Keywords: کم کاری تیروئید مادرزادی; ACTH; adrenocorticotropin hormone; ALGS; arteriohepatic dysplasia; CH; central hypothyroidism; DWS; Dandy-Walker syndrome; FT3; free triiodothyronine; FT4; free thyroxine; GH; growth hormone; HCG; human chorionic gonadotropin; IGDF1; immunogobulin superfa
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: کم کاری تیروئید مادرزادی; congenital hypothyroidism; thyroid; goiter; next generation sequencing; systemic disease complications; complication prevention;
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Neonatal intensive care unit; Preterm infants; Thyroid screening; Thyroid function testing; Thyroid testing artifacts;
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Neonatal thyroid; Development; Levothyroxine; Dysgenesis; Dyshormonogenesis;
Keywords: کم کاری تیروئید مادرزادی; congenital hypothyroidism; preterm; low birth weight; very low birth weight; thyroxine; thyroid stimulating hormone;
Keywords: کم کاری تیروئید مادرزادی; thyroid-stimulating hormone receptor; G protein; Cre/loxP-system; microRNA; Dicer1; congenital hypothyroidism;
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Thyroid dysgenesis; Ectopic thyroid gland; Children;
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Gene mutations; Next-generation sequencing; China;
Keywords: کم کاری تیروئید مادرزادی; congenital hypothyroidism; levothyroxine; permanent; transient;
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Newborn screening; Neonatal screening; Thyrotropin; Hipotireoidismo congênito; Triagem de recém-nascidos; Triagem neonatal; Tirotropina;
Keywords: کم کاری تیروئید مادرزادی; Thyroid hormone receptors; Deiodinase; Resistance to thyroid hormone; Congenital hypothyroidism; Goiter; Dyshormonogenesis; Dysgenesis;
Keywords: کم کاری تیروئید مادرزادی; TSHR; PAX8; mutations; congenital hypothyroidism; subclinical hypothyroidism; hormone resistance;
Keywords: کم کاری تیروئید مادرزادی; congenital hypothyroidism; development; thyroid dysgenesis;
Keywords: کم کاری تیروئید مادرزادی; congenital hypothyroidism; Down syndrome; T4; TSH; fT4; Free T4; SZMC; Shaare Zedek Medical Center; T4; Thyroxine; TSH; Thyroid stimulating hormone; tT4; Total T4;
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Thyroglobulin gene; Genetic screening; Variants interpretationTG, thyroglobulin; CH, congenital hypothyroidism; PCH, permanent congenital hypothyroidism; VUS, variants of unknown significance; ACHE, acetylcholinesterase; TSH, th
Keywords: کم کاری تیروئید مادرزادی; CI; confidence interval; POPS; Project on Preterm and Small-for-gestational-age; THoP; transient hypothyroxinemia of prematurity; CHT; congenital hypothyroidism; YASR; Young Adult Self Report; YABCL; Young Adult Behavioral Checklist; SGA; small-for-gestat
Keywords: کم کاری تیروئید مادرزادی; congenital hypothyroidism; Down syndrome; T4; TSH; ASHIP; Associations of Statutory Health Insurance Physician; VE; Vaccine effectiveness;
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Incidence rate; Neonatal screening; France;
Keywords: کم کاری تیروئید مادرزادی; Thyroid gland; Thyroid development; Thyroid dysgenesis; Transcription factors; Congenital hypothyroidism; Mendelian inheritance; Genetics; Epigenetics;
Keywords: کم کاری تیروئید مادرزادی; CH; congenital hypothyroidism; dB; decibel; FT4; free thyroxine; Hz; Hertz; LT4; l-thyroxine; TH; thyroid hormone; TSH; thyrotropin; Ï2; chi-square;
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Thyroid hormone resistance; Deiodinase; Thyroid hormone transporter; Thyroid hormone receptor
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Neonatal hyperthyrotropinemia; Thyrotropin-releasing hormone test
Keywords: کم کاری تیروئید مادرزادی; CH; Congenital hypothyroidism; FS; Functional sensitivity; fT4; Free thyroxine; T4; Thyroxine; Tg; Thyroglobulin; TPO; Thyroid peroxidase; TSH; Thyroid-stimulating hormone;
Keywords: کم کاری تیروئید مادرزادی; newborn screening; congenital hypothyroidism; central (secondary) congenital hypothyroidism; “gland-in-situ”; TSH cutoff; neurodevelopment; cost-effectiveness
Keywords: کم کاری تیروئید مادرزادی; thyroid development; thyroid dysgenesis; congenital hypothyroidism; thyroxine; neonatal screening; endoderm; epigenetics; Mendelian inheritance
The Protective effect of P7C3 against DNA and neuron damage in rat pups with congenital hypothyroidism
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; DNA damage; NSE; P7C3; Rat;
Mutation screening of the GLIS3 gene in a cohort of 592 Chinese patients with congenital hypothyroidism
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; GLIS3; Gene mutations; China; Next-generation sequencing;
Tamizaje neonatal de hipotiroidismo congénito, análisis de la evidencia actual y propuesta de tamizaje para la población mexicana
Keywords: کم کاری تیروئید مادرزادی; Hipotiroidismo congénito; Tamiz neonatal; Hipotiroidismo subclÃnico; Levotiroxina; Congenital hypothyroidism; Neonatal screening; Subclinical hypothyroidism; Levothyroxine;
A further case of brain-lung-thyroid syndrome with deletion proximal to NKX2-1
Keywords: کم کاری تیروئید مادرزادی; Brain-lung-thyroid syndrome; NKX2-1; Congenital hypothyroidism; Array-CGH;
