スポンサーリンク
Second Department of Pediatrics, Toho University School of Medicine | 論文
- Molecular diagnosis for presymptomatic patients with Wilson disease
- Molecular analysis and diagnosis in Japanese patients with Wilson's disease
- Point mutation in intron 11 of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia
- Mass screening for Wilson's disease : Results and recommendations
- Wolff-Parkinson-White(WPW) Syndrome in Isolated Noncompaction of the Ventricular Myocardium(INVM) : Three Cases
- Foreword
- Treatment and management of Wilson's disease
- Wilson Disease Patients with Atypical Psychiatric Symptoms
- Efficacy of D-penicillamine Challenge Test for Diagnosis of Wilson Disease
- Two families with Wilson disease in which siblings showed different phenotypes
- EYA1 gene nonsense mutation in a Japanese family with branchio-oto-renal syndrome
- Genotype-Phenotype Analysis of Mutation R778L in the ATP7B Gene