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Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan

Endocrine Journal, 2024, Vol.71(5), pp.471-480

2024

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A case of congenital hyperinsulinism presenting with diabetes after long-term diazoxide therapy

Diabetology international, 2024-07, Vol.15 (3), p.600-604

2024

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Two Cases of New-onset Pediatric Diabetes With Delayed Diagnosis and Treatment Due to the Coronavirus Disease 2019 Pandemic

Journal of the Japan Diabetes Society, 2023/01/30, Vol.66(1), pp.26-31

2023

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Questionnaire survey on severe hypoglycemia in pediatric patients with diabetes-English version

Diabetology international, 2024-10, Vol.15 (4), p.666-672

2024

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Clinical and Genetic Characteristics in Patients With Gitelman Syndrome

Kidney international reports, 2019-01, Vol.4 (1), p.119-125

2019

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Age-Related Clinical Characteristics of Isolated Congenital Unilateral Absence of a Pulmonary Artery

Pediatric cardiology, 2010-11, Vol.31 (8), p.1186-1190

2010

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A Retrospective Analysis of the Growth Pattern in Patients with Salt-wasting 21-Hydroxylase Deficiency

Clinical Pediatric Endocrinology, 2014, Vol.23(2), pp.27-34

2014

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Improving circulatory disturbance in transient abnormal myelopoiesis

Journal of pediatric hematology/oncology, 2012-05, Vol.34 (4), p.e149-e151

2012

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PAPA-1 Is a Nuclear Binding Partner of IGFBP-2 and Modulates Its Growth-Promoting Actions

Molecular endocrinology (Baltimore, Md.), 2009-02, Vol.23 (2), p.169-175

2009

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A Retrospective Analysis of the Growth Pattern in Patients with Salt-wasting 21-Hydroxylase Deficiency

Clinical Pediatric Endocrinology, 2014-04, Vol.23 (2), p.27-34

2014

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Vitamin D deficiency presenting in an infant with neonatal lupus erythematosus

Pediatrics international, 2011-04, Vol.53 (2), p.255-258

2011

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Predisposition to Subdural Hemorrhage in X-Linked Myotubular Myopathy

Pediatric neurology, 2012-05, Vol.46 (5), p.332-334

2012

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Hypocalcemia and Graves' disease associated with 22q11.2 deletion syndrome

Pediatrics international, 2023-01, Vol.65 (1), p.e15709-n/a

2023

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Clinical Features of 57 Patients with Lipoid Congenital Adrenal Hyperplasia: Criteria for Nonclassic Form Revisited

The journal of clinical endocrinology and metabolism, 2020-11, Vol.105 (11), p.1-e3937

2020

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Vitamin D deficiency rickets caused by improper lifestyle in Japanese children

Pediatrics international, 2005-04, Vol.47 (2), p.142-146

2005

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Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan

Endocrine Journal, 2024, pp.EJ23-0391

2024

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Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan

ENDOCRINE JOURNAL, 2024, Vol.71 (5), p.471-480

2024

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Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities

Nature genetics, 2024-05, Vol.56 (5), p.869-876

2024

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In Vivo Determination of Replication Origins of Human Mitochondrial DNA by Ligation-mediated Polymerase Chain Reaction

The Journal of biological chemistry, 1997-06, Vol.272 (24), p.15275-15279

1997

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Two Cases of Allgrove Syndrome with Mutations in the AAAS Gene

Endocrine Journal, 2004, Vol.51(5), pp.473-477

2004

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MON-261 Investigation of GNAS1 Gene Mutations and Expression Patterns of Fibroblast Growth Factor 23 Protein in McCune-Albright Syndrome

Journal of the Endocrine Society, 2019-04, Vol.3 (Supplement_1)

2019

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Association Study of Human MTH1 Gene Polymorphisms with Type 1 Diabetes Mellitus

Endocrine Journal, 2004, Vol.51(5), pp.493-498

2004

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A Case of Diabetic Lipemia at the Onset of Type 1 Diabetes Mellitus in 4-Year-Old Girl

Journal of the Japan Diabetes Society, 2016/08/20, Vol.59(8), pp.576-581

2016

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Case Report: Adjuvant Therapy with a High Dose of Mitotane for Adrenocortical Carcinoma in a 4-year-old Boy

Clinical Pediatric Endocrinology, 2008, Vol.17(3), pp.71-74

2008

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Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan

A case of congenital hyperinsulinism presenting with diabetes after long-term diazoxide therapy

Two Cases of New-onset Pediatric Diabetes With Delayed Diagnosis and Treatment Due to the Coronavirus Disease 2019 Pandemic

Questionnaire survey on severe hypoglycemia in pediatric patients with diabetes-English version

Clinical and Genetic Characteristics in Patients With Gitelman Syndrome

Age-Related Clinical Characteristics of Isolated Congenital Unilateral Absence of a Pulmonary Artery

A Retrospective Analysis of the Growth Pattern in Patients with Salt-wasting 21-Hydroxylase Deficiency

Improving circulatory disturbance in transient abnormal myelopoiesis

PAPA-1 Is a Nuclear Binding Partner of IGFBP-2 and Modulates Its Growth-Promoting Actions

A Retrospective Analysis of the Growth Pattern in Patients with Salt-wasting 21-Hydroxylase Deficiency

Vitamin D deficiency presenting in an infant with neonatal lupus erythematosus

Predisposition to Subdural Hemorrhage in X-Linked Myotubular Myopathy

Hypocalcemia and Graves' disease associated with 22q11.2 deletion syndrome

SAMD9 mutations cause a novel multisystem disorder, MIRAGE syndrome, and are associated with loss of chromosome 7

Clinical Features of 57 Patients with Lipoid Congenital Adrenal Hyperplasia: Criteria for Nonclassic Form Revisited

Vitamin D deficiency rickets caused by improper lifestyle in Japanese children

Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan

Clinical and molecular analyses of isolated central congenital hypothyroidism based on a survey conducted in Japan

Functional variants in a TTTG microsatellite on 15q26.1 cause familial nonautoimmune thyroid abnormalities

In Vivo Determination of Replication Origins of Human Mitochondrial DNA by Ligation-mediated Polymerase Chain Reaction

Two Cases of Allgrove Syndrome with Mutations in the AAAS Gene

MON-261 Investigation of GNAS1 Gene Mutations and Expression Patterns of Fibroblast Growth Factor 23 Protein in McCune-Albright Syndrome

Association Study of Human MTH1 Gene Polymorphisms with Type 1 Diabetes Mellitus

A Case of Diabetic Lipemia at the Onset of Type 1 Diabetes Mellitus in 4-Year-Old Girl

Case Report: Adjuvant Therapy with a High Dose of Mitotane for Adrenocortical Carcinoma in a 4-year-old Boy

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