IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

PAGLIARANI, SERENA
 Distribuzione geografica
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Continente #
EU - Europa 2.022
NA - Nord America 1.617
AS - Asia 585
SA - Sud America 42
OC - Oceania 11
AF - Africa 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 4.282
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Nazione #
US - Stati Uniti d'America 1.539
GB - Regno Unito 684
DE - Germania 336
CN - Cina 324
IT - Italia 318
SE - Svezia 270
IN - India 84
CA - Canada 70
IE - Irlanda 69
UA - Ucraina 64
FR - Francia 63
TR - Turchia 60
KR - Corea 53
FI - Finlandia 49
EU - Europa 39
DK - Danimarca 38
NL - Olanda 32
RU - Federazione Russa 25
BE - Belgio 23
SG - Singapore 23
CO - Colombia 21
BR - Brasile 19
CH - Svizzera 17
HK - Hong Kong 11
AU - Australia 10
GR - Grecia 10
ID - Indonesia 10
RO - Romania 10
JP - Giappone 5
ES - Italia 4
PT - Portogallo 4
MX - Messico 3
SC - Seychelles 3
TW - Taiwan 3
CL - Cile 2
PH - Filippine 2
QA - Qatar 2
UZ - Uzbekistan 2
A1 - Anonimo 1
AT - Austria 1
CR - Costa Rica 1
CZ - Repubblica Ceca 1
EE - Estonia 1
GL - Groenlandia 1
HN - Honduras 1
HU - Ungheria 1
IR - Iran 1
LB - Libano 1
LK - Sri Lanka 1
MY - Malesia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PA - Panama 1
PR - Porto Rico 1
RS - Serbia 1
SA - Arabia Saudita 1
VN - Vietnam 1
Totale 4.320
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Città #
Southend 623
Chandler 262
Seattle 120
Milan 101
Ann Arbor 94
Ashburn 88
Beijing 88
Fairfield 84
Wilmington 83
Princeton 79
Dublin 69
Toronto 51
Dearborn 50
Jacksonville 47
Mountain View 42
Woodbridge 40
Houston 39
Nanjing 38
Redmond 29
Bengaluru 28
Somerville 28
Boardman 27
Des Moines 27
Frankfurt am Main 27
Cambridge 24
Redwood City 21
Andover 20
Sakarya 20
Bogotá 19
Helsinki 17
Berlin 16
Shenyang 16
Jinan 15
Margão 15
New York 15
Ottawa 15
Serra 15
Brussels 14
Phoenix 14
Shanghai 14
Kiez 13
Scranton 13
Hebei 12
Medford 12
Nanchang 12
Nürnberg 12
Tianjin 12
Bitonto 10
Hong Kong 10
Athens 9
Changsha 9
Guangzhou 9
Rome 9
San Diego 9
Durham 8
Bologna 7
Roxbury 7
Grafing 6
Lanzhou 6
Ningbo 6
Silver Spring 6
Zhengzhou 6
Haikou 5
Melzo 5
Pskov 5
Zurich 5
Auburn Hills 4
Bühl 4
Frankfurt Am Main 4
Hangzhou 4
Hanover 4
Kent 4
Lisbon 4
London 4
Philadelphia 4
Seoul 4
Trieste 4
Verona 4
Waanrode 4
Boston 3
Eitensheim 3
Frankfurt 3
Goiânia 3
Gussago 3
Kunming 3
Mahé 3
Norristown 3
Padova 3
Palermo 3
Pozzo Di Gotto 3
Pune 3
Rho 3
San Francisco 3
Bari 2
Buffalo 2
Busto Arsizio 2
Cajàzeiras 2
Changchun 2
Columbus 2
Den Bosch 2
Totale 2.765
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Nome #
La canalopatia del cloro : diagnosi clinica differenziale 317
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion 235
Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches 224
Caratterizzazione molecolare dei geni CLCN1, SCN4A, KCNJ2, CACNA1S in pazienti con canalopatie muscolari 163
Glucose-free/high-protein diet improves hepatomegaly and exercise intolerance in glycogen storage disease type III mice 154
Clinical, biochemical and genetic features of glycogen debranching enzyme deficiency 144
Myotonia congenita : novel mutations in CLCN1 gene and functional characterizations in Italian patients 138
Redefining clinical phenotype in a large color of Italian non-dystrophic myotonic patients. 131
Clinical, molecular, and protein correlations in a large sample of genetically diagnosed Italian limb girdle muscular dystrophy patients 131
