IRIS
PREVITALI, STEFANO CARLO
 Distribuzione geografica
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Continente #
NA - Nord America 218
EU - Europa 217
AS - Asia 91
SA - Sud America 1
Totale 527
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Nazione #
US - Stati Uniti d'America 218
SE - Svezia 97
RU - Federazione Russa 46
CN - Cina 43
SG - Singapore 41
IT - Italia 35
FI - Finlandia 7
IE - Irlanda 7
DE - Germania 5
GB - Regno Unito 5
SI - Slovenia 5
NL - Olanda 4
CZ - Repubblica Ceca 2
FR - Francia 2
HK - Hong Kong 2
IN - India 2
JP - Giappone 2
RO - Romania 2
AR - Argentina 1
IR - Iran 1
Totale 527
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Città #
Ashburn 67
Lawrence 33
Princeton 33
Shanghai 23
Singapore 21
Milan 20
Moscow 17
New York 12
Boardman 10
Washington 8
Dublin 7
Helsinki 7
Dallas 5
Rome 4
Islington 3
Seattle 3
Auray 2
Beijing 2
Brno 2
Jiaxing 2
Los Angeles 2
Meppel 2
Munich 2
Nerviano 2
Oradea 2
Pune 2
Salerno 2
Xi'an 2
Blackburn 1
Buenos Aires 1
Cambridge 1
Central 1
Central District 1
Erlangen 1
Evanston 1
Falkenstein 1
Hefei 1
Kish 1
Legnano 1
Ljubljana 1
Mountain View 1
Nantong 1
Pusiano 1
Quanzhou 1
Rockville 1
Santa Clara 1
Shenzhen 1
Tokyo 1
Wuhu 1
Totale 318
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Nome #
JAB1 deletion in oligodendrocytes causes senescence-induced inflammation and neurodegeneration in mice 36
Cardiac and Neuromuscular Features of Patients with LMNA-Related Cardiomyopathy 27
Jab1 regulates Schwann cell proliferation and axonal sorting through p27. 20
Analyzing histopathological features of rare charcot-marie-tooth neuropathies to unravel their pathogenesis 20
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy 20
A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs) 19
Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutation 19
Neuromyelitis optica and myotonic dystrophy type 2: a rare association with diagnostic implications 18
Rebalancing expression of HMGB1 redox isoforms to counteract muscular dystrophy 18
Charcot-Marie-Tooth type 4B demyelinating neuropathy: deciphering the role of MTMR phosphatases 17
The mitochondrial protease AFG3L2 is essential for axonal development 17
A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation. 17
Protein profiling reveals energy metabolism and cytoskeletal protein alterations in LMNA mutation carriers. 17
Begelomab for severe refractory dermatomyositis: A case report 17
Hypokalemic periodic paralysis in a patient with acquired growth hormone deficiency 13
A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2 12
Diffuse intraneural leiomyoma in a case of sensorimotor neuropathy 12
Hypogonadotropic hypogonadism and peripheral neuropathy in Ebf2-null mice 12
Loss of glial fibrillary acidic protein (GFAP) impairs Schwann cell proliferation and delays nerve regeneration after damage 11
Expanding the spectrum of genes responsible for hereditary motor neuropathies 11
Muscle MRI findings in facioscapulohumeral muscular dystrophy 10
Niacin-mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination 10
Longitudinal MRI quantification of muscle degeneration in Duchenne muscular dystrophy 10
Urokinase Plasminogen Receptor and the Fibrinolytic Complex Play a Role in Nerve Repair after Nerve Crush in Mice, and in Human Neuropathies 9
The extracellular matrix affects axonal regeneration in peripheral neuropathies 9
Disruption of Mtmr2 produces CMT4B1-like neuropathy with myelin outfolding and impaired spermatogenesis 9
Vocal cord paralysis in Charcot–Marie–Tooth type 4b1 disease associated with a novel mutation in the myotubularin-related protein 2 gene: A case report and review of the literature 9
Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerve 8
Role of the extracellular matrix in regenerating and non-regenerating axonal neuropathies 8
Dlg1, Sec8, and Mtmr2 Regulate Membrane Homeostasis in Schwann Cell Myelination 8
Vimentin regulates peripheral nerve myelination 8
Mutation of the small HSP27/HSPB1 causes CMT neuropathy with abnormal neurofilament assembly 8
Expression analysis in the peripheral nerve of the myotubularin-related 2 protein phosphatase, mutated in CMT4B1 8
Brain connectivity abnormalities extend beyond the sensorimotor network in peripheral neuropathy 8
Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1A 8
Loss of Fig4 in both Schwann cells and motor neurons contributes to CMT4J neuropathy 7
HIGH POROSITY COLLAGEN TUBE: AN INNOVATIVE MEDICAL DEVICE FOR NERVE REGENERATION 7
Intravenous immunoglobulin treatment in patients with chronic inflammatory demyelinating neuropathy not responsive to other treatments 7
Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures. 7
Loss of Mtmr2 phosphatase in Schwann cells but not in motor neurons causes Charcot-Marie-tooth type 4B1 neuropathy with myelin outfoldings 6
Motor nerve biopsy: clinical usefulness and histopathological criteria 6
Dominant LMNA mutations can cause combined muscular dystrophy and peripheral neuropathy 6
Lymphomatous Neuropathy in cold agglutinin disease 6
Foot pad skin biopsy in mouse models of hereditary neuropathy 6
Functional MRI correlates of fatigue in patients with hereditary and acquired peripheral neuropathy 6
