Koji Muroya
Yokohama, Japan
Last Updated: 09/26/2026
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Found 87 publications
Health-Related Quality of Life and Its Related Factors in Adolescents and Adults With Prader-Willi Syndrome in Japan.
Journal: American journal of medical genetics. Part A
Published: January 06, 2026
Long-term effectiveness and safety of daily growth hormone therapy in Japanese children with Noonan syndrome: a post-marketing surveillance study.
Journal: Endocrine journal
Published: November 24, 2025
Age-related changes in thyroid hormone profile in pediatric patients with Down syndrome.
Journal: Endocrine journal
Published: November 05, 2025
A questionnaire-based survey on hyperphagia in individuals with Prader-Willi syndrome in Japan.
Journal: Endocrine journal
Published: July 24, 2025
Improvement in body composition of Japanese participants with Prader-Willi syndrome following somatropin treatment: an open-label, multi cohort Phase 3 study.
Journal: Endocrine journal
Published: May 28, 2025
Necrotizing enterocolitis following a single very low dose of octreotide in a patient with congenital hyperinsulinism: a case successfully managed with 18F-DOPA PET/CT-guided surgery.
Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: February 16, 2025
Letter to the Editor: Familial and early recurrent pheochromocytoma in a child with a novel in-frame duplication variant of VHL.
Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: February 04, 2025
Clinicopathological and genomic analysis of pediatric pheochromocytoma and sympathetic paraganglioma.
Journal: Endocrine journal
Published: February 02, 2025
Genetic and Clinical Characteristics of 185 Japanese Children With 46,XY Differences of Sex Development.
Journal: The Journal of clinical endocrinology and metabolism
Published: August 16, 2024
Psychiatric symptoms in children and adolescents with Graves' disease: A retrospective study and a prospective study.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: July 18, 2024
Molecular and Clinical Features of Congenital Hypothyroidism Due to Multiple DUOX2 Variants.
Journal: Thyroid : official journal of the American Thyroid Association
Published: May 17, 2024
Noonan syndrome-like phenotype associated with an ERF frameshift variant.
Journal: American journal of medical genetics. Part A
Published: December 20, 2023
Last Updated: 09/26/2026