about
Motor neuron derivation from human embryonic and induced pluripotent stem cells: experimental approaches and clinical perspectivesiPSC-Based Models to Unravel Key Pathogenetic Processes Underlying Motor Neuron Disease DevelopmentMolecular, genetic and stem cell-mediated therapeutic strategies for spinal muscular atrophy (SMA)Direct reprogramming of human astrocytes into neural stem cells and neurons.Minimally invasive transplantation of iPSC-derived ALDHhiSSCloVLA4+ neural stem cells effectively improves the phenotype of an amyotrophic lateral sclerosis model.Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy.Stem cell transplantation for amyotrophic lateral sclerosis: therapeutic potential and perspectives on clinical translation.The wide spectrum of clinical phenotypes of spinal muscular atrophy with respiratory distress type 1: a systematic review.Pluripotent stem cell-based models of spinal muscular atrophy.Neurological counterparts of hyponatremia: pathological mechanisms and clinical manifestations.Human pluripotent stem cells as tools for neurodegenerative and neurodevelopmental disease modeling and drug discovery.Experimental Advances Towards Neural Regeneration from Induced Stem Cells to Direct In Vivo Reprogramming.Spinal muscular atrophy--recent therapeutic advances for an old challenge.MicroRNA Metabolism and Dysregulation in Amyotrophic Lateral Sclerosis.MicroRNA-Directed Neuronal Reprogramming as a Therapeutic Strategy for Neurological Diseases.Exertional rhabdomyolysis leading to acute kidney injury: when genetic defects are diagnosed in adult life.Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the LiteratureCentral Nervous System Involvement in Common Variable Immunodeficiency: A Case of Acute Unilateral Optic Neuritis in a 26-Year-Old Italian PatientSubclinical Leber's hereditary optic neuropathy with pediatric acute spinal cord onset: more than meets the eyeCan Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the LiteratureKey role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neuronsNusinersen treatment and cerebrospinal fluid neurofilaments: An explorative study on Spinal Muscular Atrophy type 3 patientsiPSCs-Based Neural 3D Systems: A Multidimensional Approach for Disease Modeling and Drug DiscoveryBack to the origins: Human brain organoids to investigate neurodegenerationOphthalmoplegia Due to Miller Fisher Syndrome in a Patient With Myasthenia GravisPediatric anti-HMGCR necrotizing myopathy: diagnostic challenges and literature review
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description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Irene Faravelli
@en
Irene Faravelli
@nl
type
label
Irene Faravelli
@en
Irene Faravelli
@nl
prefLabel
Irene Faravelli
@en
Irene Faravelli
@nl
P31
P496
0000-0001-8126-7353