Page last updated: 2024-10-18

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

ExcerptRelevanceReference
"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."8.80Syndromes 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."5.25Effect 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."4.82Pendred 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."4.80Syndromes 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."3.74Analysis 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."3.72Neuro-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."3.68The 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."3.64Sporadic 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."2.55Pendred syndrome. ( Kopp, P; Wémeau, JL, 2017)
"Pendred syndrome is often associated with inner ear malformations, especially enlarged vestibular aqueduct (EVA)."1.31Phenotypes 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."1.28Short-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."1.25Effect 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."1.25Pituitary-thyroid function in Pendred's syndrome. ( Evered, DC; Gomez-Pan, A; Hall, R, 1974)

Research

Studies (83)

TimeframeStudies, this research(%)All Research%
pre-199050 (60.24)18.7374
1990's13 (15.66)18.2507
2000's15 (18.07)29.6817
2010's5 (6.02)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Wémeau, JL2
Kopp, P3
Macías, EM1
Muñoz-Bellido, FJ1
Velasco, A1
Moreno, E1
Dávila, I1
Bizhanova, A1
Asakura, Y1
Narumi, S1
Muroya, K1
Fujita, K1
Aida, N1
Hasagawa, T1
Adachi, M1
Luxon, LM1
Cohen, M1
Coffey, RA1
Phelps, PD1
Britton, KE1
Jan, H1
Trembath, RC1
Reardon, W1
ZARA, M1
CHIMENES, H1
GALI, P1
STANBURY, JB2
OHELA, K1
PITT-RIVERS, R1
ABALLI, AJ1
COSTALES, F1
PRENDES, Z1
SCHULTZ, AL1
FLINK, EB1
KENNEDY, BJ1
ZIEVE, L1
CASSANO, C1
BASCHIERI, L1
ANDREANI, D1
MOSIER, HD1
GARDNER, JU1
HAYLES, AB1
WOOLNER, LB1
OWEN, CA1
CHAVARRIA, C1
MUNOS-FERREIRA, G1
GUEVARA, G1
RUPP, JJ1
PASCHKIS, KE1
DEGROOT, LJ2
von HARNACK, G1
HORST, W1
LENZ, W1
REINWEIN, D1
KLEIN, E1
CURZON, G1
WALD, I1
KVICALA, V1
KOLAR, M1
Hiyoshi, M1
Yamane, H1
Glaser, B2
Lai, CC1
Chiu, CY1
Shiao, AS1
Tso, YC1
Wu, YC1
Tu, TY1
Jap, TS1
Palos, F1
García-Rendueles, ME1
Araujo-Vilar, D1
Obregon, MJ1
Calvo, RM1
Cameselle-Teijeiro, J1
Bravo, SB1
Perez-Guerra, O1
Loidi, L1
Czarnocka, B1
Alvarez, P1
Refetoff, S2
Dominguez-Gerpe, L1
Alvarez, CV1
Lado-Abeal, J1
Medeiros-Neto, G2
McCoy, MA1
Smyth, JA1
Ellis, WA1
Kennedy, DG1
al-Jaberi, TM1
Hussein, AD1
Heis, HA1
Sheffield, VC1
Kraiem, Z1
Beck, JC1
Nishimura, D1
Stone, EM1
Salameh, M1
Sadeh, O1
