“Ataxia”的搜索结果，显示 1-10 项，共有 6204 项

1. 共济失调- 症状与病因- 妙佑医疗国际

   Ataxia classification. National Ataxia Foundation. https://ataxia.org/fact-sheets/. Accessed March 21, 2022. Ataxia telangiectasia information page.

2. Friedreich's Ataxia Clinic - 概述 - 妙佑医疗国际

   Friedreich's ataxia (FA) is a common form of inherited ataxia. In most cases, symptoms appear before the age of 25. Signs and symptoms of FA include a ...

3. 共济失调- 诊断与治疗- 妙佑医疗国际

   Ataxia classification. National Ataxia Foundation. https://ataxia.org/fact-sheets/. Accessed March 21, 2022. Ataxia telangiectasia information page.

4. 神经科- 临床试验- 妙佑医疗国际

   The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

5. 神经科- 临床试验- 妙佑医疗国际

   The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

6. 神经科- 临床试验- 妙佑医疗国际

   The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

7. 神经科- 临床试验- 妙佑医疗国际

   The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

8. 神经科- 临床试验- 妙佑医疗国际

   The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

9. 神经科- 临床试验- 妙佑医疗国际

   The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...

10. 神经科- 临床试验- 妙佑医疗国际

    The purpose of this study is to create a repository for cerebellar ataxia and nucleotide repeat diseases in order to fully investigate the genetic and ...