CATALOGO DEI PRODOTTI DELLA RICERCA

DARRA, Francesca
 Distribuzione geografica
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Continente #
EU - Europa 5.311
NA - Nord America 4.483
AS - Asia 3.594
SA - Sud America 597
AF - Africa 88
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 3
Totale 14.096
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Nazione #
US - Stati Uniti d'America 4.406
RU - Federazione Russa 2.006
SG - Singapore 1.585
CN - Cina 1.059
GB - Regno Unito 969
IT - Italia 753
BR - Brasile 494
HK - Hong Kong 359
FR - Francia 315
IE - Irlanda 264
DE - Germania 252
SE - Svezia 245
VN - Vietnam 241
FI - Finlandia 215
KR - Corea 106
UA - Ucraina 70
AR - Argentina 46
NL - Olanda 44
AT - Austria 43
IN - India 38
CA - Canada 34
ID - Indonesia 34
JP - Giappone 30
MX - Messico 30
PL - Polonia 29
TR - Turchia 29
BD - Bangladesh 21
ES - Italia 21
IQ - Iraq 20
TG - Togo 18
ZA - Sudafrica 18
AU - Australia 16
EC - Ecuador 16
BE - Belgio 15
MA - Marocco 13
BJ - Benin 12
CL - Cile 11
LT - Lituania 11
PY - Paraguay 11
CO - Colombia 10
SA - Arabia Saudita 10
CH - Svizzera 9
GR - Grecia 7
HU - Ungheria 7
KE - Kenya 7
PK - Pakistan 7
AE - Emirati Arabi Uniti 6
RO - Romania 6
UZ - Uzbekistan 6
AM - Armenia 5
CZ - Repubblica Ceca 5
DZ - Algeria 5
AL - Albania 3
AZ - Azerbaigian 3
EG - Egitto 3
IL - Israele 3
KH - Cambogia 3
LV - Lettonia 3
MD - Moldavia 3
PE - Perù 3
SK - Slovacchia (Repubblica Slovacca) 3
SY - Repubblica araba siriana 3
VE - Venezuela 3
DK - Danimarca 2
ET - Etiopia 2
EU - Europa 2
GY - Guiana 2
HR - Croazia 2
IR - Iran 2
JM - Giamaica 2
JO - Giordania 2
KG - Kirghizistan 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
NI - Nicaragua 2
NP - Nepal 2
OM - Oman 2
PA - Panama 2
PH - Filippine 2
TH - Thailandia 2
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BW - Botswana 1
BY - Bielorussia 1
BZ - Belize 1
DO - Repubblica Dominicana 1
EE - Estonia 1
GA - Gabon 1
GD - Grenada 1
GE - Georgia 1
GN - Guinea 1
IS - Islanda 1
KI - Kiribati 1
KY - Cayman, isole 1
LI - Liechtenstein 1
LK - Sri Lanka 1
LU - Lussemburgo 1
Totale 14.077
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Città #
Southend 785
Singapore 744
Moscow 638
Chandler 528
Jacksonville 503
Ashburn 361
Dallas 359
Hong Kong 358
Woodbridge 315
Dublin 256
Beijing 222
Ann Arbor 161
Houston 116
The Dalles 115
Lawrence 105
Princeton 105
Los Angeles 98
Wilmington 96
Verona 88
New York 78
Ho Chi Minh City 74
Shenyang 61
Jinan 60
Nanjing 58
Buffalo 56
Hanoi 52
Munich 51
São Paulo 51
Milan 50
Helsinki 45
Lancaster 41
Redmond 41
Redondo Beach 39
Tianjin 39
Sindelfingen 38
Columbus 37
Bologna 32
Changsha 32
Nanchang 32
Boardman 30
Tokyo 30
Rome 28
Santa Clara 28
Council Bluffs 27
Seattle 26
Vienna 25
Zhengzhou 25
Guangzhou 24
Hebei 24
Taizhou 23
London 22
Rio de Janeiro 22
Warsaw 22
Amsterdam 21
Norwalk 21
Taiyuan 21
Seoul 20
Denver 19
Dong Ket 19
Hangzhou 19
Jakarta 19
Haikou 18
Jiaxing 18
Lomé 18
Falkenstein 17
Nuremberg 17
Turku 15
Kent 14
Ningbo 14
Padova 14
San Francisco 14
Stockholm 14
Chicago 13
Boston 12
Brooklyn 12
Brussels 12
Campinas 12
Cotonou 12
Haiphong 12
Johannesburg 12
Atlanta 11
Falls Church 11
Frankfurt am Main 11
Phoenix 11
Boydton 10
Brasília 10
Dhaka 10
Guarulhos 10
Hyderabad 10
Lappeenranta 10
Orem 10
Redwood City 10
Charlotte 9
Curitiba 9
Lanzhou 9
Montreal 9
Salvador 9
Washington 9
Auburn Hills 8
Baghdad 8
Totale 7.899
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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] 501
Epilessia mioclono-astatica (EMA): studio elettroclinico longitudinale di 25 soggetti 321
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] 187
BERS-like epilepsy in subjects with focal gyral anomalies: electroclinical findings. 182
Alternating Hemiplegia of childhood: epilepsy and electroencephalographic investigations. 179
Postural control in childhood: investigating the neurodevelopmental gradient hypothesis 175
[Neurologic outcome in infants surgically treated for congenital cardiopathy: preliminary data]. 170
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 169
