BALESTRI, PAOLO
 Distribuzione geografica
Continente #
NA - Nord America 10.523
EU - Europa 6.347
AS - Asia 3.530
SA - Sud America 576
AF - Africa 154
OC - Oceania 17
Continente sconosciuto - Info sul continente non disponibili 1
Totale 21.148
Nazione #
US - Stati Uniti d'America 10.400
RU - Federazione Russa 1.506
CN - Cina 1.321
GB - Regno Unito 1.275
SG - Singapore 1.055
IE - Irlanda 988
UA - Ucraina 627
BR - Brasile 487
SE - Svezia 452
FR - Francia 385
DE - Germania 361
VN - Vietnam 347
HK - Hong Kong 298
IT - Italia 262
FI - Finlandia 259
KR - Corea 122
BD - Bangladesh 98
ZA - Sudafrica 74
CA - Canada 72
IN - India 68
ES - Italia 56
NG - Nigeria 39
TR - Turchia 39
PL - Polonia 38
BE - Belgio 32
MX - Messico 31
IQ - Iraq 30
NL - Olanda 29
CZ - Repubblica Ceca 28
AR - Argentina 25
JP - Giappone 25
EC - Ecuador 16
ID - Indonesia 16
AU - Australia 14
CL - Cile 13
PK - Pakistan 12
SA - Arabia Saudita 12
UZ - Uzbekistan 12
CO - Colombia 11
AT - Austria 10
VE - Venezuela 10
EG - Egitto 9
JO - Giordania 9
MA - Marocco 9
KZ - Kazakistan 8
KE - Kenya 7
AE - Emirati Arabi Uniti 6
PY - Paraguay 6
AZ - Azerbaigian 5
BG - Bulgaria 5
LT - Lituania 5
NP - Nepal 5
OM - Oman 5
PE - Perù 5
AL - Albania 4
BH - Bahrain 4
CI - Costa d'Avorio 4
GR - Grecia 4
HU - Ungheria 4
IL - Israele 4
JM - Giamaica 4
MY - Malesia 4
TN - Tunisia 4
BB - Barbados 3
BN - Brunei Darussalam 3
CR - Costa Rica 3
IR - Iran 3
PH - Filippine 3
PT - Portogallo 3
RO - Romania 3
TH - Thailandia 3
BO - Bolivia 2
ET - Etiopia 2
HN - Honduras 2
LB - Libano 2
LU - Lussemburgo 2
LV - Lettonia 2
NI - Nicaragua 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
PS - Palestinian Territory 2
QA - Qatar 2
TT - Trinidad e Tobago 2
AI - Anguilla 1
AM - Armenia 1
AO - Angola 1
BY - Bielorussia 1
CG - Congo 1
CY - Cipro 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EU - Europa 1
GA - Gabon 1
GE - Georgia 1
IM - Isola di Man 1
KG - Kirghizistan 1
LA - Repubblica Popolare Democratica del Laos 1
MD - Moldavia 1
PA - Panama 1
PR - Porto Rico 1
Totale 21.140
Città #
Dallas 1.199
Fairfield 1.188
Southend 1.080
Dublin 985
Ashburn 943
Chandler 577
Woodbridge 545
Singapore 523
Jacksonville 501
Seattle 482
Houston 476
Wilmington 476
Cambridge 433
Santa Clara 422
Ann Arbor 393
Moscow 368
Beijing 291
Hong Kong 278
San Jose 278
Princeton 201
Nanjing 179
Hefei 141
The Dalles 133
New York 130
Seoul 122
Ho Chi Minh City 117
Los Angeles 115
Helsinki 113
Menlo Park 97
Lauterbourg 92
Munich 91
Hanoi 84
Siena 83
San Diego 80
Boardman 78
Johannesburg 68
Nanchang 57
Council Bluffs 56
Buffalo 54
Shenyang 52
Norwalk 43
San Mateo 43
Shanghai 43
Tianjin 43
Turku 43
São Paulo 40
Abuja 39
Columbus 35
Málaga 35
Orem 34
Warsaw 28
Changsha 26
Hebei 26
Montreal 26
Milan 24
Toronto 24
Brno 22
Brussels 22
Chicago 22
Lancaster 22
Tokyo 22
Denver 21
Rio de Janeiro 20
San Francisco 20
Zhengzhou 20
Chennai 19
Jiaxing 19
Redondo Beach 19
Brooklyn 18
Guangzhou 18
Izmir 18
London 18
Poplar 18
Da Nang 17
Haiphong 17
Jinan 17
Stockholm 17
Frankfurt am Main 15
Ningbo 15
Atlanta 14
Hangzhou 13
Manchester 13
Nuremberg 13
Belo Horizonte 12
Dearborn 12
Kunming 12
Phoenix 11
Rome 11
Baghdad 10
Ottawa 10
Tashkent 10
Washington 10
Amsterdam 9
Brasília 9
Mexico City 9
Naples 9
Redwood City 9
Roubaix 9
Amman 8
Ankara 8
Totale 14.790
Nome #
Chromosome 18 aberrations and epilepsy: a review 385
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability. 381
3.2 Mb microdeletion in chromosome 7 bands q22.2-q22.3 associated with overgrowth and delayed bone age 331
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features 325
A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb 313
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 311
A child with vestibular neuritis. Is adenovirus implicated? 306
2q24-q31 deletion: report of a case and review of the literature 306
A new case of severe congenital nemaline myopathy 303
Private inherited microdeletion/microduplications: implications in clinical practice 273
