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Thyroid function tests and thyroid autoantibody tests, a review

Nihon rinshō, 2012-11, Vol.70 (11), p.1892

Ieiri, Tamio

2012

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Partial iodide organification defect caused by a novel mutation of the thyroid peroxidase gene in three siblings

Clinical endocrinology (Oxford), 2003-08, Vol.59 (2), p.198-206

2003

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A novel compound heterozygous mutation in the thyroglobulin gene resulting in congenital goitrous hypothyroidism with high serum triiodothyronine levels

Journal of human genetics, 2006-04, Vol.51 (4), p.379-382

2006

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Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene

Pediatrics international, 2005-02, Vol.47 (1), p.105-108

2005

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Clinical significance of measurement of plasma annexin V concentration of patients in the emergency room

Resuscitation, 2003-05, Vol.57 (2), p.171-177

2003

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Report of the IFCC Working Group for Standardization of Thyroid Function Tests; Part 1: Thyroid-Stimulating Hormone

Clinical chemistry (Baltimore, Md.), 2010-06, Vol.56 (6), p.902-911

2010

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Report of the IFCC Working Group for Standardization of Thyroid Function Tests; Part 2: Free Thyroxine and Free Triiodothyronine

Clinical chemistry (Baltimore, Md.), 2010-06, Vol.56 (6), p.912-920

2010

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Thyroxine binding globulin (TBG), triiodothyronine uptake (T3U), thyroxine binding capacity (TBC)

Nihon rinshō, 2010-07, Vol.68 Suppl 7, p.300

Ieiri, Tamio

2010

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Total triiodothyronine (TT3), free triiodothyronine (FT3), reverse T3 (rT3)

Nihon rinshō, 2010-07, Vol.68 Suppl 7, p.284

Ieiri, Tamio

2010

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Does smoking cessation with varenicline worsen vascular endothelial function?

BMJ open, 2013-06, Vol.3 (6), p.e003052

2013

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High Incidence of Thyroid Cancer in Long-Standing Goiters with Thyroglobulin Mutations

Thyroid (New York, N.Y.), 2005-09, Vol.15 (9), p.179-1084

2005

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Thyroglobulin Gene Mutations Producing Defective Intracellular Transport of Thyroglobulin Are Associated with Increased Thyroidal Type 2 Iodothyronine Deiodinase Activity

The journal of clinical endocrinology and metabolism, 2007-04, Vol.92 (4), p.1451-1457

2007

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Haplotype Analysis Reveals Founder Effects of Thyroglobulin Gene Mutations C1058R and C1977S in Japan

The journal of clinical endocrinology and metabolism, 2006-08, Vol.91 (8), p.3100-3104

2006

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A novel homozygous missense mutation of the dual oxidase 2 (DUOX2) gene in an adult patient with large goiter

Thyroid (New York, N.Y.), 2008-05, Vol.18 (5), p.561-566

2008

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Ectopic thyroid

Nihon rinshō, 2006-05, Vol.Suppl 1, p.539

Ieiri, Tamio

2006

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Defects in the coupling of iodotyrosyl residues

Nihon rinshō, 2006-05, Vol.Suppl 1, p.367

Ieiri, Tamio

2006

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Report of the IFCC Working Group for Standardization of Thyroid Function Tests; Part 3: Total Thyroxine and Total Triiodothyronine

Clinical chemistry (Baltimore, Md.), 2010-06, Vol.56 (6), p.921-929

2010

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Thyroxine binding globulin (TBG), triiodothyronine uptake (T3U), thyroxine binding capacity (TBC)

Nihon rinshō, 2005-08, Vol.63 Suppl 8, p.272

Ieiri, Tamio

2005

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Total triiodothyronine (TT3), free triiodothyronine (FT3), reverse T3 (rT3)

Nihon rinshō, 2005-08, Vol.63 Suppl 8, p.258

Ieiri, Tamio

2005

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Missense Mutation (C1263R) in the Thyroglobulin Gene Causes Congenital Goiter with Mild Hypothyroidism by Impaired Intracellular Transport

