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Steroid-induced diabetes: a clinical and molecular approach to understanding and treatment

Diabetes/metabolism research and reviews, 2014-02, Vol.30 (2), p.96-102

2014

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A study of recurrence and death from papillary thyroid cancer with 27 years of median follow-up

Surgery, 2013-12, Vol.154 (6), p.1436-1447

2013

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American Thyroid Association Guide to investigating thyroid hormone economy and action in rodent and cell models

Thyroid (New York, N.Y.), 2014-01, Vol.24 (1), p.88

2014

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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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Homozygous Thyroid Hormone Receptor β-Gene Mutations in Resistance to Thyroid Hormone: Three New Cases and Review of the Literature

The journal of clinical endocrinology and metabolism, 2012-04, Vol.97 (4), p.1328-1336

2012

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Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing Congenital Hypothyroidism

Thyroid (New York, N.Y.), 2021-10, Vol.31 (10), p.1589

2021

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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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Defects of Thyroid Hormone Synthesis and Action

Endocrinology and metabolism clinics of North America, 2017-06, Vol.46 (2), p.375-388

2017

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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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Approach to the Patient with Resistance to Thyroid Hormone and Pregnancy

The journal of clinical endocrinology and metabolism, 2010-07, Vol.95 (7), p.3094-3102

2010

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Measurement of Reverse Triiodothyronine Level and the Triiodothyronine to Reverse Triiodothyronine Ratio in Dried Blood Spot Samples at Birth May Facilitate Early Detection of Monocarboxylate Transporter 8 Deficiency

Thyroid (New York, N.Y.), 2021-09, Vol.31 (9), p.1316-1321

2021

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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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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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A Novel Missense Mutation in the SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism

Thyroid (New York, N.Y.), 2018-08, Vol.28 (8), p.1068-1070

2018

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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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Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C)

Thyroid (New York, N.Y.), 2023-02, Vol.33 (2), p.261

2023

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Adeno Associated Virus 9-Based Gene Therapy Delivers a Functional Monocarboxylate Transporter 8, Improving Thyroid Hormone Availability to the Brain of Mct8-Deficient Mice

Thyroid (New York, N.Y.), 2016-09, Vol.26 (9), p.1311-1319

2016

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Prenatal Diagnosis of Resistance to Thyroid Hormone and Its Clinical Implications

The journal of clinical endocrinology and metabolism, 2017-10, Vol.102 (10), p.3775-3782

2017

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Mutations in SECISBP2 result in abnormal thyroid hormone metabolism

Nature genetics, 2005-11, Vol.37 (11), p.1247-1252

2005

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Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital Hypothyroidism

Thyroid (New York, N.Y.), 2020-05, Vol.30 (5), p.780-782

2020

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Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese Families

Thyroid (New York, N.Y.), 2019-02, Vol.29 (2), p.302-304

2019

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The Thyroid Hormone Analog DITPA Ameliorates Metabolic Parameters of Male Mice With Mct8 Deficiency

Endocrinology (Philadelphia), 2015-11, Vol.156 (11), p.3889-3894

2015

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Steroid-induced diabetes: a clinical and molecular approach to understanding and treatment

A study of recurrence and death from papillary thyroid cancer with 27 years of median follow-up

American Thyroid Association Guide to investigating thyroid hormone economy and action in rodent and cell models

Diiodothyropropionic Acid (DITPA) in the Treatment of MCT8 Deficiency

Homozygous Thyroid Hormone Receptor β-Gene Mutations in Resistance to Thyroid Hormone: Three New Cases and Review of the Literature

Novel DIO1 Gene Mutation Acting as Phenotype Modifier for Novel Compound Heterozygous TPO Gene Mutations Causing Congenital Hypothyroidism

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

Defects of Thyroid Hormone Synthesis and Action

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

Approach to the Patient with Resistance to Thyroid Hormone and Pregnancy

Measurement of Reverse Triiodothyronine Level and the Triiodothyronine to Reverse Triiodothyronine Ratio in Dried Blood Spot Samples at Birth May Facilitate Early Detection of Monocarboxylate Transporter 8 Deficiency

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

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

A Novel Missense Mutation in the SLC5A5 Gene in a Sudanese Family with Congenital Hypothyroidism

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

Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion

STR mutations on chromosome 15q cause thyrotropin resistance by activating a primate-specific enhancer of MIR7-2/MIR1179

Congenital Hypothyroidism in Two Sudanese Families Harboring a Novel Iodotyrosine Deiodinase Mutation (IYD R279C)

Adeno Associated Virus 9-Based Gene Therapy Delivers a Functional Monocarboxylate Transporter 8, Improving Thyroid Hormone Availability to the Brain of Mct8-Deficient Mice

Prenatal Diagnosis of Resistance to Thyroid Hormone and Its Clinical Implications

Mutations in SECISBP2 result in abnormal thyroid hormone metabolism

Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital Hypothyroidism

Congenital Hypothyroidism due to Oligogenic Mutations in Two Sudanese Families

The Thyroid Hormone Analog DITPA Ameliorates Metabolic Parameters of Male Mice With Mct8 Deficiency

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