Neonatal screening: 9% of children with filter paper thyroid-stimulating hormone levels between 5 and 10 μIU/mL have congenital hypothyroidism
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Neonatal screening; Infant; Newborn; Thyroid diseases; Hipotireoidismo congênito; Triagem neonatal; Lactente; Recém-nascido; Doenças da glândula tireoide;
Neonatal screening: 9% of children with filter paper thyroidâstimulating hormone levels between 5 and 10 μIU/mL have congenital hypothyroidism
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Neonatal screening; Infant; Newborn; Thyroid diseases; Hipotireoidismo congênito; Triagem neonatal; Lactente; Recémânascido; Doenças da glândula tireoide;
Detecting congenital hypothyroidism with newborn screening: the relevance of thyroidâstimulating hormone cutoff values
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Newborn screening; Neonatal screening; Thyrotropin; Hipotireoidismo congênito; Triagem de recémânascidos; Triagem neonatal; Tirotropina;
Disorders of H2O2 generation
Keywords: کم کاری تیروئید مادرزادی; DUOX; DUOXA; congenital hypothyroidism; dyshormonogenesis;
Next-generation sequencing of NKX2.1, FOXE1, PAX8, NKX2.5, and TSHR in 100 Chinese patients with congenital hypothyroidism and athyreosis
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Athyreosis; Next-generation sequencing; Mutation; Genotype-phenotype;
Pendred syndrome
Keywords: کم کاری تیروئید مادرزادی; Pendred syndrome; sensorineural deafness; goiter; congenital hypothyroidism; thyroid hormone; iodide;
Perfluoroalkyl substances in serum from South Korean infants with congenital hypothyroidism and healthy infants - Its relationship with thyroid hormones
Keywords: کم کاری تیروئید مادرزادی; Perfluoroalkyl substances; Congenital hypothyroidism; Infant; Serum; South Korea;
Carcinoma papilar de tiroides en un niño con hipotiroidismo congénito dishormonogénico. Reporte de un caso
Keywords: کم کاری تیروئید مادرزادی; Cáncer de tiroides; Niños; Hipotiroidismo congénito; Radiación ionizante; Thyroid cancer; Children; Congenital hypothyroidism; Ionising radiation;
High prevalence of DUOX2 gene mutations among children with congenital hypothyroidism in central China
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; DUOX2; Dyshormonogenesis; NGS; Ampliseq;
Can One Predict Resolution of Neonatal Hyperthyrotropinemia?
Keywords: کم کاری تیروئید مادرزادی; congenital hypothyroidism; neonatal hyperthyrotropinemia; perinatal stress; BW; Birth weight; GA; Gestational age; NBS; Newborn screening; NICU; Neonatal intensive care unit; ROP; Retinopathy of prematurity; T4; Thyroxine; TSH; Thyrotropin;
Compound heterozygous DUOX2 gene mutations (c.2335-1G>C/c.3264_3267delCAGC) associated with congenital hypothyroidism. Characterization of complex cryptic splice sites by minigene analysis
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; DUOX2 gene; Mutation; Compound heterozygous mutations; Cryptic splice site
PAX8 pathogenic variants in Chinese patients with congenital hypothyroidism
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Paired box gene 8; Next-generation sequencing; Chinese patients
Novel compound heterozygous Thyroglobulin mutations c.745+1G>A/c.7036+2T>A associated with congenital goiter and hypothyroidism in a Vietnamese family. Identification of a new cryptic 5′ splice site in the exon 6
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Thyroglobulin gene; Mutation; Compound heterozygous mutations; Cryptic splice site
Tetrabromobisphenol A and hexabromocyclododecane flame retardants in infant-mother paired serum samples, and their relationships with thyroid hormones and environmental factors
Keywords: کم کاری تیروئید مادرزادی; Organohalogen; Human monitoring; Congenital hypothyroidism; Infant; Environmental factors;
Towards the pre-clinical diagnosis of hypothyroidism caused by iodotyrosine deiodinase (DEHAL1) defects
Keywords: کم کاری تیروئید مادرزادی; iodide recycling; DEHAL1 gene; congenital hypothyroidism; neonatal screening; mass spectrometry; mental retardation; IYD
Hipotiroidismo congénito
Keywords: کم کاری تیروئید مادرزادی; Disgenesia tiroideia; Dishormonogénese; Hipotiroidismo congénitoThyroid dysgenesis; Dyshormonogenesis; Congenital hypothyroidism
Novel mutational mechanism in the thyroglobulin gene: Imperfect DNA inversion as a cause for hereditary hypothyroidism
Keywords: کم کاری تیروئید مادرزادی; Thyroglobulin gene; Mutation; Inversion; Deletion; Congenital hypothyroidism;
The association between some endocrine disruptors in human plasma and the occurrence of congenital hypothyroidism
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Endocrine disruptors; Isoflavones; Association; GC-MS;
Neurodevelopment evaluation in children with congenital hypothyroidism by Bayley-III
Keywords: کم کاری تیروئید مادرزادی; Congenital hypothyroidism; Bayley-III score; Neurological development
Early Adiposity Rebound and Obesity in Children with Congenital Hypothyroidism
Keywords: کم کاری تیروئید مادرزادی; adiposity rebound; congenital hypothyroidism; obesity
Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism
Keywords: کم کاری تیروئید مادرزادی; CH; Congenital hypothyroidism; DQ; Developmental quotient; fT3; Free triiodothyronine; fT4; Free thyroxine; L-T4; Levothyroxine; TSH; Thyrotropin;