IRIS
VEGGIOTTI, PIERANGELO
 Distribuzione geografica
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Continente #
NA - Nord America 6.889
AS - Asia 5.194
EU - Europa 4.106
SA - Sud America 553
AF - Africa 175
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 9
Totale 16.946
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Nazione #
US - Stati Uniti d'America 6.736
CN - Cina 2.594
SG - Singapore 1.198
IE - Irlanda 891
IT - Italia 556
UA - Ucraina 548
HK - Hong Kong 531
DE - Germania 465
FI - Finlandia 444
RU - Federazione Russa 399
VN - Vietnam 375
BR - Brasile 373
FR - Francia 266
GB - Regno Unito 185
SE - Svezia 165
IN - India 105
ZA - Sudafrica 93
CA - Canada 74
AR - Argentina 68
BD - Bangladesh 68
MX - Messico 52
JP - Giappone 48
IQ - Iraq 41
PK - Pakistan 39
NL - Olanda 32
PL - Polonia 30
CO - Colombia 26
BE - Belgio 24
AT - Austria 23
TR - Turchia 23
PH - Filippine 21
VE - Venezuela 21
EC - Ecuador 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
LT - Lituania 10
EU - Europa 9
IR - Iran 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
CH - Svizzera 5
IL - Israele 5
KR - Corea 5
LB - Libano 5
NG - Nigeria 5
PA - Panama 5
CR - Costa Rica 4
DK - Danimarca 4
DO - Repubblica Dominicana 4
JM - Giamaica 4
KG - Kirghizistan 4
OM - Oman 4
CI - Costa d'Avorio 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
SK - Slovacchia (Repubblica Slovacca) 2
TW - Taiwan 2
AM - Armenia 1
BG - Bulgaria 1
BY - Bielorussia 1
CD - Congo 1
Totale 16.925
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Città #
Dublin 890
Chandler 883
San Jose 834
Jacksonville 673
Singapore 608
Ashburn 576
Nanjing 550
Hong Kong 526
Beijing 443
Dallas 417
Boardman 293
Nanchang 237
Princeton 185
Lawrence 179
Medford 174
Lauterbourg 167
Hebei 162
Wilmington 158
Changsha 155
Shenyang 150
Los Angeles 149
Ho Chi Minh City 138
Jiaxing 121
Helsinki 107
New York 105
Munich 89
Tianjin 89
Ann Arbor 88
Milan 87
Council Bluffs 83
Buffalo 81
Hangzhou 80
Johannesburg 76
Hanoi 75
Shanghai 72
Moscow 65
Redondo Beach 65
Pavia 46
Orem 44
Rome 43
Tokyo 43
São Paulo 41
Woodbridge 39
Verona 38
Santa Clara 35
Turku 33
Falkenstein 30
Houston 30
Seattle 30
Frankfurt am Main 29
Da Nang 25
Norwalk 24
Brussels 23
Warsaw 23
Atlanta 22
The Dalles 22
Chennai 21
Denver 21
Palermo 20
Tashkent 20
Mexico City 19
Toronto 19
Washington 19
Chicago 18
Kunming 18
Montreal 18
Stockholm 18
Zhengzhou 18
Brooklyn 17
Fairfield 17
Haiphong 16
London 16
Baghdad 15
Jinan 15
Nuremberg 15
Amsterdam 14
Boston 14
Florence 14
Guangzhou 14
San Francisco 14
Manchester 13
Phoenix 13
Rio de Janeiro 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
Columbus 9
Istanbul 9
Nairobi 9
Quito 9
Redwood City 9
Totale 11.082
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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* 280
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 190
Caratteristiche EEG e loro evoluzione nella lissencefalia classica 163
19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias. 157
La dieta chetogenica nel trattamento dell' epilessia farmaco-resistente. Studio pilota di 10 pazienti 154
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients 141
Acute chorea in a child receiving second dose of human papilloma virus vaccine 137
Therapy of encephalopathy with status epilepticus during sleep (ESES/CSWS syndrome): an update 135
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 132
Evaluation of food intake in disabled children 131
Atypical Manifestations in Glut1 Deficiency Syndrome 131
A pilot study of ketogenic diet in patients with Lafora body disease. 128
Drug-resistant epilepsy treated with ketogenic diet 128
A pilot study of a ketogenic diet in patients with Lafora body disease 125
ANDAMENTO DELL’INDICE GLUCO-CHETONICO IN CORSO DI TRATTAMENTO DIEPILESSIA REFRATTARIA CON DIETA CHETOGENICA 125
Evaluation of food intake and nutritional status in children with refractory status epilepticus 122
The epileptology of Aicardi-Goutières syndrome: electro-clinical-radiological findings 122
Paroxysmal tonic eye deviation: an atypical presentation of hypothalamic hamartoma 119
Post-operative benefits of animal-assisted therapy in pediatric surgery: a randomised study. 114
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 113
Quality of life in chronic ketogenic diet treatment: she GLUT1DS population perspective 113
Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case. 111
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 110
Neurofunctional correlates of vulnerability to psychosis: a systematic review and meta-analysis 109
Ketogenic Diet in Lafora Disease: A Pilot Study 109
Auditory attention at the onset of West syndrome: correlation with EEG patternsand visual function. 108
Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and geneticheterogeneity. 108
Ataxia-without-telangiectasia in two sisters with rearrangements of chromosomes 7 and 14. 108
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 107
Impact of the ketogenic diet on linear growth in children: A single-center retrospective analysis of 34 cases 107
Acquired epileptic frontal syndrome as long-term outcome in two children withCSWS. 106
Intravenous methylprednisolone pulse therapy for children with epileptic encephalopathy 104
Overall cognitive profiles in patients with GLUT1 Deficiency Syndrome 104
Long-term cognitive and behavioural follow-up in three patients with eyeclosure-triggered paroxysmal activity 104
Measuring the Outcomes of Maternal COVID-19-related Prenatal Exposure (MOM-COPE): Study protocol for a multicentric longitudinal project 104
Long-term cognitive and behavioural follow-up in three patients with eye closure-triggered paroxysmal activity. 103
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 103