Disruption of MTMR2 in Schwann cells produces CMT4B1-like neuropathy with myelin outfoldings 5
Functional changes in Duchenne muscular dystrophy; a 12-month longitudinal cohort study 5
Phenotypic clustering of lamin A/C mutations in neuromuscular patients 5
LMNA-associated myopathies: The Italian experience in a large cohort of patients. 4
Kif13b Regulates PNS and CNS Myelination through the Dlg1 Scaffold 4
DEFINING GENOTYPE-PHENOTYPE CORRELATIONS IN THE CMT NEUROPATHIES 3
LAMA2 Neuropathies: Human Findings and Pathomechanisms From Mouse Models 1
SINGLE-FIBER ELECTROMYOGRAPHY STUDY OF RECOVERY AFTER NERVE CRUSH AND CARDIOTOXIN MUSCLE INJURY IN EXPERIMENTAL MOUSE MODEL 1
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements 1
IT'S TOO EASY TO MAKE IT SIMPLE: HNPP DIAGNOSIS 1
Longitudinal evaluation of axonal regeneration in mouse after nerve crush: a stimulated single-fibre electromyography study 1
Autocrine and immune cell-derived BDNF in human skeletal muscle: implications for myogenesis and tissue regeneration 1
Expanding the central nervous system disease spectrum associated with FLNC mutation 1
Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis 1
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4 1
Registries versus tertiary care centers: How do we measure standards of care in Duchenne muscular dystrophy 1
The empowerment of translational research: lessons from laminopathies 1
Increased expression of Myosin binding protein H in the skeletal muscle of amyotrophic lateral sclerosis patients 1
Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophy 1
Long Term Natural History Data in Ambulant Boys with Duchenne Muscular Dystrophy: 36-Month Changes 1
Out-of-Frame Mutations in ACTN2 Last Exon Cause a Dominant Distal Myopathy With Facial Weakness 1
The nonsense mutation stop+4 model correlates with motor changes in Duchenne muscular dystrophy 1
STIMULATED SINGLE-FIBER ELECTROMYOGRAPHY EVALUATION OF AXONAL REGENERATION IN ANIMAL MODELS 1
Rimeporide as a first- in-class NHE-1 inhibitor: Results of a phase Ib trial in young patients with Duchenne Muscular Dystrophy 1
Muscle inflammatory pattern in alpha- and gamma-sarcoglycanopathies 1
Osteopontin in Duchenne Muscular Dystrophy 1
The expanding spectrum of PRPS1-associated phenotypes: three novel mutations segregating with X-linked hearing loss and mild peripheral neuropathy 1
Categorizing natural history trajectories of ambulatory function measured by the 6-minute walk distance in patients with Duchenne muscular dystrophy 1
North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow up 1
DLG1 COORDINATES A HOMEOSTATIC CONTROL OF MYELINATION VIA SEC8 AND MTMR2 INTERACTION 1
Novel Splice-Site Mutation in SMN1 Associated with a very Severe SMA-I Phenotype 1
SKIN BIOPSY IN ANIMAL MODELS OF HEREDITARY NEUROPATHIES 1
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases 1
CSN5/JAB1 REGULATES SCHWANN CELL-AXON INTERACTION AND PLAYS A ROLE IN PERIPHERAL NERVE DEVELOPMENT AND FUNCTION 1
Alteration of the late endocytic pathway in Charcot-Marie-Tooth type 2B disease 1
HEREDITARY NEURALGIC AMYOTROPHY: A CASE REPORT 1
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy 1
Prostaglandin D2 synthase modulates macrophage activity and accumulation in injured peripheral nerves 1
Categorizing natural history trajectories of ambulatory function measured by the 6-minute walk distance in patients with Duchenne muscular dystrophy 1
A whole-brain network analysis in patients with hereditary and acquired peripheral neuropathy 1
A 5-year clinical follow-up study from the Italian National Registry for FSHD 1
Loss of function MPZ mutation causes milder CMT1B neuropathy 1
Longitudinal follow-up and muscle MRI pattern of two siblings with polyglucosan body myopathy due to glycogenin-1 mutation 1
Peripheral Nerve Development and the Pathogenesis of Peripheral Neuropathy: the Sorting Point 1
Timed Rise from Floor as a Predictor of Disease Progression in Duchenne Muscular Dystrophy: An Observational Study 1
Outcome Measures Validation Study for Mesoangioblasts Transplantation in Children Affected by Duchenne Muscular Dystrophy 1
6 Minute Walk Test in Duchenne MD Patients with Different Mutations: 12 Month Changes 1
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy 1
Animal Models as a Tool to Design Therapeutical Strategies for CMT-like Hereditary Neuropathies 1
Genetic modifiers of respiratory function in Duchenne muscular dystrophy 1
Matrix Metalloproteinase-2 Is Involved in Myelination of Dorsal Root Ganglia Neurons 1
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 1
How Schwann Cells Sort Axons: New Concepts 1
Myogenic Cell Transplantation in Genetic and Acquired Diseases of Skeletal Muscle 1
New Mutations in SCN4A and Their Biophysical Properties 1
Totale 622
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Categoria #
all - tutte 9.691
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 9.691
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20206 0 0 2 1 0 1 0 0 0 1 0 1
2020/20215 0 0 1 0 1 1 1 0 0 0 0 1
2021/202230 0 0 0 4 0 8 7 2 3 0 6 0
2022/2023203 73 40 20 0 2 19 11 10 6 18 0 4
2023/2024182 1 8 24 32 19 47 3 14 0 4 4 26
2024/2025189 83 14 92 0 0 0 0 0 0 0 0 0
Totale 638