Muscle mitochondrial dysfunction due to defective mitochondrial biogenesis in SMA patients. Beta-lactam antibiotics offer neuroprotection in a spinal muscular atrophy mouse model by multiple mechanisms. Glycogen storage disease type III: Motoneuron transplantation rescue the phenotype of spinal muscular atrophy with respiratory distress type 1 SMARD1. Tyr78Phe transthyretin mutation with motor-predominant neuropathy as the initial presentation Case Reports in Neurology Feb 23;3 1: Journal of Histochemistry and Cytochemistry, Oct;52
Journal of Clinical Investigation, Oct 1; Aggiungere questo documento salvato. Skin-derived stem cells transplanted into resorbable guides provide functional nerve regeneration after sciatic nerve resection. Firenze, 14 February Fulvio Guatelli ……. Fas siRNA mediated interference reduces motor neuron death in amyotrophic lateral sclerosis mouse model.
Epub Jul Questo progetto prevede la creazione di una piattaforma per la sintesi di nuovi composti farmacologici ad impiego clinico.
J Cell Mol Med. Neurology, vol 72, suppl.
currixulum Aldehyde dehydrogenase positive neuronal stem cells generate motor neurons and promote functional recovery in an animal model of Spinal Muscular Atrophy with Respiratory Distress type 1. Journal of the Neurological Sciences, Oct 15; Fibroblasts mediated gene transfer to skeletal muscle: Remember me on this computer. Genetic distribution and unusual phenotypes in a periodic paralysis color.
Crash course in progettazione editoriale. Translations —— translations into Cufriculum of essays of B. American Journal of Human Genetics, May;84 5: Epub Sep 8.
Open Access, valutazione, distribuzione Padova, 28 Novembre La Spezia — Italy. Cognitive and Behavioral Neurolology, Mar;23 1: Beta-lactam antibiotic offer neuroprotection in a spinal muscular atrophy mouse model by multiple mechanisms, Experimental Neurology Malattie del sistema nervoso centrale e periferico.
Epub Sep 24 Ex-Articolo 56, Basi molecolari delle malattie del motoneuron Nuclear Medicine and Biology, 28 8: Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches.
Abstract book 33 Cagliani R. Skin-derived stem cells transplanted into resorbable guides provide functional nerve regeneration after sciatic nerve resection.
Transplantation of neural stem cells derived ffirenze murine embryonic stem cells ameliorates spinal muscular atrophy phenotype.
Progetto di Ricerca dell’Istituto Scientifico E. Neural stem cell population deriving from SOX2-dependent dedifferentiated human astrocytes as possible cell source for cell mediated therapy in neurodegenerative diseases.
Peter Mohobi Bako | Università degli Studi di Firenze (University of Florence) –
Muscle-specific genes are expressed in a fraction of mouse bone marrow cells. The proposal of Saul Kripke]. Targeted gene correction of spinal muscular atrophy—induced pluripotent stem cells and motor neurons as a model and for cell therapy.
Expert Opin Drug Discov.
Tyr78Phe transthyretin mutation with motor-predominant neuropathy as the initial presentation Case Reports in Neurology Feb 23;3 1: Genotype and phenotype characterization in a large dystrophinopathic firdnze with extended follow-up. SOD1 misplacing and mitochondrial dysfunction in amyotrophic lateral sclerosis pathogenesis. Telethon Scientific Convention, Salsomaggiore Terme, marzo The role of innervation in a mouse “in vitro” model of merosin negative congenital muscular dystrophy.
Epub Apr 4.