IRIS
PREVITALI, STEFANO CARLO
 Distribuzione geografica
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Continente #
NA - Nord America 4.719
EU - Europa 3.810
AS - Asia 3.295
SA - Sud America 722
Continente sconosciuto - Info sul continente non disponibili 355
AF - Africa 68
OC - Oceania 4
Totale 12.973
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Nazione #
US - Stati Uniti d'America 4.439
RU - Federazione Russa 1.820
SG - Singapore 1.202
IT - Italia 1.177
CN - Cina 1.056
BR - Brasile 620
HK - Hong Kong 378
VN - Vietnam 300
FR - Francia 162
SE - Svezia 133
CA - Canada 129
GB - Regno Unito 117
DE - Germania 116
IN - India 88
BD - Bangladesh 77
NL - Olanda 60
AT - Austria 48
FI - Finlandia 48
MX - Messico 39
AR - Argentina 35
ES - Italia 27
JP - Giappone 25
TR - Turchia 24
ZA - Sudafrica 23
PL - Polonia 21
EC - Ecuador 19
JM - Giamaica 19
CR - Costa Rica 18
IQ - Iraq 18
ID - Indonesia 17
TT - Trinidad e Tobago 15
NI - Nicaragua 13
UZ - Uzbekistan 13
CO - Colombia 12
IE - Irlanda 11
SA - Arabia Saudita 11
LT - Lituania 10
PY - Paraguay 10
GT - Guatemala 9
PR - Porto Rico 9
RO - Romania 9
VE - Venezuela 9
IR - Iran 8
PH - Filippine 8
PK - Pakistan 8
CL - Cile 7
DZ - Algeria 7
NP - Nepal 7
AE - Emirati Arabi Uniti 6
BE - Belgio 6
GR - Grecia 6
HN - Honduras 6
KE - Kenya 6
LB - Libano 6
MA - Marocco 6
TN - Tunisia 6
UA - Ucraina 6
CZ - Repubblica Ceca 5
GP - Guadalupe 5
IL - Israele 5
JO - Giordania 5
PS - Palestinian Territory 5
SI - Slovenia 5
AU - Australia 4
CW - ???statistics.table.value.countryCode.CW??? 4
MY - Malesia 4
PE - Perù 4
SC - Seychelles 4
AL - Albania 3
BB - Barbados 3
BG - Bulgaria 3
BO - Bolivia 3
CG - Congo 3
EG - Egitto 3
HR - Croazia 3
HU - Ungheria 3
SN - Senegal 3
SV - El Salvador 3
TH - Thailandia 3
UY - Uruguay 3
BH - Bahrain 2
CH - Svizzera 2
DM - Dominica 2
DO - Repubblica Dominicana 2
GE - Georgia 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
Totale 12.605
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Città #
Dallas 753
Ashburn 692
Singapore 582
San Jose 530
Moscow 378
Hong Kong 374
Milan 292
Council Bluffs 235
Beijing 172
Shanghai 165
Hefei 149
Lauterbourg 129
Phoenix 124
Ho Chi Minh City 118
New York 98
Los Angeles 87
Santa Clara 87
Rome 84
Orem 69
São Paulo 61
Hanoi 59
Naples 46
Princeton 45
Lawrence 43
Nuremberg 39
Miano 37
Montreal 35
Chicago 33
Chennai 28
Helsinki 28
North Bergen 28
Denver 26
Amsterdam 25
Bologna 25
Washington 24
Brooklyn 23
Tokyo 23
Boardman 22
Manchester 22
Vienna 22
Toronto 21
Atlanta 19
Boston 19
Poplar 19
Warsaw 18
Belo Horizonte 17
Houston 17
Munich 17
Seattle 17
Turin 17
Brescia 16
London 16
San José 16
Carrboro 15
Hangzhou 15
Mumbai 15
San Francisco 15
Shenzhen 15
Cesano Boscone 14
Guangzhou 14
Charlotte 13
Da Nang 13
Florence 13
Haiphong 13
Johannesburg 13
Kingston 13
Lappeenranta 13
Managua 13
Rio de Janeiro 13
Zhengzhou 13
Curitiba 12
Biên Hòa 11
Buffalo 11
Catania 11
Falkenstein 11
Frankfurt am Main 11
Randolph Township 11
Stockholm 11
Bari 10
Brasília 10
Dublin 10
Philadelphia 10
Tashkent 10
Vancouver 10
Ankara 9
Detroit 9
Guayaquil 9
Mexico City 9
Omaha 9
Pittsburgh 9
West Roxbury 9
Assago 8
Cleveland 8
Des Moines 8
Madrid 8
Queens 8
Salvador 8
Baghdad 7
Bengaluru 7
Buenos Aires 7
Totale 6.555
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Nome #
Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13 344
Multidisciplinary Screening of a Novel Founder LMNA Mutation Associated With Cardiomyopathy in a Geographic Isolate 294
Genotype and phenotype spectrum of Charcot-Marie-Tooth disease due to mutations in SORD 257
LAMA2 Neuropathies: Human Findings and Pathomechanisms From Mouse Models 190
JAB1 deletion in oligodendrocytes causes senescence-induced inflammation and neurodegeneration in mice 189
Niacin ameliorates Charcot-Marie-Tooth 4B1 neuropathy without interfering with nerve regeneration 188
A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs) 188
Jab1 regulates Schwann cell proliferation and axonal sorting through p27. 157
Nusinersen safety and effects on motor function in adult spinal muscular atrophy type 2 and 3 148
Cardiac and Neuromuscular Features of Patients with LMNA-Related Cardiomyopathy 147
Rebalancing expression of HMGB1 redox isoforms to counteract muscular dystrophy 141
