IRIS
BALESTRI, PAOLO
 Distribuzione geografica
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Continente #
NA - Nord America 7.418
EU - Europa 4.659
AS - Asia 911
OC - Oceania 12
SA - Sud America 7
AF - Africa 4
Continente sconosciuto - Info sul continente non disponibili 1
Totale 13.012
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Nazione #
US - Stati Uniti d'America 7.395
GB - Regno Unito 1.203
IE - Irlanda 985
CN - Cina 671
UA - Ucraina 613
SE - Svezia 435
RU - Federazione Russa 384
FR - Francia 252
DE - Germania 246
IT - Italia 211
FI - Finlandia 205
SG - Singapore 192
ES - Italia 36
BE - Belgio 31
CZ - Repubblica Ceca 24
CA - Canada 22
TR - Turchia 21
NL - Olanda 16
AU - Australia 10
HK - Hong Kong 5
JP - Giappone 4
AE - Emirati Arabi Uniti 3
CI - Costa d'Avorio 3
CL - Cile 3
IR - Iran 3
PL - Polonia 3
AR - Argentina 2
BR - Brasile 2
GR - Grecia 2
HU - Ungheria 2
IN - India 2
LU - Lussemburgo 2
LV - Lettonia 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
VN - Vietnam 2
AT - Austria 1
BN - Brunei Darussalam 1
CY - Cipro 1
EU - Europa 1
ID - Indonesia 1
IL - Israele 1
IM - Isola di Man 1
LT - Lituania 1
MX - Messico 1
NG - Nigeria 1
PH - Filippine 1
RO - Romania 1
SA - Arabia Saudita 1
SI - Slovenia 1
TH - Thailandia 1
UZ - Uzbekistan 1
Totale 13.012
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Città #
Fairfield 1.188
Southend 1.080
Dublin 982
Ashburn 655
Chandler 577
Woodbridge 544
Jacksonville 497
Seattle 478
Wilmington 476
Houston 468
Cambridge 433
Ann Arbor 393
Princeton 201
Santa Clara 187
Nanjing 178
Singapore 150
Beijing 113
Helsinki 102
Menlo Park 97
Siena 93
Boardman 78
San Diego 78
New York 75
Nanchang 56
Shenyang 52
Norwalk 43
San Mateo 43
Shanghai 39
Tianjin 38
Málaga 35
Moscow 34
Hebei 26
Brno 22
Changsha 22
Brussels 21
Lancaster 21
Izmir 18
Jiaxing 17
Milan 17
Zhengzhou 17
Jinan 16
Ningbo 15
London 14
San Francisco 13
Dearborn 12
Guangzhou 12
Toronto 12
Hangzhou 11
Kunming 11
Munich 10
Redwood City 9
Los Angeles 8
Ottawa 8
Prescot 8
Tappahannock 8
Waanrode 8
Washington 8
Lanzhou 7
Rome 7
Naples 6
Taizhou 6
Canberra 5
Düsseldorf 5
Falls Church 5
Auburn Hills 4
Chiswick 4
Florence 4
Hounslow 4
Kilburn 4
Abidjan 3
Andover 3
Bonndorf 3
Cassino 3
Changchun 3
Chicago 3
Città di Castello 3
Duncan 3
Haikou 3
Miami 3
Mountain View 3
Somerville 3
Susegana 3
Sydney 3
Trieste 3
Warsaw 3
Zanjan 3
Buenos Aires 2
Central 2
Clifton 2
Corciano 2
Dallas 2
Dubai 2
Falkenstein 2
Fremont 2
Hong Kong 2
Indiana 2
Las Vegas 2
Leawood 2
Leuven 2
Luxembourg 2
Totale 9.967
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Nome #
Chromosome 18 aberrations and epilepsy: a review 297
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability. 255
SCN1A mutation associated with atypical Panayiotopoulos syndrome 192
Quantification of psychosine in the serum of twitcher mouse by LC-ESI-tandem-MS analysis 184
Recurrent Miller Fisher syndrome in children 177
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 175
3.2 Mb microdeletion in chromosome 7 bands q22.2-q22.3 associated with overgrowth and delayed bone age 172
Private inherited microdeletion/microduplications: implications in clinical practice 169
Precocious puberty with trisomy X syndrome 165
Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy 163
A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb 163
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 159
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features 159
De novo complete trisomy 5p clinical and neuroradiological findings 158
Hot water epilepsy and focal malformation of the parietal cortex development 157
Topiramate effects on plasma serotonin levels in children with epilepsy 152
Optic perineuritis: A further cause of visual loss and disc edema in children 150
Oxidative stress in children affected by epileptic encephalopathies 149
A child with vestibular neuritis. Is adenovirus implicated? 148
The phenotype of floating-harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP. 148
2q24-q31 deletion: report of a case and review of the literature 148
Typical absence seizures associated with localization-related epilepsy: a clinical and electroencephalographic characterization 143
Cerebral glucose metabolism in neurofibromatosis type 1 assessed with (18f)-2-FLUORO-2-DEOXY-d-GLUCOSE AND pet 142
Overlapping microdeletions involving 15q22.2 narrow the critical region for intellectual disability to NARG2 and RORA 142
Serum levels of chitotriosidase as a marker of disease activity and clinical stage in sarcoidosis. 142
Celiac disease with cerebral calcium and silica deposits: x-ray spectroscopic findings, an autopsy study 141
Efficacy and safety of topiramate in infants according to epilepsy syndromes 141
Aicardi syndrome with favorable outcome: case report and review 140
Epilepsy, progressive cerebral calcifications, and coeliac disease 139
A novel homozygous ISPD gene mutation causing phenotype variability in a consanguineous family 138
Schinzel-Giedion syndrome: a further cause of West syndrome 135
Zonisamide in children and young adults with refractory epilepsy: an open label, multicenter Italian study 134
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria 134
Dexfenfluramine effective in drug-resistant temporal lobe epilepsy 133
Craniofacial dyssynostosis: case report and review 133
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss a provisionally unique genetic syndrome 133
Epilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy 132
Esantema in un bambino con puntura di zecca: rickettsiosi? 132
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 131
Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation 131
Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures 131
A new case of severe congenital nemaline myopathy 130
Central precocious puberty and abnormal chromosomal patterns 129
Epilepsy in neurofibromatosis 1 128
Lacosamide in children with refractory status epilepticus. A multicenter Italian experience 127
Linear scleroderma associated with progressive brain atrophy 125
Brain mitochondrial impairment in ethylmalonic encephalopathy 124
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review 124
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity? 124
Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature 123
Late-onset childhood occipital epilepsy(Gastaut type): a family study 123
Quantitative ultrasound and dual-energy x-ray absorptiometry in children and adolescents with neurofibromatosis of type 1. 122
Lacosamide efficacy in epileptic syndromes with continuous spike and waves during slow sleep (CSWS) 122
Clinical features of psychogenic non-epileptic seizures in prepubertal and pubertal patients with idiopathic epilepsy 122
Plasmapheresis in a child affected by acute disseminated encephalomyelitis 122
Multiple neuroendocrine disorder in Salla disease 122
Alternating hemiplegia of childhood or Hashimoto’s encephalopathy? 121
Childhood absence epilepsy: evolution and prognostic factors 120
Bathing epilepsy: report of two Caucasian cases 119
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy 119
Efficacy and tolerability of add-on Lacosamide in children with Lennox-Gastaut syndrome 119
null 118
Endocrine disorders in two sisters affected by MELAS syndrome 118
Inter-ictal and post-ictal circulating levels of allopregnanolone, an anticonvulsant metabolite of progesterone, in epileptic children 118
Levetiracetam monotherapy for children and adolescents with benign rolandic seizures 117
Elettroencephalographic and epileptic patterns in x chromosome anomalies 116
Efficacy and tolerability of add-on lacosamide in children with Lennox-Gastaut syndrome 116
A comparative study of hydrocortisone versus deflazacort in drug-resistant epilepsy of childhood 116
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity? 115
Body mass index and serum lipid changes during treatment with valproic acid in children with epilepsy 115
Pubertal disorders in inv dup(15) syndrome 115
Efficacy and safety of levetiracetam in infants and young children with refractory epilepsy 111
Efficacy and safety of rufinamide in children under four years of age with drug-resistant epilepsies 111
Spermatogenesis in a man with complete deletion of USP9Y 110
Photoparoxysmal responses in children with chromosomal aberrations 110
Epilepsy and vaccinations: Italian guidelines 110
Seizures and electroencephalographic findings in CDKL5 mutations: case report and review 110
Management of status dystonicus in children. Cases reportand review 108
Epilepsy and elettroencephalographic finding in pericentric inversion of chromosome 12 108
Petechial rash associated with Parvovirus B19 in children: case report and literature review 107
Levetiracetam monotherapy for childhood occipital epilepsy of gastaut 106
Intractable reflex audiogenic seizures in Aicardi syndrome 105
Oxcarbazepine and atypical evolution of benign idiopathic focal epilepsy of childhood 103
Clinical and neuroradiologic findings in three cases of fucosidosis 102
null 102
Efficacy and safety of lacosamide in infants and young children with refractory focal epilepsy 102
Recurrent torticollis caused by dissecting vertebral artery aneurysm in a pediatric patient results of endovascular treatment by use of coil embolization case report 101
MR brain imaging of fucosidosis type I 97
Progressive cerebral calcification ,epilepsy,and celiac disease 95
Association of Chiari I malformation, mental retardation, speech delay and epilepsy: a specific desorder ? 95
Ethylmalonic encephalopathy: further clinical and neuroradiological characterization 94
Long-term follow-up in children with benign convulsions associated with gastroenteritis 93
Severe Metabolic Abnormalities in the White Matter of Patients with Vacuolating Leukoencephalopathy with Subcortical Cysts. A Proton MR Spectroscopic Imaging Study 88
Malformation of the cortical development in Neurofibromatosis type 1 88
Epilepsy and electroencephalographic anomalies in chromosome 2 aberrations. A review 86
Isoprostanes in distrophynopathy: evidence of increased oxidative stress 83
Oxidative stress in children with epileptic encephalopathy 82
GM2 gangliosidosis variant B1 neuroradiological findings 81
Efficacy and safety of topiramate in refractory epilepsy of childhood: long-term follow-up study 79
Pontocerebellar hypoplasia type 2: further clinical characterization and evidence of positive response of dyskinesia to levodopa 79
Totale 12.842
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Categoria #
all - tutte 45.861
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 45.861
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.712 0 0 0 0 225 217 226 377 247 198 56 166
2020/20212.055 65 291 124 232 94 240 62 279 156 166 275 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
2024/2025826 50 127 272 146 231 0 0 0 0 0 0 0
Totale 13.119