Two families with Wilson disease in which siblings showed different phenotypes
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概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2002-10-01
著者
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SHIMIZU Norikazu
Second Department of Pediatrics, Toho University School of Medicine
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TAKESHITA Yukiko
Second Department of Pediatrics, Toho University School of Medicine
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AOKI Tsugutoshi
Second Department of Pediatrics, Toho University School of Medicine
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NAKAZONO Hiroki
Second Department of Pediatrics, Toho University School of Medicines
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YAMAGUCHI Yukitoshi
Second Department of Pediatrics, Toho University School of Medicines
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Aoki Tsugutoshi
Second Department Of Pediatrics Toho University School Of Medicine
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Saitou Miyuki
Second Department Of Pediatrics Toho University School Of Medicine Ohashi Hospital
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FUJIKAWA Yoshinao
Second Department of Pediatrics, Toho University School of Medicine, Ohashi Hospital
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Yamaguchi Yukitoshi
Second Department Of Pediatrics Toho University School Of Medicine Ohashi Hospital
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Yamaguchi Yukitoshi
Second Department Of Pediatrics School Of Medicine Toho University
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Fujikawa Yoshinao
Second Department Of Pediatrics Toho University School Of Medicine Ohashi Hospital
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Nakazono Hiroki
Second Department Of Pediatrics Toho University School Of Medicine
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Shimizu Norikazu
Second Department Of Pediatrics Toho University School Of Medicine
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Takeshita Yukiko
Second Department Of Pediatrics Toho University School Of Medicine
関連論文
- 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
- Genotype-Phenotype Analysis of Mutation R778L in the ATP7B Gene