Aicardi syndrome with favorable outcome: case report and review 271
Celiac disease with cerebral calcium and silica deposits: x-ray spectroscopic findings, an autopsy study 258
Cerebral glucose metabolism in neurofibromatosis type 1 assessed with (18f)-2-FLUORO-2-DEOXY-d-GLUCOSE AND pet 256
Efficacy and safety of topiramate in infants according to epilepsy syndromes 253
De novo complete trisomy 5p clinical and neuroradiological findings 250
Recurrent Miller Fisher syndrome in children 247
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 246
A comparative study of hydrocortisone versus deflazacort in drug-resistant epilepsy of childhood 244
SCN1A mutation associated with atypical Panayiotopoulos syndrome 240
Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy 240
Oxidative stress in children affected by epileptic encephalopathies 239
Hot water epilepsy and focal malformation of the parietal cortex development 238
Epilepsy, progressive cerebral calcifications, and coeliac disease 237
Quantification of psychosine in the serum of twitcher mouse by LC-ESI-tandem-MS analysis 237
A novel homozygous ISPD gene mutation causing phenotype variability in a consanguineous family 236
Central precocious puberty and abnormal chromosomal patterns 232
Elettroencephalographic and epileptic patterns in x chromosome anomalies 230
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 229
Optic perineuritis: A further cause of visual loss and disc edema in children 229
Precocious puberty with trisomy X syndrome 228
Serum levels of chitotriosidase as a marker of disease activity and clinical stage in sarcoidosis. 225
Typical absence seizures associated with localization-related epilepsy: a clinical and electroencephalographic characterization 223
Overlapping microdeletions involving 15q22.2 narrow the critical region for intellectual disability to NARG2 and RORA 221
Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation 221
Childhood absence epilepsy: evolution and prognostic factors 220
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria 220
Craniofacial dyssynostosis: case report and review 218
Schinzel-Giedion syndrome: a further cause of West syndrome 217
Epilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy 216
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity? 211
Epilepsy in neurofibromatosis 1 210
Bathing epilepsy: report of two Caucasian cases 209
Association of Chiari I malformation, mental retardation, speech delay and epilepsy: a specific desorder ? 209
Dexfenfluramine effective in drug-resistant temporal lobe epilepsy 208
Lacosamide efficacy in epileptic syndromes with continuous spike and waves during slow sleep (CSWS) 205
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss a provisionally unique genetic syndrome 204
Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature 203
Spermatogenesis in a man with complete deletion of USP9Y 202
Lacosamide in children with refractory status epilepticus. A multicenter Italian experience 202
Brain mitochondrial impairment in ethylmalonic encephalopathy 202
Epilepsy and elettroencephalographic finding in pericentric inversion of chromosome 12 200
The phenotype of floating-harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP. 197
Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures 196
Topiramate effects on plasma serotonin levels in children with epilepsy 195
Multiple neuroendocrine disorder in Salla disease 194
Quantitative ultrasound and dual-energy x-ray absorptiometry in children and adolescents with neurofibromatosis of type 1. 193
Late-onset childhood occipital epilepsy(Gastaut type): a family study 192
Body mass index and serum lipid changes during treatment with valproic acid in children with epilepsy 192
Esantema in un bambino con puntura di zecca: rickettsiosi? 190
Clinical features of psychogenic non-epileptic seizures in prepubertal and pubertal patients with idiopathic epilepsy 184
