CATALOGO DEI PRODOTTI DELLA RICERCA

DARRA, Francesca
 Distribuzione geografica
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Continente #
EU - Europa 3.236
NA - Nord America 3.167
AS - Asia 1.446
SA - Sud America 51
AF - Africa 27
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 2
Totale 7.942
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Nazione #
US - Stati Uniti d'America 3.152
GB - Regno Unito 909
CN - Cina 818
IT - Italia 691
SG - Singapore 478
FR - Francia 301
RU - Federazione Russa 295
IE - Irlanda 265
SE - Svezia 234
FI - Finlandia 196
DE - Germania 171
UA - Ucraina 63
BR - Brasile 42
VN - Vietnam 30
NL - Olanda 21
AT - Austria 20
HK - Hong Kong 20
KR - Corea 18
TG - Togo 18
ID - Indonesia 17
BE - Belgio 16
JP - Giappone 15
AU - Australia 12
CA - Canada 11
TR - Turchia 11
PL - Polonia 8
IN - India 7
CH - Svizzera 6
GR - Grecia 6
CL - Cile 5
ES - Italia 5
HU - Ungheria 5
MA - Marocco 5
RO - Romania 5
BD - Bangladesh 4
SA - Arabia Saudita 4
AM - Armenia 3
CZ - Repubblica Ceca 3
AL - Albania 2
AR - Argentina 2
EG - Egitto 2
EU - Europa 2
HR - Croazia 2
IL - Israele 2
KG - Kirghizistan 2
LA - Repubblica Popolare Democratica del Laos 2
LV - Lettonia 2
MD - Moldavia 2
MX - Messico 2
TH - Thailandia 2
AE - Emirati Arabi Uniti 1
AZ - Azerbaigian 1
BG - Bulgaria 1
BN - Brunei Darussalam 1
BZ - Belize 1
EC - Ecuador 1
EE - Estonia 1
IQ - Iraq 1
IR - Iran 1
IS - Islanda 1
JO - Giordania 1
KE - Kenya 1
KZ - Kazakistan 1
LI - Liechtenstein 1
LK - Sri Lanka 1
LT - Lituania 1
LU - Lussemburgo 1
MZ - Mozambico 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PA - Panama 1
PE - Perù 1
PH - Filippine 1
PK - Pakistan 1
PT - Portogallo 1
TW - Taiwan 1
UZ - Uzbekistan 1
Totale 7.942
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Città #
Southend 785
Chandler 538
Jacksonville 503
Singapore 379
Woodbridge 315
Dublin 258
Ashburn 179
Ann Arbor 161
Beijing 158
Lawrence 106
Princeton 106
Houston 105
Wilmington 97
Verona 83
Shenyang 61
Jinan 59
Nanjing 57
Helsinki 46
New York 45
Milan 42
Redmond 42
Lancaster 41
Sindelfingen 39
Tianjin 34
Nanchang 32
Bologna 29
Changsha 28
Boardman 24
Hebei 24
Seattle 24
Zhengzhou 24
Taizhou 23
Norwalk 21
Hong Kong 20
Taiyuan 20
Dong Ket 19
Rome 19
Haikou 18
Jiaxing 18
Lomé 18
Seoul 18
Guangzhou 17
Hangzhou 15
Jakarta 15
Ningbo 15
Santa Clara 15
Tokyo 15
Dallas 14
Kent 14
Moscow 14
Padova 14
Brussels 13
Vienna 13
Chicago 12
Falls Church 11
Boydton 10
Los Angeles 10
Redwood City 10
Fairfield 9
Lanzhou 9
San Francisco 9
Auburn Hills 8
Bari 8
Dongguan 8
Washington 8
Amsterdam 7
Falkenstein 7
Lappeenranta 7
Brescia 6
Detroit 6
Melbourne 6
São Paulo 6
Torino 6
Gothenburg 5
Groningen 5
Nuremberg 5
Paris 5
Toronto 5
Torrile 5
Atlanta 4
Berlin 4
Bussolengo 4
Cambridge 4
Edinburgh 4
Florence 4
Frankfurt am Main 4
Fuzhou 4
Lapeer 4
London 4
Mantova 4
Napoli 4
Novokuznetsk 4
Ottawa 4
Palermo 4
Phoenix 4
Pisa 4
Puerto Varas 4
Riyadh 4
San Diego 4
Sant'Ambrogio di Valpolicella 4
Totale 5.069
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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] 413
Epilessia mioclono-astatica (EMA): studio elettroclinico longitudinale di 25 soggetti 289
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 115
BERS-like epilepsy in subjects with focal gyral anomalies: electroclinical findings. 107
Utilizzo di lamotrigina come terapia aggiuntiva in età pediatrica: revisione della letteratura. 105
EEG diagnostic helpfulness in childhood epilepsies with focal cortical dysplasias. Electroclinical study of 62 personal cases 104
Encephalopathy related to status epilepticus during slow sleep (ESES) including Landau-Kleffner syndrome 102
Cromosoma 20 ad anello: studio elettroclinico di 3 osservazioni personali. 100
Alternating Hemiplegia of childhood: epilepsy and electroencephalographic investigations. 97
Clinical and EEG Features of Idiopathic Focal Epilepsies in Childhood 97
