IRIS
PREVITALI, STEFANO CARLO
 Distribuzione geografica
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Continente #
AS - Asia 3.109
EU - Europa 2.952
NA - Nord America 2.377
SA - Sud America 707
AF - Africa 65
OC - Oceania 4
Continente sconosciuto - Info sul continente non disponibili 1
Totale 9.215
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Nazione #
US - Stati Uniti d'America 2.277
RU - Federazione Russa 1.817
SG - Singapore 1.160
CN - Cina 995
BR - Brasile 611
IT - Italia 389
HK - Hong Kong 363
VN - Vietnam 294
FR - Francia 159
SE - Svezia 131
DE - Germania 109
GB - Regno Unito 98
IN - India 86
NL - Olanda 52
AT - Austria 48
FI - Finlandia 48
CA - Canada 46
MX - Messico 37
BD - Bangladesh 35
AR - Argentina 34
JP - Giappone 24
TR - Turchia 23
ZA - Sudafrica 23
ES - Italia 21
EC - Ecuador 19
IQ - Iraq 17
PL - Polonia 17
ID - Indonesia 15
UZ - Uzbekistan 13
SA - Arabia Saudita 11
CO - Colombia 10
IE - Irlanda 10
PY - Paraguay 10
VE - Venezuela 9
IR - Iran 8
LT - Lituania 8
PK - Pakistan 8
CL - Cile 7
DZ - Algeria 7
KE - Kenya 6
LB - Libano 6
MA - Marocco 6
NP - Nepal 6
TN - Tunisia 6
UA - Ucraina 6
AE - Emirati Arabi Uniti 5
CZ - Repubblica Ceca 5
JO - Giordania 5
PS - Palestinian Territory 5
SI - Slovenia 5
AU - Australia 4
JM - Giamaica 4
PH - Filippine 4
RO - Romania 4
BG - Bulgaria 3
BO - Bolivia 3
CG - Congo 3
EG - Egitto 3
HR - Croazia 3
HU - Ungheria 3
MY - Malesia 3
PE - Perù 3
SN - Senegal 3
AL - Albania 2
BE - Belgio 2
BH - Bahrain 2
CH - Svizzera 2
DO - Repubblica Dominicana 2
GE - Georgia 2
GR - Grecia 2
GT - Guatemala 2
HN - Honduras 2
IL - Israele 2
KG - Kirghizistan 2
KW - Kuwait 2
KZ - Kazakistan 2
LK - Sri Lanka 2
MD - Moldavia 2
NG - Nigeria 2
OM - Oman 2
PA - Panama 2
RS - Serbia 2
AO - Angola 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BF - Burkina Faso 1
BN - Brunei Darussalam 1
BS - Bahamas 1
BW - Botswana 1
BY - Bielorussia 1
BZ - Belize 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
CY - Cipro 1
MT - Malta 1
PT - Portogallo 1
RE - Reunion 1
SC - Seychelles 1
SV - El Salvador 1
TH - Thailandia 1
Totale 9.209
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Città #
Dallas 725
Singapore 547
Ashburn 391
Moscow 378
Hong Kong 359
San Jose 258
Shanghai 163
Beijing 155
Hefei 149
Lauterbourg 129
Ho Chi Minh City 118
Milan 118
New York 72
Orem 62
São Paulo 61
Hanoi 55
Los Angeles 54
Lawrence 43
Princeton 43
Nuremberg 39
Chennai 28
Helsinki 28
Amsterdam 24
Santa Clara 24
Rome 22
Tokyo 22
Vienna 22
Boardman 21
Brooklyn 21
Montreal 20
Denver 19
Manchester 19
Poplar 19
Washington 19
Belo Horizonte 17
Chicago 17
Munich 17
Hangzhou 15
London 15
Mumbai 15
Phoenix 15
Shenzhen 15
Cesano Boscone 14
Warsaw 14
Boston 13
Da Nang 13
Guangzhou 13
Haiphong 13
Johannesburg 13
Lappeenranta 13
Zhengzhou 13
Curitiba 12
Rio de Janeiro 12
Biên Hòa 11
Falkenstein 11
Houston 11
Randolph Township 11
Seattle 11
Toronto 11
Atlanta 10
Brasília 10
Council Bluffs 10
Dublin 10
Frankfurt am Main 10
Tashkent 10
Guayaquil 9
Naples 9
Stockholm 9
Ankara 8
Assago 8
Salvador 8
Baghdad 7
Bengaluru 7
Buenos Aires 7
Des Moines 7
Mexico City 7
Santo André 7
Thái Bình 7
Asunción 6
Barnet 6
Brescia 6
Charlotte 6
Guarulhos 6
Nairobi 6
Querétaro 6
Riyadh 6
San Francisco 6
Skokie 6
Turku 6
Xi'an 6
Amman 5
Catanzaro 5
Duque de Caxias 5
Fortaleza 5
Goiânia 5
Ha Long 5
Islington 5
Jinan 5
New Delhi 5
Porto Alegre 5
Totale 4.844
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Nome #
Multidisciplinary Screening of a Novel Founder LMNA Mutation Associated With Cardiomyopathy in a Geographic Isolate 261
JAB1 deletion in oligodendrocytes causes senescence-induced inflammation and neurodegeneration in mice 162
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD 158
Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13 157
Niacin ameliorates Charcot-Marie-Tooth 4B1 neuropathy without interfering with nerve regeneration 156
LAMA2 Neuropathies: Human Findings and Pathomechanisms From Mouse Models 134
Jab1 regulates Schwann cell proliferation and axonal sorting through p27. 133
Nusinersen safety and effects on motor function in adult spinal muscular atrophy type 2 and 3 129
Rebalancing expression of HMGB1 redox isoforms to counteract muscular dystrophy 123
Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutation 120
Cardiac and Neuromuscular Features of Patients with LMNA-Related Cardiomyopathy 119
A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation. 115
