IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

VEGGIOTTI, PIERANGELO
 Distribuzione geografica
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Continente #
NA - Nord America 9.217
AS - Asia 8.954
EU - Europa 7.295
SA - Sud America 1.104
AF - Africa 189
OC - Oceania 167
Continente sconosciuto - Info sul continente non disponibili 10
Totale 26.936
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Nazione #
US - Stati Uniti d'America 8.841
CN - Cina 2.795
SG - Singapore 2.624
IT - Italia 2.167
GB - Regno Unito 1.448
BR - Brasile 816
HK - Hong Kong 742
RU - Federazione Russa 718
VN - Vietnam 689
BD - Bangladesh 587
DE - Germania 507
FR - Francia 447
IE - Irlanda 357
IN - India 356
SE - Svezia 331
JP - Giappone 242
CA - Canada 234
NL - Olanda 231
ES - Italia 199
ID - Indonesia 196
FI - Finlandia 163
TR - Turchia 163
AU - Australia 149
KR - Corea 140
AR - Argentina 123
AT - Austria 82
BE - Belgio 82
DK - Danimarca 79
MX - Messico 79
NO - Norvegia 63
UA - Ucraina 62
CH - Svizzera 59
TW - Taiwan 58
PL - Polonia 52
CI - Costa d'Avorio 50
PT - Portogallo 47
IQ - Iraq 40
IR - Iran 39
CO - Colombia 38
GR - Grecia 38
EC - Ecuador 37
RO - Romania 33
IL - Israele 32
CL - Cile 30
MY - Malesia 30
ZA - Sudafrica 28
EU - Europa 26
MA - Marocco 26
SA - Arabia Saudita 26
PH - Filippine 24
PK - Pakistan 24
EG - Egitto 23
JO - Giordania 22
TH - Thailandia 21
CZ - Repubblica Ceca 20
AE - Emirati Arabi Uniti 19
NZ - Nuova Zelanda 18
VE - Venezuela 18
HR - Croazia 16
LT - Lituania 16
PE - Perù 16
UZ - Uzbekistan 16
HU - Ungheria 15
KE - Kenya 15
UY - Uruguay 14
CR - Costa Rica 13
SI - Slovenia 13
TN - Tunisia 12
PY - Paraguay 11
KW - Kuwait 10
NP - Nepal 10
AL - Albania 9
JM - Giamaica 9
LB - Libano 9
AZ - Azerbaigian 8
KZ - Kazakistan 8
DO - Repubblica Dominicana 7
EE - Estonia 7
ET - Etiopia 7
LV - Lettonia 6
SC - Seychelles 6
TT - Trinidad e Tobago 6
BB - Barbados 5
HN - Honduras 5
SK - Slovacchia (Repubblica Slovacca) 5
A2 - ???statistics.table.value.countryCode.A2??? 4
BA - Bosnia-Erzegovina 4
BG - Bulgaria 4
DZ - Algeria 4
LU - Lussemburgo 4
MK - Macedonia 4
PA - Panama 4
BY - Bielorussia 3
KG - Kirghizistan 3
NG - Nigeria 3
BN - Brunei Darussalam 2
CY - Cipro 2
GT - Guatemala 2
LA - Repubblica Popolare Democratica del Laos 2
LK - Sri Lanka 2
Totale 26.911
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Città #
Singapore 1.407
Southend 1.094
Ashburn 910
Hong Kong 629
Milan 580
Fairfield 518
San Jose 510
Beijing 468
Council Bluffs 379
Chandler 359
Dublin 352
Princeton 307
Wilmington 304
Woodbridge 299
Seattle 285
Los Angeles 271
Hefei 248
Dallas 247
Houston 235
Santa Clara 217
Boardman 195
New York 194
Cambridge 189
Ho Chi Minh City 189
Lauterbourg 183
Redwood City 180
Ann Arbor 179
Guangzhou 168
Bengaluru 167
Dearborn 166
Buffalo 154
Hanoi 144
Moscow 141
Rome 137
Nanjing 129
Jakarta 128
Des Moines 113
Frankfurt am Main 107
Helsinki 101
Shanghai 82
Tokyo 78
São Paulo 75
Phoenix 73
Tianjin 67
Seoul 65
Madrid 64
Chicago 62
Hangzhou 60
London 60
Cangzhou 59
Columbus 57
Toronto 57
Shenzhen 54
Atlanta 53
Naples 51
Oslo 51
Ottawa 51
Abidjan 50
Istanbul 50
Central District 49
Nuremberg 48
Jinan 47
Munich 47
Edinburgh 46
Shenyang 46
Vienna 46
Sydney 45
Changsha 42
The Dalles 41
Da Nang 39
Washington 39
Berlin 36
Bologna 35
Silver Spring 35
Chengdu 34
Norwalk 34
Melbourne 33
Redmond 33
Rio de Janeiro 33
Dong Ket 31
Athens 30
Brussels 30
Denver 30
Belo Horizonte 29
Cleveland 29
Nanchang 28
Buenos Aires 27
Taipei 27
Turin 27
Bari 26
Boston 26
Mountain View 26
San Diego 26
Paris 25
Florence 24
Philadelphia 24
Zhengzhou 24
Amsterdam 23
Fuzhou 23
Montreal 23
Totale 15.168
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Nome #
The phenotype of SCN8A developmental and epileptic encephalopathy 1.350
