mimicking cystic fibrosis.
Topics: Adrenal Glands; Child, Preschool; Chlorides; Cystic Fibrosis; Diagnosis, Differential; Esophageal Ac | 2000 |
False positive sweat test, malnutrition, and the Mauriac syndrome.
Topics: Child; Chlorides; Cystic Fibrosis; Diabetes Mellitus, Type 1; Dwarfism; False Positive Reactions; Fe | 1979 |
Short-lasting unilateral neuralgiform headache attacks with tearing and conjunctival injection: the first "symptomatic" case?
Topics: Adult; Cluster Headache; Conjunctival Diseases; Functional Laterality; Humans; Intracranial Arteriov | 1991 |
Recurrent respiratory disease, azoospermia, and nasal polyposis. A syndrome that mimics cystic fibrosis and immotile cilia syndrome.
Topics: Adult; Chronic Disease; Ciliary Motility Disorders; Cystic Fibrosis; Diagnosis, Differential; Humans | 1985 |
Autonomic neuropathy of acute onset.
Topics: Acute Disease; Adult; Autonomic Nervous System; Child; Female; Humans; Hypotension; Intestinal Obstr | 1974 |
[Sodium and potassium ion concentration in the eccrine sweat of hand palm in pregnant women with late toxemia syndrome].
Topics: Adolescent; Adult; Female; Humans; Potassium; Pre-Eclampsia; Pregnancy; Sodium; Sweat; Syndrome | 1973 |
Odontotrichomelic hypohidrotic dysplasia. A clinical reappraisal.
Topics: Abnormalities, Multiple; Arm; Breast; Child; Cleft Lip; Ear; Ectodermal Dysplasia; Face; Female; Hai | 1972 |