CATALOGO DEI PRODOTTI DELLA RICERCA

DARRA, Francesca
 Distribuzione geografica
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Continente #
NA - Nord America 3.030
EU - Europa 2.835
AS - Asia 908
SA - Sud America 13
OC - Oceania 8
AF - Africa 6
Continente sconosciuto - Info sul continente non disponibili 2
Totale 6.802
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Nazione #
US - Stati Uniti d'America 3.022
GB - Regno Unito 903
CN - Cina 690
IT - Italia 647
FR - Francia 301
IE - Irlanda 261
SE - Svezia 225
FI - Finlandia 174
DE - Germania 159
SG - Singapore 99
UA - Ucraina 63
VN - Vietnam 30
RU - Federazione Russa 24
HK - Hong Kong 18
KR - Corea 18
BE - Belgio 16
NL - Olanda 16
JP - Giappone 15
TR - Turchia 9
AT - Austria 8
AU - Australia 8
CA - Canada 6
IN - India 6
PL - Polonia 6
BR - Brasile 5
CH - Svizzera 5
CL - Cile 5
ES - Italia 5
GR - Grecia 5
HU - Ungheria 4
SA - Arabia Saudita 4
MA - Marocco 3
RO - Romania 3
AL - Albania 2
AR - Argentina 2
BD - Bangladesh 2
CZ - Repubblica Ceca 2
EU - Europa 2
IL - Israele 2
KG - Kirghizistan 2
LA - Repubblica Popolare Democratica del Laos 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
BG - Bulgaria 1
BZ - Belize 1
EC - Ecuador 1
EG - Egitto 1
ID - Indonesia 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
LU - Lussemburgo 1
MD - Moldavia 1
MZ - Mozambico 1
PA - Panama 1
PH - Filippine 1
PT - Portogallo 1
TH - Thailandia 1
UZ - Uzbekistan 1
Totale 6.802
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Città #
Southend 785
Chandler 538
Jacksonville 503
Woodbridge 315
Dublin 254
Ann Arbor 161
Beijing 157
Ashburn 154
Lawrence 106
Princeton 106
Houston 105
Wilmington 97
Verona 75
Shenyang 61
Jinan 59
Singapore 59
Nanjing 57
New York 45
Redmond 42
Lancaster 41
Sindelfingen 39
Tianjin 34
Milan 33
Nanchang 32
Bologna 29
Changsha 27
Helsinki 25
Boardman 24
Hebei 24
Seattle 23
Zhengzhou 23
Taizhou 22
Norwalk 21
Dong Ket 19
Taiyuan 19
Haikou 18
Hong Kong 18
Jiaxing 18
Seoul 18
Rome 16
Hangzhou 15
Ningbo 15
Tokyo 15
Kent 14
Padova 14
Brussels 13
Falls Church 11
Guangzhou 11
Boydton 10
Redwood City 10
Fairfield 9
Auburn Hills 8
Dongguan 8
Los Angeles 8
Vienna 8
Washington 8
Lanzhou 7
San Francisco 7
Bari 6
Brescia 6
Chicago 6
Detroit 6
Lappeenranta 6
Torino 6
Paris 5
Torrile 5
Amsterdam 4
Atlanta 4
Berlin 4
Bussolengo 4
Edinburgh 4
Florence 4
Fuzhou 4
Groningen 4
Lapeer 4
Melbourne 4
Moscow 4
Napoli 4
Novokuznetsk 4
Palermo 4
Pisa 4
Puerto Varas 4
Riyadh 4
San Diego 4
Sant'Ambrogio di Valpolicella 4
Taranto 4
Chions 3
Clearwater 3
Cork 3
Faenza 3
Frankfurt am Main 3
Kemerovo 3
Madrid 3
Nuremberg 3
Palo Del Colle 3
Phoenix 3
Prato 3
Tappahannock 3
Trebaseleghe 3
Voronezh 3
Totale 4.561
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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] 401
Epilessia mioclono-astatica (EMA): studio elettroclinico longitudinale di 25 soggetti 284
Utilizzo di lamotrigina come terapia aggiuntiva in età pediatrica: revisione della letteratura. 98
BERS-like epilepsy in subjects with focal gyral anomalies: electroclinical findings. 98
EEG diagnostic helpfulness in childhood epilepsies with focal cortical dysplasias. Electroclinical study of 62 personal cases 96
Cromosoma 20 ad anello: studio elettroclinico di 3 osservazioni personali. 93
Encephalopathy related to status epilepticus during slow sleep (ESES) including Landau-Kleffner syndrome 91
Electroclinical findings in childhood epilepsy with focal cortical dysplasia. (Abstract) 89
Clinical and EEG Features of Idiopathic Focal Epilepsies in Childhood 89
Alternating Hemiplegia of childhood: epilepsy and electroencephalographic investigations. 84
Benign myoclonic epilepsy in infancy (BMEI): a longitudinal electroclinical study of 22 cases. 83
Myoclonic status in non-progressive encephalopaties (MSNPE) 83
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] 83
Clinical dissection of early onset absence epilepsy in children and prognostic implications. 82
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 79
Epilepsy and disorders of cortical development in children with congenital cytomegalovirus infection 78
Congenital hemiplegia and epilepsy: a retrospective clinical study of 78 patients 78
Chiari 1 malformation in a child with febrile seizures, parasomnias, and sleep apnea syndrome 78
Epileptic spasms: interictal patterns. 77
A study of 63 cases with eyelid mioclonia with or without absences: type of seizure or an epileptic syndrome? 76
Are there other types of benign focal epilepsies in childhood? 75
Congenital disorders of glycosylation presenting as epileptic encephalopathy with migrating partial seizures in infancy 75
Efficacy of Levetiracetam in treatment of continous spike wave during sleep (CSWS) 71
Somatic mosaicism of PCDH19 mutation in a family with low-penetrance EFMR. 70
Tuberous sclerosis and epilepsy: Longitudinal electroclinical and neuroradiological study of 55 subjects [EPILESSIA E SCLEROSI TUBEROSA: STUDIO ELETTROCLINICO E NEURORADIOLOGICO DI 55 SOGGETTI] 70