Analyzing histopathological features of rare charcot-marie-tooth neuropathies to unravel their pathogenesis 136
Muscle hypertrophy following acquired neurogenic injury: systematic review and analysis of existing literature 134
Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutation 133
Overcoming therapeutic challenges: Successful management of a supposedly triple seronegative, refractory generalized myasthenia gravis patient with efgartigimod 132
Mutations in MYO9B are associated with Charcot–Marie–Tooth disease type 2 neuropathies and isolated optic atrophy 128
A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation. 126
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)) 124
Prostaglandin D2 synthase modulates macrophage activity and accumulation in injured peripheral nerves 115
Begelomab for severe refractory dermatomyositis: A case report 111
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) 109
Brain connectivity abnormalities extend beyond the sensorimotor network in peripheral neuropathy 109
Charcot-Marie-Tooth type 4B demyelinating neuropathy: deciphering the role of MTMR phosphatases 108
A novel heat shock protein 27 homozygous mutation: widening of the continuum between MND/dHMN/CMT2 106
Rimeporide as a first- in-class NHE-1 inhibitor: Results of a phase Ib trial in young patients with Duchenne Muscular Dystrophy 104
Going for a stroll on lurasidone: Considerations on an atypical case of acute compartment syndrome of both legs 104
The mitochondrial protease AFG3L2 is essential for axonal development 104
Mesoangioblasts at 20: From the embryonic aorta to the patient bed 103
Alteration of the late endocytic pathway in Charcot-Marie-Tooth type 2B disease 100
A GENOMIC APPROACH TO IDENTIFY NEW GENES RESPONSIBLE FOR INHERITED MOTOR AND CMT2 NEUROPATHIES: A COLLABORATIVE STUDY 100
Expanding the spectrum of genes responsible for hereditary motor neuropathies 97
CLINICAL AND MOLECULAR CHARACTERIZATION OF A COHORT OF PATIENTS WITH DISTAL MOTOR NEUROPATHY 94
CLINICAL CHARACTERIZATION OF A PATIENT CARRYING HINT1 MUTATION 93
Neuromyelitis optica and myotonic dystrophy type 2: a rare association with diagnostic implications 93
A 5-year clinical follow-up study from the Italian National Registry for FSHD 91
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy 90
CHARCOT-MARIE-TOOTH DISEASE TYPE 4B: A MULTICENTRE RETROSPECTIVE STUDY 89
Intra-arterial transplantation of HLA-matched donor mesoangioblasts in Duchenne muscular dystrophy 88
Dipeptidyl peptidase 4/CD26 expression in human idiopathic inflammatory myopathies reveals skeletal muscle injury and vascular inflammation 88
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) 86
24 Month Longitudinal Data in Ambulant Boys with Duchenne Muscular Dystrophy 85
Autocrine and immune cell-derived BDNF in human skeletal muscle: implications for myogenesis and tissue regeneration 81
Animal Models as a Tool to Design Therapeutical Strategies for CMT-like Hereditary Neuropathies 79
The extracellular matrix affects axonal regeneration in peripheral neuropathies 78
Vimentin regulates peripheral nerve myelination 76
Kif13b Regulates PNS and CNS Myelination through the Dlg1 Scaffold 76
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 75
Urokinase Plasminogen Receptor and the Fibrinolytic Complex Play a Role in Nerve Repair after Nerve Crush in Mice, and in Human Neuropathies 74
Loss of Mtmr2 phosphatase in Schwann cells but not in motor neurons causes Charcot-Marie-tooth type 4B1 neuropathy with myelin outfoldings 74
Abnormal Schwann cell-axon interaction in EBF-2 "knock out" mice 74
Disruption of Mtmr2 produces CMT4B1-like neuropathy with myelin outfolding and impaired spermatogenesis 73
Categorizing natural history trajectories of ambulatory function measured by the 6-minute walk distance in patients with Duchenne muscular dystrophy 72
Hypokalemic periodic paralysis in a patient with acquired growth hormone deficiency 72
Monophasic multifocal motor neuropathy with concomitant central nervous system demyelination following anti-TNFα therapy 70
Molecular mechanisms and therapeutic strategies for neuromuscular diseases. 70
Protein profiling reveals energy metabolism and cytoskeletal protein alterations in LMNA mutation carriers. 70
