Mushiake Sotaro | Department Of Pediatrics D-5 Developmental Medicine Osaka University Graduate School Of Medical Scie

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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
Treatment with recombinant IL-2 for recurrent respiratory infection in a case of cartilage-hair hypoplasia with autoimmune hemolytic anemia
A Case of Pediatric Virilizing Adrenocortical Tumor Resulting in Hypothalamic-pituitary Activation and Central Precocious Puberty Following Surgical Removal
Alendronate and pharmacological doses of 1α OHD_3 therapy in a patient with McCune-Albright syndrome and accompanying hypophosphatemia
A patient with Shiga toxin-associated hemolytic uremic syndrome who developed hyperkalemia in the recovery period
Hypophosphatemic rickets accompanying McCune-Albright syndrome : evidence that a humoral factor causes hypophosphatemia
Blunted effect of parathyroid hormone on adenosine 3',5'-cyclic monophosphate production is derived from ATP depletion in proximal convoluted tubules of hypophosphatemic mice
The role of IGF-I in phosphate therapy for the short stature of patients with hypophosphatemic vitamin D-resistant rickets
The Rat Intrinsic Factor Gene: Its 5'-Upstream Region and Chief Cell-Specific Transcription
Long-term hospitalization during pregnancy is a risk factor for vitamin D deficiency in neonates
Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome
A Patient with Sotos Syndrome Who Reached Final Height
Histological findings in the livers of patients with neonatal intrahepatic cholestasis caused by citrin deficiency
A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia
Major role of apolipoprotein B in cycloheximide-induced acute hepatic steatosis in mice

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