Tatsuo Ogawa

Shizuoka, 4208527, Japan

Last Updated: 09/26/2026

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Found 9 publications

Acute Autonomic Sensory Neuropathy Causing Severe Hyponatremia: A Rare Cause of Syndrome of Inappropriate Antidiuresis.

Acute Autonomic Sensory Neuropathy Causing Severe Hyponatremia: A Rare Cause of Syndrome of Inappropriate Antidiuresis.

Journal: JCEM case reports

Published: August 26, 2025

A case of hypophysitis after COVID-19 vaccination with a detection of anti-pituitary antibody, with review of literature.

A case of hypophysitis after COVID-19 vaccination with a detection of anti-pituitary antibody, with review of literature.

Journal: Endocrine journal

Published: May 06, 2024

An Asymptomatic Case With MEN1 Slipping Through Genetic Screening by SNV-dependent Allelic Dropout.

An Asymptomatic Case With MEN1 Slipping Through Genetic Screening by SNV-dependent Allelic Dropout.

Journal: Journal of the Endocrine Society

Published: April 04, 2022

Comparisons of plasma aldosterone and renin data between an automated chemiluminescent immunoanalyzer and conventional radioimmunoassays in the screening and diagnosis of primary aldosteronism.

Comparisons of plasma aldosterone and renin data between an automated chemiluminescent immunoanalyzer and conventional radioimmunoassays in the screening and diagnosis of primary aldosteronism.

Journal: PloS one

Published: February 21, 2021

Parameters of captopril challenge test can predict results of other confirmatory tests for primary aldosteronism and propose the next test to be done.

Parameters of captopril challenge test can predict results of other confirmatory tests for primary aldosteronism and propose the next test to be done.

Journal: Endocrine journal

Published: April 07, 2020

ARMC5 Alterations in Primary Macronodular Adrenal Hyperplasia (PMAH) and the Clinical State of Variant Carriers.

ARMC5 Alterations in Primary Macronodular Adrenal Hyperplasia (PMAH) and the Clinical State of Variant Carriers.

Journal: Journal of the Endocrine Society

Published: May 31, 2019

Novel germline variant of TMEM127 gene in a patient with familial pheochromocytoma.

Novel germline variant of TMEM127 gene in a patient with familial pheochromocytoma.

Journal: Endocrinology, diabetes & metabolism case reports

Published: February 21, 2017

Asymptomatic Congenital Hyperinsulinism due to a Glucokinase-Activating Mutation, Treated as Adrenal Insufficiency for Twelve Years.

Asymptomatic Congenital Hyperinsulinism due to a Glucokinase-Activating Mutation, Treated as Adrenal Insufficiency for Twelve Years.

Journal: Case reports in endocrinology

Published: November 15, 2016

Low-dose glimepiride with sitagliptin improves glycemic control without dose-dependency in patients with type 2 diabetes inadequately controlled on high-dose glimepiride.

Low-dose glimepiride with sitagliptin improves glycemic control without dose-dependency in patients with type 2 diabetes inadequately controlled on high-dose glimepiride.

Journal: Endocrine journal

Published: August 30, 2014

Showing 1-9 of 9

Last Updated: 09/26/2026