VEGGIOTTI, PIERANGELO
 Distribuzione geografica
Continente #
NA - Nord America 6.477
AS - Asia 5.115
EU - Europa 4.078
SA - Sud America 552
AF - Africa 175
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 9
Totale 16.426
Nazione #
US - Stati Uniti d'America 6.338
CN - Cina 2.574
SG - Singapore 1.168
IE - Irlanda 891
UA - Ucraina 548
IT - Italia 532
HK - Hong Kong 530
DE - Germania 465
FI - Finlandia 444
RU - Federazione Russa 399
BR - Brasile 373
VN - Vietnam 373
FR - Francia 266
GB - Regno Unito 185
SE - Svezia 165
IN - India 105
ZA - Sudafrica 93
AR - Argentina 68
CA - Canada 64
MX - Messico 50
BD - Bangladesh 47
JP - Giappone 45
IQ - Iraq 41
PK - Pakistan 39
NL - Olanda 31
PL - Polonia 30
CO - Colombia 25
BE - Belgio 24
AT - Austria 23
TR - Turchia 23
VE - Venezuela 21
EC - Ecuador 20
PH - Filippine 20
UZ - Uzbekistan 20
ES - Italia 19
MA - Marocco 19
ID - Indonesia 18
JO - Giordania 14
CL - Cile 13
KE - Kenya 13
NZ - Nuova Zelanda 12
PY - Paraguay 11
SA - Arabia Saudita 11
TN - Tunisia 11
EU - Europa 9
IR - Iran 9
LT - Lituania 9
RO - Romania 9
BO - Bolivia 8
MY - Malesia 8
AE - Emirati Arabi Uniti 7
NP - Nepal 7
PE - Perù 7
AU - Australia 6
EG - Egitto 6
MU - Mauritius 6
PS - Palestinian Territory 6
UY - Uruguay 6
AZ - Azerbaigian 5
IL - Israele 5
LB - Libano 5
NG - Nigeria 5
PA - Panama 5
CH - Svizzera 4
DK - Danimarca 4
DO - Repubblica Dominicana 4
JM - Giamaica 4
KG - Kirghizistan 4
KR - Corea 4
OM - Oman 4
CI - Costa d'Avorio 3
CR - Costa Rica 3
CY - Cipro 3
ET - Etiopia 3
GR - Grecia 3
HN - Honduras 3
HU - Ungheria 3
LV - Lettonia 3
LY - Libia 3
NO - Norvegia 3
PT - Portogallo 3
RS - Serbia 3
SN - Senegal 3
TT - Trinidad e Tobago 3
AL - Albania 2
DZ - Algeria 2
EE - Estonia 2
GA - Gabon 2
GE - Georgia 2
KH - Cambogia 2
KZ - Kazakistan 2
LK - Sri Lanka 2
NI - Nicaragua 2
QA - Qatar 2
TW - Taiwan 2
AM - Armenia 1
BG - Bulgaria 1
BY - Bielorussia 1
CD - Congo 1
CG - Congo 1
Totale 16.406
Città #
Dublin 890
Chandler 883
Jacksonville 673
San Jose 640
Singapore 603
Nanjing 550
Ashburn 532
Hong Kong 525
Beijing 438
Dallas 411
Boardman 292
Nanchang 237
Princeton 185
Lawrence 179
Medford 174
Lauterbourg 167
Hebei 162
Wilmington 158
Changsha 155
Shenyang 150
Los Angeles 143
Ho Chi Minh City 137
Jiaxing 121
Helsinki 107
New York 92
Munich 89
Tianjin 89
Ann Arbor 88
Milan 87
Buffalo 79
Hangzhou 79
Johannesburg 76
Hanoi 74
Shanghai 72
Moscow 65
Redondo Beach 65
Pavia 46
Rome 42
São Paulo 41
Tokyo 41
Orem 40
Woodbridge 39
Verona 38
Turku 33
Falkenstein 30
Seattle 30
Frankfurt am Main 29
Houston 29
Santa Clara 29
Da Nang 25
Norwalk 24
Brussels 23
Warsaw 23
The Dalles 22
Atlanta 21
Chennai 21
Denver 20
Palermo 20
Tashkent 20
Kunming 18
Stockholm 18
Washington 18
Zhengzhou 18
Brooklyn 17
Fairfield 17
Mexico City 17
Toronto 17
Chicago 16
Haiphong 16
London 16
Montreal 16
Baghdad 15
Jinan 15
Nuremberg 15
Amsterdam 14
Florence 14
Guangzhou 14
Rio de Janeiro 13
Boston 12
Council Bluffs 12
Dearborn 12
Des Moines 12
Lahore 12
Manchester 12
Medellín 12
Ningbo 12
Poplar 12
Vienna 12
Amman 11
Auburn Hills 11
Cascina 11
Mumbai 11
Phoenix 10
San Francisco 10
Columbus 9
Istanbul 9
Nairobi 9
Quito 9
Redwood City 9
Rotorua 9
Totale 10.695
Nome #
La sincope in età pediatrica. Linee Guida a cura di SIP, SIMEUP, SICP, FMSI, AIAC SIC SPORT, FIMP, GSCP, GSMESPO, SINPIA, SINC* 278
Caratteristiche EEG e loro evoluzione nella lissencefalia classica 159
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 158
19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias. 153
La dieta chetogenica nel trattamento dell' epilessia farmaco-resistente. Studio pilota di 10 pazienti 152
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients 140
Therapy of encephalopathy with status epilepticus during sleep (ESES/CSWS syndrome): an update 134
Acute chorea in a child receiving second dose of human papilloma virus vaccine 134
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 131
Evaluation of food intake in disabled children 130
Atypical Manifestations in Glut1 Deficiency Syndrome 130
A pilot study of ketogenic diet in patients with Lafora body disease. 127
Drug-resistant epilepsy treated with ketogenic diet 126
