Miho Yamashita
Okayama, 7000013, Japan
Last Updated: 09/26/2026
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Found 10 publications
Relationships of Exercise and Dietary Intake with Bone Density in Young Adult Women
Journal: Nihon eiseigaku zasshi. Japanese journal of hygiene
Published: May 24, 2023
Nutrients Associated with Sleep Bruxism.
Journal: Journal of clinical medicine
Published: February 20, 2023
Genetic analysis in Japanese patients with osteogenesis imperfecta: Genotype and phenotype spectra in 96 probands.
Journal: Molecular genetics & genomic medicine
Published: August 24, 2020
Urinary Cross-linked N-terminal Telopeptide of Type I Collagen Levels of Infants with Osteogenesis Imperfecta and Healthy Infants.
Journal: Acta medica Okayama
Published: December 23, 2016
A novel mutation in the COL2A1 gene in a patient with Stickler syndrome type 1: a case report and review of the literature.
Journal: Journal of medical case reports
Published: November 12, 2016
Neonatal-Onset Hereditary Coproporphyria: A New Variant of Hereditary Coproporphyria.
Journal: JIMD reports
Published: November 04, 2016
A novel mutation p.Ser348Cys in FGFR3 causes achondroplasia.
Journal: American journal of medical genetics. Part A
Published: November 10, 2015
HDR syndrome in a Japanese girl with biliary atresia: a case report.
Journal: BMC pediatrics
Published: July 02, 2015
Japanese familial case with metaphyseal dysplasia, Schmid Type caused by the p.T555P mutation in the COL10A1 gene.
Journal: Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology
Published: June 13, 2014
Showing 1-10 of 10
Last Updated: 09/26/2026