スポンサーリンク
Department Of Pediatrics D-5 Developmental Medicine Osaka University Graduate School Of Medical Scie | 論文
- Mutation analysis of Japanese patient with fucosidosis
- Zonisamide Monotherapy in Newly Diagnosed Infantile Spasms
- 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
- 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
- Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndrome
- A Case of Primary Hyperparathyroidism in Childhood Found by a Chance Hematuria
- 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
- Decrease in serum FGF23 levels after intravenous infusion of pamidronate in patients with osteogenesis imperfecta
- Major role of apolipoprotein B in cycloheximide-induced acute hepatic steatosis in mice