IRIS
VEGGIOTTI, PIERANGELO
 Distribuzione geografica
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Continente #
NA - Nord America 5.512
AS - Asia 4.236
EU - Europa 3.768
SA - Sud America 417
AF - Africa 70
OC - Oceania 17
Continente sconosciuto - Info sul continente non disponibili 9
Totale 14.029
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Nazione #
US - Stati Uniti d'America 5.405
CN - Cina 2.488
SG - Singapore 921
IE - Irlanda 885
UA - Ucraina 543
IT - Italia 497
HK - Hong Kong 472
FI - Finlandia 439
DE - Germania 437
RU - Federazione Russa 395
BR - Brasile 321
SE - Svezia 164
GB - Regno Unito 161
VN - Vietnam 128
FR - Francia 92
CA - Canada 58
IN - India 50
AR - Argentina 43
MX - Messico 37
JP - Giappone 32
PL - Polonia 27
ZA - Sudafrica 27
BE - Belgio 23
NL - Olanda 23
AT - Austria 22
BD - Bangladesh 22
IQ - Iraq 17
PK - Pakistan 17
ES - Italia 15
CO - Colombia 13
EC - Ecuador 12
NZ - Nuova Zelanda 12
EU - Europa 9
IR - Iran 9
LT - Lituania 9
TR - Turchia 9
UZ - Uzbekistan 9
JO - Giordania 8
RO - Romania 8
PY - Paraguay 7
AE - Emirati Arabi Uniti 6
ID - Indonesia 6
MU - Mauritius 6
TN - Tunisia 6
VE - Venezuela 6
BO - Bolivia 5
KE - Kenya 5
MA - Marocco 5
AU - Australia 4
CH - Svizzera 4
KR - Corea 4
PE - Perù 4
PS - Palestinian Territory 4
CI - Costa d'Avorio 3
CL - Cile 3
DK - Danimarca 3
EG - Egitto 3
KG - Kirghizistan 3
MY - Malesia 3
NO - Norvegia 3
NP - Nepal 3
OM - Oman 3
SA - Arabia Saudita 3
SN - Senegal 3
TT - Trinidad e Tobago 3
UY - Uruguay 3
AZ - Azerbaigian 2
CR - Costa Rica 2
EE - Estonia 2
ET - Etiopia 2
GA - Gabon 2
GE - Georgia 2
GR - Grecia 2
HN - Honduras 2
LK - Sri Lanka 2
LY - Libia 2
NG - Nigeria 2
PH - Filippine 2
PT - Portogallo 2
RS - Serbia 2
TW - Taiwan 2
AL - Albania 1
BG - Bulgaria 1
BY - Bielorussia 1
CG - Congo 1
CZ - Repubblica Ceca 1
DO - Repubblica Dominicana 1
GT - Guatemala 1
HU - Ungheria 1
IL - Israele 1
JM - Giamaica 1
KH - Cambogia 1
KI - Kiribati 1
KZ - Kazakistan 1
LB - Libano 1
LU - Lussemburgo 1
LV - Lettonia 1
MK - Macedonia 1
ML - Mali 1
MM - Myanmar 1
Totale 14.019
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Città #
Dublin 884
Chandler 883
Jacksonville 673
Nanjing 550
Hong Kong 470
Beijing 423
Ashburn 417
Dallas 409
Singapore 399
Boardman 290
Nanchang 237
Princeton 185
Lawrence 179
Medford 174
Hebei 162
Wilmington 158
Changsha 155
Shenyang 150
Los Angeles 134
Jiaxing 121
Helsinki 102
Munich 89
Tianjin 89
Ann Arbor 88
New York 84
Milan 82
Hangzhou 79
Buffalo 76
Shanghai 71
Moscow 65
Redondo Beach 65
Ho Chi Minh City 48
Pavia 41
Rome 40
Woodbridge 39
Verona 38
São Paulo 35
Turku 33
Falkenstein 30
Seattle 30
Houston 29
Tokyo 29
Norwalk 24
Brussels 23
Warsaw 23
Hanoi 21
Johannesburg 21
Denver 20
The Dalles 20
Kunming 18
Santa Clara 18
Zhengzhou 18
Fairfield 17
Stockholm 17
Brooklyn 16
Orem 16
Chicago 15
Jinan 15
Toronto 15
Washington 15
Atlanta 14
Florence 14
Guangzhou 14
Montreal 14
Chennai 13
Mexico City 13
Palermo 13
Boston 12
Dearborn 12
London 12
Ningbo 12
Nuremberg 12
Rio de Janeiro 12
Auburn Hills 11
Cascina 11
Poplar 11
Vienna 11
Des Moines 10
San Francisco 10
Columbus 9
Mumbai 9
Phoenix 9
Redwood City 9
Rotorua 9
Tashkent 9
Amman 8
Charlotte 8
Lissone 8
Porto Alegre 8
Vancouver 8
Amsterdam 7
Bologna 7
Changchun 7
Da Nang 7
Frankfurt am Main 7
Fuzhou 7
Haiphong 7
Quito 7
San Jose 7
Secaucus 7
Totale 9.062
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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* 264
Caratteristiche EEG e loro evoluzione nella lissencefalia classica 146
La dieta chetogenica nel trattamento dell' epilessia farmaco-resistente. Studio pilota di 10 pazienti 141
19q13.11 cryptic deletion: description of two new cases and indication for a role of WTIP haploinsufficiency in hypospadias. 133
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 130
Cognitive development in Dravet syndrome: a retrospective, multicenter study of 26 patients 123
Acute chorea in a child receiving second dose of human papilloma virus vaccine 118
Evaluation of food intake in disabled children 115
Therapy of encephalopathy with status epilepticus during sleep (ESES/CSWS syndrome): an update 112
Drug-resistant epilepsy treated with ketogenic diet 112
