Hiroshi Yoshida

Phylogenetic and antigenic analyses of coxsackievirus A6 isolates in Yamagata, Japan between 2001 and 2017.

K. Mizuta, Y. Katsushima, Y. Aoki, 2019, Vaccine.

Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate‐glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese

K. Hayasaka, K. Akaba, H. Chiba, 1998, Biochemistry and molecular biology international.

Relation between Delayed Superfluous Insulin Secretion during An Oral Glucose Tolerance Test and Metabolic Disorders in Obese Japanese Children

M. Uchiyama, T. Kikuchi, W. Harada, 2011, Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Acanthosis nigricans is a reliable cutaneous marker of insulin resistance in obese Japanese children

Hiroshi Yoshida, S. Ito, Hajime Yamazaki, 2003, Pediatrics international : official journal of the Japan Pediatric Society.

Medium-chain triglycerides supplement therapy with a low-carbohydrate formula can supply energy and enhance ammonia detoxification in the hepatocytes of patients with adult–onset type II citrullinemia

Hiroaki Haga, H. Ohira, M. Yamakawa, 2018, Journal of Inherited Metabolic Disease.

Asymmetrical Graves’ disease in children: potential usefulness of potassium iodide monotherapy

K. Nagasaki, Kentaro Sawano, Hiroshi Yoshida, 2022, BMJ Case Reports.

Soluble LR11 as a Novel Biomarker in Acute Kawasaki Disease.

Kenichi Watanabe, Soichiro Okubo, H. Bujo, 2021, Circulation journal : official journal of the Japanese Circulation Society.