Ross, DS1
Bidart, JM1
Lacroix, L1
Evain-Brion, D1
Caillou, B1
Lazar, V1
Frydman, R1
Bellet, D1
Filetti, S1
Schlumberger, M1
Gonzalez Trevino, O1
Karamanoglu Arseven, O1
Ceballos, CJ1
Vives, VI1
Ramirez, RC1
Gomez, VV1
Sato, E1
Nakashima, T1
Miura, Y1
Furuhashi, A1
Nakayama, A1
Mori, N1
Murakami, H1
Naganawa, S1
Tadokoro, M1
Vlaeminck-Guillem, V1
Dubrulle, F1
Dumur, V1
Vincent, C1
von Deuster, C1
Wolford, JH1
Polin, D1
Buletsa, BA1
Pashchenko, AE1
Fabri, ZI1
Litvinova, LA1
Semenchuk, MM1
Niepomniszcze, H1
Coleoni, AH1
Degrossi, OJ1
Scavini, LM1
Curutchet, HP1
David, M1
Madjar, JJ1
Floret, D1
Sann, L1
Terrier, M1
Jeune, M1
Chan, V1
Wang, C1
Yeung, RT1
Harms, RH1
Roland, DA1
Simpson, CF1
Mutiga, ER1
Hornabrook, RW1
Kapoor, A1
Godbole, M1
Chauhan, S1
Ghosh, BK1
Rao, B1
Crisalli, M1
Chiossi, FM1
Monteverde, R1
Scafidi, M1
Cave, WT1
Dunn, JT1
Halpern, JP1
Boyages, SC1
Maberly, GF1
Collins, JK1
Eastman, CJ1
Morris, JG1
Herrero, C1
Font, J1
Bielsa, I1
Coca, A1
Lamberg, BA1
Gomez-Pan, A1
Evered, DC1
Hall, R1
Illum, P1
Kiaer, HW1
Hvidberg-Hansen, J1
Sondergaard, G1
Purves, RD1
Desai, KB1
Mehta, MN1
Patel, MC1
Ramanna, L1
Ganatra, RD1
Fielden, ED1
Macmillan, KL1
Watson, JD1
Bastenie, PA1
Ectors, M1
Thys, JP1
Vanhaelst, L1
Muri, P1
Benard, B1
DeWind, LT1
Leon, HA1
Brooksby, GA1
Chackerian, MJ1
Staley, RW1
Williams, SN1
Nussbaum, E1
Chin, TW1
Do, PC1
Singh, KE1
Randhawa, I1
Eisenhardt, S1
Fleckenstein, J1
Brown, SM1
Buchdahl, R1
FANCONI, A1
PRADER, A1
ISLER, W1
LUETHY, F1
SIEBENMANN, R1
DAVIES, DF1
CLARK, HE1
Xiaoming, S1
Du, Y1
Shi, X1
Hussain, W1
Layton, A1
Baral, V1
Connett, G1
DEGOS, R1
Stern, RC1
Boat, TF1
Doershuk, CF1
Hillemeier, AC1
Hen, J1
Riely, CA1
Dolan, TF1
Gryboski, JD1
Rosenstein, BJ1
Langbaum, TS1
Feingold, M1
Bartoshesky, L1
Geis, N1
Ruocco, V1
Florio, M1
Polack, FP1
Transue, DJ1
Belknap, WM1
Freij, BJ1
Aughton, DJ1
Leonard, NJ1
Hughes, HE1
Main, KM1
Price, DA1
Savage, MO1
Skakkebae, NE1
Mitchell, SC2
Zhang, A1
Smith, RL1
Kumar, SA1
Lester, MR1
Bratton, DL1
Cesur, Y1
Bereket, A1
Anadol, D1
Kiper, N1
Gocmen, A1
Yordam, N1
Rosenfeld, R1
Spigelblatt, L1
Chicoine, R1
Bussone, G1
Leone, M1
Dalla Volta, G1
Strada, L1
Gasparotti, R1
Di Monda, V1
Schanker, HM1
Rajfer, J1
Saxon, A1
Hopkins, A1
Neville, B1
Bannister, R1
Ostrzeński, A1
Cat, I1
Costa, O1
Freire-Maia, N1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Study on the Compensatory Mechanism of Iodine Nutrition and the Optimal Intake Level of Lactating Women[NCT04492657]600 participants (Anticipated)Observational2020-01-01Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Reviews