A pilot study of a ketogenic diet in patients with Lafora body disease 122
ANDAMENTO DELL’INDICE GLUCO-CHETONICO IN CORSO DI TRATTAMENTO DIEPILESSIA REFRATTARIA CON DIETA CHETOGENICA 122
Evaluation of food intake and nutritional status in children with refractory status epilepticus 120
The epileptology of Aicardi-Goutières syndrome: electro-clinical-radiological findings 120
Paroxysmal tonic eye deviation: an atypical presentation of hypothalamic hamartoma 118
Post-operative benefits of animal-assisted therapy in pediatric surgery: a randomised study. 113
Quality of life in chronic ketogenic diet treatment: she GLUT1DS population perspective 111
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 110
Long-term effects of a ketogenic diet on body composition and bone mineralization in GLUT-1 deficiency syndrome: A case series 110
Uncovering the neural correlates of the ketogenic diet: the contribution of functional neuroimaging 109
Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case. 108
Auditory attention at the onset of West syndrome: correlation with EEG patternsand visual function. 108
Ataxia-without-telangiectasia in two sisters with rearrangements of chromosomes 7 and 14. 108
Ketogenic Diet in Lafora Disease: A Pilot Study 108
Acquired epileptic frontal syndrome as long-term outcome in two children withCSWS. 106
Neurofunctional correlates of vulnerability to psychosis: a systematic review and meta-analysis 106
Impact of the ketogenic diet on linear growth in children: A single-center retrospective analysis of 34 cases 105
Intravenous methylprednisolone pulse therapy for children with epileptic encephalopathy 103
Long-term cognitive and behavioural follow-up in three patients with eyeclosure-triggered paroxysmal activity 103
Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and geneticheterogeneity. 102
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 102
Long-term evolution of neuropsychological competences in encephalopathy with status epilepticus during sleep: a variable prognosis. 101
Overall cognitive profiles in patients with GLUT1 Deficiency Syndrome 101
Measuring the Outcomes of Maternal COVID-19-related Prenatal Exposure (MOM-COPE): Study protocol for a multicentric longitudinal project 101
Dietary Treatments and New Therapeutic Perspective in GLUT1 Deficiency Syndrome 101
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 100
Evaluation of nutritional status in children with refractory epilepsy. 99
A correlated fluctuation of language and EEG abnormalities in a case of the Landau-Kleffner syndrome. 98
Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs 98
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 98
Prevalence of anti-cardiolipin, anti-beta2 glycoprotein I, and anti-prothrombin antibodies in young patients with epilepsy. 97
Ketogenic Diet in Lafora Disease: A Pilot Study 97
Abnormal visual habituation in pediatric photosensitive epilepsy 96
Extrastriate visual cortex in idiopathic occipital epilepsies: The contribution of retinotopic areas to spike generation 96
Ketogenic diets in the treatment of epilepsy: preliminary data 95
Regional hippocampal involvement and cognitive impairment in pediatric multiple sclerosis 95
Abnormal cerebellar functional MRI connectivity in patients with paediatric multiple sclerosis 95
Ketogenic Diet: Electrophysiological Effects on the Normal Human Cortex. 94
The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: an Italian consensus 94
Nutritional and pharmacological management of childhood epilepsy: ketogenic diets and common AEDs 94
Sporadic and familial glut1ds Italian patients: A wide clinical variability 94
: Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity 94
The ketogenic diet in children, adolescents and young adults with refractory epilepsy: an Italian multicentric experience. 94
Novel insight into GLUT1 Deficiency Syndrome: screening for emotional and behavioral problems in youths following ketogenic diet 94
La gestione del bambino con convulsioni febbrili: linee guida sulle convulsioni febbrili. 93
Ketogenic diet in Lafora disease: a long term follow-up pilot study 93