Plasmapheresis in a child affected by acute disseminated encephalomyelitis 184
Efficacy and safety of levetiracetam in infants and young children with refractory epilepsy 183
Ethylmalonic encephalopathy: further clinical and neuroradiological characterization 180
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity? 179
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review 179
Alternating hemiplegia of childhood or Hashimoto’s encephalopathy? 179
Progressive cerebral calcification ,epilepsy,and celiac disease 178
Efficacy and safety of topiramate in refractory epilepsy of childhood: long-term follow-up study 175
Zonisamide in children and young adults with refractory epilepsy: an open label, multicenter Italian study 175
Petechial rash associated with Parvovirus B19 in children: case report and literature review 173
Intractable reflex audiogenic seizures in Aicardi syndrome 169
Photoparoxysmal responses in children with chromosomal aberrations 168
Malformation of the cortical development in Neurofibromatosis type 1 168
Endocrine disorders in two sisters affected by MELAS syndrome 167
Seizures and electroencephalographic findings in CDKL5 mutations: case report and review 166
Linear scleroderma associated with progressive brain atrophy 166
Levetiracetam monotherapy for children and adolescents with benign rolandic seizures 165
Recurrent torticollis caused by dissecting vertebral artery aneurysm in a pediatric patient results of endovascular treatment by use of coil embolization case report 165
L-2 Hydroxyglutaric Aciduria Magnetization Transfer Contrast and Diffusion Weighted Magnetic Resonance Imaging Findings. A case Report 165
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy 164
Clinical and neuroradiologic findings in three cases of fucosidosis 161
Long-term follow-up in children with benign convulsions associated with gastroenteritis 160
Inter-ictal and post-ictal circulating levels of allopregnanolone, an anticonvulsant metabolite of progesterone, in epileptic children 160
Pubertal disorders in inv dup(15) syndrome 160
GM2 gangliosidosis variant B1 neuroradiological findings 159
Severe Metabolic Abnormalities in the White Matter of Patients with Vacuolating Leukoencephalopathy with Subcortical Cysts. A Proton MR Spectroscopic Imaging Study 158
Medial temporal lobe dysgenesis in Muenke sindrome and hypochondrolplasia 158
Epilepsy and electroencephalographic anomalies in chromosome 2 aberrations. A review 158
Management of status dystonicus in children. Cases reportand review 157
Oxcarbazepine and atypical evolution of benign idiopathic focal epilepsy of childhood 155
Oxidative stress in children with epileptic encephalopathy 154
Levetiracetam monotherapy for childhood occipital epilepsy of gastaut 153
Pontocerebellar hypoplasia type 2: further clinical characterization and evidence of positive response of dyskinesia to levodopa 152
Efficacy and safety of rufinamide in children under four years of age with drug-resistant epilepsies 149
Efficacy and tolerability of add-on lacosamide in children with Lennox-Gastaut syndrome 149
Efficacy and safety of lacosamide in infants and young children with refractory focal epilepsy 147
Efficacy and tolerability of add-on Lacosamide in children with Lennox-Gastaut syndrome 146
Epilepsy and vaccinations: Italian guidelines 144
MR brain imaging of fucosidosis type I 141
HLA-DQ typing in the diagnostic algorithm of celiac disease 137
Totale 20.759
Categoria #
all - tutte 68.771
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 68.771


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202171 0 0 0 0 0 0 0 0 0 0 0 71
2021/20221.223 61 140 54 75 17 51 59 145 67 103 111 340
2022/20231.920 117 169 257 262 201 378 38 156 206 52 49 35
2023/20241.398 54 46 119 94 35 395 531 17 4 11 13 79
2024/20252.581 50 127 272 146 335 148 25 153 288 103 305 629
2025/20266.391 437 949 913 843 1.381 275 682 154 165 307 189 96
Totale 21.255