IRIS
BALESTRI, PAOLO
 Distribuzione geografica
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Continente #
NA - Nord America 7.176
EU - Europa 4.380
AS - Asia 774
OC - Oceania 12
SA - Sud America 4
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
Totale 12.348
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Nazione #
US - Stati Uniti d'America 7.160
GB - Regno Unito 1.194
IE - Irlanda 984
CN - Cina 655
UA - Ucraina 613
SE - Svezia 435
FR - Francia 252
DE - Germania 241
IT - Italia 208
FI - Finlandia 203
RU - Federazione Russa 131
SG - Singapore 75
ES - Italia 36
BE - Belgio 29
CZ - Repubblica Ceca 24
TR - Turchia 21
NL - Olanda 16
CA - Canada 15
AU - Australia 10
HK - Hong Kong 5
JP - Giappone 4
IR - Iran 3
PL - Polonia 3
AE - Emirati Arabi Uniti 2
BR - Brasile 2
CL - Cile 2
GR - Grecia 2
IN - India 2
LU - Lussemburgo 2
NZ - Nuova Zelanda 2
AT - Austria 1
BN - Brunei Darussalam 1
CY - Cipro 1
EU - Europa 1
HU - Ungheria 1
ID - Indonesia 1
IL - Israele 1
IM - Isola di Man 1
LT - Lituania 1
LV - Lettonia 1
MX - Messico 1
NG - Nigeria 1
PH - Filippine 1
RO - Romania 1
SA - Arabia Saudita 1
SI - Slovenia 1
TH - Thailandia 1
Totale 12.348
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Città #
Fairfield 1.188
Southend 1.080
Dublin 981
Ashburn 653
Chandler 577
Woodbridge 544
Jacksonville 497
Seattle 478
Wilmington 476
Houston 468
Cambridge 433
Ann Arbor 393
Princeton 201
Nanjing 178
Beijing 113
Helsinki 100
Menlo Park 97
Siena 93
Boardman 78
San Diego 78
New York 74
Nanchang 56
Shenyang 52
Singapore 47
Norwalk 43
San Mateo 43
Tianjin 38
Shanghai 37
Málaga 35
Moscow 34
Hebei 26
Brno 22
Changsha 22
Lancaster 21
Brussels 19
Izmir 18
Jiaxing 17
Milan 17
Zhengzhou 17
Jinan 16
Ningbo 15
San Francisco 13
Dearborn 12
Hangzhou 11
Kunming 11
London 11
Guangzhou 10
Redwood City 9
Prescot 8
Tappahannock 8
Waanrode 8
Washington 8
Lanzhou 7
Rome 7
Toronto 7
Ottawa 6
Taizhou 6
Canberra 5
Düsseldorf 5
Falls Church 5
Los Angeles 5
Munich 5
Auburn Hills 4
Chiswick 4
Florence 4
Hounslow 4
Kilburn 4
Naples 4
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
Central 2
Clifton 2
Corciano 2
Dallas 2
Falkenstein 2
Fremont 2
Hong Kong 2
Indiana 2
Las Vegas 2
Leawood 2
Leuven 2
Luxembourg 2
Marcon 2
Melbourne 2
Paris 2
Prague 2
Totale 9.646
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Nome #
Chromosome 18 aberrations and epilepsy: a review 288
Coffin-Siris and Nicolaides-Baraitser syndromes are a common well recognizable cause of intellectual disability. 245
SCN1A mutation associated with atypical Panayiotopoulos syndrome 188
Quantification of psychosine in the serum of twitcher mouse by LC-ESI-tandem-MS analysis 179
Recurrent Miller Fisher syndrome in children 170
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome 167
3.2 Mb microdeletion in chromosome 7 bands q22.2-q22.3 associated with overgrowth and delayed bone age 162
Private inherited microdeletion/microduplications: implications in clinical practice 161
Precocious puberty with trisomy X syndrome 158
Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy 157
De novo complete trisomy 5p clinical and neuroradiological findings 150
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features 150
A 9.3 Mb microdeletion of 3q27.3q29 associated with psychomotor and growth delay, tricuspid valve dysplasia and bifid thumb 150
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 149
Hot water epilepsy and focal malformation of the parietal cortex development 149
Topiramate effects on plasma serotonin levels in children with epilepsy 148
Optic perineuritis: A further cause of visual loss and disc edema in children 144
The phenotype of floating-harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP. 143
Oxidative stress in children affected by epileptic encephalopathies 142
2q24-q31 deletion: report of a case and review of the literature 141
A child with vestibular neuritis. Is adenovirus implicated? 139
Overlapping microdeletions involving 15q22.2 narrow the critical region for intellectual disability to NARG2 and RORA 136
Typical absence seizures associated with localization-related epilepsy: a clinical and electroencephalographic characterization 136
Serum levels of chitotriosidase as a marker of disease activity and clinical stage in sarcoidosis. 134
Cerebral glucose metabolism in neurofibromatosis type 1 assessed with (18f)-2-FLUORO-2-DEOXY-d-GLUCOSE AND pet 133
Celiac disease with cerebral calcium and silica deposits: x-ray spectroscopic findings, an autopsy study 133
Epilepsy, progressive cerebral calcifications, and coeliac disease 132
Aicardi syndrome with favorable outcome: case report and review 132
Efficacy and safety of topiramate in infants according to epilepsy syndromes 132
A novel homozygous ISPD gene mutation causing phenotype variability in a consanguineous family 131
Zonisamide in children and young adults with refractory epilepsy: an open label, multicenter Italian study 131
Dexfenfluramine effective in drug-resistant temporal lobe epilepsy 127
Craniofacial dyssynostosis: case report and review 127
Esantema in un bambino con puntura di zecca: rickettsiosi? 127
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria 127
Schinzel-Giedion syndrome: a further cause of West syndrome 126
Benign convulsions associated with mild gastroenteritis: a multicenter clinical study 124