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 111
Atypical Manifestations in Glut1 Deficiency Syndrome 110
Evaluation of food intake and nutritional status in children with refractory status epilepticus 107
A pilot study of a ketogenic diet in patients with Lafora body disease 106
A pilot study of ketogenic diet in patients with Lafora body disease. 103
Paroxysmal tonic eye deviation: an atypical presentation of hypothalamic hamartoma 102
Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case. 99
The epileptology of Aicardi-Goutières syndrome: electro-clinical-radiological findings 99
Neurofunctional correlates of vulnerability to psychosis: a systematic review and meta-analysis 98
ANDAMENTO DELL’INDICE GLUCO-CHETONICO IN CORSO DI TRATTAMENTO DIEPILESSIA REFRATTARIA CON DIETA CHETOGENICA 97
Ataxia-without-telangiectasia in two sisters with rearrangements of chromosomes 7 and 14. 96
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 95
Ketogenic Diet in Lafora Disease: A Pilot Study 95
Long-term effects of a ketogenic diet on body composition and bone mineralization in GLUT-1 deficiency syndrome: A case series 94
Uncovering the neural correlates of the ketogenic diet: the contribution of functional neuroimaging 94
Acquired epileptic frontal syndrome as long-term outcome in two children withCSWS. 93
Long-term cognitive and behavioural follow-up in three patients with eyeclosure-triggered paroxysmal activity 93
Auditory attention at the onset of West syndrome: correlation with EEG patternsand visual function. 92
Long-term evolution of neuropsychological competences in encephalopathy with status epilepticus during sleep: a variable prognosis. 92
Quality of life in chronic ketogenic diet treatment: she GLUT1DS population perspective 92
Dietary Treatments and New Therapeutic Perspective in GLUT1 Deficiency Syndrome 92
Evaluation of nutritional status in children with refractory epilepsy. 89
Intravenous methylprednisolone pulse therapy for children with epileptic encephalopathy 89
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 89
Prevalence of anti-cardiolipin, anti-beta2 glycoprotein I, and anti-prothrombin antibodies in young patients with epilepsy. 88
Post-operative benefits of animal-assisted therapy in pediatric surgery: a randomised study. 88
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 88
Abnormal cerebellar functional MRI connectivity in patients with paediatric multiple sclerosis 87
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 86
Overall cognitive profiles in patients with GLUT1 Deficiency Syndrome 86
The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: an Italian consensus 85
Ketogenic diet in farmacoresistant epilecties 85
Abnormal visual habituation in pediatric photosensitive epilepsy 85
A correlated fluctuation of language and EEG abnormalities in a case of the Landau-Kleffner syndrome. 85
Impact of the ketogenic diet on linear growth in children: A single-center retrospective analysis of 34 cases 85
Benign partial epilepsies of adolescence: a report of 37 new cases 85
Ketogenic Diet: Electrophysiological Effects on the Normal Human Cortex. 84
Ketogenic Diet in Lafora Disease: A Pilot Study 83
Ketogenic diet in Lafora disease: a long term follow-up pilot study 82
Extrastriate visual cortex in idiopathic occipital epilepsies: The contribution of retinotopic areas to spike generation 82
Measuring the Outcomes of Maternal COVID-19-related Prenatal Exposure (MOM-COPE): Study protocol for a multicentric longitudinal project 82
La gestione del bambino con convulsioni febbrili: linee guida sulle convulsioni febbrili. 81
Nutritional and pharmacological management of childhood epilepsy: ketogenic diets and common AEDs 80
Epilepsy surgery in tuberous sclerosis complex: early predictive elements and outcome 80
Long-term neuropsychological follow-up and nosological considerations in five patients with continuous spikes and waves during slow sleep 79
Familial severe myoclonic epilepsy of infancy: truncation of Nav1.1 and geneticheterogeneity. 79
Ketogenic diets in the treatment of epilepsy: preliminary data 79
: Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity 79
