IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

PAGLIARANI, SERENA
 Distribuzione geografica
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Continente #
NA - Nord America 2.867
EU - Europa 2.692
AS - Asia 2.643
SA - Sud America 231
AF - Africa 53
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.512
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Nazione #
US - Stati Uniti d'America 2.731
SG - Singapore 820
CN - Cina 755
GB - Regno Unito 707
IT - Italia 498
DE - Germania 401
SE - Svezia 273
BD - Bangladesh 228
HK - Hong Kong 221
RU - Federazione Russa 200
VN - Vietnam 193
BR - Brasile 177
FR - Francia 140
IN - India 136
CA - Canada 99
NL - Olanda 99
FI - Finlandia 74
TR - Turchia 74
IE - Irlanda 73
KR - Corea 70
UA - Ucraina 67
DK - Danimarca 40
EU - Europa 39
ID - Indonesia 37
JP - Giappone 27
CO - Colombia 26
BE - Belgio 25
AU - Australia 22
CI - Costa d'Avorio 22
MX - Messico 18
CH - Svizzera 17
PL - Polonia 15
ES - Italia 12
ZA - Sudafrica 11
GR - Grecia 10
RO - Romania 10
AR - Argentina 9
IQ - Iraq 8
PH - Filippine 8
PK - Pakistan 8
AE - Emirati Arabi Uniti 6
AT - Austria 6
SA - Arabia Saudita 6
EC - Ecuador 5
IR - Iran 5
MY - Malesia 5
TW - Taiwan 5
CL - Cile 4
EG - Egitto 4
LB - Libano 4
PA - Panama 4
PT - Portogallo 4
PY - Paraguay 4
UZ - Uzbekistan 4
VE - Venezuela 4
AZ - Azerbaigian 3
CR - Costa Rica 3
EE - Estonia 3
JO - Giordania 3
NO - Norvegia 3
QA - Qatar 3
SC - Seychelles 3
AM - Armenia 2
BG - Bulgaria 2
BW - Botswana 2
CZ - Repubblica Ceca 2
DZ - Algeria 2
ET - Etiopia 2
GE - Georgia 2
HN - Honduras 2
IL - Israele 2
JM - Giamaica 2
KE - Kenya 2
LU - Lussemburgo 2
NZ - Nuova Zelanda 2
PE - Perù 2
PR - Porto Rico 2
SI - Slovenia 2
SV - El Salvador 2
A1 - Anonimo 1
AL - Albania 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
DO - Repubblica Dominicana 1
GA - Gabon 1
GL - Groenlandia 1
GT - Guatemala 1
HU - Ungheria 1
KG - Kirghizistan 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LT - Lituania 1
MA - Marocco 1
MD - Moldavia 1
MK - Macedonia 1
MN - Mongolia 1
NI - Nicaragua 1
NP - Nepal 1
OM - Oman 1
Totale 8.546
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Città #
Southend 623
Singapore 462
Ashburn 324
Chandler 262
Hong Kong 205
Dallas 175
Beijing 167
Milan 145
Seattle 123
San Jose 120
Ann Arbor 94
Fairfield 84
Wilmington 83
Princeton 79
Council Bluffs 78
Dublin 72
New York 67
Ho Chi Minh City 59
Los Angeles 57
Toronto 54
Santa Clara 53
Bengaluru 52
Hanoi 51
Dearborn 50
Frankfurt am Main 50
Hefei 47
Jacksonville 47
Buffalo 42
Mountain View 42
Lauterbourg 41
Houston 40
Woodbridge 40
Nanjing 39
Boardman 36
Des Moines 29
Guangzhou 29
Redmond 29
Shanghai 28
Somerville 28
Cambridge 27
Rome 26
Helsinki 24
Moscow 24
Jakarta 23
Abidjan 22
Cangzhou 22
Redwood City 21
Andover 20
Bogotá 20
Columbus 20
Sakarya 20
Tokyo 19
Jinan 18
Phoenix 18
Shenyang 18
Tianjin 18
Berlin 17
Ottawa 16
São Paulo 16
Margão 15
Munich 15
Serra 15
Bologna 14
Brussels 14
Seoul 14
Kiez 13
Scranton 13
Warsaw 13
Changsha 12
Hebei 12
Medford 12
Nanchang 12
Nürnberg 12
The Dalles 12
Turku 12
Bitonto 11
Shenzhen 10
Athens 9
Brooklyn 9
Düsseldorf 9
Nuremberg 9
San Diego 9
Boston 8
Da Nang 8
Durham 8
San Francisco 8
Amsterdam 7
Falkenstein 7
Haiphong 7
Mumbai 7
Roxbury 7
Zhengzhou 7
Belo Horizonte 6
Chennai 6
Grafing 6
Johannesburg 6
Lanzhou 6
Lappeenranta 6
Lecce 6
London 6
Totale 4.913
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Nome #
La canalopatia del cloro : diagnosi clinica differenziale 386
Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches 377
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion 358
Myotonia congenita : novel mutations in CLCN1 gene and functional characterizations in Italian patients 292
MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form 256
Glucose-free/high-protein diet improves hepatomegaly and exercise intolerance in glycogen storage disease type III mice 253
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4 247
Caratterizzazione molecolare dei geni CLCN1, SCN4A, KCNJ2, CACNA1S in pazienti con canalopatie muscolari 245
Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients 244
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies 239
