about
Mutations in the motor and stalk domains of KIF5A in spastic paraplegia type 10 and in axonal Charcot-Marie-Tooth type 2.Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures.Urokinase plasminogen receptor and the fibrinolytic complex play a role in nerve repair after nerve crush in mice, and in human neuropathies.ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy casesIntra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy.Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15Hereditary Spastic Paraplegia: Beyond Clinical Phenotypes toward a Unified Pattern of Central Nervous System Damage.Polyneuropathy in POEMS syndrome: role of angiogenic factors in the pathogenesis.Is M129V of PRNP gene associated with Alzheimer's disease? A case-control study and a meta-analysis.Exome sequencing reveals a novel homozygous mutation in ACP33 gene in the first Italian family with SPG21.Spontaneous intracerebral hemorrhage in Urbach-Wiethe disease.CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.The extracellular matrix affects axonal regeneration in peripheral neuropathies.Clinical phenotype variability in patients with hereditary spastic paraplegia type 5 associated with CYP7B1 mutations.Induction of neuropilins-1 and -2 and their ligands, Sema3A, Sema3F, and VEGF, during Wallerian degeneration in the peripheral nervous system.A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2.Vascular endothelial growth factor gene variability is associated with increased risk for AD.Analyzing Histopathological Features of Rare Charcot-Marie-Tooth Neuropathies to Unravel Their PathogenesisA fatal case of Churg–Strauss syndrome presenting with acute polyneuropathy mimicking Guillain–Barré syndromeMotor nerve biopsy: Clinical usefulness and histopathological criteriaDiffuse intraneural leiomyoma in a case of sensorimotor neuropathyNeurolupus is associated with anti-ribosomal P protein antibodies: An inception cohort studyA new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutationRole of VEGF gene variability in longevity: A lesson from the Italian populationPentraxin-3 and VEGF in POEMS syndrome: a 2-year longitudinal studyIs erythropoietin gene a modifier factor in amyotrophic lateral sclerosis?Absence of angiogenic genes modification in Italian ALS patientsVEGF gene variability and type 1 diabetes: evidence for a protective roleVascular endothelial growth factor helps differentiate neuropathies in rare plasma cell dyscrasiasSubcutaneous immunoglobulin therapy for the treatment of multifocal motor neuropathy: a case reportMuscle MRI findings in facioscapulohumeral muscular dystrophy
P50
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P50
description
hulumtuese
@sq
researcher
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wetenschapper
@nl
հետազոտող
@hy
name
Marina Scarlato
@ast
Marina Scarlato
@en
Marina Scarlato
@es
Marina Scarlato
@nl
type
label
Marina Scarlato
@ast
Marina Scarlato
@en
Marina Scarlato
@es
Marina Scarlato
@nl
prefLabel
Marina Scarlato
@ast
Marina Scarlato
@en
Marina Scarlato
@es
Marina Scarlato
@nl
P106
P1153
8953893700
P21
P31
P496
0000-0003-1060-8207