The ketogenic diet in children, adolescents and young adults with refractory epilepsy: an Italian multicentric experience. 78
Reversibility of vigabratin-induced visual-field defect. 77
Encopresi 77
Atypical onset of multiple sclerosis in an adolescent with monosymptomatic chronic tension-type headache. 77
Epilepsy in patients with GRIN2A alterations: Genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs 77
Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene. 76
Long-term cognitive and behavioural follow-up in three patients with eye closure-triggered paroxysmal activity. 76
Regional hippocampal involvement and cognitive impairment in pediatric multiple sclerosis 76
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 76
Evaluation of nutritional status in children with refractory epilepsy 75
Optimal clinical management of children receiving the ketogenic diet: recommendations of the International Ketogenic Diet Study Group. 75
Chorea mollis: long-term follow-up of an infantile case. 75
Sporadic and familial glut1ds Italian patients: A wide clinical variability 75
Spontaneous MRI improvement and absence of cerebral calcification in Aicardi-Goutières syndrome: Diagnostic and disease-monitoring implications 75
Rhythmic movement disorder and cyclic alternating pattern during sleep: a video-polysomnographic study in a 9-year-old boy 75
Generalized epilepsy with febrile seizures plus (GEFS+): clinical spectrum in seven Italian families unrelated to SCN1A, SCN1B, and GABRG2 gene mutations. 74
Dravet phenotype in a subject with a der(4)t(4;8)(p16.3;p23.3) without the involvement of the LETM1 gene 74
Hydrocephalus and porencephaly 73
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 73
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsyof infancy (SMEI) patients with SCN1A mutations. 72
The ketogenic diet for Dravet syndrome and other epileptic encephalopathies: An Italian consensus 72
Mutational scanning of potassium, sodium and chloride ion channels in malignant migrating partial seizures in infancy 72
Topiramate as add-on drug in children, adolescents and young adults with Lennox-Gastaut syndrome: an Italian multicentric study 71
Immunomodulatory treatment of early onset multiple sclerosis: Results of an Italian Co-operative Study 71
Lamotrigine in infantile spasms. 71
Epilepsy surgery in children: Evaluation of seizure outcome and predictive elements 71
Cognitive impairment in paediatric multiple sclerosis patients is not related to cortical lesions 71
Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients. 71
Novel insight into GLUT1 Deficiency Syndrome: screening for emotional and behavioral problems in youths following ketogenic diet 71
Somatic and germline mosaicisms in severe myoclonic epilepsy of infancy. 70
Motor impairment on awakening in a patient with an EEG pattern of "unilateral,continuous spikes and waves during slow sleep". 70
Germ-line mutation of the NRAS gene may be responsible for the development of juvenile myelomonocytic leukaemia 70
The ketogenic diet in children, adolescents and young adults with refractory epilepsy: an italian multicentric experience 70
Early-onset occipital idiopathic epilepsy: a syndrome to be treated? 70
Brain macro- and microscopic damage in patients with paediatric MS. 70
Brain correlates of spike and wave discharges in GLUT1 deficiency syndrome 70
CHD2 variants are a risk factor for photosensitivity in epilepsy 70
Continuous spikes and wave activity during slow wave sleep: syndrome or eeg pattern 69
Generalized epilepsy with febrile seizures plus and severe myoclonic epilepsy in infancy: a case report of two Italian families. 69
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G>A mitochondrial DNA mutation: a case report 69
Clinical, cytogenetic and immunological aspects in 4 cases resembling ataxia telangiectasia. 69
Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance. 69
Totale 8.776
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Categoria #
all - tutte 61.440
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 61.440
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021630 0 0 0 0 0 135 9 157 42 143 121 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
2025/20262.998 480 389 620 598 684 227 0 0 0 0 0 0
Totale 14.166