GOVONI, ALESSANDRA
 Distribuzione geografica
Continente #
EU - Europa 4.306
NA - Nord America 4.156
AS - Asia 3.410
SA - Sud America 430
AF - Africa 103
OC - Oceania 71
Continente sconosciuto - Info sul continente non disponibili 15
Totale 12.491
Nazione #
US - Stati Uniti d'America 3.935
CN - Cina 1.040
GB - Regno Unito 996
IT - Italia 924
SG - Singapore 812
DE - Germania 594
SE - Svezia 328
BR - Brasile 269
HK - Hong Kong 263
FR - Francia 260
JP - Giappone 255
RU - Federazione Russa 246
BD - Bangladesh 215
IN - India 173
CA - Canada 168
VN - Vietnam 168
ES - Italia 128
NL - Olanda 126
FI - Finlandia 113
TR - Turchia 106
KR - Corea 98
CH - Svizzera 94
IE - Irlanda 87
ID - Indonesia 63
AR - Argentina 62
AU - Australia 61
PL - Polonia 58
BE - Belgio 54
UA - Ucraina 51
TW - Taiwan 47
CO - Colombia 44
AT - Austria 39
MX - Messico 37
TH - Thailandia 32
DK - Danimarca 31
GR - Grecia 30
CI - Costa d'Avorio 25
EU - Europa 23
RO - Romania 23
CL - Cile 20
NO - Norvegia 19
CZ - Repubblica Ceca 18
EG - Egitto 18
IL - Israele 18
PT - Portogallo 17
PH - Filippine 16
HU - Ungheria 14
IQ - Iraq 14
PE - Perù 14
TN - Tunisia 14
AE - Emirati Arabi Uniti 12
BG - Bulgaria 11
DZ - Algeria 11
SA - Arabia Saudita 11
AP - ???statistics.table.value.countryCode.AP??? 10
CY - Cipro 10
NZ - Nuova Zelanda 10
ZA - Sudafrica 10
EC - Ecuador 9
MY - Malesia 9
HR - Croazia 8
PK - Pakistan 7
UY - Uruguay 6
LK - Sri Lanka 5
LV - Lettonia 5
ML - Mali 5
MO - Macao, regione amministrativa speciale della Cina 5
PA - Panama 5
SK - Slovacchia (Repubblica Slovacca) 5
UZ - Uzbekistan 5
BY - Bielorussia 4
IR - Iran 4
LU - Lussemburgo 4
MA - Marocco 4
SC - Seychelles 4
SI - Slovenia 4
VE - Venezuela 4
KE - Kenya 3
NP - Nepal 3
PR - Porto Rico 3
RS - Serbia 3
SN - Senegal 3
AM - Armenia 2
AZ - Azerbaigian 2
CR - Costa Rica 2
EE - Estonia 2
JM - Giamaica 2
KZ - Kazakistan 2
LB - Libano 2
LT - Lituania 2
MD - Moldavia 2
ME - Montenegro 2
MK - Macedonia 2
PS - Palestinian Territory 2
PY - Paraguay 2
QA - Qatar 2
AL - Albania 1
BS - Bahamas 1
BT - Bhutan 1
CG - Congo 1
Totale 12.494
Città #
Southend 659
Singapore 485
Ashburn 382
Chandler 255
Dallas 255
Hong Kong 218
Milan 205
San Jose 182
Beijing 180
Fairfield 151
Frankfurt am Main 149
Redwood City 148
Wilmington 128
Seattle 115
New York 106
Los Angeles 101
Council Bluffs 97
Woodbridge 96
Houston 95
Princeton 88
Ann Arbor 85
Dublin 78
Helsinki 70
Tokyo 70
Toronto 66
Moscow 61
Hefei 58
Shanghai 57
Columbus 51
London 51
Cambridge 50
Rome 50
Santa Clara 50
Bengaluru 48
Hanoi 47
Jakarta 44
Boardman 43
Lauterbourg 42
Munich 41
Nanjing 41
Ho Chi Minh City 40
Buffalo 36
São Paulo 36
Madrid 35
Phoenix 35
Bogotá 33
Des Moines 32
Grafing 32
Taipei 31
Jinan 30
Atlanta 29
Brussels 29
Guangzhou 29
Istanbul 28
Seoul 28
Vienna 28
Zurich 28
The Dalles 27
Buenos Aires 26
Changsha 26
Abidjan 25
Hangzhou 25
Mountain View 25
Somerville 24
Sydney 24
Ottawa 23
Warsaw 23
Berlin 22
Chicago 22
Dearborn 22
Fuzhou 22
Paris 22
Amsterdam 20
Mumbai 19
Shenyang 19
Redmond 18
Santiago 18
Duncan 17
Seongnam 17
Ankara 16
Boston 16
Cangzhou 16
Osaka 16
Tianjin 16
Turin 16
Bangkok 15
Naples 15
Andover 14
Kyiv 14
Las Vegas 14
Shenzhen 14
Eitensheim 13
Genoa 13
Hamburg 13
Hanover 13
Silver Spring 13
Vancouver 13
Zhengzhou 13
Bologna 12
Central District 12
Totale 6.520
Nome #
Time Is Motor Neuron: Therapeutic Window and Its Correlation with Pathogenetic Mechanisms in Spinal Muscular Atrophy 2.085
The Italian limb girdle muscular dystrophy registry : relative frequency, clinical features, and differential diagnosis 1.566
Current understanding of and emerging treatment options for spinal muscular atrophy with respiratory distress type 1 (SMARD1) 667
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 422
Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanisms 394
Nusinersen treatment and cerebrospinal fluid neurofilaments : An explorative study on Spinal Muscular Atrophy type 3 patients 356
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature 353
Central nervous system involvement in common variable immunodeficiency: A case of acute unilateral optic neuritis in a 26 -year-old Italian Patient 331
