CATALOGO DEI PRODOTTI DELLA RICERCA

DARRA, Francesca
 Distribuzione geografica
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Continente #
EU - Europa 5.027
NA - Nord America 4.355
AS - Asia 3.325
SA - Sud America 580
AF - Africa 82
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 3
Totale 13.392
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Nazione #
US - Stati Uniti d'America 4.285
RU - Federazione Russa 1.747
SG - Singapore 1.385
CN - Cina 1.036
GB - Regno Unito 966
IT - Italia 747
BR - Brasile 481
HK - Hong Kong 359
FR - Francia 315
IE - Irlanda 264
DE - Germania 249
SE - Svezia 243
VN - Vietnam 215
FI - Finlandia 213
KR - Corea 103
UA - Ucraina 69
AR - Argentina 45
NL - Olanda 42
AT - Austria 41
IN - India 38
ID - Indonesia 34
CA - Canada 32
TR - Turchia 29
JP - Giappone 28
MX - Messico 28
PL - Polonia 28
ES - Italia 21
TG - Togo 18
ZA - Sudafrica 17
AU - Australia 16
BD - Bangladesh 16
BE - Belgio 15
EC - Ecuador 14
IQ - Iraq 13
BJ - Benin 12
CL - Cile 11
PY - Paraguay 11
CO - Colombia 10
LT - Lituania 10
MA - Marocco 10
SA - Arabia Saudita 10
CH - Svizzera 9
GR - Grecia 7
HU - Ungheria 7
KE - Kenya 7
PK - Pakistan 6
RO - Romania 6
UZ - Uzbekistan 6
AE - Emirati Arabi Uniti 5
AM - Armenia 5
CZ - Repubblica Ceca 5
DZ - Algeria 4
AL - Albania 3
AZ - Azerbaigian 3
EG - Egitto 3
IL - Israele 3
KH - Cambogia 3
LV - Lettonia 3
MD - Moldavia 3
PE - Perù 3
SY - Repubblica araba siriana 3
DK - Danimarca 2
EU - Europa 2
GY - Guiana 2
HR - Croazia 2
IR - Iran 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
PA - Panama 2
PH - Filippine 2
SK - Slovacchia (Repubblica Slovacca) 2
TH - Thailandia 2
VE - Venezuela 2
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BW - Botswana 1
BZ - Belize 1
DO - Repubblica Dominicana 1
EE - Estonia 1
ET - Etiopia 1
GA - Gabon 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
MG - Madagascar 1
MR - Mauritania 1
MU - Mauritius 1
MY - Malesia 1
Totale 13.376
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Città #
Southend 785
Moscow 559
Singapore 544
Chandler 528
Jacksonville 503
Dallas 358
Hong Kong 358
Ashburn 321
Woodbridge 315
Dublin 256
Beijing 222
Ann Arbor 161
Houston 115
Lawrence 105
Princeton 105
Wilmington 96
Los Angeles 95
Verona 88
New York 76
Ho Chi Minh City 69
The Dalles 65
Shenyang 61
Jinan 60
Nanjing 58
Buffalo 56
Munich 51
Milan 50
São Paulo 50
Helsinki 45
Hanoi 44
Lancaster 41
Redmond 41
Redondo Beach 39
Tianjin 39
Sindelfingen 38
Columbus 37
Bologna 32
Changsha 32
Nanchang 32
Boardman 30
Rome 28
Santa Clara 28
Tokyo 28
Council Bluffs 27
Seattle 26
Zhengzhou 25
Hebei 24
Taizhou 23
Vienna 23
Guangzhou 21
London 21
Norwalk 21
Rio de Janeiro 21
Taiyuan 21
Warsaw 21
Amsterdam 20
Seoul 20
Dong Ket 19
Hangzhou 19
Jakarta 19
Denver 18
Haikou 18
Jiaxing 18
Lomé 18
Falkenstein 17
Nuremberg 16
Turku 15
Kent 14
Ningbo 14
Padova 14
San Francisco 14
Chicago 13
Brooklyn 12
Brussels 12
Campinas 12
Cotonou 12
Stockholm 12
Atlanta 11
Boston 11
Falls Church 11
Johannesburg 11
Boydton 10
Brasília 10
Hyderabad 10
Lappeenranta 10
Phoenix 10
Redwood City 10
Charlotte 9
Curitiba 9
Frankfurt am Main 9
Guarulhos 9
Lanzhou 9
Montreal 9
Orem 9
Salvador 9
Washington 9
Auburn Hills 8
Bari 8
Belo Horizonte 8
Dhaka 8
Totale 7.481
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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] 489
Epilessia mioclono-astatica (EMA): studio elettroclinico longitudinale di 25 soggetti 317
BERS-like epilepsy in subjects with focal gyral anomalies: electroclinical findings. 173
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] 172
Alternating Hemiplegia of childhood: epilepsy and electroencephalographic investigations. 169
Postural control in childhood: investigating the neurodevelopmental gradient hypothesis 167
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 159
[Neurologic outcome in infants surgically treated for congenital cardiopathy: preliminary data]. 158
A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy. 148
