Sako Masahiro | Department Of Pediatrics Osaka University Graduate School Of Medicine

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概要

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著作論文

Endocrinological Analysis of 122 Japanese Childhood Cancer Survivors in a Single Hospital
A Case of Persistent Hyperinsulinemic Hypoglycemia of Infancy Successfully Managed with Subcutaneous Octreotide Injection and Nocturnal Intravenous Glucose Supply
Lack of Puberty Despite Elevated Estradiol in a 46,XY Phenotypic Female with Frasier Syndrome
A Spectrum of Clinical Presentations in Seven Japanese Patients with Vitamin D Deficiency
Novel mutation of gene coding for glial fibrillary acidic protein in a Japanese patient with Alexander disease
Longitudinal Observation of a Patient with Leri-Weill Dyschondrosteosis and SHOX Haploinsufficiency
Hormonal and Genetical Assessment of a Japanese Girl with Weaver Syndrome
A Case of Pediatric Virilizing Adrenocortical Tumor Resulting in Hypothalamic-pituitary Activation and Central Precocious Puberty Following Surgical Removal
Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome
A Patient with Sotos Syndrome Who Reached Final Height
A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia

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