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability 238
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability 219
Myotonia permanens with neonatal onset associated with a p.Gly1306Glu mutation in the SCN4A gene. 213
Adult polyglucosan body disease in a patient originally diagnosed with Fabry's disease 213
Redefining clinical phenotype in a large color of Italian non-dystrophic myotonic patients. 211
Longitudinal follow-up and muscle MRI pattern of two siblings with polyglucosan body myopathy due to glycogenin-1 mutation 204
Clinical, biochemical and genetic features of glycogen debranching enzyme deficiency 203
Molecular epidemiology and clinical features of a large Italian cohort of 291 dystrophinopathic patients. 203
Case report: Sodium and chloride muscle channelopathy coexistence: A complicated phenotype and a challenging diagnosis 199
Elucidating the role of Agl in bladder carcinogenesis by generation and characterization of genetically engineered mice 197
Glycogen storage disease type III : A novel Agl knockout mouse model 196
New mutations in SCN4A and their biophysical properties 194
Glicogenosi di tipo III: rivalutazione delle caratteristiche cliniche e genetiche dei pazienti e stato dell’arte sul modello murino knock-out. 192
Disease natural history in a large group of genetically diagnosed glycogen storage disease type III. 179
One gene, two clinical profiles:novel GBE1 mutations in GSD type IV and Adult Polyglucosan Body Disease. 179
Molecular characterization of CLCN1, SCN4A, KCNJ2, CACNA1S genes in patients with muscle channelopathies. 176
Myotonic dystrophy type 2: clinical, neurophysiological mnd muscular features of a family with short CCTG expansion. 174
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy 173
Phenotypic heterogeneity of GBE1 mutations: congenital glycogen storage disease type IV and adult polyglucosan body disease. 166
Adult polyglucosan body disease: clinical and histological heterogeneity of a large Italian family 163
Novel CLCN1 gene mutation associated with myotonia congenita in Italian patients. 159
Myotonic dystrophies: an update on clinical features, molecular mechanisms, management, and gene therapy 157
Case report: Multiple approach analysis in a case of clinically assessed myotonia congenita 157
Hepatic and neuromuscular forms of glycogenosis Type III : nine mutations in AGL Gene 154
Genetic distribution and unusual phenotypes in a periodic paralysis 149
Mutations in DNA2 cause progressive myopathy with mtDNA instability 148
Hypokalaemic periodic paralysis: a new nonsense mutation in KCNJ 2 gene 143
Clinical, biochemical and genetic features of Glycogen Debrancher Enzyme deficiency 138
Rescue of GSDIII Phenotype with Gene Transfer Requires Liver- and Muscle-Targeted GDE Expression 131
Case report: Clinical and molecular characterization of two siblings affected by Brody myopathy 128
Case report: Dihydropyridine receptor (CACNA1S) congenital myopathy, a novel phenotype with early onset periodic paralysis 122
Clinical, histological and molecular features of two italian families with mutations in CAV3 gene 122
A severe pediatric case of congenital Myastenic Syndrome due to a novel mutation in COLQ gene 122
LONG-NEXT: A new accurate and efficient NGS-based method for GBA1 analysis in Parkinson disease 105
Myotonic Dystrophy type 2 unmasked by physical activity resumption following COVID-19 lockdown: case discussion and review of the literature 88
Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III 87
A new MYH2 variant in an Italian patient expanding the clinical spectrum of MYH2-related myopathy 9
Expanding the genetic landscape of Dusty Core Disease: new RYR1 variants in Italian patients 9
null 3
Totale 8.920
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Categoria #
all - tutte 23.024
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 23.024
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021135 0 0 0 0 0 0 0 0 0 0 98 37
2021/2022567 34 35 32 21 40 36 40 20 86 69 30 124
2022/2023754 96 99 65 84 94 135 14 39 84 8 21 15
2023/2024432 8 27 27 30 109 34 18 51 17 14 40 57
2024/20251.292 57 123 35 130 73 34 58 101 79 151 140 311
2025/20262.917 321 225 338 228 233 171 334 119 229 234 485 0
Totale 8.920