Okada Shintaro | The Research Foundation For Microbial Diseases Of Osaka University

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著作論文

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
Difficulty in differential diagnosis of atypical absence seizures and complex partial seizures in childhood
Mutation analysis of Japanese patient with fucosidosis
Zonisamide Monotherapy in Newly Diagnosed Infantile Spasms
Human herpesvirus-6 infection in neonates : Not protected by only humoral immunity
Decreased frequency of seizures in infantile spasms associated with lissencephaly by human herpes virus 7 infection
Mutational analysis of MECP2 in Japanese patients with atypical Rett syndrome
Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence
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
A novel activating mutation (C129S) in the calcium-sensing receptor gene in a Japanese family with autosomal dominant hypocalcemia
Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome
ALLELE FREQUENCIES OF INTRAGENIC, AND 5' AND 3' MARKERS OF THE DYSTROPHIN GENE IN JAPANESE FAMILIES AFFLICTED WITH DUCHENNE OR BECKER MUSCULAR DYSTROPHY
A case of chronic infantile type of fucosidosis : clinical and magnetic resonance in image findings

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