CATALOGO DEI PRODOTTI DELLA RICERCA

DARRA, Francesca
 Distribuzione geografica
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Continente #
NA - Nord America 3.891
EU - Europa 3.471
AS - Asia 2.752
SA - Sud America 414
AF - Africa 51
OC - Oceania 18
Continente sconosciuto - Info sul continente non disponibili 2
Totale 10.599
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Nazione #
US - Stati Uniti d'America 3.850
SG - Singapore 1.185
GB - Regno Unito 926
CN - Cina 880
IT - Italia 735
BR - Brasile 363
HK - Hong Kong 353
FR - Francia 315
RU - Federazione Russa 300
IE - Irlanda 264
DE - Germania 238
SE - Svezia 237
FI - Finlandia 212
KR - Corea 91
VN - Vietnam 73
UA - Ucraina 65
AT - Austria 38
NL - Olanda 36
IN - India 30
TR - Turchia 26
AR - Argentina 20
ID - Indonesia 20
CA - Canada 19
TG - Togo 18
JP - Giappone 17
PL - Polonia 17
ES - Italia 16
AU - Australia 15
BE - Belgio 15
BD - Bangladesh 12
MX - Messico 12
IQ - Iraq 10
MA - Marocco 9
SA - Arabia Saudita 9
CL - Cile 8
ZA - Sudafrica 8
CH - Svizzera 7
PY - Paraguay 7
EC - Ecuador 6
GR - Grecia 6
HU - Ungheria 6
RO - Romania 6
AM - Armenia 5
CO - Colombia 5
CZ - Repubblica Ceca 5
LT - Lituania 5
UZ - Uzbekistan 5
AE - Emirati Arabi Uniti 3
AL - Albania 3
AZ - Azerbaigian 3
DZ - Algeria 3
IL - Israele 3
KE - Kenya 3
LV - Lettonia 3
MD - Moldavia 3
PK - Pakistan 3
DK - Danimarca 2
EG - Egitto 2
EU - Europa 2
HR - Croazia 2
JO - Giordania 2
KG - Kirghizistan 2
KH - Cambogia 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
LB - Libano 2
NI - Nicaragua 2
PA - Panama 2
PE - Perù 2
SK - Slovacchia (Repubblica Slovacca) 2
SY - Repubblica araba siriana 2
TH - Thailandia 2
VE - Venezuela 2
BB - Barbados 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BZ - Belize 1
DO - Repubblica Dominicana 1
EE - Estonia 1
ET - Etiopia 1
GA - Gabon 1
GE - Georgia 1
GN - Guinea 1
GY - Guiana 1
IR - Iran 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
MZ - Mozambico 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PH - Filippine 1
PT - Portogallo 1
SN - Senegal 1
Totale 10.593
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Città #
Southend 785
Chandler 528
Singapore 527
Jacksonville 503
Hong Kong 352
Dallas 323
Woodbridge 315
Dublin 256
Ashburn 211
Beijing 170
Ann Arbor 161
Houston 106
Lawrence 105
Princeton 105
Wilmington 96
Verona 88
The Dalles 65
Shenyang 61
Jinan 60
Nanjing 58
New York 53
Munich 51
Milan 46
Helsinki 45
Los Angeles 45
Lancaster 41
Redmond 41
Sindelfingen 38
Columbus 37
Tianjin 34
Bologna 32
Nanchang 32
São Paulo 32
Changsha 31
Boardman 27
Buffalo 27
Council Bluffs 25
Hebei 24
Rome 24
Seattle 24
Zhengzhou 24
Santa Clara 23
Taizhou 23
Vienna 23
Norwalk 21
Guangzhou 20
Taiyuan 20
Dong Ket 19
Ho Chi Minh City 19
Seoul 19
Haikou 18
Jiaxing 18
Lomé 18
Rio de Janeiro 18
Tokyo 17
Hangzhou 16
Nuremberg 16
Amsterdam 15
Jakarta 15
Moscow 15
Turku 15
Kent 14
Ningbo 14
Padova 14
San Francisco 13
Brussels 12
Chicago 11
Falls Church 11
Redondo Beach 11
Warsaw 11
Boydton 10
Campinas 10
Hyderabad 10
Redwood City 10
Brooklyn 9
Frankfurt am Main 9
Lanzhou 9
Lappeenranta 9
Washington 9
Auburn Hills 8
Bari 8
Curitiba 8
Dhaka 8
Fairfield 8
Hanoi 8
London 8
Brasília 7
Dongguan 7
Falkenstein 7
Phoenix 7
Riyadh 7
Stockholm 7
Toronto 7
Belo Horizonte 6
Boston 6
Brescia 6
Detroit 6
Florence 6
Goiânia 6
Guarulhos 6
Totale 6.319
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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] 449
Epilessia mioclono-astatica (EMA): studio elettroclinico longitudinale di 25 soggetti 307
BERS-like epilepsy in subjects with focal gyral anomalies: electroclinical findings. 135
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 132
Encephalopathy related to status epilepticus during slow sleep (ESES) including Landau-Kleffner syndrome 130
EEG diagnostic helpfulness in childhood epilepsies with focal cortical dysplasias. Electroclinical study of 62 personal cases 122
Alternating Hemiplegia of childhood: epilepsy and electroencephalographic investigations. 122