Myotonia permanens with neonatal onset associated with a p.Gly1306Glu mutation in the SCN4A gene. 130
New mutations in SCN4A and their biophysical properties 129
Molecular epidemiology and clinical features of a large Italian cohort of 291 dystrophinopathic patients. 128
Glicogenosi di tipo III: rivalutazione delle caratteristiche cliniche e genetiche dei pazienti e stato dell’arte sul modello murino knock-out. 121
Disease natural history in a large group of genetically diagnosed glycogen storage disease type III. 118
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability 112
Mutations in DNA2 link progressive myopathy to mitochondrial DNA instability 112
Glycogen storage disease type III : A novel Agl knockout mouse model 112
Molecular characterization of CLCN1, SCN4A, KCNJ2, CACNA1S genes in patients with muscle channelopathies. 111
One gene, two clinical profiles:novel GBE1 mutations in GSD type IV and Adult Polyglucosan Body Disease. 111
Hypokalaemic periodic paralysis: a new nonsense mutation in KCNJ 2 gene 110
Longitudinal follow-up and muscle MRI pattern of two siblings with polyglucosan body myopathy due to glycogenin-1 mutation 108
Hepatic and neuromuscular forms of glycogenosis Type III : nine mutations in AGL Gene 107
Novel CLCN1 gene mutation associated with myotonia congenita in Italian patients. 100
Myotonic dystrophy type 2: clinical, neurophysiological mnd muscular features of a family with short CCTG expansion. 98
Sodium Channel Myotonia Due to Novel Mutations in Domain I of Nav1.4 98
Clinical, biochemical and genetic features of Glycogen Debrancher Enzyme deficiency 97
A severe pediatric case of congenital Myastenic Syndrome due to a novel mutation in COLQ gene 96
Phenotypic heterogeneity of GBE1 mutations: congenital glycogen storage disease type IV and adult polyglucosan body disease. 94
MYH2 myopathy, a new case expands the clinical and pathological spectrum of the recessive form 94
Genetic distribution and unusual phenotypes in a periodic paralysis 93
Mutations in DNA2 cause progressive myopathy with mtDNA instability 88
Early Findings in Neonatal Cases of RYR1-Related Congenital Myopathies 88
Adult polyglucosan body disease: clinical and histological heterogeneity of a large Italian family 86
Adult polyglucosan body disease in a patient originally diagnosed with Fabry's disease 82
Elucidating the role of Agl in bladder carcinogenesis by generation and characterization of genetically engineered mice 79
Clinical, histological and molecular features of two italian families with mutations in CAV3 gene 72
CACNA1S mutation associated with a case of juvenile-onset congenital myopathy 59
Rescue of GSDIII Phenotype with Gene Transfer Requires Liver- and Muscle-Targeted GDE Expression 57
Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III 44
Case report: Sodium and chloride muscle channelopathy coexistence: A complicated phenotype and a challenging diagnosis 34
Case report: Clinical and molecular characterization of two siblings affected by Brody myopathy 6
null 3
Totale 4.614
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Categoria #
all - tutte 11.077
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 11.077
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019100 0 0 0 0 0 0 0 0 0 0 38 62
2019/2020584 82 13 27 30 26 59 58 31 131 77 36 14
2020/2021559 16 38 60 31 41 42 64 51 50 31 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
2023/2024335 8 27 27 30 109 34 18 51 17 14 0 0
Totale 4.614