Efficacy of Levetiracetam in treatment of continous spike wave during sleep (CSWS) 156
A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy. 155
Benign myoclonic epilepsy in infancy (BMEI): a longitudinal electroclinical study of 22 cases. 150
Chiari 1 malformation in a child with febrile seizures, parasomnias, and sleep apnea syndrome 150
Encephalopathy related to status epilepticus during slow sleep (ESES) including Landau-Kleffner syndrome 149
The transition from pediatric to adult age in patients with Dravet Syndrome: A study on the current management pathways and the challenges ahead 149
Are there other types of benign focal epilepsies in childhood? 147
CDKL5 deficiency disorder in males: Five new variants and review of the literature 144
EEG diagnostic helpfulness in childhood epilepsies with focal cortical dysplasias. Electroclinical study of 62 personal cases 141
A study of 63 cases with eyelid mioclonia with or without absences: type of seizure or an epileptic syndrome? 141
Cromosoma 20 ad anello: studio elettroclinico di 3 osservazioni personali. 140
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 139
Utilizzo di lamotrigina come terapia aggiuntiva in età pediatrica: revisione della letteratura. 137
Epileptic spasms: interictal patterns. 133
Myoclonic status in non-progressive encephalopaties (MSNPE) 130
The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy 129
Clinical and EEG Features of Idiopathic Focal Epilepsies in Childhood 125
Electroclinical findings in childhood epilepsy with focal cortical dysplasia. (Abstract) 123
3D facial morphometry in Italian patients affected by Aicardi syndrome 123
Clinical dissection of early onset absence epilepsy in children and prognostic implications. 122
Adaptive behaviour in adolescents and adults with Dravet syndrome 121
Diaper changing-induced reflex seizures in CDKL5-related epilepsy 121
Brain MRI findings in Severe Myoclonic Epilepsy in Infancy and genotype-phenotype correlations. 120
EEG findings during "paroxysmal hemiplegia" in a patient with GLUT1-deficiency 120
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy 120
Non-convulsive febrile status epilepticus mimicking a postictal state after a febrile seizure: an ictal electroclinical and evolutive study 119
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 119
Absence seizures in the first 3 years of life: An electroclinical study of 46 cases 118
Aicardi Syndrome: Key Fetal MRI Features and Prenatal Differential Diagnosis 117
Myoclonic Status in Nonprogressive Encephalopathies 116
Epilepsy and disorders of cortical development in children with congenital cytomegalovirus infection 114
Tuberous sclerosis and epilepsy: Longitudinal electroclinical and neuroradiological study of 55 subjects [EPILESSIA E SCLEROSI TUBEROSA: STUDIO ELETTROCLINICO E NEURORADIOLOGICO DI 55 SOGGETTI] 114
Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center study 114
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. 111
SYNGAP1-related developmental and epileptic encephalopathy: The impact on daily life 110
Congenital hemiplegia and epilepsy: a retrospective clinical study of 78 patients 109
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. 109
Remote Teamwork Management of NORSE During the COVID-19 Lockdown 109
Epilessia e sclerosi tuberosa: studio elettroclinico e neuroradiologico di 55 soggetti. 108
Progressive myoclonic epilepsy and spinal muscular atrophy: One case report and review of the literature 108
Mioclonic-astatic epilepsy (MAE): Longitudinal electroclinical study of 25 subjects,Epilessia Mioclono-Astatica (EMA): Studio elettroclinico longitudinale di 25 soggetti 108
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome 107
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 107
Restless legs sindrome and attention-deficit/hyperactivity disorder: a review of the literature. 105
Childhood absence epilepsy and electroencephalographic focal abnormalities with or without clinical manifestations. 105
