Yasuko Shoji
Izumi, Japan
Last Updated: 09/26/2026
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Found 15 publications
Genetic backgrounds and genotype-phenotype relationships in anthropometric parameters of 116 Japanese individuals with Noonan syndrome.
Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: January 09, 2024
Diagnostic Pitfall: Mosaic Turner syndrome with a 46, XY lymphocyte karyotype.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: October 01, 2020
Renal function in short-statured children born small for gestational age and treated with growth hormone.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: August 26, 2020
Visceral adipose tissue resides within the reference range in children with Prader-Willi syndrome receiving nutritional intervention on a regular basis.
Journal: Endocrine journal
Published: June 23, 2020
Central hypothyroidism improves with age in very young children with Prader-Willi syndrome.
Journal: Clinical endocrinology
Published: May 25, 2020
Fat distribution in short-stature children born small for gestational age.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: March 10, 2020
MIRAGE syndrome caused by a novel missense variant (p.Ala1479Ser) in the SAMD9 gene.
Journal: Human genome variation
Published: October 08, 2019
Growth hormone treatment for extremely low birthweight children born small for gestational age.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: August 22, 2019
Genotype-phenotype correlation analysis in Japanese patients with Noonan syndrome.
Journal: Endocrine journal
Published: July 12, 2019
Early ileostomy in a 419 g infant and long-term follow up: A case report.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: March 16, 2019
Thyroid hormone status in patients with severe selenium deficiency.
Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: July 12, 2017
Last Updated: 09/26/2026