Long Term Observations and Mortality Rates in ALS Patients Treated with Autologous Mesenchymal Cell Transplantations
Survival in ALS is highly variable, ranging from a few months to many years. Population-based prospective registries showed that up to a third of the patients die within one year from diagnosis [1-3]. In this short communication we present our long-term observations (~15 years) in terms of severe adverse events and survival rates, in patients treated with autologous mesenchymal stem cells, who participated in 3 previous open-label studies, in our center at Hadassah Medical Organization in Jerusalem, Israel.
Authors
- Petrou Panayiota
Publication Details
- Journal
- Open access Journal of Neurology & Neurosurgery
- Published
- 2025-04-17
- DOI
- https://doi.org/10.19080/oajnn.2025.19.556017
- Primary Topic
- Amyotrophic Lateral Sclerosis Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00