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing 319
Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis 315
Bridging the Gap : Gene Therapy in a Spinal Muscular Atrophy Type 1 Patient 284
Bilateral Cavernous Carotid Aneurysms: Atypical Presentation of a Rare Cause of Mass Effect. A Case Report and a Review of the Literature 266
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies 241
Genotype and phenotype characterization in a large dystrophinopathic cohort with extended follow-up 233
Growing evidence about the relationship between vessel dissection and Scuba diving 225
Spinal muscular atrophy with respiratory distress type 1: Clinical phenotypes, molecular pathogenesis and therapeutic insights 222
Molecular analysis of SMARD1 patient-derived cells demonstrates that nonsense-mediated mRNA decay is impaired 220
Stormorken syndrome caused by a p.R304W STIM1 mutation: The first Italian patient and a review of the literature 216
Diagnostic and prognostic value of CSF neurofilaments in a cohort of patients with motor neuron disease: A cross-sectional study 216
Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanisms 209
Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients 204
A new case of limb girdle muscular dystrophy 2G in a Greek patient, founder effect and review of the literature 202
The expanding spectrum of LAMA2 gene mutations : from congenital muscular dystrophy 1A to limb girdle muscular dystrophy 2R 189
The Italian registry of limb girdle muscular dystrophy : natural history, genotype-phenotype correlations and outcome measures 183
Genetic correction of spinal muscular atrophy-induced pluripotent stem cells and motoneurons as a disease model and cell source for transplantation 179
Adults with spinal muscular atrophy: a large-scale natural history study shows gender effect on disease 176
Multi-omics profiling of CSF from spinal muscular atrophy type 3 patients after nusinersen treatment: a 2-year follow-up multicenter retrospective study 174
Nuova mutazione intronica nel gene della distrofina determinante inserzione di un pseudo esone in paziente DMD 170
Congenital myopathies : clinical, morphological and molecular findings in a sample of 29 Italian patients 168
Systemic transplantation of c-kit+ cells exerts a therapeutic effect in a model of amyotrophic lateral sclerosis 166
The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairment 164
Nusinersen safety and effects on motor function in adult spinal muscular atrophy type 2 and 3 164
Frequency and characterization of anoctamin 5 mutations in Italian limb girdle muscular dystrophy patients 160
LAMA2 gene mutations are cause of congenital and limb-girdle muscular dystrophies 159
The Italian limb girdle muscular dystrophies (LGMD) registry : molecular and clinical data 159
A novel CHRNE gene mutation associated with congenital myasthenia: case report and review of the literature 154
A novel intronic DYS gene mutation leading to a pseudoexon insertion in a DMD patient 146
MRI patterns of muscle involvement in type 2 and 3 spinal muscular atrophy patients 141
Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy 134
Dystrophin gene mutations and their clinical correlates in 319 Italian patients affected with dystrophinopathy 130
Proposal of a new clinical protocol for evaluating fatigability in adult SMA patients 128
Respiratory function in a large cohort of treatment-naïve adult spinal muscular atrophy patients: a cross-sectional study 119
CPEO due to mutations in the tRNA for isolucine : two additional Italian cases. 117
Revised genetic classification of limb girdle muscular dystrophies 101
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Totale 12.936
Categoria #
all - tutte 30.715
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 30.715


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021164 0 0 0 0 0 0 0 0 0 0 0 164
2021/20221.202 107 114 91 119 83 84 83 84 130 88 91 128
2022/20231.215 163 127 85 93 85 177 100 93 118 63 74 37
2023/20241.062 51 70 78 90 158 79 88 84 40 96 112 116
2024/20251.782 92 155 56 186 122 101 100 159 127 175 195 314
2025/20263.526 312 252 438 269 305 237 387 147 355 240 399 185
Totale 12.936