Yuki Sonoyama-Kawashima - Publications

First Japanese Case of Hereditary Transthyretin Amyloid Cardiomyopathy with an Ile68Leu Variant: A Case Report.

Journal: Internal medicine (Tokyo, Japan)

Published: June 10, 2026

A New Program for Determining Abnormal Growth Curves in School Health Checkups.

Journal: The Journal of school health

Published: April 24, 2025

Clinical characteristics of and growth hormone treatment effects on short stature with type 1 insulin-like growth factor receptor (IGF1R) gene alteration.

Journal: Endocrine journal

Published: May 06, 2024

MELAS-Derived Neurons Functionally Improve by Mitochondrial Transfer from Highly Purified Mesenchymal Stem Cells (REC).

Journal: International journal of molecular sciences

Published: November 17, 2023

Extracellular Vesicles and Cx43-Gap Junction Channels Are the Main Routes for Mitochondrial Transfer from Ultra-Purified Mesenchymal Stem Cells, RECs.

Journal: International journal of molecular sciences

Published: April 21, 2023

Various phenotypes of short stature with heterozygous IGF-1 receptor (IGF1R) mutations.

Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology

Published: October 20, 2021

The case of a patient with MIRAGE syndrome with familial dysautonomia-like symptoms.

Journal: Human genome variation

Published: March 04, 2021

Cord Blood from SGA Preterm Infants Exhibits Increased GLUT4 mRNA Expression.

Journal: Yonago acta medica

Published: November 17, 2020

Genotype-Structure-Phenotype Correlations of Disease-Associated IGF1R Variants and Similarities to Those of INSR Variants.

Journal: Diabetes

Published: November 12, 2020

IGF2 Mutations.

Journal: The Journal of clinical endocrinology and metabolism

Published: April 10, 2019

A novel frameshift mutation in NR3C2 leads to decreased expression of mineralocorticoid receptor: a family with renal pseudohypoaldosteronism type 1.

Journal: Endocrine journal

Published: October 12, 2016

Heterozygous nonsense mutations near the C-terminal region of IGF1R in two patients with small-for-gestational-age-related short stature.

Journal: Clinical endocrinology

Published: January 26, 2015