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Polymorphism of the polyalanine tract of thyroid transcription factor-2 gene in patients with thyroid dysgenesis.
- Published in:
- European Journal of Endocrinology, 2001, v. 145, n. 4, p. 385, doi. 10.1530/eje.0.1450385
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- Publication type:
- Article
PTEN mutation in a Japanese boy with autonomously functioning thyroid nodule.
- Published in:
- Pediatrics International, 2017, v. 59, n. 11, p. 1223, doi. 10.1111/ped.13427
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- Publication type:
- Article
Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene.
- Published in:
- Pediatrics International, 2005, v. 47, n. 1, p. 105, doi. 10.1111/j.1442-200x.2005.02020.x
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- Publication type:
- Article
A novel compound heterozygous mutation in the thyroglobulin gene resulting in congenital goitrous hypothyroidism with high serum triiodothyronine levels.
- Published in:
- Journal of Human Genetics, 2006, v. 51, n. 4, p. 379, doi. 10.1007/s10038-006-0360-2
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- Publication type:
- Article
Complete Sequencing of the bla<sub>NDM-1</sub>-Positive IncA/C Plasmid from Escherichia coli ST38 Isolate Suggests a Possible Origin from Plant Pathogens.
- Published in:
- PLoS ONE, 2011, v. 6, n. 9, p. 1, doi. 10.1371/journal.pone.0025334
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- Publication type:
- Article
Thyroglobulin Gene Mutations Producing Defective Intracellular Transport of Thyroglobulin Are Associated with Increased Thyroidal Type 2 Iodothyronine Deiodinase Activity.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 4, p. 1451, doi. 10.1210/jc.2006-1242
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- Publication type:
- Article
Haplotype Analysis Reveals Founder Effects of Thyroglobulin Gene Mutations C1058R and C1977S in Japan.
- Published in:
- Journal of Clinical Endocrinology & Metabolism, 2006, v. 91, n. 8, p. 3100, doi. 10.1210/jc.2005-2702
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- Publication type:
- Article
Adult Thyroid Outcomes of Congenital Hypothyroidism.
- Published in:
- Thyroid, 2023, v. 33, n. 5, p. 556, doi. 10.1089/thy.2022.0481
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- Publication type:
- Article
Seasonal Changes in Serum Thyrotropin Concentrations Observed from Big Data Obtained During Six Consecutive Years from 2010 to 2015 at a Single Hospital in Japan.
- Published in:
- Thyroid, 2018, v. 28, n. 4, p. 429, doi. 10.1089/thy.2017.0600
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- Publication type:
- Article
Measurement of serum low density lipoprotein-cholesterol in patients with hypertriglycemia.
- Published in:
- Electrophoresis, 2000, v. 21, n. 2, p. 293, doi. 10.1002/(SICI)1522-2683(20000101)21:2<293::AID-ELPS293>3.0.CO;2-9
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- Publication type:
- Article
Painless destructive thyroiditis in a patient with resistance to thyroid hormone: a case report.
- Published in:
- Thyroid Research, 2019, v. 12, n. 1, p. N.PAG, doi. 10.1186/s13044-019-0072-2
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- Publication type:
- Article
Evaluation of the double-disk synergy test for New Delhi metallo-β-lactamase-1 and other metallo-β-lactamase producing gram-negative bacteria by using metal-ethylenediaminetetraacetic acid complexes.
- Published in:
- Microbiology & Immunology, 2013, v. 57, n. 5, p. 346, doi. 10.1111/1348-0421.12042
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- Publication type:
- Article
Standardization of Free Thyroxine Measurements Allows the Adoption of a More Uniform Reference Interval.
- Published in:
- Clinical Chemistry, 2017, v. 63, n. 10, p. 1642, doi. 10.1373/clinchem.2017.274407
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- Publication type:
- Article
Harmonization of Serum Thyroid-Stimulating Hormone Measurements Paves the Way for the Adoption of a More Uniform Reference Interval.
- Published in:
- Clinical Chemistry, 2017, v. 63, n. 7, p. 1248, doi. 10.1373/clinchem.2016.269456
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- Publication type:
- Article
A case of hypoparathyroidism, deafness, and renal dysplasia (HDR) syndrome with a novel frameshift variant in GATA3, p.W10Cfs40, lacks kidney malformation.
- Published in:
- Clinical Case Reports, 2020, v. 8, n. 12, p. 2619, doi. 10.1002/ccr3.3186
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- Publication type:
- Article
A Japanese Family with DICER1 Syndrome Found in Childhood-Onset Multinodular Goitre.
- Published in:
- Hormone Research in Paediatrics, 2020, v. 93, n. 7/8, p. 477, doi. 10.1159/000511140
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- Publication type:
- Article
Prevalence of Thyrotropin Receptor Germline Mutations and Clinical Courses in 89 Hyperthyroid Patients with Diffuse Goiter and Negative Anti-Thyrotropin Receptor Antibodies.