A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs) 114
Corrigendum to “Going for a stroll on lurasidone: Considerations on an atypical case of acute compartment syndrome of both legs” [Heliyon 9(4) (April 2023) e15047] (Heliyon (2023) 9(4), (S2405844023022545), (10.1016/j.heliyon.2023.e15047)) 108
Overcoming therapeutic challenges: Successful management of a supposedly triple seronegative, refractory generalized myasthenia gravis patient with efgartigimod 107
Mutations in MYO9B are associated with Charcot–Marie–Tooth disease type 2 neuropathies and isolated optic atrophy 103
Analyzing histopathological features of rare charcot-marie-tooth neuropathies to unravel their pathogenesis 103
Prostaglandin D2 synthase modulates macrophage activity and accumulation in injured peripheral nerves 100
Brain connectivity abnormalities extend beyond the sensorimotor network in peripheral neuropathy 98
Charcot-Marie-Tooth type 4B demyelinating neuropathy: deciphering the role of MTMR phosphatases 96
Muscle hypertrophy following acquired neurogenic injury: systematic review and analysis of existing literature 95
A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2 94
Begelomab for severe refractory dermatomyositis: A case report 94
A GENOMIC APPROACH TO IDENTIFY NEW GENES RESPONSIBLE FOR INHERITED MOTOR AND CMT2 NEUROPATHIES: A COLLABORATIVE STUDY 92
Going for a stroll on lurasidone: Considerations on an atypical case of acute compartment syndrome of both legs 91
The mitochondrial protease AFG3L2 is essential for axonal development 91
Alteration of the late endocytic pathway in Charcot-Marie-Tooth type 2B disease 90
Mesoangioblasts at 20: From the embryonic aorta to the patient bed 87
CLINICAL AND MOLECULAR CHARACTERIZATION OF A COHORT OF PATIENTS WITH DISTAL MOTOR NEUROPATHY 85
Corrigendum to “Going for a stroll on lurasidone: Considerations on an atypical case of acute compartment syndrome of both legs” [Heliyon Volume 9, Issue 4, April 2023, Article e15047](S2405844023022545)(10.1016/j.heliyon.2023.e15047) 85
CLINICAL CHARACTERIZATION OF A PATIENT CARRYING HINT1 MUTATION 84
Expanding the spectrum of genes responsible for hereditary motor neuropathies 82
CHARCOT-MARIE-TOOTH DISEASE TYPE 4B: A MULTICENTRE RETROSPECTIVE STUDY 81
Rimeporide as a first- in-class NHE-1 inhibitor: Results of a phase Ib trial in young patients with Duchenne Muscular Dystrophy 78
Neuromyelitis optica and myotonic dystrophy type 2: a rare association with diagnostic implications 78
24 Month Longitudinal Data in Ambulant Boys with Duchenne Muscular Dystrophy 75
A 5-year clinical follow-up study from the Italian National Registry for FSHD 74
Correction to: Molecular mechanisms and therapeutic strategies for neuromuscular diseases (Cellular and Molecular Life Sciences, (2024), 81, 1, (198), 10.1007/s00018-024-05229-9) 73
Animal Models as a Tool to Design Therapeutical Strategies for CMT-like Hereditary Neuropathies 72
Autocrine and immune cell-derived BDNF in human skeletal muscle: implications for myogenesis and tissue regeneration 71
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy 70
Dipeptidyl peptidase 4/CD26 expression in human idiopathic inflammatory myopathies reveals skeletal muscle injury and vascular inflammation 68
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy 67
Abnormal Schwann cell-axon interaction in EBF-2 "knock out" mice 66
The extracellular matrix affects axonal regeneration in peripheral neuropathies 65
Vimentin regulates peripheral nerve myelination 64
DEFINING GENOTYPE-PHENOTYPE CORRELATIONS IN THE CMT NEUROPATHIES 63
Categorizing natural history trajectories of ambulatory function measured by the 6-minute walk distance in patients with Duchenne muscular dystrophy 62
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 62
Protein profiling reveals energy metabolism and cytoskeletal protein alterations in LMNA mutation carriers. 62
6 Minute Walk Test in Duchenne MD Patients with Different Mutations: 12 Month Changes 60
Hypokalemic periodic paralysis in a patient with acquired growth hormone deficiency 60
Autoimmunity in the peripheral nervous system 60
A whole-brain functional network connectivity analysis in patients with hereditary and acquired peripheral neuropathy. 60
Facioscapulohumeral dystrophy 60
Loss of Mtmr2 phosphatase in Schwann cells but not in motor neurons causes Charcot-Marie-tooth type 4B1 neuropathy with myelin outfoldings 58