[Neurologic outcome in infants surgically treated for congenital cardiopathy: preliminary data]. 105
Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20. 104
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 103
Ring chromosome 20 syndrome: Report of 3 cases,Cromosoma 20 ad anello: Studio elettroclinico di 3 osservazioni personali 103
Candidate biomarkers from the integration of methylation and gene expression in discordant autistic sibling pairs 102
Individually tailored extratemporal epilepsy surgery in children: anatomo-electro-clinical features and outcome predictors in a population of 53 cases. 102
Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients 102
Somatic mosaicism of PCDH19 mutation in a family with low-penetrance EFMR. 101
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 101
Sociodemographic and clinical changes in pediatric in-patient admissions for mental health emergencies during the COVID-19 pandemic: March 2020 to June 2021 101
EEG features in Encephalopathy related to Status Epilepticus during slow Sleep 99
A registry for Dravet syndrome: The Italian experience 98
Myoclonic status in non-progressive encephalopathies 98
Neuroimaging Changes in Menkes Disease, Part 2 98
Temporal lobe epilepsy in children: electroclinical and neuroradiological study of 62 cases. 97
Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients. 97
Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance. 97
KETASER01 protocol: What went right and what went wrong 96
The partial occipital epilepsies in childhood: electroclinical delineation from the symptomatic to idiopatic cases. 96
Neuroimaging Changes in Menkes Disease, Part 1 96
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 96
The phenotype of SCN8A developmental and epileptic encephalopathy 95
Myoclonic status in non progressive encephalopathies. 94
Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients. 94
Epilepsy with myoclonic atonic seizures: an electroclinical study of 69 patients. 94
Pediatric Epilepsy - Myoclonic Status in Nonprogressive Encephalopathies 93
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy. 92
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective study 92
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. 91
Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study. 91
Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature. 91
SEPs in the congenital hemiplegia [APPORTO DEI POTENZIALI EVOCATI SOMESTESICI NELLO STUDIO DELLE EMIPLEGIE CONGENITE] 91
Is there a benign limbic epilepsy in children? 90
Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locus. 90
Epilepsy features in ARID1B-related Coffin-Siris syndrome 90
Clinical Reasoning: Hyperventilation-Induced Alternating Hemiplegia With Concomitant Hemispheric EEG Slowing in a 7-Year-Old Girl With Headache 89
Clinical characteristics of 80 subjects with KCNQ2-related encephalopathy: Results from a family-driven survey 89
Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome. 89
Epilepsy-related brain networks in ring chromosome 20 syndrome: An EEG-fMRI study. 89
Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life 89
Head circumferences of patients with Dravet syndrome show growth slowdown 88
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations. 86
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] 86
Gelastic seizures and “smiling spasms”: A peculiar ictal pattern 85
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations. 85
Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boys 85
Scotosensitive and photosensitive myoclonic seizures in an infant with trisomy 13. 84
Totale 11.920
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Categoria #
all - tutte 51.055
article - articoli 46.113
book - libri 0
conference - conferenze 917
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 4.025
Totale 102.110
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021354 0 0 0 0 0 74 13 64 64 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
2025/20264.728 548 322 498 1.121 1.827 412 0 0 0 0 0 0
Totale 14.301