IRIS
VEGGIOTTI, PIERANGELO
 Distribuzione geografica
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Continente #
NA - Nord America 7.263
AS - Asia 5.217
EU - Europa 4.126
SA - Sud America 563
AF - Africa 175
Continente sconosciuto - Info sul continente non disponibili 147
OC - Oceania 20
Totale 17.511
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Nazione #
US - Stati Uniti d'America 7.091
CN - Cina 2.597
SG - Singapore 1.207
IE - Irlanda 892
IT - Italia 570
UA - Ucraina 548
HK - Hong Kong 534
DE - Germania 465
FI - Finlandia 444
RU - Federazione Russa 399
VN - Vietnam 378
BR - Brasile 377
FR - Francia 266
GB - Regno Unito 187
SE - Svezia 165
IN - India 105
ZA - Sudafrica 93
CA - Canada 82
BD - Bangladesh 72
AR - Argentina 70
MX - Messico 52
JP - Giappone 48
IQ - Iraq 41
PK - Pakistan 39
NL - Olanda 33
PL - Polonia 30
CO - Colombia 28
BE - Belgio 24
AT - Austria 23
TR - Turchia 23
EC - Ecuador 21
PH - Filippine 21
VE - Venezuela 21
ES - Italia 20
UZ - Uzbekistan 20
MA - Marocco 19
ID - Indonesia 18
JO - Giordania 14
CL - Cile 13
KE - Kenya 13
NZ - Nuova Zelanda 12
PY - Paraguay 12
SA - Arabia Saudita 11
TN - Tunisia 11
LT - Lituania 10
RO - Romania 10
CR - Costa Rica 9
EU - Europa 9
IR - Iran 9
BO - Bolivia 8
MY - Malesia 8
AE - Emirati Arabi Uniti 7
JM - Giamaica 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
CH - Svizzera 5
HN - Honduras 5
IL - Israele 5
KR - Corea 5
LB - Libano 5
NG - Nigeria 5
PA - Panama 5
DK - Danimarca 4
DO - Repubblica Dominicana 4
KG - Kirghizistan 4
OM - Oman 4
CI - Costa d'Avorio 3
CY - Cipro 3
ET - Etiopia 3
GR - Grecia 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
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
TW - Taiwan 2
AM - Armenia 1
BG - Bulgaria 1
BM - Bermuda 1
Totale 17.351
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Città #
Dublin 890
Chandler 883
San Jose 851
Jacksonville 673
Singapore 612
Ashburn 596
Nanjing 550
Hong Kong 529
Beijing 443
Dallas 419
Boardman 293
Council Bluffs 272
Nanchang 237
Princeton 185
Lawrence 179
Medford 174
Lauterbourg 167
Hebei 162
Wilmington 158
Changsha 155
Los Angeles 153
Shenyang 150
Ho Chi Minh City 138
Jiaxing 121
Helsinki 107
New York 107
Milan 90
Munich 89
Tianjin 89
Ann Arbor 88
Buffalo 81
Hangzhou 80
Hanoi 77
Johannesburg 76
Shanghai 73
Moscow 65
Redondo Beach 65
Santa Clara 49
Pavia 46
Orem 44
Rome 44
Tokyo 43
São Paulo 41
Verona 39
Woodbridge 39
Houston 33
Turku 33
Falkenstein 30
Seattle 30
Frankfurt am Main 29
Da Nang 25
Norwalk 24
Atlanta 23
Brussels 23
The Dalles 23
Warsaw 23
Chennai 21
Denver 21
Washington 21
Palermo 20
Tashkent 20
Mexico City 19
Montreal 19
Toronto 19
Brooklyn 18
Chicago 18
Kunming 18
Stockholm 18
Zhengzhou 18
Columbus 17
Fairfield 17
San Francisco 17
Haiphong 16
London 16
Phoenix 16
Baghdad 15
Jinan 15
Nuremberg 15
Amsterdam 14
Boston 14
Florence 14
Guangzhou 14
Rio de Janeiro 14
Manchester 13
Dearborn 12
Des Moines 12
Lahore 12
Medellín 12
Ningbo 12
Poplar 12
Vienna 12
Amman 11
Auburn Hills 11
Cascina 11
Mumbai 11
Charlotte 10
Quito 10
Istanbul 9
Nairobi 9
Redwood City 9
Totale 11.370
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Nome #
La sincope in età pediatrica. Linee Guida a cura di SIP, SIMEUP, SICP, FMSI, AIAC SIC SPORT, FIMP, GSCP, GSMESPO, SINPIA, SINC* 282
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 192
Caratteristiche EEG e loro evoluzione nella lissencefalia classica 165
19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias. 159
La dieta chetogenica nel trattamento dell' epilessia farmaco-resistente. Studio pilota di 10 pazienti 157
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients 142
Therapy of encephalopathy with status epilepticus during sleep (ESES/CSWS syndrome): an update 138
Acute chorea in a child receiving second dose of human papilloma virus vaccine 138
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 134
Atypical Manifestations in Glut1 Deficiency Syndrome 133
Evaluation of food intake in disabled children 132
A pilot study of ketogenic diet in patients with Lafora body disease. 130
Drug-resistant epilepsy treated with ketogenic diet 129