Cryptogenic Epileptic Syndromes Related to SCN1A Twelve Novel Mutations Identified 585
MRI substrates of sustained attention system and cognitive impairment in pediatric MS patients 451
Ictal EEG patterns in epilepsy with centro-temporal spikes 421
Posterior brain damage and cognitive impairment in pediatric multiple sclerosis 381
3D facial morphometry in Italian patients affected by Aicardi syndrome 356
Post-operative benefits of animal-assisted therapy in pediatric surgery : A randomised study 332
Diagnostic boundaries of autism disorder vs pervasive developmental disorder nos comparative observational study and literature review 329
The face of Glut1-DS patients : A 3D craniofacial morphometric analysis 322
Optimal clinical management of children receiving dietary therapies for epilepsy : Updated recommendations of the International Ketogenic Diet Study Group 321
Long-Term Effects of a Classic Ketogenic Diet on Ghrelin and Leptin Concentration : a 12-Month Prospective Study in a Cohort of Italian Children and Adults with GLUT1-Deficiency Syndrome and Drug Resistant Epilepsy 310
Evaluation of nutritional status in children with refractory epilepsy 286
Treatment of electrical status epilepticus in sleep : A pooled analysis of 575 cases 281
Newborn screening for X-linked adrenoleukodystrophy in Italy: Diagnostic algorithm and disease monitoring 278
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations 276
Stroke and Stroke-Like Episodes: Recurrent Manifestations in GLUT1 Deficiency Syndrome 268
Germ-line mutation of the NRAS gene may be responsible for the development of juvenile myelomonocytic leukaemia 253
CNS involvement in a cohort of pediatric patients affected with mitochondrial disorders caused by heterogeneous biochemical and genetic defects 245
GLUT1 deficiency syndrome 2013 : current state of the art 232
The effect of chronic neuroglycopenia on resting state networks in GLUT1 syndrome across the lifespan 231
Food and Food Products on the Italian Market for Ketogenic Dietary Treatment of Neurological Diseases 224
Mapping the Effect of Interictal Epileptic Activity Density During Wakefulness on Brain Functioning in Focal Childhood Epilepsies With Centrotemporal Spikes 223
Impact of the Ketogenic Diet on Linear Growth in Children: A Single-Center Retrospective Analysis of 34 Cases 215
Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations : Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy 213
Glut1 Deficiency Syndrome (Glut1DS ) : State of the art in 2020 and recommendations of the international Glut1DS study group 213
Neurological Involvement in Multisystem Inflammatory Syndrome in Children: Clinical, Electroencephalographic and Magnetic Resonance Imaging Peculiarities and Therapeutic Implications. An Italian Single-Center Experience 209
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment 209
Biochemical phenotyping unravels novel metabolic abnormalities and potential biomarkers associated with treatment of GLUT1 deficiency with ketogenic diet 208
Acute encephalitis in pediatric multisystem inflammatory syndrome associated with COVID-19 208
Quality of Life in Chronic Ketogenic Diet Treatment : the GLUT1DS Population Perspective 203
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implications 199
Aspetti clinici e molecolari in un paziente pediatrico affetto da Sindrome di Leigh associata alla mutazione mitocondriale m.14459G>A 199
Glucose transporter 1 deficiency syndrome: nutritional and growth pattern phenotypes at diagnosis 199
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation :aA case report 198
Glut1 deficiency syndrome throughout life: clinical phenotypes, intelligence, life achievements and quality of life in familial cases 194