Longitudinal MRI quantification of muscle degeneration in Duchenne muscular dystrophy 57
Kif13b Regulates PNS and CNS Myelination through the Dlg1 Scaffold 57
Urokinase Plasminogen Receptor and the Fibrinolytic Complex Play a Role in Nerve Repair after Nerve Crush in Mice, and in Human Neuropathies 56
Disruption of Mtmr2 produces CMT4B1-like neuropathy with myelin outfolding and impaired spermatogenesis 56
CYTOSKELETON AND PERIPHERAL NERVE MYELINATION: A NOVEL ROLE FOR VIMENTIN 56
Expression analysis in the peripheral nerve of the myotubularin-related 2 protein phosphatase, mutated in CMT4B1 55
Correction: Increased Serum Hepcidin Levels in Subjects with the Metabolic Syndrome: A Population Stydy. 55
LOSS OF FIG4 IN BOTH SCHWANN CELLS AND MOTOR NEURONS CONTRIBUTES TO CMT4J NEUROPATHY 54
A whole-brain network analysis in patients with hereditary and acquired peripheral neuropathy 54
Loss of glial fibrillary acidic protein (GFAP) impairs Schwann cell proliferation and delays nerve regeneration after damage 54
Intravenous immunoglobulin treatment in patients with chronic inflammatory demyelinating neuropathy not responsive to other treatments 54
The exctracellular matrix affects axonal regeneration in peripheral neuropathies 54
Hypogonadotropic hypogonadism and peripheral neuropathy in Ebf2-null mice 54
Pregnancy in Charcot-Marie-Tooth disease: Data from the Italian CMT national registry 54
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements 53
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 LITERATUREPPP 53
Muscle MRI findings in facioscapulohumeral muscular dystrophy 53
Increased serum hepcidin levels in subjects with the metabolic syndrome: a population study 53
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4 52
Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerve 52
Peripheral Nerve Development and the Pathogenesis of Peripheral Neuropathy: the Sorting Point 52
Genetic modifiers of respiratory function in Duchenne muscular dystrophy 52
CSN5/JAB1 PLAYS A ROLE IN AXONAL SORTING AND MYELINATION IN PERIPHERAL NERVE 52
POEMS syndrome: the matter-of-fact approach 52
Merosin deficient congenital muscular dystrophy type 1A: An international workshop on the road to therapy 15-17 November 2019, Maastricht, the Netherlands 52
Niacin-mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination 52
Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53 51
MODULATION OF NEUREGULIN 1 TYPE III PATHWAY TO TREAT HEREDITARY DEMYELINATING NEUROPATHIES 50
TRAFFICKING THROUGH THE ENDO-LYSOSOMAL AXIS REGULATES MYELINATION AND REPAIR IN THE PERIPHERAL NERVOUS SYSTEM 50
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 50
Molecular mechanisms and therapeutic strategies for neuromuscular diseases. 50
Editorial: Current Insights Into LAMA2 Disease. 50
Role of the extracellular matrix in regenerating and non-regenerating axonal neuropathies 49
Loss of function MPZ mutation causes milder CMT1B neuropathy 49
Loss of Fig4 in both Schwann cells and motor neurons contributes to CMT4J neuropathy 49
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 48
How Schwann Cells Sort Axons: New Concepts 48
Diffuse intraneural leiomyoma in a case of sensorimotor neuropathy 48
Foot pad skin biopsy in mouse models of hereditary neuropathy 48
P3170Innovative approach for risk stratification of LMNA-related cardiomyopathy: results from an integrated cardiological and neurological 10-year follow-up multicentre study 48
Quantitative muscle strength assessment in duchenne muscular dystrophy: longitudinal study and correlation with functional measures. 48
CSN5/JAB1 REGULATES SCHWANN CELL-AXON INTERACTION AND PLAYS A ROLE IN PERIPHERAL NERVE DEVELOPMENT AND FUNCTION 47
Mutation of the small HSP27/HSPB1 causes CMT neuropathy with abnormal neurofilament assembly 47
Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1A 47
Totale 7.550
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Categoria #
all - tutte 43.411
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 43.411
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211 0 0 0 0 0 0 0 0 0 0 0 1
2021/202234 0 0 0 7 0 8 7 2 4 0 6 0
2022/2023269 98 49 22 0 3 23 12 14 11 31 1 5
2023/2024324 7 17 40 55 31 89 8 22 0 4 6 45
2024/20252.239 128 25 114 239 110 176 396 228 318 193 142 170
2025/20266.553 541 491 792 860 555 204 682 484 1.695 249 0 0
Totale 9.458