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The syndromes of reduced sensitivity to thyroid hormone

Biochimica et biophysica acta, 2013-07, Vol.1830 (7), p.3987-4003

2013

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Generation of functional thyroid from embryonic stem cells

Nature (London), 2012-11, Vol.491 (7422), p.66-71

2012

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Paradigms of Dynamic Control of Thyroid Hormone Signaling

Endocrine reviews, 2019-08, Vol.40 (4), p.1000-1047

2019

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Syndromes of reduced sensitivity to thyroid hormone: genetic defects in hormone receptors, cell transporters and deiodination

Baillière's best practice & research. Clinical endocrinology & metabolism, 2007-06, Vol.21 (2), p.277-305

2007

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Reduced Sensitivity to Thyroid Hormone as a Transgenerational Epigenetic Marker Transmitted Along the Human Male Line

Thyroid (New York, N.Y.), 2019-06, Vol.29 (6), p.778-782

2019

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Effect of the Fetal THRB Genotype on the Placenta

The journal of clinical endocrinology and metabolism, 2023-09, Vol.108 (10), p.e944-e948

2023

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Diiodothyropropionic Acid (DITPA) in the Treatment of MCT8 Deficiency

The journal of clinical endocrinology and metabolism, 2012-12, Vol.97 (12), p.4515-4523

2012

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Extended Absorption of Liothyronine from Poly-Zinc-Liothyronine: Results from a Phase 1, Double-Blind, Randomized, and Controlled Study in Humans

Thyroid (New York, N.Y.), 2022-02, Vol.32 (2), p.196-205

2022

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A Novel Pathogenic Variant in PAX8 Leads to Familial Congenital Hypothyroidism

Thyroid (New York, N.Y.), 2022-08, Vol.32 (8), p.1000-1002

2022

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Tissue-Specific Thyroid Hormone Deprivation and Excess in Monocarboxylate Transporter (Mct) 8-Deficient Mice

Endocrinology (Philadelphia), 2006-09, Vol.147 (9), p.4036-4043

2006

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Very Severe Resistance to Thyroid Hormone β in One of Three Affected Members of a Family with a Novel Mutation in the THRB Gene

Thyroid (New York, N.Y.), 2019-10, Vol.29 (10), p.1518-1520

2019

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The Relationship Between Fetal THRB Genotype and Maternal Thyroid Function

Thyroid (New York, N.Y.), 2023-10, Vol.33 (10), p.1255-1258

2023

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Cerebral cortex hyperthyroidism of newborn mct8-deficient mice transiently suppressed by lat2 inactivation

PloS one, 2014-05, Vol.9 (5), p.e96915-e96915

2014

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Early Diagnosis and Treatment of an Infant with a Novel Thyroid Hormone Receptor α Gene (pC380SfsX9) Mutation

Thyroid (New York, N.Y.), 2021-06, Vol.31 (6), p.1003-1005

2021

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Human Type 1 Iodothyronine Deiodinase ( DIO1 ) Mutations Cause Abnormal Thyroid Hormone Metabolism

Thyroid (New York, N.Y.), 2021-02, Vol.31 (2), p.202-207

2021

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Graves’ disease and papillary thyroid carcinoma: case report and literature review of a single academic center

BMC endocrine disorders, 2022-08, Vol.22 (1), p.1-199, Article 199

2022

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Combined Levothyroxine and Propylthiouracil Treatment in Children with Monocarboxylate Transporter 8 Deficiency: A Multicenter Case Series of 12 Patients

Thyroid (New York, N.Y.), 2024-09

2024

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Inherited defects in thyroid hormone cell-membrane transport and metabolism

Baillière's best practice & research. Clinical endocrinology & metabolism, 2014-03, Vol.28 (2), p.189-201

2014

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Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation

Thyroid (New York, N.Y.), 2021-05, Vol.31 (5), p.713-720

2021

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Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism

The journal of clinical endocrinology and metabolism, 2020-05, Vol.105 (5), p.1564-1572

2020

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Role of the Thyroid Gland in Expression of the Thyroid Phenotype of Sbp2-Deficient Mice

Endocrinology (Philadelphia), 2020-05, Vol.161 (5), p.1

2020

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Changes in Thyroid Status During Perinatal Development of MCT8-Deficient Male Mice

Endocrinology (Philadelphia), 2013-07, Vol.154 (7), p.2533-2541

2013

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Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion

The Journal of clinical investigation, 2010-09, Vol.120 (9), p.3377-3388

2010

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Year in Thyroidology: Basic Science

Thyroid (New York, N.Y.), 2023-01, Vol.33 (1), p.16-20

Dumitrescu, Alexandra

2023

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Importance of Monocarboxylate Transporter 8 for the Blood-Brain Barrier-Dependent Availability of 3,5,3′-Triiodo-l-Thyronine

Endocrinology (Philadelphia), 2009-05, Vol.150 (5), p.2491-2496

2009

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The syndromes of reduced sensitivity to thyroid hormone

Generation of functional thyroid from embryonic stem cells

Paradigms of Dynamic Control of Thyroid Hormone Signaling

Syndromes of reduced sensitivity to thyroid hormone: genetic defects in hormone receptors, cell transporters and deiodination

Reduced Sensitivity to Thyroid Hormone as a Transgenerational Epigenetic Marker Transmitted Along the Human Male Line

Effect of the Fetal THRB Genotype on the Placenta

Diiodothyropropionic Acid (DITPA) in the Treatment of MCT8 Deficiency

Extended Absorption of Liothyronine from Poly-Zinc-Liothyronine: Results from a Phase 1, Double-Blind, Randomized, and Controlled Study in Humans

A Novel Pathogenic Variant in PAX8 Leads to Familial Congenital Hypothyroidism

Tissue-Specific Thyroid Hormone Deprivation and Excess in Monocarboxylate Transporter (Mct) 8-Deficient Mice

Very Severe Resistance to Thyroid Hormone β in One of Three Affected Members of a Family with a Novel Mutation in the THRB Gene

The Relationship Between Fetal THRB Genotype and Maternal Thyroid Function

Cerebral cortex hyperthyroidism of newborn mct8-deficient mice transiently suppressed by lat2 inactivation

Early Diagnosis and Treatment of an Infant with a Novel Thyroid Hormone Receptor α Gene (pC380SfsX9) Mutation

Human Type 1 Iodothyronine Deiodinase ( DIO1 ) Mutations Cause Abnormal Thyroid Hormone Metabolism

Graves’ disease and papillary thyroid carcinoma: case report and literature review of a single academic center

Combined Levothyroxine and Propylthiouracil Treatment in Children with Monocarboxylate Transporter 8 Deficiency: A Multicenter Case Series of 12 Patients

Inherited defects in thyroid hormone cell-membrane transport and metabolism

Prenatal Treatment of Thyroid Hormone Cell Membrane Transport Defect Caused by MCT8 Gene Mutation

Increased Prevalence of TG and TPO Mutations in Sudanese Children With Congenital Hypothyroidism

Role of the Thyroid Gland in Expression of the Thyroid Phenotype of Sbp2-Deficient Mice

Changes in Thyroid Status During Perinatal Development of MCT8-Deficient Male Mice

Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion

Year in Thyroidology: Basic Science

Importance of Monocarboxylate Transporter 8 for the Blood-Brain Barrier-Dependent Availability of 3,5,3′-Triiodo-l-Thyronine

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