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Human umbilical cord blood-derived mononuclear cell transplantation: case series of 30 subjects with Hereditary Ataxia

BACKGROUND: The differential diagnosis for hereditary ataxia encompasses a variety of diseases characterized by both autosomal dominant and recessive inheritance. There are no curative treatments available for these neurodegenerative conditions. This open label treatment study used human umbilical c...

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Detalhes bibliográficos
Main Authors: Yang, Wan-Zhang, Zhang, Yun, Wu, Fang, Zhang, Min, Cho, SC, Li, Chun-Zhen, Li, Shao-Hui, Shu, Guo-Jian, Sheng, You-Xiang, Zhao, Ning, Tang, Ying, Jiang, Shu, Jiang, Shan, Gandjian, Matthew, Ichim, Thomas E, Hu, Xiang
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2011
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3112442/
https://ncbi.nlm.nih.gov/pubmed/21575250
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1479-5876-9-65
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