Encephalopathy related to status epilepticus during slow sleep (ESES) including Landau-Kleffner syndrome 146
Efficacy of Levetiracetam in treatment of continous spike wave during sleep (CSWS) 145
Chiari 1 malformation in a child with febrile seizures, parasomnias, and sleep apnea syndrome 144
Benign myoclonic epilepsy in infancy (BMEI): a longitudinal electroclinical study of 22 cases. 143
Are there other types of benign focal epilepsies in childhood? 141
The transition from pediatric to adult age in patients with Dravet Syndrome: A study on the current management pathways and the challenges ahead 139
CDKL5 deficiency disorder in males: Five new variants and review of the literature 138
Cromosoma 20 ad anello: studio elettroclinico di 3 osservazioni personali. 137
A study of 63 cases with eyelid mioclonia with or without absences: type of seizure or an epileptic syndrome? 133
EEG diagnostic helpfulness in childhood epilepsies with focal cortical dysplasias. Electroclinical study of 62 personal cases 132
Utilizzo di lamotrigina come terapia aggiuntiva in età pediatrica: revisione della letteratura. 131
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 131
Epileptic spasms: interictal patterns. 126
Myoclonic status in non-progressive encephalopaties (MSNPE) 126
The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy 123
Clinical and EEG Features of Idiopathic Focal Epilepsies in Childhood 122
Electroclinical findings in childhood epilepsy with focal cortical dysplasia. (Abstract) 120
Clinical dissection of early onset absence epilepsy in children and prognostic implications. 118
3D facial morphometry in Italian patients affected by Aicardi syndrome 118
EEG findings during "paroxysmal hemiplegia" in a patient with GLUT1-deficiency 115
Diaper changing-induced reflex seizures in CDKL5-related epilepsy 115
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 115
Adaptive behaviour in adolescents and adults with Dravet syndrome 114
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy 114
Brain MRI findings in Severe Myoclonic Epilepsy in Infancy and genotype-phenotype correlations. 113
Absence seizures in the first 3 years of life: An electroclinical study of 46 cases 113
Epilepsy and disorders of cortical development in children with congenital cytomegalovirus infection 111
Myoclonic Status in Nonprogressive Encephalopathies 111
Non-convulsive febrile status epilepticus mimicking a postictal state after a febrile seizure: an ictal electroclinical and evolutive study 110
Aicardi Syndrome: Key Fetal MRI Features and Prenatal Differential Diagnosis 109
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. 108
Tuberous sclerosis and epilepsy: Longitudinal electroclinical and neuroradiological study of 55 subjects [EPILESSIA E SCLEROSI TUBEROSA: STUDIO ELETTROCLINICO E NEURORADIOLOGICO DI 55 SOGGETTI] 108
Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center study 108
Congenital hemiplegia and epilepsy: a retrospective clinical study of 78 patients 105
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. 104
Epilessia e sclerosi tuberosa: studio elettroclinico e neuroradiologico di 55 soggetti. 103
Restless legs sindrome and attention-deficit/hyperactivity disorder: a review of the literature. 103
Remote Teamwork Management of NORSE During the COVID-19 Lockdown 103
Mioclonic-astatic epilepsy (MAE): Longitudinal electroclinical study of 25 subjects,Epilessia Mioclono-Astatica (EMA): Studio elettroclinico longitudinale di 25 soggetti 103
Childhood absence epilepsy and electroencephalographic focal abnormalities with or without clinical manifestations. 102
Progressive myoclonic epilepsy and spinal muscular atrophy: One case report and review of the literature 102
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome 102
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 102
Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20. 100
SYNGAP1-related developmental and epileptic encephalopathy: The impact on daily life 100
Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients 99