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 93
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 93
Atypical onset of multiple sclerosis in an adolescent with monosymptomatic chronic tension-type headache. 92
Benign partial epilepsies of adolescence: a report of 37 new cases 92
Ketogenic diet in farmacoresistant epilecties 91
Epilepsy surgery in tuberous sclerosis complex: early predictive elements and outcome 91
CHD2 variants are a risk factor for photosensitivity in epilepsy 90
Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations. 88
Long-term neuropsychological follow-up and nosological considerations in five patients with continuous spikes and waves during slow sleep 88
Spontaneous MRI improvement and absence of cerebral calcification in Aicardi-Goutières syndrome: Diagnostic and disease-monitoring implications 88
Rhythmic movement disorder and cyclic alternating pattern during sleep: a video-polysomnographic study in a 9-year-old boy 88
Evaluation of nutritional status in children with refractory epilepsy 86
Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients. 86
Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene. 85
Reversibility of vigabratin-induced visual-field defect. 85
The phenotype of SCN8A developmental and epileptic encephalopathy 85
Sex-dependent association between variability in infants’ OXTR methylation at birth and negative affectivity at 3 months 84
Optimal clinical management of children receiving the ketogenic diet: recommendations of the International Ketogenic Diet Study Group. 84
The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: An Italian consensus 84
Chorea mollis: long-term follow-up of an infantile case. 84
Hydrocephalus and porencephaly 84
Encopresi 83
Germ-line mutation of the NRAS gene may be responsible for the development of juvenile myelomonocytic leukaemia 83
Long-term cognitive and behavioural follow-up in three patients with eye closure-triggered paroxysmal activity. 83
Dravet phenotype in a subject with a der(4)t(4;8)(p16.3;p23.3) without the involvement of the LETM1 gene 83
Cognitive impairment in paediatric multiple sclerosis patients is not related to cortical lesions 83
Brain correlates of spike and wave discharges in GLUT1 deficiency syndrome 83
A real‐life pilot study of the clinical application of pharmacogenomics testing on saliva in epilepsy 82
Glucose transporter 1 deficiency syndrome: nutritional and growth pattern phenotypes at diagnosis 82
Lamotrigine in infantile spasms. 81
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsyof infancy (SMEI) patients with SCN1A mutations. 80
Diagnostic boundaries of autism disorder vs pervasive developmental disorder nos comparative observational study and literature review. 80
Topiramate as add-on drug in children, adolescents and young adults with Lennox-Gastaut syndrome: an Italian multicentric study 79
Somatic and germline mosaicisms in severe myoclonic epilepsy of infancy. 79
Motor impairment on awakening in a patient with an EEG pattern of "unilateral,continuous spikes and waves during slow sleep". 79
Epidemiologia delle sindromi epilettiche nel primo anno di vita: analisi delle coorti di utenti di quattro centri specialistici italiani. 79
Eye-closure-triggered paroxysmal activity and cognitive impairment: a case report 79
Brain macro- and microscopic damage in patients with paediatric MS. 79
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations 79
Clinical, cytogenetic and immunological aspects in 4 cases resembling ataxia telangiectasia. 78
The ketogenic diet in children, adolescents and young adults with refractory epilepsy: an italian multicentric experience 78
Totale 10.131
Categoria #
all - tutte 65.200
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 65.200


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021287 0 0 0 0 0 0 0 0 0 143 121 23
2021/2022747 10 2 9 4 9 6 16 38 59 18 127 449
2022/20232.554 281 168 31 205 313 246 13 154 1.036 12 64 31
2023/2024877 89 155 29 100 68 193 27 87 5 17 24 83
2024/20252.466 66 205 149 81 69 114 118 176 554 54 276 604
2025/20265.396 480 389 620 598 684 267 1.238 257 527 336 0 0
Totale 16.564