CATALOGO DEI PRODOTTI DELLA RICERCA

DARRA, Francesca
 Distribuzione geografica
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Continente #
EU - Europa 5.597
NA - Nord America 5.595
AS - Asia 4.261
SA - Sud America 654
AF - Africa 149
OC - Oceania 23
Continente sconosciuto - Info sul continente non disponibili 3
Totale 16.282
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Nazione #
US - Stati Uniti d'America 5.506
RU - Federazione Russa 2.010
SG - Singapore 1.877
CN - Cina 1.113
GB - Regno Unito 994
IT - Italia 947
BR - Brasile 528
HK - Hong Kong 400
VN - Vietnam 358
FR - Francia 326
DE - Germania 267
IE - Irlanda 266
SE - Svezia 248
FI - Finlandia 223
KR - Corea 155
UA - Ucraina 72
IN - India 68
AR - Argentina 56
NL - Olanda 48
AT - Austria 44
ID - Indonesia 41
CA - Canada 38
JP - Giappone 38
MX - Messico 37
TR - Turchia 33
BD - Bangladesh 30
PL - Polonia 30
IQ - Iraq 29
ZA - Sudafrica 28
ES - Italia 26
NG - Nigeria 26
AU - Australia 19
EC - Ecuador 18
TG - Togo 18
BE - Belgio 16
PK - Pakistan 16
SA - Arabia Saudita 16
CL - Cile 14
MA - Marocco 14
CO - Colombia 13
LT - Lituania 13
BJ - Benin 12
PY - Paraguay 12
CH - Svizzera 10
EG - Egitto 10
UZ - Uzbekistan 10
DZ - Algeria 9
HU - Ungheria 9
KE - Kenya 8
AE - Emirati Arabi Uniti 7
GR - Grecia 7
RO - Romania 7
AM - Armenia 6
ET - Etiopia 6
PH - Filippine 6
CZ - Repubblica Ceca 5
IL - Israele 5
JO - Giordania 5
NP - Nepal 5
TN - Tunisia 5
VE - Venezuela 5
AZ - Azerbaigian 4
KZ - Kazakistan 4
LB - Libano 4
SN - Senegal 4
SY - Repubblica araba siriana 4
AL - Albania 3
BY - Bielorussia 3
IR - Iran 3
KH - Cambogia 3
LV - Lettonia 3
MD - Moldavia 3
OM - Oman 3
PE - Perù 3
SK - Slovacchia (Repubblica Slovacca) 3
TH - Thailandia 3
UY - Uruguay 3
DK - Danimarca 2
EU - Europa 2
GA - Gabon 2
GE - Georgia 2
GY - Guiana 2
HR - Croazia 2
JM - Giamaica 2
KG - Kirghizistan 2
LA - Repubblica Popolare Democratica del Laos 2
MY - Malesia 2
NI - Nicaragua 2
NO - Norvegia 2
PA - Panama 2
AF - Afghanistan, Repubblica islamica di 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BW - Botswana 1
BZ - Belize 1
DO - Repubblica Dominicana 1
EE - Estonia 1
Totale 16.257
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Città #
Singapore 997
Southend 785
Ashburn 661
Moscow 638
San Jose 605
Chandler 528
Jacksonville 503
Hong Kong 396
Dallas 361
Woodbridge 315
Dublin 258
Verona 240
Beijing 228
The Dalles 199
Ann Arbor 161
Houston 117
Ho Chi Minh City 111
Lawrence 105
Princeton 105
Los Angeles 102
Wilmington 96
Hanoi 83
New York 83
Shenyang 61
Jinan 60
Milan 59
Nanjing 58
Buffalo 57
São Paulo 54
Munich 51
Helsinki 50
Council Bluffs 46
Lancaster 41
Redmond 41
Santa Clara 41
Tianjin 40
Redondo Beach 39
Sindelfingen 38
Tokyo 38
Columbus 37
Bologna 35
Changsha 32
Nanchang 32
Boardman 31
Rome 30
Guangzhou 27
Seattle 27
Abuja 26
Vienna 26
London 25
Zhengzhou 25
Amsterdam 24
Hebei 24
Rio de Janeiro 24
Frankfurt am Main 23
Orem 23
Taizhou 23
Warsaw 22
Denver 21
Jakarta 21
Norwalk 21
Taiyuan 21
Seoul 20
Dong Ket 19
Hangzhou 19
Haikou 18
Jiaxing 18
Lomé 18
Falkenstein 17
Johannesburg 17
Nuremberg 17
Stockholm 17
Haiphong 15
San Francisco 15
Turku 15
Baghdad 14
Chennai 14
Chicago 14
Kent 14
Ningbo 14
Padova 14
Boston 13
Brooklyn 13
Brussels 13
Da Nang 13
Lappeenranta 13
Atlanta 12
Campinas 12
Cotonou 12
Manchester 12
Falls Church 11
Guarulhos 11
Hyderabad 11
Phoenix 11
Boydton 10
Brasília 10
Curitiba 10
Dhaka 10
Montreal 10
Redwood City 10
Totale 9.577
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Nome #
Applicazione della tecnica MLPA (Multiplex Ligation-Dependent Probe Amplification) per lo screening dei riarrangiamenti subtelomerici in pazienti pediatrici con ritardo mentale | [Application of MLPA (Multiplex Ligation-Dependent Probe Amplification) for the screening of subtelomeric rearrangements in children with mental retardation] 529
Epilessia mioclono-astatica (EMA): studio elettroclinico longitudinale di 25 soggetti 329
Acute aphasia and psychosis: A peculiar type of partial complex epileptic status with favourable outcome (Conference Paper) [AFASIA E PSICOSI ACUTE: UNA FORMA PARTICOLARE DI STATO DI MALE PARZIALE AD EVOLUZIONE FAVOREVOLE] 207
Postural control in childhood: investigating the neurodevelopmental gradient hypothesis 195
Alternating Hemiplegia of childhood: epilepsy and electroencephalographic investigations. 194
BERS-like epilepsy in subjects with focal gyral anomalies: electroclinical findings. 193