11 reviews available for iodine and Syndrome

ArticleYear
Pendred syndrome.
    Best practice & research. Clinical endocrinology & metabolism, 2017, Volume: 31, Issue:2

    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.
    Endocrinology, 2009, Volume: 150, Issue:3

    Topics: Animals; Gene Expression Regulation; Homeostasis; Humans; Iodine; Membrane Transport Proteins; Metab

2009
Pendred syndrome.
    Pediatric endocrinology reviews : PER, 2003, Volume: 1 Suppl 2

    Topics: Biological Transport; Goiter; Hearing Loss, Sensorineural; Humans; Iodine; Membrane Transport Protei

2003
Unusual manifestations of thyrotoxicosis.
    Progress in clinical and biological research, 1983, Volume: 116

    Topics: Adenocarcinoma; Dexamethasone; Female; Glycoprotein Hormones, alpha Subunit; Humans; Hyperthyroidism

1983
Syndromes of thyrotoxicosis with low radioactive iodine uptake.
    Endocrinology and metabolism clinics of North America, 1998, Volume: 27, Issue:1

    Topics: Humans; Hyperthyroidism; Iodine; Iodine Radioisotopes; Syndrome; Thyroiditis, Subacute; Thyrotoxicos

1998
[Pendred's syndrome. Current features].
    Presse medicale (Paris, France : 1983), 2001, Nov-17, Volume: 30, Issue:34

    Topics: Carrier Proteins; Deafness; Goiter; Humans; Iodine; Membrane Transport Proteins; Sulfate Transporter

2001
Endemic Cretinism.
    Contemporary neurology series, 1975, Volume: 12

    Topics: Adolescent; Adult; Aged; Brain; Child; Child, Preschool; Congenital Hypothyroidism; Congo; Deafness;

1975
[Spontaneous hypothyroidism after 50].
    Problemes actuels d'endocrinologie et de nutrition, 1973, Volume: SERIE 17

    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.
    Archives of gynecology and obstetrics, 2016, Volume: 294, Issue:1

    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.
    The Journal of pediatrics, 1995, Volume: 126, Issue:2

    Topics: Child; Chlorides; Diabetes Complications; Diabetes Mellitus; Diabetes Mellitus, Type 1; Dwarfism; Fe

1995
The fish-odor syndrome.
    Perspectives in biology and medicine, 1996,Summer, Volume: 39, Issue:4

    Topics: Diet; Halitosis; Humans; Metabolism, Inborn Errors; Methylamines; Odorants; Sweat; Syndrome

1996

Trials

1 trial available for iodine and Syndrome

ArticleYear
Parenteral iodine and selenium supplementation in stillbirth/perinatal weak calf syndrome.
    The Veterinary record, 1995, Feb-04, Volume: 136, Issue:5

    Topics: Animals; Animals, Newborn; Cattle; Cattle Diseases; Female; Fetal Death; Injections; Iodine; Pregnan

1995

Other Studies

71 other studies available for iodine and Syndrome

ArticleYear
DRESS syndrome involving 2 unrelated substances: imipenem and iodinated contrast media.
    Journal of investigational allergology & clinical immunology, 2013, Volume: 23, Issue:1

    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.
    American journal of medical genetics. Part A, 2010, Volume: 152A, Issue:7

    Topics: Abnormalities, Multiple; Adolescent; Adult; Amino Acid Sequence; Base Sequence; Child; Child, Presch

2010
Neuro-otological findings in Pendred syndrome.
    International journal of audiology, 2003, Volume: 42, Issue:2

    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].
    Annales d'endocrinologie, 1954, Volume: 15, Issue:2

    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.
    The Journal of clinical endocrinology and metabolism, 1955, Volume: 15, Issue:1

    Topics: Abnormalities, Multiple; Antithyroid Agents; Congenital Hypothyroidism; Humans; Iodine; Iodine Radio

1955
[Sporadic cretinism with goiter].
    Revista cubana de pediatria, 1955, Volume: 27, Issue:9

    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.
    The Journal of clinical endocrinology and metabolism, 1957, Volume: 17, Issue:3

    Topics: Congenital Hypothyroidism; Humans; Iodine; Iodine Radioisotopes; Radioisotopes; Syndrome

1957
[Research on the metabolism of iodine in goiters & hyperadrenalism syndromes].
    Helvetica medica acta, 1957, Volume: 24, Issue:3

    Topics: Adrenal Gland Diseases; Adrenal Medulla; Adrenocortical Hyperfunction; Disease; Goiter; Humans; Iodi

1957
Sporadic goitrous cretinism.
    California medicine, 1959, Volume: 90, Issue:1

    Topics: Congenital Hypothyroidism; Goiter; Humans; Hypothyroidism; Infant; Iodides; Iodine; Iodine Radioisot

1959
Iodine metabolism in goitrous cretins.
    The Journal of clinical endocrinology and metabolism, 1959, Volume: 19, Issue:6

    Topics: Abnormalities, Multiple; Congenital Hypothyroidism; Humans; Iodine; Minerals; Syndrome

