CATALOGO DEI PRODOTTI DELLA RICERCA

DARRA, Francesca
 Distribuzione geografica
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Continente #
NA - Nord America 5.986
EU - Europa 5.711
AS - Asia 4.420
SA - Sud America 663
Continente sconosciuto - Info sul continente non disponibili 214
AF - Africa 149
OC - Oceania 23
Totale 17.166
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Nazione #
US - Stati Uniti d'America 5.878
RU - Federazione Russa 2.010
SG - Singapore 1.894
CN - Cina 1.131
IT - Italia 1.050
GB - Regno Unito 994
BR - Brasile 534
HK - Hong Kong 406
VN - Vietnam 358
FR - Francia 326
DE - Germania 268
IE - Irlanda 267
SE - Svezia 250
FI - Finlandia 223
KR - Corea 155
BD - Bangladesh 140
UA - Ucraina 73
IN - India 68
AR - Argentina 56
CA - Canada 49
NL - Olanda 48
AT - Austria 44
JP - Giappone 43
ID - Indonesia 42
MX - Messico 40
TR - Turchia 34
PL - Polonia 31
IQ - Iraq 29
ZA - Sudafrica 28
ES - Italia 27
NG - Nigeria 26
AU - Australia 19
EC - Ecuador 18
TG - Togo 18
BE - Belgio 16
CL - Cile 16
PK - Pakistan 16
SA - Arabia Saudita 16
CO - Colombia 14
MA - Marocco 14
LT - Lituania 13
BJ - Benin 12
CH - Svizzera 12
PY - Paraguay 12
EG - Egitto 10
HU - Ungheria 10
UZ - Uzbekistan 10
DZ - Algeria 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
JM - Giamaica 4
KZ - Kazakistan 4
LB - Libano 4
MD - Moldavia 4
SN - Senegal 4
SY - Repubblica araba siriana 4
TH - Thailandia 4
AL - Albania 3
BY - Bielorussia 3
IR - Iran 3
KH - Cambogia 3
LV - Lettonia 3
OM - Oman 3
PE - Perù 3
SK - Slovacchia (Repubblica Slovacca) 3
UY - Uruguay 3
DK - Danimarca 2
EU - Europa 2
GA - Gabon 2
GE - Georgia 2
GY - Guiana 2
HR - Croazia 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
CR - Costa Rica 1
DO - Repubblica Dominicana 1
Totale 16.927
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Città #
Singapore 1.004
Southend 785
Ashburn 698
San Jose 653
Moscow 638
Chandler 528
Jacksonville 503
Hong Kong 399
Dallas 368
Woodbridge 315
Dublin 259
Verona 240
Beijing 238
The Dalles 199
Ann Arbor 161
Council Bluffs 135
Houston 117
Los Angeles 117
Ho Chi Minh City 111
Lawrence 105
Princeton 105
New York 102
Wilmington 99
Hanoi 83
Milan 79
Buffalo 67
Shenyang 61
Jinan 60
Nanjing 58
Santa Clara 57
São Paulo 54
Munich 51
Helsinki 50
Columbus 41
Lancaster 41
Redmond 41
Bologna 40
Tianjin 40
Redondo Beach 39
Rome 39
Tokyo 39
Sindelfingen 38
Changsha 32
Nanchang 32
Boardman 31
Seattle 28
Guangzhou 27
Abuja 26
Rio de Janeiro 26
Vienna 26
London 25
Zhengzhou 25
Amsterdam 24
Hebei 24
Denver 23
Frankfurt am Main 23
Orem 23
Taizhou 23
Warsaw 22
Jakarta 21
Norwalk 21
Taiyuan 21
Seoul 20
Dong Ket 19
Hangzhou 19
Chicago 18
Haikou 18
Jiaxing 18
Lomé 18
Falkenstein 17
Johannesburg 17
Nuremberg 17
Stockholm 17
San Francisco 16
Boston 15
Haiphong 15
Turku 15
Atlanta 14
Baghdad 14
Brooklyn 14
Chennai 14
Kent 14
Manchester 14
Montreal 14
Ningbo 14
Padova 14
Brussels 13
Da Nang 13
Lappeenranta 13
Phoenix 13
Toronto 13
Campinas 12
Cotonou 12
Palermo 12
Falls Church 11
Guarulhos 11
Hyderabad 11
Bari 10
Boydton 10
Brasília 10
Totale 9.909
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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] 534
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] 213
Alternating Hemiplegia of childhood: epilepsy and electroencephalographic investigations. 199
The transition from pediatric to adult age in patients with Dravet Syndrome: A study on the current management pathways and the challenges ahead 198
Postural control in childhood: investigating the neurodevelopmental gradient hypothesis 197
BERS-like epilepsy in subjects with focal gyral anomalies: electroclinical findings. 195
[Neurologic outcome in infants surgically treated for congenital cardiopathy: preliminary data]. 192
Chiari 1 malformation in a child with febrile seizures, parasomnias, and sleep apnea syndrome 188
Efficacy of Levetiracetam in treatment of continous spike wave during sleep (CSWS) 184
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 179