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss a provisionally unique genetic syndrome 124
Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures 124
Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation 123
A new case of severe congenital nemaline myopathy 122
Lacosamide in children with refractory status epilepticus. A multicenter Italian experience 122
Linear scleroderma associated with progressive brain atrophy 122
Epilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy 121
Central precocious puberty and abnormal chromosomal patterns 121
null 118
Clinical features of psychogenic non-epileptic seizures in prepubertal and pubertal patients with idiopathic epilepsy 118
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review 118
Lacosamide efficacy in epileptic syndromes with continuous spike and waves during slow sleep (CSWS) 117
Loss-of-function mutation of the AF9/MLLT3 gene in a girl with neuromotor development delay, cerebellar ataxia, and epilepsy 117
Brain mitochondrial impairment in ethylmalonic encephalopathy 117
Epilepsy in neurofibromatosis 1 117
Endocrine disorders in two sisters affected by MELAS syndrome 116
Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature 116
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity? 116
Efficacy and tolerability of add-on Lacosamide in children with Lennox-Gastaut syndrome 115
Plasmapheresis in a child affected by acute disseminated encephalomyelitis 115
Late-onset childhood occipital epilepsy(Gastaut type): a family study 115
Multiple neuroendocrine disorder in Salla disease 115
Alternating hemiplegia of childhood or Hashimoto’s encephalopathy? 115
Quantitative ultrasound and dual-energy x-ray absorptiometry in children and adolescents with neurofibromatosis of type 1. 114
Childhood absence epilepsy: evolution and prognostic factors 113
Levetiracetam monotherapy for children and adolescents with benign rolandic seizures 113
Inter-ictal and post-ictal circulating levels of allopregnanolone, an anticonvulsant metabolite of progesterone, in epileptic children 113
Efficacy and tolerability of add-on lacosamide in children with Lennox-Gastaut syndrome 113
Bathing epilepsy: report of two Caucasian cases 112
Pubertal disorders in inv dup(15) syndrome 112
Elettroencephalographic and epileptic patterns in x chromosome anomalies 109
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity? 109
A comparative study of hydrocortisone versus deflazacort in drug-resistant epilepsy of childhood 108
Epilepsy and vaccinations: Italian guidelines 107
Efficacy and safety of rufinamide in children under four years of age with drug-resistant epilepsies 107
Body mass index and serum lipid changes during treatment with valproic acid in children with epilepsy 106
Levetiracetam monotherapy for childhood occipital epilepsy of gastaut 105
Management of status dystonicus in children. Cases reportand review 104
Seizures and electroencephalographic findings in CDKL5 mutations: case report and review 104
Spermatogenesis in a man with complete deletion of USP9Y 103
Photoparoxysmal responses in children with chromosomal aberrations 103
Efficacy and safety of levetiracetam in infants and young children with refractory epilepsy 103
Petechial rash associated with Parvovirus B19 in children: case report and literature review 103
null 102
Intractable reflex audiogenic seizures in Aicardi syndrome 102
Clinical and neuroradiologic findings in three cases of fucosidosis 99
Oxcarbazepine and atypical evolution of benign idiopathic focal epilepsy of childhood 99
Efficacy and safety of lacosamide in infants and young children with refractory focal epilepsy 98
Epilepsy and elettroencephalographic finding in pericentric inversion of chromosome 12 98
Recurrent torticollis caused by dissecting vertebral artery aneurysm in a pediatric patient results of endovascular treatment by use of coil embolization case report 96
MR brain imaging of fucosidosis type I 95
Progressive cerebral calcification ,epilepsy,and celiac disease 91
Long-term follow-up in children with benign convulsions associated with gastroenteritis 90
Association of Chiari I malformation, mental retardation, speech delay and epilepsy: a specific desorder ? 87
Ethylmalonic encephalopathy: further clinical and neuroradiological characterization 85
Severe Metabolic Abnormalities in the White Matter of Patients with Vacuolating Leukoencephalopathy with Subcortical Cysts. A Proton MR Spectroscopic Imaging Study 82
Malformation of the cortical development in Neurofibromatosis type 1 81
Isoprostanes in distrophynopathy: evidence of increased oxidative stress 80
Epilepsy and electroencephalographic anomalies in chromosome 2 aberrations. A review 80
GM2 gangliosidosis variant B1 neuroradiological findings 75
Oxidative stress in children with epileptic encephalopathy 74
Efficacy and safety of topiramate in refractory epilepsy of childhood: long-term follow-up study 72
Pontocerebellar hypoplasia type 2: further clinical characterization and evidence of positive response of dyskinesia to levodopa 71
Totale 12.210
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Categoria #
all - tutte 42.163
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 42.163
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.529 0 111 214 492 225 217 226 377 247 198 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
2024/2025162 50 112 0 0 0 0 0 0 0 0 0 0
Totale 12.455