1959
Butanol-insoluble iodinated compound in the plasma of a goitrous cretin.
    The Journal of clinical endocrinology and metabolism, 1960, Volume: 20

    Topics: 1-Butanol; Butanols; Congenital Hypothyroidism; Goiter; Humans; Iodine; Syndrome

1960
The syndrome of congenital goiter with butanol-insoluble serum iodine.
    The American journal of medicine, 1959, Volume: 27

    Topics: Butanols; Goiter; Humans; Iodine; Syndrome

1959
[The hereditary syndrome of inner ear deafness and faulty iodine utilization with goiter].
    Deutsche medizinische Wochenschrift (1946), 1961, Dec-15, Volume: 86

    Topics: Ear, Inner; Goiter; Humans; Iodine; Syndrome

1961
[A SPECIAL FORM OF IODINE USE IN SPORADIC CRETINISM. CLINICAL AND BIOCHEMICAL STUDY RESULTS].
    Schweizerische medizinische Wochenschrift, 1963, Aug-31, Volume: 93

    Topics: Abnormalities, Multiple; Congenital Hypothyroidism; Goiter; Humans; Iodides; Iodine; Syndrome

1963
A QUANTITATIVE SIMOLA TEST AND ITS APPLICATION TO THE INVESTIGATION OF EXTRAPYRAMIDAL SYNDROMES.
    Clinica chimica acta; international journal of clinical chemistry, 1963, Volume: 8

    Topics: Catecholamines; Central Nervous System Diseases; Chorea; Extrapyramidal Tracts; Hepatolenticular Deg

1963
[I-131 MUSCLE CLEARANCE IN RADICULAR LUMBOSACRAL SYNDROMES].
    Ceskoslovenska neurologie, 1964, Volume: 27

    Topics: Humans; Intervertebral Disc Displacement; Iodine; Iodine Isotopes; Lumbosacral Region; Muscles; Poly

1964
[Syndrome of local and general intolerance after intrabronchial lipiodol].
    Paris medical, 1951, Jan-20, Volume: 41, Issue:3

    Topics: Bronchi; Ethiodized Oil; Iodides; Iodine; Iodine Isotopes; Syndrome

1951
A pedigree with Pendred syndrome: case report and discussion on hereditary hearing loss.
    Acta oto-laryngologica. Supplementum, 2004, Issue:554

    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.
    Metabolism: clinical and experimental, 2007, Volume: 56, Issue:9

    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.
    The Journal of clinical endocrinology and metabolism, 2008, Volume: 93, Issue:1

    Topics: Adult; Amino Acid Sequence; Female; Goiter, Nodular; Haplotypes; Hearing Loss, Sensorineural; Humans

2008
Management of goitre in Pendred's syndrome.
    The British journal of surgery, 1994, Volume: 81, Issue:10

    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.
    Nature genetics, 1996, Volume: 12, Issue:4

    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.
    The Journal of clinical endocrinology and metabolism, 2000, Volume: 85, Issue:11

    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.
    European journal of endocrinology, 2001, Volume: 144, Issue:6

    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.
    European journal of endocrinology, 2001, Volume: 145, Issue:6

    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)].
    HNO, 1976, Volume: 24, Issue:4

    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.
    Poultry science, 1975, Volume: 54, Issue:4

    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].
    Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952), 1978, Volume: 78, Issue:11

    Topics: Cerebral Hemorrhage; Cerebral Infarction; Cerebrovascular Disorders; Humans; Hypertension; Iodine; I

1978
Biochemical studies on the iodine organification defect of Pendred's syndrome.
    Acta endocrinologica, 1978, Volume: 89, Issue:1

    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].
    Archives francaises de pediatrie, 1977, Volume: 34, Issue:2

    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.
    Clinical endocrinology, 1979, Volume: 11, Issue:3

    Topics: Adolescent; Adult; Congenital Hypothyroidism; Deafness; Female; Goiter; Humans; Iodine; Male; Pedigr

1979
Experimentally induced "fatty liver syndrome" condition in laying hens.
    Poultry science, 1977, Volume: 56, Issue:2

    Topics: Animals; Body Weight; Chickens; Cholesterol; Estradiol; Fatty Liver; Female; Iodine; Liver; Poultry

