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Factors and impact of physicians’ diagnostic errors in malpractice claims in Japan

PloS one, 2020-08, Vol.15 (8), p.e0237145

2020

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Cognitive Bias and Diagnostic Errors among Physicians in Japan: A Self-Reflection Survey

International journal of environmental research and public health, 2022-04, Vol.19 (8), p.4645

2022

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Clinical and genetic aspects of hypophosphatasia in Japanese patients

Archives of disease in childhood, 2014-03, Vol.99 (3), p.211-215

2014

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Survey of potentially inappropriate prescriptions for common cold symptoms in Japan: A cross-sectional study

PloS one, 2022-05, Vol.17 (5), p.e0265874

2022

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Japan's Academic Barriers to Gender Equality as Seen in a Comparison of Public and Private Medical Schools: A Cross-Sectional Study

Women's health reports (New Rochelle, N.Y.), 2022-01, Vol.3 (1), p.115-123

2022

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Background factors associated with academic motivation for attending medical school immediately after admission in Japan: A single‐center study

Journal of general and family medicine, 2022-05, Vol.23 (3), p.164-171

2022

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Novel compound heterozygous mutations in the SBP2 gene: characteristic clinical manifestations and the implications of GH and triiodothyronine in longitudinal bone growth and maturation

European journal of endocrinology, 2012-04, Vol.166 (4), p.757-764

2012

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Biallelic Inactivation of the Dual Oxidase Maturation Factor 2 (DUOXA2) Gene as a Novel Cause of Congenital Hypothyroidism

The journal of clinical endocrinology and metabolism, 2008-02, Vol.93 (2), p.605-610

2008

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Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision)

Clinical Pediatric Endocrinology, 2015, Vol.24(3), pp.77-105

2015

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Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision)

Clinical Pediatric Endocrinology, 2015, Vol.24(3), pp.107-133

2015

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Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan

Clinical Pediatric Endocrinology, 2015, Vol.24(4), pp.167-173

2015

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P229: Non-coding variants create an enhancer cluster that causes resistance to thyrotropin via long-range interactions with a microRNA promoter

Genetics in Medicine Open, 2024, Vol.2, p.101126, Article 101126

2024

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A case of an infant with congenital combined pituitary hormone deficiency and normalized liver histology of infantile cholestasis after hormone replacement therapy

Clinical Pediatric Endocrinology, 2017, Vol.26(4), pp.251-257

2017

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Japan can learn from the Swedish primary care doctor fostering system

Journal of general and family medicine, 2018-09, Vol.19 (5), p.183-184

2018

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Primary care doctor fostering and clinical research training in Sweden: Implications for Japan

Journal of general and family medicine, 2019-01, Vol.20 (1), p.4-8

2019

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The Utility of Virtual Patient Simulations for Clinical Reasoning Education

International journal of environmental research and public health, 2020-08, Vol.17 (15), p.5325

2020

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A case of an infant with congenital combined pituitary hormone deficiency and normalized liver histology of infantile cholestasis after hormone replacement therapy

Clinical Pediatric Endocrinology, 2017-10, Vol.26 (4), p.251-257

2017

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Mutations in the Small Heterodimer Partner Gene are Associated with Mild Obesity in Japanese subjects

Proceedings of the National Academy of Sciences - PNAS, 2001-01, Vol.98 (2), p.575-580

2001

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Association of the CTLA-4 Gene 49 A/G Polymorphism With Type 1 Diabetes and Autoimmune Thyroid Disease in Japanese Children

Diabetes care, 2003-03, Vol.26 (3), p.843-847

2003

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Thyroid hormone and skeletal metabolism

Clinical calcium, 2014-06, Vol.24 (6), p.821

Onigata, Kazumichi

2014

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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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Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese

Endocrine, 2006-12, Vol.30 (3), p.383-388

2006

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Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan

Clinical Pediatric Endocrinology, 2015-10, Vol.24 (4), p.167-173

2015

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Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision)

Clinical Pediatric Endocrinology, 2015-07, Vol.24 (3), p.107-133

2015

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Resistance to thyroid hormone

Endocrine development, 2014, Vol.26, p.118

2014

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Factors and impact of physicians’ diagnostic errors in malpractice claims in Japan

Cognitive Bias and Diagnostic Errors among Physicians in Japan: A Self-Reflection Survey

Clinical and genetic aspects of hypophosphatasia in Japanese patients

Survey of potentially inappropriate prescriptions for common cold symptoms in Japan: A cross-sectional study

Japan's Academic Barriers to Gender Equality as Seen in a Comparison of Public and Private Medical Schools: A Cross-Sectional Study

Background factors associated with academic motivation for attending medical school immediately after admission in Japan: A single‐center study

Novel compound heterozygous mutations in the SBP2 gene: characteristic clinical manifestations and the implications of GH and triiodothyronine in longitudinal bone growth and maturation

Biallelic Inactivation of the Dual Oxidase Maturation Factor 2 (DUOXA2) Gene as a Novel Cause of Congenital Hypothyroidism

Guidelines for diagnosis and treatment of 21-hydroxylase deficiency (2014 revision)

Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision)

Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan

P229: Non-coding variants create an enhancer cluster that causes resistance to thyrotropin via long-range interactions with a microRNA promoter

A case of an infant with congenital combined pituitary hormone deficiency and normalized liver histology of infantile cholestasis after hormone replacement therapy

Japan can learn from the Swedish primary care doctor fostering system

Primary care doctor fostering and clinical research training in Sweden: Implications for Japan

The Utility of Virtual Patient Simulations for Clinical Reasoning Education

A case of an infant with congenital combined pituitary hormone deficiency and normalized liver histology of infantile cholestasis after hormone replacement therapy

Mutations in the Small Heterodimer Partner Gene are Associated with Mild Obesity in Japanese subjects

Association of the CTLA-4 Gene 49 A/G Polymorphism With Type 1 Diabetes and Autoimmune Thyroid Disease in Japanese Children

Thyroid hormone and skeletal metabolism

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

Clinical significance of heterozygous carriers associated with compensated hypothyroidism in R450H, a common inactivating mutation of the thyrotropin receptor gene in Japanese

Frequencies of spontaneous breast development and spontaneous menarche in Turner syndrome in Japan

Guidelines for Mass Screening of Congenital Hypothyroidism (2014 revision)

Resistance to thyroid hormone

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