IRIS
MORGESE, GUIDO
 Distribuzione geografica
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Continente #
NA - Nord America 2.416
EU - Europa 1.476
AS - Asia 217
OC - Oceania 5
AF - Africa 1
SA - Sud America 1
Totale 4.116
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Nazione #
US - Stati Uniti d'America 2.411
GB - Regno Unito 386
IE - Irlanda 377
UA - Ucraina 210
CN - Cina 201
SE - Svezia 138
DE - Germania 115
FR - Francia 91
FI - Finlandia 79
IT - Italia 48
ES - Italia 20
TR - Turchia 7
CA - Canada 5
RU - Federazione Russa 4
AU - Australia 3
BE - Belgio 2
HK - Hong Kong 2
JP - Giappone 2
NZ - Nuova Zelanda 2
PL - Polonia 2
AE - Emirati Arabi Uniti 1
CL - Cile 1
CZ - Repubblica Ceca 1
ID - Indonesia 1
IM - Isola di Man 1
IN - India 1
IR - Iran 1
LU - Lussemburgo 1
LV - Lettonia 1
NG - Nigeria 1
SA - Arabia Saudita 1
Totale 4.116
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Città #
Fairfield 411
Dublin 375
Southend 357
Chandler 220
Ashburn 201
Wilmington 191
Jacksonville 169
Woodbridge 169
Seattle 158
Cambridge 152
Houston 152
Ann Arbor 121
Princeton 68
Nanjing 58
Helsinki 44
New York 35
San Diego 29
Beijing 28
Boardman 27
Siena 25
Nanchang 24
Málaga 20
Shenyang 20
San Mateo 17
Shanghai 14
Tianjin 13
Izmir 7
Jiaxing 6
Lancaster 6
Venezia 6
Zhengzhou 6
Changsha 5
Falls Church 5
Menlo Park 5
Ningbo 5
Norwalk 5
San Francisco 5
Tappahannock 5
Hebei 4
Jinan 4
Kunming 4
Washington 4
Andover 3
Città di Castello 3
Falkenstein 3
Hangzhou 3
London 3
Prescot 3
Toronto 3
Brussels 2
Canberra 2
Fremont 2
Guangzhou 2
Hounslow 2
Kilburn 2
Redwood City 2
Taizhou 2
Abuja 1
Arezzo 1
Atlanta 1
Auckland 1
Bangalore 1
Cattolica 1
Central 1
Changchun 1
Chicago 1
Chiyoda-ku 1
Dubai 1
Duncan 1
Düsseldorf 1
Edinburgh 1
Gdynia 1
Henderson 1
Islington 1
Jinhua 1
Lanzhou 1
Leawood 1
Lincoln 1
Luxembourg 1
Markham 1
Melbourne 1
Paris 1
Pisa 1
Prague 1
Riga 1
Riyadh 1
Rome 1
Sacramento 1
Setagaya-ku 1
Spoleto 1
Warsaw 1
Winnipeg 1
Zanjan 1
Totale 3.253
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Nome #
Chromosome 18 aberrations and epilepsy: a review 285
18q-syndrome and ectodermal dysplasia syndrome: description of a child and his family 196
Efficacy and safety of levetiracetam: an add-on trial in children with refractory epilepsy 155
Hereditary neuronal intranuclear inclusion disease with autonomic failure and cerebellar degeneration. 151
De novo complete trisomy 5p clinical and neuroradiological findings 149
Hot water epilepsy and focal malformation of the parietal cortex development 146
A child with vestibular neuritis. Is adenovirus implicated? 134
Typical absence seizures associated with localization-related epilepsy: a clinical and electroencephalographic characterization 132
Transient neonatal hypothyroidism after gestational exposure to amiodarone: a follow-up of two cases 130
Efficacy and safety of topiramate in infants according to epilepsy syndromes 129
Aicardi syndrome with favorable outcome: case report and review 128
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria 126
Craniofacial dyssynostosis: case report and review 123
Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures 123
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss a provisionally unique genetic syndrome 122
Central precocious puberty and abnormal chromosomal patterns 118
Non-progressive leukoencephalopathy with bilateral anterior temporal cysts: a case report and review of the literature 115
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity? 115
Epilepsy in neurofibromatosis 1 115
Inter-ictal and post-ictal circulating levels of allopregnanolone, an anticonvulsant metabolite of progesterone, in epileptic children 111
Childhood absence epilepsy: evolution and prognostic factors 110
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity? 107
Seizures and electroencephalographic findings in CDKL5 mutations: case report and review 102
Photoparoxysmal responses in children with chromosomal aberrations 101
Intractable reflex audiogenic seizures in Aicardi syndrome 101
Efficacy and safety of levetiracetam in infants and young children with refractory epilepsy 100
Elettroencephalographic and epileptic patterns in x chromosome anomalies 96
Epilepsy and elettroencephalographic finding in pericentric inversion of chromosome 12 95
Association of Chiari I malformation, mental retardation, speech delay and epilepsy: a specific desorder ? 84
Ethylmalonic encephalopathy: further clinical and neuroradiological characterization 82
Malformation of the cortical development in Neurofibromatosis type 1 78
GM2 gangliosidosis variant B1 neuroradiological findings 73
Pontocerebellar hypoplasia type 2: further clinical characterization and evidence of positive response of dyskinesia to levodopa 69
Efficacy and safety of topiramate in refractory epilepsy of childhood: long-term follow-up study 67
Medial temporal lobe dysgenesis in Muenke sindrome and hypochondrolplasia 67
A unified standard of obesity. 2
Totale 4.137
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Categoria #
all - tutte 13.756
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 13.756
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019316 0 0 0 0 0 0 0 0 0 58 122 136
2019/2020911 118 30 67 157 73 69 64 121 87 56 16 53
2020/2021726 27 95 98 94 22 78 11 92 51 45 87 26
2021/2022415 14 53 19 11 9 18 20 68 13 29 42 119
2022/2023704 36 71 100 99 61 136 16 61 73 25 19 7
2023/2024499 24 13 41 39 14 132 228 4 1 3 0 0
Totale 4.137