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] 122
Utilizzo di lamotrigina come terapia aggiuntiva in età pediatrica: revisione della letteratura. 119
Cromosoma 20 ad anello: studio elettroclinico di 3 osservazioni personali. 116
Benign myoclonic epilepsy in infancy (BMEI): a longitudinal electroclinical study of 22 cases. 115
Clinical and EEG Features of Idiopathic Focal Epilepsies in Childhood 113
Myoclonic status in non-progressive encephalopaties (MSNPE) 112
The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy 112
Electroclinical findings in childhood epilepsy with focal cortical dysplasia. (Abstract) 111
Chiari 1 malformation in a child with febrile seizures, parasomnias, and sleep apnea syndrome 110
Postural control in childhood: investigating the neurodevelopmental gradient hypothesis 110
[Neurologic outcome in infants surgically treated for congenital cardiopathy: preliminary data]. 109
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 109
Efficacy of Levetiracetam in treatment of continous spike wave during sleep (CSWS) 108
Clinical dissection of early onset absence epilepsy in children and prognostic implications. 107
The transition from pediatric to adult age in patients with Dravet Syndrome: A study on the current management pathways and the challenges ahead 107
Are there other types of benign focal epilepsies in childhood? 106
A study of 63 cases with eyelid mioclonia with or without absences: type of seizure or an epileptic syndrome? 106
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy 105
Epilepsy and disorders of cortical development in children with congenital cytomegalovirus infection 104
Epileptic spasms: interictal patterns. 101
Tuberous sclerosis and epilepsy: Longitudinal electroclinical and neuroradiological study of 55 subjects [EPILESSIA E SCLEROSI TUBEROSA: STUDIO ELETTROCLINICO E NEURORADIOLOGICO DI 55 SOGGETTI] 98
A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy. 98
Progressive myoclonic epilepsy and spinal muscular atrophy: One case report and review of the literature 97
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. 97
Congenital hemiplegia and epilepsy: a retrospective clinical study of 78 patients 96
Epilessia e sclerosi tuberosa: studio elettroclinico e neuroradiologico di 55 soggetti. 95
Childhood absence epilepsy and electroencephalographic focal abnormalities with or without clinical manifestations. 93
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome 92
Brain MRI findings in Severe Myoclonic Epilepsy in Infancy and genotype-phenotype correlations. 90
Absence seizures in the first 3 years of life: An electroclinical study of 46 cases 90
Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20. 90
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 90
Somatic mosaicism of PCDH19 mutation in a family with low-penetrance EFMR. 89
Individually tailored extratemporal epilepsy surgery in children: anatomo-electro-clinical features and outcome predictors in a population of 53 cases. 88
EEG findings during "paroxysmal hemiplegia" in a patient with GLUT1-deficiency 88
CDKL5 deficiency disorder in males: Five new variants and review of the literature 88
Restless legs sindrome and attention-deficit/hyperactivity disorder: a review of the literature. 87
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. 87
Myoclonic Status in Nonprogressive Encephalopathies 87
Temporal lobe epilepsy in children: electroclinical and neuroradiological study of 62 cases. 85
Diaper changing-induced reflex seizures in CDKL5-related epilepsy 84
Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients. 83
The partial occipital epilepsies in childhood: electroclinical delineation from the symptomatic to idiopatic cases. 83
Myoclonic status in non-progressive encephalopathies 82
Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance. 82
SEPs in the congenital hemiplegia [APPORTO DEI POTENZIALI EVOCATI SOMESTESICI NELLO STUDIO DELLE EMIPLEGIE CONGENITE] 82
Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center study 82
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy. 81
Mioclonic-astatic epilepsy (MAE): Longitudinal electroclinical study of 25 subjects,Epilessia Mioclono-Astatica (EMA): Studio elettroclinico longitudinale di 25 soggetti 81
Aicardi Syndrome: Key Fetal MRI Features and Prenatal Differential Diagnosis 80
3D facial morphometry in Italian patients affected by Aicardi syndrome 80
Epilepsy with myoclonic atonic seizures: an electroclinical study of 69 patients. 78
Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients 78
SYNGAP1-related developmental and epileptic encephalopathy: The impact on daily life 78
Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study. 77
Neuroimaging Changes in Menkes Disease, Part 2 77
Epilepsy-related brain networks in ring chromosome 20 syndrome: An EEG-fMRI study. 77
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. 76
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations. 75
Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome. 75
Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature. 75
Remote Teamwork Management of NORSE During the COVID-19 Lockdown 75
Myoclonic status in non progressive encephalopathies. 73
Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients. 73
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 73
Is there a benign limbic epilepsy in children? 72
Uncombable hair syndrome, mental retardation, single palmar crease and arched palate in a patient with neurofibromatosis type I 72
Pediatric Epilepsy - Myoclonic Status in Nonprogressive Encephalopathies 72
EEG features in Encephalopathy related to Status Epilepticus during slow Sleep 72
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations. 71
Neuroimaging Changes in Menkes Disease, Part 1 71
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 71
Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boys 71
Adaptive behaviour in adolescents and adults with Dravet syndrome 70
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15) 70
Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locus. 69
Scotosensitive and photosensitive myoclonic seizures in an infant with trisomy 13. 69
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] 69
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective study 69
Ring chromosome 20 syndrome: a link between epilepsy onset and neuropsychological impairment in three children. 68
Clinical spectrum of STX1B-related epileptic disorders 68
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 66
[Neurologic outcome in infants surgically treated for congenital cardiopathy: preliminary data]. 65
Sociodemographic and clinical changes in pediatric in-patient admissions for mental health emergencies during the COVID-19 pandemic: March 2020 to June 2021 65
Different clinical and immunological presentation of ataxia-telangiectasia within the same family. 64
Ring chromosome 20 syndrome: Report of 3 cases,Cromosoma 20 ad anello: Studio elettroclinico di 3 osservazioni personali 64
Periventricular heterotopia in fragile X sindrome. 63
Refining the phenotype associated with MEF2C haploinsufficiency 63
The phenotype of SCN8A developmental and epileptic encephalopathy 63
Familial Ohtahara syndrome due to a novel ARX gene mutation 62
Electroclinical findings in four patients with karyotype 47,XYY 61
Epilepsy features in ARID1B-related Coffin-Siris syndrome 61
Candidate biomarkers from the integration of methylation and gene expression in discordant autistic sibling pairs 60
Totale 9.265
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Categoria #
all - tutte 43.298
article - articoli 39.038
book - libri 0
conference - conferenze 779
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 3.481
Totale 86.596
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021562 0 0 27 72 109 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
2025/20261.229 548 322 359 0 0 0 0 0 0 0 0 0
Totale 10.802