- Published in:
- Thyroid, 2014, v. 24, n. 5, p. 789, doi. 10.1089/thy.2013.0431
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- Publication type:
- Article
Diagnosis of Iodide Transport Defect: Do We Need to Measure the Saliva/Serum Radioactive Iodide Ratio to Diagnose Iodide Transport Defect?
- Published in:
- Thyroid, 2010, v. 20, n. 12, p. 1419, doi. 10.1089/thy.2010.0069
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- Publication type:
- Article
A Novel Homozygous Missense Mutation of the Dual Oxidase 2 (DUOX2) Gene in an Adult Patient with Large Goiter.
- Published in:
- Thyroid, 2008, v. 18, n. 5, p. 561, doi. 10.1089/thy.2007.0258
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- Publication type:
- Article
High Incidence of Thyroid Cancer in Long-Standing Goiterswith Thyroglobulin Mutations.
- Published in:
- Thyroid, 2005, v. 15, n. 9, p. 1079
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- Publication type:
- Article
Transient Hypothyroidism or Persistent Hyperthyrotropinemia in Neonates Born to Mothers with Excessive Iodine Intake.
- Published in:
- Thyroid, 2004, v. 14, n. 12, p. 1077
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- Publication type:
- Article
Analysis of the Promoter of the Thyrotropin Receptor Gene and the Entire Genomic Sequence of Thyroid Transcription Factor-1 in Familial Congenital Hypothyroidism due to Thyrotropin Unresponsiveness.
- Published in:
- Thyroid, 1998, v. 8, n. 4, p. 305, doi. 10.1089/thy.1998.8.305
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- Publication type:
- Article
Different Growth Control of the Two Human Thyroid Cell Lines of Adenomatous Goiter and Papillary Carcinoma.
- Published in:
- Thyroid, 1995, v. 5, n. 1, p. 41, doi. 10.1089/thy.1995.5.41
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- Publication type:
- Article
Effects of Epidermal Growth Factor, Phorbol Ester, and Retinole Acid on Hormone Synthesis and Morphology in Porcine Thyroid Follicles Cultured in Collagen Gel.
- Published in:
- Thyroid, 1992, v. 2, n. 4, p. 351, doi. 10.1089/thy.1992.2.351
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- Publication type:
- Article
Papillary thyroid carcinoma in one of identical twin patients with Pendred syndrome.
- Published in:
- Endocrine Journal, 2013, v. 60, n. 6, p. 805, doi. 10.1507/endocrj.ej12-0396
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- Publication type:
- Article
Goiter in a 6-year-old patient with novel thyroglobulin gene variant (Gly145Glu) causing intracellular thyroglobulin transport disorder: Correlation between goiter size and the free T3 to free T4 ratio.
- Published in:
- Clinical Pediatric Endocrinology, 2022, v. 31, n. 3, p. 185, doi. 10.1297/cpe.2022-0006
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- Publication type:
- Article
Emergence of NDM-1-positive capsulated Escherichia coli with high resistance to serum killing in Japan.
- Published in:
- Journal of Infection & Chemotherapy (Springer Science & Business Media B.V.), 2011, v. 17, n. 3, p. 435, doi. 10.1007/s10156-011-0232-3
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- Publication type:
- Article
A Novel Germline Mutation of KEAP 1 (R483H) Associated with a Non-Toxic Multinodular Goiter.
- Published in:
- 2016
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- Publication type:
- Case Study
Breakthrough viridans streptococcal bacteremia in allogeneic hematopoietic stem cell transplant recipients receiving levofloxacin prophylaxis in a Japanese hospital.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Complete sequencing of an IncFII NDM-1 plasmid in Klebsiella pneumoniae shows structural features shared with other multidrug resistance plasmids.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Complete sequencing of an IncFII NDM-1 plasmid in Klebsiella pneumoniae shows structural features shared with other multidrug resistance plasmids.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Graves' disease and Gitelman syndrome.
- Published in:
- 2016
- By:
- Publication type:
- Letter to the Editor
A Japanese family with familial nonautoimmune hyperthyroidism with a novel mutation (Asn406Ser) in extracellular domain of thyrotrophin receptor.
- Published in:
- Clinical Endocrinology, 2012, v. 77, n. 2, p. 329, doi. 10.1111/j.1365-2265.2011.04324.x
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- Publication type:
- Article
Partial iodide organification defect caused by a novel mutation of the thyroid peroxidase gene in three siblings.
- Published in:
- Clinical Endocrinology, 2003, v. 59, n. 2, p. 198, doi. 10.1046/j.1365-2265.2003.01823.x
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- Publication type:
- Article
Thyroglobulin GeneMutation with Cold Nodule on Thyroid Scintigraphy.
- Published in:
- Case Reports in Endocrinology, 2012, p. 1, doi. 10.1155/2012/280319
- By:
- Publication type:
- Article
First Case of New Delhi Metallo-β-Lactamase 1–Producing Escherichia coli Infection in Japan.
- Published in:
- 2011
- By:
- Publication type:
- Letter