Electroclinical findings in childhood epilepsy with focal cortical dysplasia. (Abstract) 96
Benign myoclonic epilepsy in infancy (BMEI): a longitudinal electroclinical study of 22 cases. 94
Myoclonic status in non-progressive encephalopaties (MSNPE) 94
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] 92
The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy 92
Clinical dissection of early onset absence epilepsy in children and prognostic implications. 89
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 89
Chiari 1 malformation in a child with febrile seizures, parasomnias, and sleep apnea syndrome 89
Epilepsy and disorders of cortical development in children with congenital cytomegalovirus infection 87
Congenital hemiplegia and epilepsy: a retrospective clinical study of 78 patients 84
Epileptic spasms: interictal patterns. 84
Are there other types of benign focal epilepsies in childhood? 83
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy 83
A study of 63 cases with eyelid mioclonia with or without absences: type of seizure or an epileptic syndrome? 79
[Neurologic outcome in infants surgically treated for congenital cardiopathy: preliminary data]. 79
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. 79
Tuberous sclerosis and epilepsy: Longitudinal electroclinical and neuroradiological study of 55 subjects [EPILESSIA E SCLEROSI TUBEROSA: STUDIO ELETTROCLINICO E NEURORADIOLOGICO DI 55 SOGGETTI] 78
Efficacy of Levetiracetam in treatment of continous spike wave during sleep (CSWS) 76
Progressive myoclonic epilepsy and spinal muscular atrophy: One case report and review of the literature 75
Somatic mosaicism of PCDH19 mutation in a family with low-penetrance EFMR. 75
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome 75
Epilessia e sclerosi tuberosa: studio elettroclinico e neuroradiologico di 55 soggetti. 73
Postural control in childhood: investigating the neurodevelopmental gradient hypothesis 73
A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy. 73
Childhood absence epilepsy and electroencephalographic focal abnormalities with or without clinical manifestations. 72
The partial occipital epilepsies in childhood: electroclinical delineation from the symptomatic to idiopatic cases. 72
Brain MRI findings in Severe Myoclonic Epilepsy in Infancy and genotype-phenotype correlations. 70
Restless legs sindrome and attention-deficit/hyperactivity disorder: a review of the literature. 69
Diaper changing-induced reflex seizures in CDKL5-related epilepsy 69
Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients. 68
SEPs in the congenital hemiplegia [APPORTO DEI POTENZIALI EVOCATI SOMESTESICI NELLO STUDIO DELLE EMIPLEGIE CONGENITE] 68
Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20. 67
Individually tailored extratemporal epilepsy surgery in children: anatomo-electro-clinical features and outcome predictors in a population of 53 cases. 67
Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance. 67
Epilepsy with myoclonic atonic seizures: an electroclinical study of 69 patients. 67
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 67
Absence seizures in the first 3 years of life: An electroclinical study of 46 cases 66
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy. 66
Myoclonic status in non-progressive encephalopathies 65
EEG findings during "paroxysmal hemiplegia" in a patient with GLUT1-deficiency 65
Temporal lobe epilepsy in children: electroclinical and neuroradiological study of 62 cases. 64
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. 64
Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study. 63
Myoclonic Status in Nonprogressive Encephalopathies 63
Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature. 62
Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients 62
3D facial morphometry in Italian patients affected by Aicardi syndrome 62
Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boys 62
