OKADA Shintaro | Department of Pediatrics, Osaka University Medical School

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概要

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著作論文

Correlation of genetic etiology with response to β-adrenergic blockade among symptomatic patients with familial long-QT syndrome
Treatment with recombinant IL-2 for recurrent respiratory infection in a case of cartilage-hair hypoplasia with autoimmune hemolytic anemia
Treatment of mitochondrial encephalomyopathy with a combination of cytochrome C and vitamins B_1 and B_2
Functional and Morphological Abnormalities of Mitochondria in Human Cells Containing Mitochondrial DNA with Pathogenic Point Mutations in tRNA Genes
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
Follow-Up Study of Hypervariable Region Sequences of the Hepatitis C Virus (HCV) Genome in an Infant with Delayed Anti-HCV Antibody Responses
Difficulty in differential diagnosis of atypical absence seizures and complex partial seizures in childhood
Postural change and pulmonary ventilation-perfusion distribution after Fontan operation
-0476-ASSESSMENT OF EXERCISE TOLERANCE BY ANAEROBIC THRESHOLD IN POST-OPERATIVE PATIENTS WITH CONGENITAL HEART DISEASE
Mutation analysis of Japanese patient with fucosidosis
Hypersensitivity to Mosquito Bites Conceals Clonal Lymphoproliferation of Epstein-Barr Viral DNA-positive Natural Killer Cells
Zonisamide Monotherapy in Newly Diagnosed Infantile Spasms
Human herpesvirus-6 infection in neonates : Not protected by only humoral immunity
Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome
Ictal Video-EEG Recording of Three Partial Seizures in a Patient with the Benign Infantile Convulsions Associated with Mild Gastroenteritis
Remission of progressive multifocal leukoencephalopathy following highly active antiretroviral therapy in a patient with HIV infection
Isolated Iissencephaly sequence with balanced chromosome translocation involving 17p13.3
Mutation analysis of two Japanese patients with Fanconi-Bickel syndrome
Gene therapy in Duchenne muscular dystrophy
AN EcoRI RFLP IN HUMAN APC GENE
EFFECTS OF SUCROSE IN CULTURED HUMAN SKIN FIBROBLASTS
A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia
A case of giant axonal neuropathy showing focal aggregation and hypophosphorylation of intermediate filaments
CORRELATION OF SUBCELLULAR LOCALIZATION OF DISEASE-SPECIFIC INCLUSIONS AND SPHINGOLIPID ACTIVATOR PROTEIN-1(SAP-1)IN SULFATIDE SULFATASE-DEFICIENT FIBROBLASTS
Localization of SAP-1 in fibroblasts of metachromatic leukodystrophy
Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome
HISTOCHEMICAL DEMONSTRATION OF ACID BETA-D-GALACTO-SIDASE ACTIVITY IN CULTURED HUMAN SKIN FIBROBLASTS AND ITS APPLICATION TO SINGLE CELL ANALYSES
Indigogenic Method for β-galactosidase in Cultured Skin Fibroblasts and its Application to Single Cell Analysis
The application of a simple assay method for lysosomal hydrolase in a single cultured skin fibroblast: Cytogenetic study of Mucolipidosis by cell fusion.

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