A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy. 173
Encephalopathy related to status epilepticus during slow sleep (ESES) including Landau-Kleffner syndrome 171
Benign myoclonic epilepsy in infancy (BMEI): a longitudinal electroclinical study of 22 cases. 169
EEG diagnostic helpfulness in childhood epilepsies with focal cortical dysplasias. Electroclinical study of 62 personal cases 165
A study of 63 cases with eyelid mioclonia with or without absences: type of seizure or an epileptic syndrome? 161
CDKL5 deficiency disorder in males: Five new variants and review of the literature 161
Are there other types of benign focal epilepsies in childhood? 160
Myoclonic status in non-progressive encephalopaties (MSNPE) 160
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 160
3D facial morphometry in Italian patients affected by Aicardi syndrome 160
Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center study 151
Diaper changing-induced reflex seizures in CDKL5-related epilepsy 150
Utilizzo di lamotrigina come terapia aggiuntiva in età pediatrica: revisione della letteratura. 147
Cromosoma 20 ad anello: studio elettroclinico di 3 osservazioni personali. 147
The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy 147
Non-convulsive febrile status epilepticus mimicking a postictal state after a febrile seizure: an ictal electroclinical and evolutive study 146
Epilepsy and disorders of cortical development in children with congenital cytomegalovirus infection 146
Adaptive behaviour in adolescents and adults with Dravet syndrome 145
Epileptic spasms: interictal patterns. 145
Clinical dissection of early onset absence epilepsy in children and prognostic implications. 145
Clinical and EEG Features of Idiopathic Focal Epilepsies in Childhood 145
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy 145
GABRA1-Related Disorders: From Genetic to Functional Pathways 142
Absence seizures in the first 3 years of life: An electroclinical study of 46 cases 141
Brain MRI findings in Severe Myoclonic Epilepsy in Infancy and genotype-phenotype correlations. 140
Aicardi Syndrome: Key Fetal MRI Features and Prenatal Differential Diagnosis 139
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. 137
Electroclinical findings in childhood epilepsy with focal cortical dysplasia. (Abstract) 135
EEG findings during "paroxysmal hemiplegia" in a patient with GLUT1-deficiency 135
Myoclonic Status in Nonprogressive Encephalopathies 134
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 132
Tuberous sclerosis and epilepsy: Longitudinal electroclinical and neuroradiological study of 55 subjects [EPILESSIA E SCLEROSI TUBEROSA: STUDIO ELETTROCLINICO E NEURORADIOLOGICO DI 55 SOGGETTI] 131
SYNGAP1-related developmental and epileptic encephalopathy: The impact on daily life 131
Candidate biomarkers from the integration of methylation and gene expression in discordant autistic sibling pairs 130
Remote Teamwork Management of NORSE During the COVID-19 Lockdown 128
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome 127
Progressive myoclonic epilepsy and spinal muscular atrophy: One case report and review of the literature 126
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. 126
EEG features in Encephalopathy related to Status Epilepticus during slow Sleep 126
Mioclonic-astatic epilepsy (MAE): Longitudinal electroclinical study of 25 subjects,Epilessia Mioclono-Astatica (EMA): Studio elettroclinico longitudinale di 25 soggetti 126
Somatic mosaicism of PCDH19 mutation in a family with low-penetrance EFMR. 125
Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients 125
Childhood absence epilepsy and electroencephalographic focal abnormalities with or without clinical manifestations. 124
The phenotype of SCN8A developmental and epileptic encephalopathy 124
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 124
[Neurologic outcome in infants surgically treated for congenital cardiopathy: preliminary data]. 123
