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Alexandra, Spinozerebelläre Ataxie Typ 1 | Stammzellenbehandlungsbericht

Wie bei vielen anderen Ataxie-Patienten, kamen die progressiven Verluste die motorischen Grundfunktionen, die Sprache und die Balance als plötzlicher Schock.

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Referenzen

  1. Human Umbilical Cord Blood Derived Mononuclear Cell Transplantation Case Series of 30 Subjects with Hereditary Ataxia
  2. Hyun-Jung Park,Giyoon Bang, Bo Ra Lee, Hyun Ok Kim, and Phil Hyu Lee. Neuroprotective Effect of Human Mesenchymal Stem Cells in an AnimalModel of Double Toxin-Induced Multiple System Atrophy Parkinsonism. Cell Transplantation, Vol. 20, pp. 827–835, 2011.
  3. Zhongling Feng & Feng Gao. Stem Cell Challenges in the Treatment of Neurodegenerative Disease. CNS Neuroscience & Therapeutics 00 (2011) 1–7.
  4. Kevin Kemp,Elizabeth Mallam, Kelly Hares, Jonathan Witherick, Neil Scolding, and Alastair Wilkins. Mesenchymal Stem Cells Restore Frataxin Expression and Increase Hydrogen Peroxide Scavenging Enzymes in Friedreich Ataxia Fibroblasts.
  5. You-Kang Chang, Ming-Hsiang Chen, Yi-Hung et al. Mesenchymal stem cell transplantation ameliorates motor function deterioration of spinocerebellar ataxia by rescuing cerebellar Purkinje cells.