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Publications by Tetsushi Maruta

Congenital Primary Hypothyroidism With the Homozygous Nonsense Mutation P.K1374* in the Thyroglobulin Gene and a Normal-Sized Thyroid Gland on Levothyroxine Replacement

Internal Medicine

Medicine

2019

English

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A Homozygous Nonsense Thyroid Peroxidase Mutation (R540X) Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous Family

JCRPE Journal of Clinical Research in Pediatric Endocrinology

English

Congenital Central Hypothyroidism Due to a Homozygous Mutation in theTSHβSubunit Gene

Case Reports in Pediatrics

2011

English

Mutation Screening of the Thyroid Peroxidase Gene in a Cohort of 55 Portuguese Patients With Congenital Hypothyroidism

European Journal of Endocrinology

English

Combined Levothyroxine Plus Liothyronine Compared With Levothyroxine Alone in Primary Hypothyroidism

JAMA - Journal of the American Medical Association

Medicine

2003

English

Severe Cystic Fibrosis in a Child Homozygous for the G542 Nonsense Mutation in the CFTR Gene.

Journal of Medical Genetics

Genetics

1993

English

The Association Between Serum TSH Levels and BMI Percentiles in Children With Primary Hypothyroidism That Are Chemically Euthyroid on Levothyroxine Replacement

JCRPE Journal of Clinical Research in Pediatric Endocrinology

English

Two Siblings With Congenital Central Hypothyroidism Caused by a Novel Mutation in the IGSF1 Gene

Clinical Pediatric Endocrinology

English

Anti-Thyroid Peroxidase and Anti-Thyroglobulin Antibodies in Patients With Hypothyroidism

Journal of Medical Science And clinical Research

2016

English

“Effects of Levothyroxine Replacement Therapy on Insulin Sensitivity in Subjects With Overt Hypothyroidism.”

International Journal of Advanced Research

2016

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Tetsushi Maruta

Congenital Primary Hypothyroidism With the Homozygous Nonsense Mutation P.K1374* in the Thyroglobulin Gene and a Normal-Sized Thyroid Gland on Levothyroxine Replacement

Related publications

A Homozygous Nonsense Thyroid Peroxidase Mutation (R540X) Consistently Causes Congenital Hypothyroidism in Two Siblings Born to a Consanguineous Family

Congenital Central Hypothyroidism Due to a Homozygous Mutation in theTSHβSubunit Gene

Mutation Screening of the Thyroid Peroxidase Gene in a Cohort of 55 Portuguese Patients With Congenital Hypothyroidism

Combined Levothyroxine Plus Liothyronine Compared With Levothyroxine Alone in Primary Hypothyroidism

Severe Cystic Fibrosis in a Child Homozygous for the G542 Nonsense Mutation in the CFTR Gene.

The Association Between Serum TSH Levels and BMI Percentiles in Children With Primary Hypothyroidism That Are Chemically Euthyroid on Levothyroxine Replacement

Two Siblings With Congenital Central Hypothyroidism Caused by a Novel Mutation in the IGSF1 Gene

Anti-Thyroid Peroxidase and Anti-Thyroglobulin Antibodies in Patients With Hypothyroidism

“Effects of Levothyroxine Replacement Therapy on Insulin Sensitivity in Subjects With Overt Hypothyroidism.”