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations. 61
Uncombable hair syndrome, mental retardation, single palmar crease and arched palate in a patient with neurofibromatosis type I 61
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations. 61
Epilepsy-related brain networks in ring chromosome 20 syndrome: An EEG-fMRI study. 61
Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome. 60
Neuroimaging Changes in Menkes Disease, Part 2 60
Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center study 60
Pediatric Epilepsy - Myoclonic Status in Nonprogressive Encephalopathies 58
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15) 57
Aicardi Syndrome: Key Fetal MRI Features and Prenatal Differential Diagnosis 57
Mioclonic-astatic epilepsy (MAE): Longitudinal electroclinical study of 25 subjects,Epilessia Mioclono-Astatica (EMA): Studio elettroclinico longitudinale di 25 soggetti 57
SYNGAP1-related developmental and epileptic encephalopathy: The impact on daily life 55
Clinical spectrum of STX1B-related epileptic disorders 54
Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients. 53
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. 53
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective study 53
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 53
Is there a benign limbic epilepsy in children? 52
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] 52
Remote Teamwork Management of NORSE During the COVID-19 Lockdown 52
CDKL5 deficiency disorder in males: Five new variants and review of the literature 52
Myoclonic status in non progressive encephalopathies. 51
Different clinical and immunological presentation of ataxia-telangiectasia within the same family. 51
Ring chromosome 20 syndrome: a link between epilepsy onset and neuropsychological impairment in three children. 51
Neuroimaging Changes in Menkes Disease, Part 1 51
Scotosensitive and photosensitive myoclonic seizures in an infant with trisomy 13. 50
Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locus. 49
Refining the phenotype associated with MEF2C haploinsufficiency 49
null 49
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 49
Efficacy of Levetiracetam in treatment of continous spike wave during sleep (CSWS),Efficacia del Levetiracetam nel trattamento dello stato di punta onda continua del sonno (POCS) 49
Periventricular heterotopia in fragile X sindrome. 48
EEG features in Encephalopathy related to Status Epilepticus during slow Sleep 48
Adaptive behaviour in adolescents and adults with Dravet syndrome 47
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 47
Ring chromosome 20 syndrome: Report of 3 cases,Cromosoma 20 ad anello: Studio elettroclinico di 3 osservazioni personali 47
The phenotype of SCN8A developmental and epileptic encephalopathy 46
The transition from pediatric to adult age in patients with Dravet Syndrome: A study on the current management pathways and the challenges ahead 46
Electroclinical findings in four patients with karyotype 47,XYY 45
Familial Ohtahara syndrome due to a novel ARX gene mutation 44
Sociodemographic and clinical changes in pediatric in-patient admissions for mental health emergencies during the COVID-19 pandemic: March 2020 to June 2021 44
Epilepsy features in ARID1B-related Coffin-Siris syndrome 40
Totale 7.290
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Categoria #
all - tutte 32.089
article - articoli 28.844
book - libri 0
conference - conferenze 562
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.683
Totale 64.178
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020450 0 0 0 0 0 0 93 48 12 100 92 105
2020/2021771 70 139 27 72 109 74 13 64 64 6 90 43
2021/2022758 82 187 4 20 21 20 16 59 26 36 76 211
2022/20231.709 128 115 161 296 168 382 43 123 193 15 57 28
2023/2024863 44 58 78 81 137 107 41 42 12 57 138 68
2024/20251.162 151 163 92 443 134 116 63 0 0 0 0 0
Totale 8.137