Endocrine Journal, 1998, Vol.45(3), pp.315-327

1998

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Sequence Analysis of Thyroid Transcription Factor-1 Gene Reveals Absence of Mutations in Patients with Thyroid Dysgenesis but Presence of Polymorphisms in the 5' Flanking Region and Intron

Endocrine Journal, 1998, Vol.45(4), pp.563-567

1998

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Proposal of a candidate international conventional reference measurement procedure for free thyroxine in serum

Clinical chemistry and laboratory medicine, 2007-01, Vol.45 (7), p.934-936

2007

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P4-16-3 Genomic microdeletion of 6,675 nucleotides encompassing exon 28 and 29 of thyroglobulin(Tg)gene was found with a compound heterozygous occurrence of single nucleotide deletion 7890delT

ENDOCRINE JOURNAL, 2010, Vol.57 (suppl.2-2), p.S478-S478

2010

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Medical technologist as a member of infection control team

Rinsho byori. The Japanese journal of clinical pathology, 2005-11, Vol.53 (11), p.1036

2005

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A case of pseudo-Bartter's syndrome induced by long-term ingestion of furosemide delivered orally through health tea

The Japanese Journal of Nephrology, 2003/07/25, Vol.45(5), pp.457-463

2003

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Thyroid function tests and thyroid autoantibody tests, a review

Partial iodide organification defect caused by a novel mutation of the thyroid peroxidase gene in three siblings

A novel compound heterozygous mutation in the thyroglobulin gene resulting in congenital goitrous hypothyroidism with high serum triiodothyronine levels

Subclinical hypothyroidism caused by a mutation of the thyrotropin receptor gene

Clinical significance of measurement of plasma annexin V concentration of patients in the emergency room

Report of the IFCC Working Group for Standardization of Thyroid Function Tests; Part 1: Thyroid-Stimulating Hormone

Report of the IFCC Working Group for Standardization of Thyroid Function Tests; Part 2: Free Thyroxine and Free Triiodothyronine

Thyroxine binding globulin (TBG), triiodothyronine uptake (T3U), thyroxine binding capacity (TBC)

Total triiodothyronine (TT3), free triiodothyronine (FT3), reverse T3 (rT3)

Does smoking cessation with varenicline worsen vascular endothelial function?

High Incidence of Thyroid Cancer in Long-Standing Goiters with Thyroglobulin Mutations

Thyroglobulin Gene Mutations Producing Defective Intracellular Transport of Thyroglobulin Are Associated with Increased Thyroidal Type 2 Iodothyronine Deiodinase Activity

Haplotype Analysis Reveals Founder Effects of Thyroglobulin Gene Mutations C1058R and C1977S in Japan

A novel homozygous missense mutation of the dual oxidase 2 (DUOX2) gene in an adult patient with large goiter

Ectopic thyroid

Defects in the coupling of iodotyrosyl residues

Report of the IFCC Working Group for Standardization of Thyroid Function Tests; Part 3: Total Thyroxine and Total Triiodothyronine

Thyroxine binding globulin (TBG), triiodothyronine uptake (T3U), thyroxine binding capacity (TBC)

Total triiodothyronine (TT3), free triiodothyronine (FT3), reverse T3 (rT3)

Missense Mutation (C1263R) in the Thyroglobulin Gene Causes Congenital Goiter with Mild Hypothyroidism by Impaired Intracellular Transport

Sequence Analysis of Thyroid Transcription Factor-1 Gene Reveals Absence of Mutations in Patients with Thyroid Dysgenesis but Presence of Polymorphisms in the 5' Flanking Region and Intron

Proposal of a candidate international conventional reference measurement procedure for free thyroxine in serum

P4-16-3 Genomic microdeletion of 6,675 nucleotides encompassing exon 28 and 29 of thyroglobulin(Tg)gene was found with a compound heterozygous occurrence of single nucleotide deletion 7890delT

Medical technologist as a member of infection control team

A case of pseudo-Bartter's syndrome induced by long-term ingestion of furosemide delivered orally through health tea

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