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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