DEFINING GENOTYPE-PHENOTYPE CORRELATIONS IN THE CMT NEUROPATHIES 70
Pregnancy in Charcot-Marie-Tooth disease: Data from the Italian CMT national registry 69
Expression analysis in the peripheral nerve of the myotubularin-related 2 protein phosphatase, mutated in CMT4B1 68
Facioscapulohumeral dystrophy 68
Diagnosis of Duchenne Muscular Dystrophy in Italy in the last decade: Critical issues and areas for improvements 67
6 Minute Walk Test in Duchenne MD Patients with Different Mutations: 12 Month Changes 67
Autoimmunity in the peripheral nervous system 67
A whole-brain functional network connectivity analysis in patients with hereditary and acquired peripheral neuropathy. 67
LOSS OF FIG4 IN BOTH SCHWANN CELLS AND MOTOR NEURONS CONTRIBUTES TO CMT4J NEUROPATHY 66
Longitudinal MRI quantification of muscle degeneration in Duchenne muscular dystrophy 66
CYTOSKELETON AND PERIPHERAL NERVE MYELINATION: A NOVEL ROLE FOR VIMENTIN 66
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 64
Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerve 64
Correction: Increased Serum Hepcidin Levels in Subjects with the Metabolic Syndrome: A Population Stydy. 64
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4 63
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 63
Loss of glial fibrillary acidic protein (GFAP) impairs Schwann cell proliferation and delays nerve regeneration after damage 63
The exctracellular matrix affects axonal regeneration in peripheral neuropathies 63
Increased serum hepcidin levels in subjects with the metabolic syndrome: a population study 63
TRAFFICKING THROUGH THE ENDO-LYSOSOMAL AXIS REGULATES MYELINATION AND REPAIR IN THE PERIPHERAL NERVOUS SYSTEM 62
A whole-brain network analysis in patients with hereditary and acquired peripheral neuropathy 62
Loss of Fig4 in both Schwann cells and motor neurons contributes to CMT4J neuropathy 62
Niacin-mediated Tace activation ameliorates CMT neuropathies with focal hypermyelination 62
Peripheral Nerve Development and the Pathogenesis of Peripheral Neuropathy: the Sorting Point 61
CSN5/JAB1 PLAYS A ROLE IN AXONAL SORTING AND MYELINATION IN PERIPHERAL NERVE 61
Long-term natural history data in Duchenne muscular dystrophy ambulant patients with mutations amenable to skip exons 44, 45, 51 and 53 61
Muscle MRI findings in facioscapulohumeral muscular dystrophy 61
MODULATION OF NEUREGULIN 1 TYPE III PATHWAY TO TREAT HEREDITARY DEMYELINATING NEUROPATHIES 60
Genetic modifiers of respiratory function in Duchenne muscular dystrophy 60
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 60
Intravenous immunoglobulin treatment in patients with chronic inflammatory demyelinating neuropathy not responsive to other treatments 60
Hypogonadotropic hypogonadism and peripheral neuropathy in Ebf2-null mice 60
Loss of function MPZ mutation causes milder CMT1B neuropathy 59
Merosin deficient congenital muscular dystrophy type 1A: An international workshop on the road to therapy 15-17 November 2019, Maastricht, the Netherlands 59
POEMS syndrome: the matter-of-fact approach 58
Editorial: Current Insights Into LAMA2 Disease. 58
Mesoangioblast delivery of miniagrin ameliorates murine model of merosin-deficient congenital muscular dystrophy type 1A 58
Suitability of external controls for drug evaluation in Duchenne muscular dystrophy 58
GENOMIC APPROACH FOR INHERITED MOTOR AND CMT2 NEUROPATHIES: A COLLABORATIVE STUDY 57
Foot pad skin biopsy in mouse models of hereditary neuropathy 57
Dlg1, Sec8, and Mtmr2 Regulate Membrane Homeostasis in Schwann Cell Myelination 56
Phenotype-Genotype Correlations in Early-Onset Myelin Protein Zero-Related Neuropathies 56
Role of the extracellular matrix in regenerating and non-regenerating axonal neuropathies 55
CSN5/JAB1 REGULATES SCHWANN CELL-AXON INTERACTION AND PLAYS A ROLE IN PERIPHERAL NERVE DEVELOPMENT AND FUNCTION 55
Totale 9.263
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Categoria #
all - tutte 64.789
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 64.789
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/20267.033 541 491 792 860 555 204 682 484 1.695 350 239 140
2026/20273.035 257 723 618 1.437 0 0 0 0 0 0 0 0
Totale 12.973