IRIS
PREVITALI, STEFANO CARLO
 Distribuzione geografica
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Continente #
NA - Nord America 292
EU - Europa 265
AS - Asia 240
SA - Sud America 2
AF - Africa 1
Totale 800
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Nazione #
US - Stati Uniti d'America 291
SG - Singapore 132
SE - Svezia 98
CN - Cina 95
IT - Italia 54
RU - Federazione Russa 47
DE - Germania 12
FI - Finlandia 9
GB - Regno Unito 9
IN - India 8
NL - Olanda 8
IE - Irlanda 7
SI - Slovenia 5
AT - Austria 4
BG - Bulgaria 3
CZ - Repubblica Ceca 3
FR - Francia 3
HK - Hong Kong 2
JP - Giappone 2
RO - Romania 2
AR - Argentina 1
BR - Brasile 1
CA - Canada 1
GR - Grecia 1
IR - Iran 1
SC - Seychelles 1
Totale 800
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Città #
Singapore 78
Ashburn 73
Lawrence 33
Milan 33
Princeton 33
Shanghai 27
Moscow 18
New York 15
Boardman 12
Randolph Township 11
Zhengzhou 10
Hangzhou 9
Shenzhen 9
Washington 9
Helsinki 8
Des Moines 7
Dublin 7
Los Angeles 6
Skokie 6
Dallas 5
Islington 5
Jinan 5
Amsterdam 4
Munich 4
Rome 4
Shantou 4
Seattle 3
Sofia 3
Vienna 3
Xi'an 3
Alpharetta 2
Auray 2
Beijing 2
Brescia 2
Brno 2
Chicago 2
Falkenstein 2
Jiaxing 2
Meppel 2
Nerviano 2
New Delhi 2
Oradea 2
Pune 2
Quanzhou 2
Salerno 2
Warren Township 2
Athens 1
Blackburn 1
Boston 1
Boydton 1
Buenos Aires 1
Cambridge 1
Central 1
Central District 1
Changsha 1
Currais Novos 1
Erlangen 1
Evanston 1
Frankfurt am Main 1
Glasgow 1
Hefei 1
Hyderabad 1
Kish 1
Lappeenranta 1
Legnano 1
Ljubljana 1
Mountain View 1
Nantong 1
Nuremberg 1
Oakland 1
Prague 1
Pusiano 1
Rockville 1
San Antonio 1
Santa Clara 1
Taizhou 1
Tokyo 1
Trieste 1
Wuhu 1
Wuxi 1
Totale 513
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Nome #
Nusinersen safety and effects on motor function in adult spinal muscular atrophy type 2 and 3 57
JAB1 deletion in oligodendrocytes causes senescence-induced inflammation and neurodegeneration in mice 52
Cardiac and Neuromuscular Features of Patients with LMNA-Related Cardiomyopathy 29
Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutation 23
Jab1 regulates Schwann cell proliferation and axonal sorting through p27. 22
Going for a stroll on lurasidone: Considerations on an atypical case of acute compartment syndrome of both legs 21
Analyzing histopathological features of rare charcot-marie-tooth neuropathies to unravel their pathogenesis 21
Charcot-Marie-Tooth type 4B demyelinating neuropathy: deciphering the role of MTMR phosphatases 20
A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs) 20
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy 20
The mitochondrial protease AFG3L2 is essential for axonal development 19
A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin 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
Begelomab for severe refractory dermatomyositis: A case report 18
Protein profiling reveals energy metabolism and cytoskeletal protein alterations in LMNA mutation carriers. 17
Hypokalemic periodic paralysis in a patient with acquired growth hormone deficiency 16
Merosin deficient congenital muscular dystrophy type 1A: An international workshop on the road to therapy 15-17 November 2019, Maastricht, the Netherlands 14
A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2 13
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy 13
Prostaglandin D2 synthase modulates macrophage activity and accumulation in injured peripheral nerves 12
Diffuse intraneural leiomyoma in a case of sensorimotor neuropathy 12
Hypogonadotropic hypogonadism and peripheral neuropathy in Ebf2-null mice 12
LAMA2 Neuropathies: Human Findings and Pathomechanisms From Mouse Models 11
Disruption of Mtmr2 produces CMT4B1-like neuropathy with myelin outfolding and impaired spermatogenesis 11
Peripheral Nerve Development and the Pathogenesis of Peripheral Neuropathy: the Sorting Point 11
Loss of glial fibrillary acidic protein (GFAP) impairs Schwann cell proliferation and delays nerve regeneration after damage 11
Niacin-mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination 11
Longitudinal MRI quantification of muscle degeneration in Duchenne muscular dystrophy 11
Expanding the spectrum of genes responsible for hereditary motor neuropathies 11
The extracellular matrix affects axonal regeneration in peripheral neuropathies 10
Loss of function MPZ mutation causes milder CMT1B neuropathy 10
Brain connectivity abnormalities extend beyond the sensorimotor network in peripheral neuropathy 10
Muscle MRI findings in facioscapulohumeral 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
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4 9
Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53 9
Editorial: Current Insights Into LAMA2 Disease. 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
Loss of Mtmr2 phosphatase in Schwann cells but not in motor neurons causes Charcot-Marie-tooth type 4B1 neuropathy with myelin outfoldings 8
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 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
Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1A 8
Suitability of external controls for drug evaluation in Duchenne muscular dystrophy 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
Foot pad skin biopsy in mouse models of hereditary neuropathy 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
Pregnancy in Charcot-Marie-Tooth disease: Data from the Italian CMT national registry 7
Expanding the central nervous system disease spectrum associated with FLNC mutation 6
Rimeporide as a first- in-class NHE-1 inhibitor: Results of a phase Ib trial in young patients with Duchenne Muscular Dystrophy 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
Functional MRI correlates of fatigue in patients with hereditary and acquired peripheral neuropathy 6
Registries versus tertiary care centers: How do we measure standards of care in Duchenne muscular dystrophy 5
Long Term Natural History Data in Ambulant Boys with Duchenne Muscular Dystrophy: 36-Month Changes 5
Genetic modifiers of respiratory function in Duchenne muscular dystrophy 5
CSN5/JAB1 PLAYS A ROLE IN AXONAL SORTING AND MYELINATION IN PERIPHERAL NERVE 5
Effects of short-to-long term enzyme replacement therapy (ERT) on skeletal muscle tissue in late onset Pompe disease (LOPD) 5
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
Muscle inflammatory pattern in alpha- and gamma-sarcoglycanopathies 4
Restoring cell-basal lamina interaction to rescue tissue degeneration in congenital muscular dystrophy 4
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 4
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements 3
Autocrine and immune cell-derived BDNF in human skeletal muscle: implications for myogenesis and tissue regeneration 3
STIMULATED SINGLE-FIBER ELECTROMYOGRAPHY EVALUATION OF AXONAL REGENERATION IN ANIMAL MODELS 3
Categorizing natural history trajectories of ambulatory function measured by the 6-minute walk distance in patients with Duchenne muscular dystrophy 3
CSN5/JAB1 REGULATES SCHWANN CELL-AXON INTERACTION AND PLAYS A ROLE IN PERIPHERAL NERVE DEVELOPMENT AND FUNCTION 3
A whole-brain network analysis in patients with hereditary and acquired peripheral neuropathy 3
POEMS syndrome: the matter-of-fact approach 3
Facioscapulohumeral dystrophy 3
Outcome measures validation study for mesoangioblasts transplantation in children affected by Duchenne muscular dystrophy 3
SINGLE-FIBER ELECTROMYOGRAPHY STUDY OF RECOVERY AFTER NERVE CRUSH AND CARDIOTOXIN MUSCLE INJURY IN EXPERIMENTAL MOUSE MODEL 2
IT'S TOO EASY TO MAKE IT SIMPLE: HNPP DIAGNOSIS 2
Longitudinal evaluation of axonal regeneration in mouse after nerve crush: a stimulated single-fibre electromyography study 2
The empowerment of translational research: lessons from laminopathies 2
Increased expression of Myosin binding protein H in the skeletal muscle of amyotrophic lateral sclerosis patients 2
Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophy 2
DLG1 COORDINATES A HOMEOSTATIC CONTROL OF MYELINATION VIA SEC8 AND MTMR2 INTERACTION 2
Novel Splice-Site Mutation in SMN1 Associated with a very Severe SMA-I Phenotype 2
SKIN BIOPSY IN ANIMAL MODELS OF HEREDITARY NEUROPATHIES 2
Expanding the phenotype of neuromuscular disorders: NGS reveals new genes responsible for recessive motor neuropathies 2
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases 2
Alteration of the late endocytic pathway in Charcot-Marie-Tooth type 2B disease 2
HEREDITARY NEURALGIC AMYOTROPHY: A CASE REPORT 2
SEVEN EXAMPLES OF EXPANDABLE CLINICAL SPECTRUM OF NEUROMUSCULAR GENES 2
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy 2
6 Minute Walk Test in Duchenne MD Patients with Different Mutations: 12 Month Changes 2
Animal Models as a Tool to Design Therapeutical Strategies for CMT-like Hereditary Neuropathies 2
Totale 927
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Categoria #
all - tutte 12.911
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 12.911
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20203 0 0 0 0 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
2022/2023205 73 40 20 0 2 19 11 10 6 19 1 4
2023/2024195 1 10 27 33 20 50 3 15 0 4 4 28
2024/2025485 84 14 91 224 72 0 0 0 0 0 0 0
Totale 949