Dietary Treatments and New Therapeutic Perspective in GLUT1 Deficiency Syndrome 102
Long-term evolution of neuropsychological competences in encephalopathy with status epilepticus during sleep: a variable prognosis. 101
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 101
Evaluation of nutritional status in children with refractory epilepsy. 100
Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs 100
A correlated fluctuation of language and EEG abnormalities in a case of the Landau-Kleffner syndrome. 99
Regional hippocampal involvement and cognitive impairment in pediatric multiple sclerosis 99
Novel insight into GLUT1 Deficiency Syndrome: screening for emotional and behavioral problems in youths following ketogenic diet 99
Prevalence of anti-cardiolipin, anti-beta2 glycoprotein I, and anti-prothrombin antibodies in young patients with epilepsy. 98
Abnormal cerebellar functional MRI connectivity in patients with paediatric multiple sclerosis 98
Sporadic and familial glut1ds Italian patients: A wide clinical variability 98
Ketogenic Diet in Lafora Disease: A Pilot Study 98
Abnormal visual habituation in pediatric photosensitive epilepsy 97
Extrastriate visual cortex in idiopathic occipital epilepsies: The contribution of retinotopic areas to spike generation 97
Ketogenic Diet: Electrophysiological Effects on the Normal Human Cortex. 96
The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: an Italian consensus 96
Ketogenic diet in Lafora disease: a long term follow-up pilot study 96
Ketogenic diets in the treatment of epilepsy: preliminary data 96
La gestione del bambino con convulsioni febbrili: linee guida sulle convulsioni febbrili. 95
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 95
Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations. 94
Nutritional and pharmacological management of childhood epilepsy: ketogenic diets and common AEDs 94
Atypical onset of multiple sclerosis in an adolescent with monosymptomatic chronic tension-type headache. 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
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 94
Benign partial epilepsies of adolescence: a report of 37 new cases 94
Epilepsy surgery in tuberous sclerosis complex: early predictive elements and outcome 92
Ketogenic diet in farmacoresistant epilecties 91
CHD2 variants are a risk factor for photosensitivity in epilepsy 91
Reversibility of vigabratin-induced visual-field defect. 90
Long-term neuropsychological follow-up and nosological considerations in five patients with continuous spikes and waves during slow sleep 90
Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients. 90
Spontaneous MRI improvement and absence of cerebral calcification in Aicardi-Goutières syndrome: Diagnostic and disease-monitoring implications 90
Rhythmic movement disorder and cyclic alternating pattern during sleep: a video-polysomnographic study in a 9-year-old boy 90
Brain correlates of spike and wave discharges in GLUT1 deficiency syndrome 89
Sex-dependent association between variability in infants’ OXTR methylation at birth and negative affectivity at 3 months 88
Encopresi 88
The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: An Italian consensus 88
A real‐life pilot study of the clinical application of pharmacogenomics testing on saliva in epilepsy 87
Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene. 87
Germ-line mutation of the NRAS gene may be responsible for the development of juvenile myelomonocytic leukaemia 87
Evaluation of nutritional status in children with refractory epilepsy 86
Chorea mollis: long-term follow-up of an infantile case. 86
Glucose transporter 1 deficiency syndrome: nutritional and growth pattern phenotypes at diagnosis 86
The phenotype of SCN8A developmental and epileptic encephalopathy 86
Optimal clinical management of children receiving the ketogenic diet: recommendations of the International Ketogenic Diet Study Group. 85
Cognitive impairment in paediatric multiple sclerosis patients is not related to cortical lesions 85
Dravet phenotype in a subject with a der(4)t(4;8)(p16.3;p23.3) without the involvement of the LETM1 gene 84
Hydrocephalus and porencephaly 84
Short-term effects of ketogenic diet on anthropometric parameters, body fat distribution, and inflammatory cytokine production in GLUT1 deficiency syndrome 84
Lamotrigine in infantile spasms. 83
Epilepsia partialis continua in a case of MELAS: clinical and neurophysiological study. 83
Topiramate as add-on drug in children, adolescents and young adults with Lennox-Gastaut syndrome: an Italian multicentric study 82
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsyof infancy (SMEI) patients with SCN1A mutations. 82
Motor impairment on awakening in a patient with an EEG pattern of "unilateral,continuous spikes and waves during slow sleep". 82
Clinical and genetic findings in 26 Italian patients with Lafora disease. 81
Eye-closure-triggered paroxysmal activity and cognitive impairment: a case report 81
Visual function in infants with west syndrome: correlation with EEG patterns. 80
Clinical, cytogenetic and immunological aspects in 4 cases resembling ataxia telangiectasia. 80
Diagnostic boundaries of autism disorder vs pervasive developmental disorder nos comparative observational study and literature review. 80
Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations 80
Totale 10.392
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Categoria #
all - tutte 70.456
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 70.456
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202123 0 0 0 0 0 0 0 0 0 0 0 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
2025/20265.916 480 389 620 598 684 267 1.238 257 527 440 296 120
Totale 17.084