Measuring the Outcomes of Maternal COVID-19-related Prenatal Exposure (MOM-COPE) : study protocol for a multicentric longitudinal project 193
Overall cognitive profiles in patients with GLUT1 Deficiency Syndrome 187
Corticosteroids versus clobazam in epileptic encephalopathy with ESES: a European multicentre randomised controlled clinical trial (RESCUE ESES*) 186
Long−term health outcome and quality of life in children with multisystem inflammatory syndrome: findings from multidisciplinary follow−up at an Italian tertiary−care paediatric hospital 185
Long-term follow-up of nutritional status in children with GLUT1 Deficiency Syndrome treated with classic ketogenic diet: a 5-year prospective study 185
Transition for patients with epilepsy due to metabolic and mitochondrial disorders 185
MeCP2 investigation in a wide cohort of italian Rett patients and array methylation assay in six cases sharing the 1164_1027del44 MeCP2 mutation 182
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification 181
Case Report: Novel Compound Heterozygous RNASEH2B Mutations Cause Aicardi–Goutières Syndrome 181
Brain correlates of spike and wave discharges in GLUT1 deficiency syndrome 180
Clinical and genetical heterogeneity in a cohort of pediatric patients affected with mitochondrial disorders 177
Three-dimensional craniofacial features of Glut1 deficiency syndrome patients 177
Eating disorder risks and psychopathological distress in Italian high school adolescents 173
19q13.11 cryptic deletion : description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias 173
Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study 171
The perceived burden of epilepsy: Impact on the quality of life of children and adolescents and their families 169
Galloway-Mowat syndrome : an early-onset progressive encephalopathy with intractable epilepsy associated to renal impairment : two novel cases and review of literature 168
A novel de novo HCN2 loss‐of‐function variant causing developmental and epileptic encephalopathy treated with a ketogenic diet 167
Basal ganglia dysmorphism in patients with Aicardi syndrome 164
Effects of adjunctive eslicarbazepine acetate on neurocognitive functioning in children with refractory focal-onset seizures 163
Successful use of perampanel in GABRA1-related myoclonic epilepsy with photosensitivity 162
Impact of COVID-19 lockdown in children with neurological disorders in Italy 159
Visual function in infants with west syndrome: correlation with EEG patterns 158
Molecular Genetics of GLUT1DS Italian Pediatric Cohort: 10 Novel Disease-Related Variants and Structural Analysis 157
Nutritional and Pharmacological Management of Childhood Epilepsy: Ketogenic Diets and Common AEDs 154
THE ELECTROCLINICAL SEIZURE PATTERN OF BENIGN EPILEPSY WITH CENTROTEMPORAL SPIKES IN 30 PATIENTS 153
Diagnostic Yield and Cost-Effectiveness of "Dynamic" Exome Analysis in Epilepsy with Neurodevelopmental Disorders: A Tertiary-Center Experience in Northern Italy 153
Facial evaluation in holoprosencephaly 152
The costs of childhood epilepsy in Italy: comparative findings from three health care settings 149
The expanding knowledge of epilepsy in leukodystrophies 148
The use of alglucosidase alfa as a treatment in two patients with Lafora Disease 145
Use of ketogenic diet in patients with SCN8A-related epilepsy: report in two clinical cases 145
Short-term effects of ketogenic diet on anthropometric parameters, body fat distribution, and inflammatory cytokine production in GLUT1 deficiency syndrome 145
The influence of wakefulness fluctuations on brain networks involved in centrotemporal spike occurrence 144