[Neurologic outcome in infants surgically treated for congenital cardiopathy: preliminary data]. 189
Efficacy of Levetiracetam in treatment of continous spike wave during sleep (CSWS) 179
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 176
Chiari 1 malformation in a child with febrile seizures, parasomnias, and sleep apnea syndrome 175
A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy. 170
The transition from pediatric to adult age in patients with Dravet Syndrome: A study on the current management pathways and the challenges ahead 170
Encephalopathy related to status epilepticus during slow sleep (ESES) including Landau-Kleffner syndrome 169
Benign myoclonic epilepsy in infancy (BMEI): a longitudinal electroclinical study of 22 cases. 166
EEG diagnostic helpfulness in childhood epilepsies with focal cortical dysplasias. Electroclinical study of 62 personal cases 162
Are there other types of benign focal epilepsies in childhood? 159
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 159
A study of 63 cases with eyelid mioclonia with or without absences: type of seizure or an epileptic syndrome? 158
3D facial morphometry in Italian patients affected by Aicardi syndrome 157
CDKL5 deficiency disorder in males: Five new variants and review of the literature 157
Myoclonic status in non-progressive encephalopaties (MSNPE) 152
Diaper changing-induced reflex seizures in CDKL5-related epilepsy 148
Utilizzo di lamotrigina come terapia aggiuntiva in età pediatrica: revisione della letteratura. 146
Cromosoma 20 ad anello: studio elettroclinico di 3 osservazioni personali. 146
Adaptive behaviour in adolescents and adults with Dravet syndrome 145
Epilepsy and disorders of cortical development in children with congenital cytomegalovirus infection 145
Epileptic spasms: interictal patterns. 144
The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy 143
Non-convulsive febrile status epilepticus mimicking a postictal state after a febrile seizure: an ictal electroclinical and evolutive study 142
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy 141
Brain MRI findings in Severe Myoclonic Epilepsy in Infancy and genotype-phenotype correlations. 139
Clinical and EEG Features of Idiopathic Focal Epilepsies in Childhood 138
Aicardi Syndrome: Key Fetal MRI Features and Prenatal Differential Diagnosis 136
Clinical dissection of early onset absence epilepsy in children and prognostic implications. 135
Electroclinical findings in childhood epilepsy with focal cortical dysplasia. (Abstract) 134
EEG findings during "paroxysmal hemiplegia" in a patient with GLUT1-deficiency 134
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. 133
Myoclonic Status in Nonprogressive Encephalopathies 131
Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center study 130
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 130
SYNGAP1-related developmental and epileptic encephalopathy: The impact on daily life 130
Absence seizures in the first 3 years of life: An electroclinical study of 46 cases 127
Tuberous sclerosis and epilepsy: Longitudinal electroclinical and neuroradiological study of 55 subjects [EPILESSIA E SCLEROSI TUBEROSA: STUDIO ELETTROCLINICO E NEURORADIOLOGICO DI 55 SOGGETTI] 127
Remote Teamwork Management of NORSE During the COVID-19 Lockdown 127
Candidate biomarkers from the integration of methylation and gene expression in discordant autistic sibling pairs 126
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome 126
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. 124
Progressive myoclonic epilepsy and spinal muscular atrophy: One case report and review of the literature 123
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 123
Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients 122
EEG features in Encephalopathy related to Status Epilepticus during slow Sleep 122
Mioclonic-astatic epilepsy (MAE): Longitudinal electroclinical study of 25 subjects,Epilessia Mioclono-Astatica (EMA): Studio elettroclinico longitudinale di 25 soggetti 122
Congenital hemiplegia and epilepsy: a retrospective clinical study of 78 patients 120
Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20. 120
Somatic mosaicism of PCDH19 mutation in a family with low-penetrance EFMR. 120
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 120
Sociodemographic and clinical changes in pediatric in-patient admissions for mental health emergencies during the COVID-19 pandemic: March 2020 to June 2021 119