Evaluation of food intake and nutritional status in children with refractory status epilepticus 127
A pilot study of a ketogenic diet in patients with Lafora body disease 127
ANDAMENTO DELL’INDICE GLUCO-CHETONICO IN CORSO DI TRATTAMENTO DIEPILESSIA REFRATTARIA CON DIETA CHETOGENICA 126
The epileptology of Aicardi-Goutières syndrome: electro-clinical-radiological findings 125
Paroxysmal tonic eye deviation: an atypical presentation of hypothalamic hamartoma 120
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 119
Post-operative benefits of animal-assisted therapy in pediatric surgery: a randomised study. 116
Quality of life in chronic ketogenic diet treatment: she GLUT1DS population perspective 114
Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case. 113
Long-term effects of a ketogenic diet on body composition and bone mineralization in GLUT-1 deficiency syndrome: A case series 113
Neurofunctional correlates of vulnerability to psychosis: a systematic review and meta-analysis 112
Impact of the ketogenic diet on linear growth in children: A single-center retrospective analysis of 34 cases 112
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 111
Uncovering the neural correlates of the ketogenic diet: the contribution of functional neuroimaging 111
Auditory attention at the onset of West syndrome: correlation with EEG patternsand visual function. 110
Ataxia-without-telangiectasia in two sisters with rearrangements of chromosomes 7 and 14. 110
Ketogenic Diet in Lafora Disease: A Pilot Study 110
Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and geneticheterogeneity. 109
Intravenous methylprednisolone pulse therapy for children with epileptic encephalopathy 109
Acquired epileptic frontal syndrome as long-term outcome in two children withCSWS. 108
Long-term cognitive and behavioural follow-up in three patients with eye closure-triggered paroxysmal activity. 107
Long-term cognitive and behavioural follow-up in three patients with eyeclosure-triggered paroxysmal activity 107
Measuring the Outcomes of Maternal COVID-19-related Prenatal Exposure (MOM-COPE): Study protocol for a multicentric longitudinal project 106
Overall cognitive profiles in patients with GLUT1 Deficiency Syndrome 105
Dietary Treatments and New Therapeutic Perspective in GLUT1 Deficiency Syndrome 105
Long-term evolution of neuropsychological competences in encephalopathy with status epilepticus during sleep: a variable prognosis. 104
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 104
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 102
Ketogenic Diet in Lafora Disease: A Pilot Study 102
Evaluation of nutritional status in children with refractory epilepsy. 101
A correlated fluctuation of language and EEG abnormalities in a case of the Landau-Kleffner syndrome. 101
Sporadic and familial glut1ds Italian patients: A wide clinical variability 101
Novel insight into GLUT1 Deficiency Syndrome: screening for emotional and behavioral problems in youths following ketogenic diet 101
Regional hippocampal involvement and cognitive impairment in pediatric multiple sclerosis 100
Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs 100
Prevalence of anti-cardiolipin, anti-beta2 glycoprotein I, and anti-prothrombin antibodies in young patients with epilepsy. 99
Abnormal cerebellar functional MRI connectivity in patients with paediatric multiple sclerosis 99
Extrastriate visual cortex in idiopathic occipital epilepsies: The contribution of retinotopic areas to spike generation 99
Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene. 98
Ketogenic Diet: Electrophysiological Effects on the Normal Human Cortex. 98
Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations. 98
Nutritional and pharmacological management of childhood epilepsy: ketogenic diets and common AEDs 98
Abnormal visual habituation in pediatric photosensitive epilepsy 98
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 98
Ketogenic diet in Lafora disease: a long term follow-up pilot study 97
Ketogenic diets in the treatment of epilepsy: preliminary data 97
