A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis
- 20/11/2013
Neurorescue effects and stem properties of chorinic villi and amniotic progenitors cells.
- 14/10/2013
Non-invasive near-infrared live imaging of human adult mesenchymal stem cells transplanted ina rodent model of Parkinson’s disease.
- 14/10/2013
Molecular signatures of ALS disease progression in hind and forelimb muscles of a SOD1G93A mouse model.
- 14/10/2013
Longitudinal tracking of human fetal cells labeled with super paramagnetic iron oxide nanoparticles in the brain of mice motor neuron disease.
- 14/10/2013
Neuroprotective effects of human mesenchymal stem cells on neuronal cultures exposed to 6-hydroxydopamine. Implications for separative therapy in Parkinson’s disease.
- 14/10/2013
Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis.
- 14/10/2013
TDP-43 and FUS RNA-binding proteins bind distinct sets of cytoplasmic messenger RNAs and differently regulate their post-transcriptional fate in motoneuron-like cells
- 14/10/2013
Screening of the PFN1 gene in sporadic ALS and FTD.
- 14/10/2013
C9ORF72 hexanucleotide repeat expansion in a large Italian cohort with amyotrophic lateral sclerosis and the evidence of a founder effect.
- 14/10/2013
Mutations in the Profilin 1 Gene Cause Familial Amyotrophic Lateral Sclerosis.
- 14/10/2013
Wake-up stroke and TIA due to paradoxical embolism during long obstructive sleep apnea: a cross-sectional study.
- 14/10/2013
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia.
- 14/10/2013
Charles Bonnet syndrome: two case reports and review of the literature.
- 14/10/2013
Intra- and interhemispheric structural network abnormalities in PLS and ALS.
- 14/10/2013
ELAV proteins and their multi-faceted RNA-binding activities in neurons.
- 14/10/2013
Vascular and parenchymal lesions along with enhanced neurogenesis characterize the brain of asymptomatic stroke-prone spontaneous hypertensive rats
- 14/10/2013
Defining the Role of the Bcl-2 Family Proteins in Huntington’s Disease. Running title: Bcl-2 Family Proteins in Huntington’s Disease
- 14/10/2013
Different mutations at V363MAPT codon are associated wtiyh atipica clinical phenotypes and sow unusual structural and functional features.
- 14/10/2013
CSF Oligoclonal bands in ALS patients with disease associated mutations.
- 14/10/2013
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