Sociodemographic and clinical changes in pediatric in-patient admissions for mental health emergencies during the COVID-19 pandemic: March 2020 to June 2021 123
Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20. 122
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 122
Congenital hemiplegia and epilepsy: a retrospective clinical study of 78 patients 120
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 120
Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance. 119
Neuroimaging Changes in Menkes Disease, Part 1 119
Refractory tonic-myoclonic status epilepticus with catamenial recurrence in epilepsy with myoclonic atonic seizures: A case report 118
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 118
Clinical characteristics of 80 subjects with KCNQ2-related encephalopathy: Results from a family-driven survey 118
Epilessia e sclerosi tuberosa: studio elettroclinico e neuroradiologico di 55 soggetti. 117
A registry for Dravet syndrome: The Italian experience 116
Restless legs sindrome and attention-deficit/hyperactivity disorder: a review of the literature. 115
Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature. 115
Individually tailored extratemporal epilepsy surgery in children: anatomo-electro-clinical features and outcome predictors in a population of 53 cases. 114
Clinical Reasoning: Hyperventilation-Induced Alternating Hemiplegia With Concomitant Hemispheric EEG Slowing in a 7-Year-Old Girl With Headache 113
KETASER01 protocol: What went right and what went wrong 113
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations. 112
Ring chromosome 20 syndrome: Report of 3 cases,Cromosoma 20 ad anello: Studio elettroclinico di 3 osservazioni personali 112
Myoclonic status in non-progressive encephalopathies 111
Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome. 111
Epilepsy with myoclonic atonic seizures: an electroclinical study of 69 patients. 111
Temporal lobe epilepsy in children: electroclinical and neuroradiological study of 62 cases. 110
Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients. 109
Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study. 109
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy. 109
Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients. 108
The partial occipital epilepsies in childhood: electroclinical delineation from the symptomatic to idiopatic cases. 108
SEPs in the congenital hemiplegia [APPORTO DEI POTENZIALI EVOCATI SOMESTESICI NELLO STUDIO DELLE EMIPLEGIE CONGENITE] 108
Pediatric Epilepsy - Myoclonic Status in Nonprogressive Encephalopathies 108
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective study 108
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. 107
Neuroimaging Changes in Menkes Disease, Part 2 107
Head circumferences of patients with Dravet syndrome show growth slowdown 107
Epilepsy features in ARID1B-related Coffin-Siris syndrome 107
Epilepsy-related brain networks in ring chromosome 20 syndrome: An EEG-fMRI study. 106
Electroclinical features of MEF2C haploinsufficiency-related epilepsy: A multicenter European study 106
Familial Ohtahara syndrome due to a novel ARX gene mutation,Sindrome di Ohtahara familiare causata da una nuova mutazione del gene ARX 104
Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life 104
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
Defining the electroclinical phenotype and outcome of PCDH19-related epilepsy: A multicenter study 103
Gelastic seizures and “smiling spasms”: A peculiar ictal pattern 102
Is there a benign limbic epilepsy in children? 102
Totale 13.932
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Categoria #
all - tutte 62.219
article - articoli 56.466
book - libri 0
conference - conferenze 1.078
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 4.675
Totale 124.438
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022668 0 186 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
2025/20267.354 548 322 498 1.121 1.827 489 730 505 502 408 178 226
2026/2027239 198 41 0 0 0 0 0 0 0 0 0 0
Totale 17.166