1977
Treatment of the repeat breeder cow syndrome in Kenya.
    Tropical animal health and production, 1978, Volume: 10, Issue:4

    Topics: Ampicillin; Animals; Breeding; Cattle; Cattle Diseases; Chloramphenicol; Estrus; Female; Fertilizati

1978
Congenital goitrous hypothyroidism due to organification defect--(a case report).
    Indian pediatrics, 1977, Volume: 14, Issue:7

    Topics: Child; Congenital Hypothyroidism; Female; Goiter; Humans; Iodine; Syndrome

1977
[Studies on our cases of central and peripheral hypothyroidism].
    Minerva pediatrica, 1976, May-26, Volume: 28, Issue:19

    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.
    The Journal of clinical endocrinology and metabolism, 1975, Volume: 41, Issue:3

    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.
    Brain : a journal of neurology, 1991, Volume: 114 ( Pt 2)

    Topics: Adult; Brain; China; Congenital Hypothyroidism; Gait; Geography; Goiter; Humans; Hypothyroidism; Ind

1991
[Treatment of Sweet's syndrome using potassium iodate].
    Medicina clinica, 1985, Feb-09, Volume: 84, Issue:5

    Topics: Adult; Female; Fever; Humans; Iodates; Iodine; Leukocytosis; Potassium; Potassium Compounds; Skin Di

1985
Congenital euthyroid goitre and partial peripheral resistance to thyroid hormones.
    Lancet (London, England), 1973, Apr-21, Volume: 1, Issue:7808

    Topics: Adult; Antibodies; Cholesterol; Female; Goiter; Humans; Hydroxyproline; Iodine; Perchlorates; Pituit

1973
Pituitary-thyroid function in Pendred's syndrome.
    British medical journal, 1974, Apr-20, Volume: 2, Issue:5911

    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.
    Archives of otolaryngology (Chicago, Ill. : 1960), 1972, Volume: 96, Issue:4

    Topics: Adenoma; Adolescent; Adult; Age Factors; Aged; Audiometry; Cochlea; Deafness; Female; Goiter; Goiter

1972
Goitre and deafness: Pendred's syndrome.
    The New Zealand medical journal, 1972, Volume: 76, Issue:483

    Topics: Adult; Deafness; Genes, Recessive; Goiter; Humans; Iodine; Male; Pedigree; Perchlorates; Syndrome; T

1972
Thyroidal iodopriteins in Pendred's syndrome.
    The Journal of endocrinology, 1974, Volume: 63, Issue:2

    Topics: Adult; Albumins; Chromatography; Deafness; Female; Goiter; Humans; Iodine; Monoiodotyrosine; Syndrom

1974
The anoestrous syndrome in New Zealand dairy cattle. 1. A preliminary investigation.
    New Zealand veterinary journal, 1973, Volume: 21, Issue:5

    Topics: Age Factors; Animals; Cattle; Cattle Diseases; Estradiol; Estrus; Female; Infertility, Female; Iodin

1973
Letter: Post-ingestion prevention of rumen overload syndrome in cattle.
    The Canadian veterinary journal = La revue veterinaire canadienne, 1974, Volume: 15, Issue:2

    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.
    Metabolism: clinical and experimental, 1972, Volume: 21, Issue:8

    Topics: Adolescent; Bone Diseases, Developmental; Child; Deafness; Erythrocytes; Female; Fibroblasts; Goiter

1972
Nutritional and hormonal aspects of the oxygen toxicity syndrome.
    Aerospace medicine, 1971, Volume: 42, Issue:5

    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.
    Pediatric pulmonology, 2014, Volume: 49, Issue:3

    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.
    Journal of the Royal Society of Medicine, 2008, Volume: 101 Suppl 1

    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?].
    Helvetica paediatrica acta, 1963, Volume: 18

    Topics: 17-Ketosteroids; Addison Disease; Adolescent; Adrenal Insufficiency; Adrenocorticotropic Hormone; Ch

1963
A hypertensive syndrome with relative adrenal cortical overactivity.
    Circulation, 1950, Volume: 2, Issue:4

    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.
    Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan, 2005, Volume: 25, Issue:2

