Progetto a Concorso IRCCS Ospedale Maggiore Policlinico , Trapianto di cellule staminali di derivazione emopoietica come strategia di rigenerazione neuronale in topi nmd, modello animale di Amiotrofia Spinale 8. Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy. Current Vascular Pharmacology, Jan;8 1: Journal of Cellular Molecular Medicine, Aug;15 8: Clinical and molecular features and therapeutic perspectives of spinal muscular atrophy with respiratory distress type 1.
Epub Feb Long-term neuropsychological deficits after cerebellar infarctions in two young adult twins. Atti, II Convegno dei Biotecnologi. Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. Identification of oculomotor-restricted genes with motor neuron protective properties for the development of ALS therapeutics. POLG1 mutations and stroke like episodes: Clinical Neuropathology, 19, , 11 Corti S.
Milano, 26 Maggio Evidence from a Cortical Blind Patient. Cariplo Foundation grant Genetic correction of spinal muscular atrophy-induced pluripotent stem cells and motoneurons as a disease model and cell source for transplantation.
Journal of the Neurological Sciences, May 15; Cellular Molecular Life Sciences, May;71 9: Clinical genetics, May;75 5: Two more Italian families.
Ubiquilin 2 mutations in 64 Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia. Natural history, genotype-phenotype correlations and outcome measures.
Log In Sign Up. Journal of Cellular Molecular Medicine, Aug;15 8: Questi risultati sono stati pubblicati in prestigiose riviste internazionali peer-reviewed tra cui Science Translational Medicine, Journal of Clinical Investigation, Stem Cell Reports, Neuron etc.
A typical cerebellar reactivity in patients sera with neurological disorders of suspected paraneoplastic nature. Atti, poster 8 29 Ronchi D. Suggest us how to improve StudyLib For complaints, use another form. Extracorporeal circulation as a new experimental approach for myoblast implantation.
A splicing site OPA1 cureiculum associated with autosomal dominant optic atrophy in an Italian family. Somatic stem cell research for neural repair: Neuromuscular Disorders, vol 17, pp In questi anni la Dott. Effect of steroid treatment in cerebellar ataxia associated with anti-GAD antibodies.
Epub Oct 4. Epub Apr 4. Remember me on this computer.
Peter Mohobi Bako | Università degli Studi di Firenze (University of Florence) –
June 20, place: Human motor neuron generation from embryonic stem cells and induced pluripotent stem cells. Dick, William Gibson, Robert A. Antisense oligonucleotides-based strategy as a therapy for the development of genetic Motor Neuron Diseases.
Medea Bosisio, Parini, Italy Neuromuscolar Disorders, Nov;22 POLG1 mutations and stroke like episodes: Towards the development of a gene therapy for mitochondrial diseases.
Epub Jan Journal of the Neurological Sciences, Jun 15; Nuclear reprogramming and adult stem cell potential. Journal of Neurology vol.