Effects of the ketogenic diet on nutritional status, resting energy expenditure, and substrate oxidation in patients with medically refractory epilepsy: a 6-month prospective observational study 143
Intravenous methylprednisolone pulse therapy for children with epileptic encephalopathy 142
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 families 142
Epilessia mioclonica e coinvolgimento del secondo motoneurone ad esordio in età infantile: un caso clinico 141
Distribution of progressive myoclonus epilepsies in Italy; positively diagnosed and unclassified patients 140
Remitting Tics and Narcolepsy Overlap Associated with Streptococcal Infection : a Case Report 138
Functional correlates of clinical phenotype and severity in recurrent SCN2A variants 137
Rufinamide in children and adults with Lennox-Gastaut syndrome : first Italian multicenter experience 136
Ruxolitinib in Aicardi-Goutières syndrome 136
Families' Perception of Classic Ketogenic Diet Management in Acute Medical Conditions: A Web-Based Survey 133
Italian cohort of Lafora disease : clinical features, disease evolution, and genotype-phenotype correlations 133
GLUT1-DS Italian registry: past, present, and future: a useful tool for rare disorders 133
Connections Between Febrile Infection-Related Epilepsy Syndrome and Autoimmune Encephalitis. A Case Report of a Child With New Anti-neuronal Antibodies 130
Pathways to quality of life in adolescents with genetic generalized epilepsy: The role of seizure features and affective symptoms 130
Topiramate efficacy in an infant with partial seizures refractory to conventional antiepileptic drugs 129
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation 128
Effectiveness of a commercially available blue lens in photosensitive epileptic patients: The results of a large multicenter Italian study 127
Terapia con everolimus in un paziente con Sindrome Polidramnios-Megaloencefalia-Epilessia Sintomatica (PMSE) con epilessia farmacoresistente 126
Efficacy of the Ketogenic Diet as Targeted Therapy in a Cohort of Patients with GLUT1-DS 126
Crisi a semeiologia minima nel secondo mese di vita: quali ipotesi diagnostiche 125
The ketogenic diet for Dravet syndrome and other epileptic encephalopathies : an Italian consensus 125
Menkes disease complicated by concurrent ACY1 deficiency: A case report 122
Acquired epileptic frontal syndrome as long-term outcome in two children with CSWS 122
Re-emergence of SSPE : Consequence of the decline of adherence to vaccination programmes? 122
EEG at onset and MRI predict long-term clinical outcome in Aicardi syndrome 121
Suppressive efficacy by a commercially available blue lens on PPR in 610 photosensitive epilepsy patients 120
Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional Study 119
Thyroid dysfunction in children and adolescents affected by undernourished and overnourished eating disorders 119
Acute chorea in a child receiving second dose of human papilloma virus vaccine 117
FDXR-associated disease: a challenging differential diagnosis with inflammatory peripheral neuropathy 116
KetoSTrENgTH (KETOgenic diet aS TheRapy for mEtabolic and NeuroloGical condiTions in cHildren): a prospective observational multicenter study 115
Totale 20.286
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Categoria #
all - tutte 83.339
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 83.339
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021236 0 0 0 0 0 0 0 0 0 0 0 236
2021/20221.898 159 123 129 103 117 209 124 118 158 149 118 391
2022/20232.155 238 133 163 196 180 445 65 146 255 82 150 102
2023/20241.823 84 134 94 128 377 229 122 108 44 94 197 212
2024/20254.551 134 504 156 397 338 264 259 456 264 473 437 869
2025/202610.861 941 732 1.035 944 884 634 1.104 687 1.199 786 1.202 713
Totale 28.167