    Topics: Acupuncture Therapy; Brain; Brain Diseases; Climacteric; Diagnosis, Differential; Dizziness; Female;

2005
'Blue sheet syndrome'.
    Journal of the European Academy of Dermatology and Venereology : JEADV, 2006, Volume: 20, Issue:6

    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.
    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2008, Volume: 7, Issue:4

    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].
    Gazeta medica portuguesa, 1948, Volume: 1, Issue:3

    Topics: Ascorbic Acid; Ascorbic Acid Deficiency; Avitaminosis; Glossitis; Humans; Sweat; Syndrome

1948
Obstructive azoospermia as a diagnostic criterion for the cystic fibrosis syndrome.
    Lancet (London, England), 1982, Jun-19, Volume: 1, Issue:8286

    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.
    Pediatrics, 1982, Volume: 69, Issue:3

    Topics: Child; Chlorides; Cholestasis, Intrahepatic; Humans; Infant, Newborn; Infant, Newborn, Diseases; Mal

1982
Incidence of meconium abnormalities in newborn infants with cystic fibrosis.
    American journal of diseases of children (1960), 1980, Volume: 134, Issue:1

    Topics: Child, Preschool; Cystic Fibrosis; Humans; Infant; Infant, Newborn; Intestinal Diseases; Intestinal

1980
TAR syndrome: Dorsal pedal edema and excessive perspiration.
    American journal of diseases of children (1960), 1980, Volume: 134, Issue:9

    Topics: Edema; Eosinophilia; Foot Diseases; Humans; Infant; Infant, Newborn; Infant, Newborn, Diseases; Lymp

1980
Fish-odor syndrome: an olfactory diagnosis.
    International journal of dermatology, 1995, Volume: 34, Issue:2

    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.
    Clinical dysmorphology, 1994, Volume: 3, Issue:4

    Topics: Child, Preschool; Chlorides; Facial Bones; Female; Hair Diseases; Humans; Osteochondrodysplasias; Ra

1994
Decreased sweating in seven patients with Laron syndrome.
    The Journal of clinical endocrinology and metabolism, 1993, Volume: 77, Issue:3

    Topics: Adolescent; Adult; Child; Female; Growth Hormone; Humans; Male; Potassium; Reference Values; Sodium;

1993
Fish-odour syndrome and impaired N-oxidation.
    Biochemical Society transactions, 1996, Volume: 24, Issue:1

    Topics: Diet; Female; Genetic Carrier Screening; Homozygote; Humans; Male; Metal Metabolism, Inborn Errors;

1996
KID syndrome associated with elevated sweat chloride.
    Pediatric pulmonology, 1996, Volume: 21, Issue:3

    Topics: Child, Preschool; Chlorides; Deafness; Humans; Ichthyosis; Keratitis; Male; Sweat; Syndrome

1996
Triple A syndrome mimicking cystic fibrosis.
    Journal of pediatric endocrinology & metabolism : JPEM, 2000, Volume: 13, Issue:3

    Topics: Adrenal Glands; Child, Preschool; Chlorides; Cystic Fibrosis; Diagnosis, Differential; Esophageal Ac

2000
False positive sweat test, malnutrition, and the Mauriac syndrome.
    The Journal of pediatrics, 1979, Volume: 94, Issue:2

    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?
    Cephalalgia : an international journal of headache, 1991, Volume: 11, Issue:3

    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.
    Archives of internal medicine, 1985, Volume: 145, Issue:12

    Topics: Adult; Chronic Disease; Ciliary Motility Disorders; Cystic Fibrosis; Diagnosis, Differential; Humans

1985
Autonomic neuropathy of acute onset.
    Lancet (London, England), 1974, Apr-27, Volume: 1, Issue:7861

    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].
    Ginekologia polska, 1973, Volume: 44, Issue:2

    Topics: Adolescent; Adult; Female; Humans; Potassium; Pre-Eclampsia; Pregnancy; Sodium; Sweat; Syndrome

1973
Odontotrichomelic hypohidrotic dysplasia. A clinical reappraisal.
    Human heredity, 1972, Volume: 22, Issue:1

    Topics: Abnormalities, Multiple; Arm; Breast; Child; Cleft Lip; Ear; Ectodermal Dysplasia; Face; Female; Hai

1972