Childhood absence epilepsy and electroencephalographic focal abnormalities with or without clinical manifestations. 118
[Neurologic outcome in infants surgically treated for congenital cardiopathy: preliminary data]. 118
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 117
An examination of the efficacy and safety of fenfluramine in adults, children, and adolescents with Dravet syndrome in a real-world practice setting: A report from the Fenfluramine European Early Access Program 116
Epilessia e sclerosi tuberosa: studio elettroclinico e neuroradiologico di 55 soggetti. 115
Neuroimaging Changes in Menkes Disease, Part 1 115
A registry for Dravet syndrome: The Italian experience 113
KETASER01 protocol: What went right and what went wrong 113
Restless legs sindrome and attention-deficit/hyperactivity disorder: a review of the literature. 113
Individually tailored extratemporal epilepsy surgery in children: anatomo-electro-clinical features and outcome predictors in a population of 53 cases. 112
Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance. 112
Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature. 112
Clinical characteristics of 80 subjects with KCNQ2-related encephalopathy: Results from a family-driven survey 111
Myoclonic status in non-progressive encephalopathies 111
Ring chromosome 20 syndrome: Report of 3 cases,Cromosoma 20 ad anello: Studio elettroclinico di 3 osservazioni personali 110
Temporal lobe epilepsy in children: electroclinical and neuroradiological study of 62 cases. 109
The phenotype of SCN8A developmental and epileptic encephalopathy 109
Clinical Reasoning: Hyperventilation-Induced Alternating Hemiplegia With Concomitant Hemispheric EEG Slowing in a 7-Year-Old Girl With Headache 108
Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients. 108
Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome. 108
The partial occipital epilepsies in childhood: electroclinical delineation from the symptomatic to idiopatic cases. 107
Epilepsy with myoclonic atonic seizures: an electroclinical study of 69 patients. 107
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective study 107
Epilepsy features in ARID1B-related Coffin-Siris syndrome 107
Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study. 106
Pediatric Epilepsy - Myoclonic Status in Nonprogressive Encephalopathies 106
Neuroimaging Changes in Menkes Disease, Part 2 106
Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients. 104
Pathogenic role of the X-linked cicli-dependent kinase-like 5 and aristaless-related homeobox genes in epileptic encephalopathy of unknown etiology with onset in the first year of life. 104
Head circumferences of patients with Dravet syndrome show growth slowdown 104
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy. 103
Quadro elettroclinico EPR-like in soggetti con disturbo della girazione focale: Elementi di diagnosi differenziale | [Bect-like epilepsy in subjects with focal gyral anomalies: Electroclinical findings for differential diagnosis] 103
Myoclonic status in non progressive encephalopathies. 101
Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life 101
Gelastic seizures and “smiling spasms”: A peculiar ictal pattern 100
Is there a benign limbic epilepsy in children? 100
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations. 100
SEPs in the congenital hemiplegia [APPORTO DEI POTENZIALI EVOCATI SOMESTESICI NELLO STUDIO DELLE EMIPLEGIE CONGENITE] 100
Epilepsy-related brain networks in ring chromosome 20 syndrome: An EEG-fMRI study. 100
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations. 99
GABRA1-Related Disorders: From Genetic to Functional Pathways 97
Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locus. 97
Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study 96
Totale 13.486
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Categoria #
all - tutte 55.550
article - articoli 50.246
book - libri 0
conference - conferenze 993
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 4.311
Totale 111.100
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021139 0 0 0 0 0 0 0 0 0 6 90 43
2021/2022748 80 186 4 20 21 20 16 58 24 35 75 209
2022/20231.688 127 112 160 289 166 378 43 123 190 15 57 28
2023/2024857 44 57 78 80 137 106 41 41 12 57 136 68
2024/20252.635 149 162 90 438 133 115 114 125 417 189 208 495
2025/20266.920 548 322 498 1.121 1.827 489 730 505 502 378 0 0
Totale 16.493