[Neurologic outcome in infants surgically treated for congenital cardiopathy: preliminary data]. 99
Individually tailored extratemporal epilepsy surgery in children: anatomo-electro-clinical features and outcome predictors in a population of 53 cases. 98
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 97
Somatic mosaicism of PCDH19 mutation in a family with low-penetrance EFMR. 97
Ring chromosome 20 syndrome: Report of 3 cases,Cromosoma 20 ad anello: Studio elettroclinico di 3 osservazioni personali 97
Sociodemographic and clinical changes in pediatric in-patient admissions for mental health emergencies during the COVID-19 pandemic: March 2020 to June 2021 97
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 96
Candidate biomarkers from the integration of methylation and gene expression in discordant autistic sibling pairs 95
Neuroimaging Changes in Menkes Disease, Part 2 95
Myoclonic status in non-progressive encephalopathies 94
EEG features in Encephalopathy related to Status Epilepticus during slow Sleep 94
KETASER01 protocol: What went right and what went wrong 93
Temporal lobe epilepsy in children: electroclinical and neuroradiological study of 62 cases. 93
Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients. 93
Neuroimaging Changes in Menkes Disease, Part 1 93
Myoclonic status in non progressive encephalopathies. 92
The partial occipital epilepsies in childhood: electroclinical delineation from the symptomatic to idiopatic cases. 92
Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance. 92
A registry for Dravet syndrome: The Italian experience 91
Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients. 91
The phenotype of SCN8A developmental and epileptic encephalopathy 91
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 91
SEPs in the congenital hemiplegia [APPORTO DEI POTENZIALI EVOCATI SOMESTESICI NELLO STUDIO DELLE EMIPLEGIE CONGENITE] 90
Pediatric Epilepsy - Myoclonic Status in Nonprogressive Encephalopathies 90
Epilepsy with myoclonic atonic seizures: an electroclinical study of 69 patients. 89
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective study 89
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy. 88
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. 87
Is there a benign limbic epilepsy in children? 86
Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study. 86
Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature. 85
Multicenter prospective longitudinal study in 34 patients with Dravet syndrome: Neuropsychological development in the first six years of life 85
Clinical characteristics of 80 subjects with KCNQ2-related encephalopathy: Results from a family-driven survey 84
Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome. 84
Head circumferences of patients with Dravet syndrome show growth slowdown 84
Epilepsy features in ARID1B-related Coffin-Siris syndrome 84
Clinical Reasoning: Hyperventilation-Induced Alternating Hemiplegia With Concomitant Hemispheric EEG Slowing in a 7-Year-Old Girl With Headache 83
Scotosensitive and photosensitive myoclonic seizures in an infant with trisomy 13. 83
Epilepsy-related brain networks in ring chromosome 20 syndrome: An EEG-fMRI study. 83
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations. 82
Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locus. 82
Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boys 82
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations. 81
Periventricular heterotopia in fragile X sindrome. 79
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] 79
Totale 11.373
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Categoria #
all - tutte 49.371
article - articoli 44.597
book - libri 0
conference - conferenze 880
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 3.894
Totale 98.742
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021463 0 0 0 0 109 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
2025/20264.024 548 322 498 1.121 1.535 0 0 0 0 0 0 0
Totale 13.597