La gestione del bambino con convulsioni febbrili: linee guida sulle convulsioni febbrili. 96
The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: an Italian consensus 96
Atypical onset of multiple sclerosis in an adolescent with monosymptomatic chronic tension-type headache. 96
: Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity 96
Ketogenic diet in farmacoresistant epilecties 95
The ketogenic diet in children, adolescents and young adults with refractory epilepsy: an Italian multicentric experience. 95
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 95
Benign partial epilepsies of adolescence: a report of 37 new cases 95
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 94
Epilepsy surgery in tuberous sclerosis complex: early predictive elements and outcome 93
Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients. 93
CHD2 variants are a risk factor for photosensitivity in epilepsy 93
Reversibility of vigabratin-induced visual-field defect. 92
Long-term neuropsychological follow-up and nosological considerations in five patients with continuous spikes and waves during slow sleep 91
Brain correlates of spike and wave discharges in GLUT1 deficiency syndrome 91
Spontaneous MRI improvement and absence of cerebral calcification in Aicardi-Goutières syndrome: Diagnostic and disease-monitoring implications 91
Rhythmic movement disorder and cyclic alternating pattern during sleep: a video-polysomnographic study in a 9-year-old boy 91
The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: An Italian consensus 90
Chorea mollis: long-term follow-up of an infantile case. 90
Sex-dependent association between variability in infants’ OXTR methylation at birth and negative affectivity at 3 months 89
Encopresi 89
Germ-line mutation of the NRAS gene may be responsible for the development of juvenile myelomonocytic leukaemia 89
A real‐life pilot study of the clinical application of pharmacogenomics testing on saliva in epilepsy 88
Evaluation of nutritional status in children with refractory epilepsy 88
Epilepsia partialis continua in a case of MELAS: clinical and neurophysiological study. 88
Glucose transporter 1 deficiency syndrome: nutritional and growth pattern phenotypes at diagnosis 88
The phenotype of SCN8A developmental and epileptic encephalopathy 88
Immunomodulatory treatment of early onset multiple sclerosis: Results of an Italian Co-operative Study 87
Dravet phenotype in a subject with a der(4)t(4;8)(p16.3;p23.3) without the involvement of the LETM1 gene 87
Cognitive impairment in paediatric multiple sclerosis patients is not related to cortical lesions 87
Optimal clinical management of children receiving the ketogenic diet: recommendations of the International Ketogenic Diet Study Group. 86
Eye-closure-triggered paroxysmal activity and cognitive impairment: a case report 86
Hydrocephalus and porencephaly 85
Topiramate as add-on drug in children, adolescents and young adults with Lennox-Gastaut syndrome: an Italian multicentric study 84
Motor impairment on awakening in a patient with an EEG pattern of "unilateral,continuous spikes and waves during slow sleep". 84
Lamotrigine in infantile spasms. 84
Short-term effects of ketogenic diet on anthropometric parameters, body fat distribution, and inflammatory cytokine production in GLUT1 deficiency syndrome 84
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsyof infancy (SMEI) patients with SCN1A mutations. 83
Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B6-Dependent Epilepsy 83
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification 83
Visual function in infants with west syndrome: correlation with EEG patterns. 82
Totale 10.623
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Categoria #
all - tutte 73.855
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 73.855
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022737 0 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
2025/20265.938 480 389 620 598 684 267 1.238 257 527 440 296 142
2026/2027405 125 280 0 0 0 0 0 0 0 0 0 0
Totale 17.511