Childhood absence epilepsy and electroencephalographic focal abnormalities with or without clinical manifestations. 69
The ketogenic diet in patients with myoclonic status in non-progressive encephalopathy 69
Epilessia e sclerosi tuberosa: studio elettroclinico e neuroradiologico di 55 soggetti. 68
Early-onset absence epilepsy: SLC2A1 gene analysis and treatment evolution. 68
[Neurologic outcome in infants surgically treated for congenital cardiopathy: preliminary data]. 67
Progressive myoclonic epilepsy and spinal muscular atrophy: One case report and review of the literature 67
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome 67
Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients. 65
The partial occipital epilepsies in childhood: electroclinical delineation from the symptomatic to idiopatic cases. 65
A multicenter, randomized, placebo-controlled trial of levetiracetam in children and adolescents with newly diagnosed absence epilepsy. 65
Postural control in childhood: investigating the neurodevelopmental gradient hypothesis 64
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 64
Brain MRI findings in Severe Myoclonic Epilepsy in Infancy and genotype-phenotype correlations. 63
Restless legs sindrome and attention-deficit/hyperactivity disorder: a review of the literature. 61
Low frequency mu-like activity characterizes cortical rhythms in epilepsy due to ring chromosome 20. 60
Genetic testing in benign familial epilepsies of the first year of life: Clinical and diagnostic significance. 60
SEPs in the congenital hemiplegia [APPORTO DEI POTENZIALI EVOCATI SOMESTESICI NELLO STUDIO DELLE EMIPLEGIE CONGENITE] 60
Diaper changing-induced reflex seizures in CDKL5-related epilepsy 60
Myoclonic status in non-progressive encephalopathies 59
Individually tailored extratemporal epilepsy surgery in children: anatomo-electro-clinical features and outcome predictors in a population of 53 cases. 59
EEG findings during "paroxysmal hemiplegia" in a patient with GLUT1-deficiency 59
Absence seizures in the first 3 years of life: An electroclinical study of 46 cases 58
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. 58
Focal seizures with affective symptoms are a major feature of PCDH19 gene-related epilepsy. 58
Familial occurrence of febrile seizures and epilepsy in severe myoclonic epilepsy of infancy (SMEI) patients with SCN1A mutations. 57
Uncombable hair syndrome, mental retardation, single palmar crease and arched palate in a patient with neurofibromatosis type I 56
Epilepsy with myoclonic atonic seizures: an electroclinical study of 69 patients. 56
Epilepsy in Menkes disease: an electroclinical long-term study of 28 patients 56
Epilepsy-related brain networks in ring chromosome 20 syndrome: An EEG-fMRI study. 56
Optimizing the molecular diagnosis of CDKL5 gene-related epileptic encephalopathy in boys 56
Neuroimaging Changes in Menkes Disease, Part 2 55
Temporal lobe epilepsy in children: electroclinical and neuroradiological study of 62 cases. 54
Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations. 54
Pediatric Epilepsy - Myoclonic Status in Nonprogressive Encephalopathies 53
Gait abnormalities in people with Dravet syndrome: A cross-sectional multi-center study 53
Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study. 52
Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1 52
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15) 51
Myoclonic Status in Nonprogressive Encephalopathies 51
Clinical spectrum of STX1B-related epileptic disorders 50
3D facial morphometry in Italian patients affected by Aicardi syndrome 50
Migrating focal seizures in infancy: analysis of the electroclinical patterns in 17 patients. 49
Molecular mechanisms generating and stabilizing terminal 22q13 deletions in 44 subjects with Phelan/McDermid syndrome. 49
null 49
Different clinical and immunological presentation of ataxia-telangiectasia within the same family. 48
Electroclinical pattern in MECP2 duplication syndrome: eight new reported cases and review of literature. 48
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] 48
Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locus. 47
Scotosensitive and photosensitive myoclonic seizures in an infant with trisomy 13. 47
Neuroimaging Changes in Menkes Disease, Part 1 47
Myoclonic status in non progressive encephalopathies. 46
Ring chromosome 20 syndrome: a link between epilepsy onset and neuropsychological impairment in three children. 46
Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. 46
Is there a benign limbic epilepsy in children? 45
Refining the phenotype associated with MEF2C haploinsufficiency 45
Symptomatic and presumed symptomatic focal epilepsies in childhood: An observational, prospective study 45
Dravet syndrome: Early electroclinical findings and long-term outcome in adolescents and adults 45
Aicardi Syndrome: Key Fetal MRI Features and Prenatal Differential Diagnosis 45
SYNGAP1-related developmental and epileptic encephalopathy: The impact on daily life 45
Periventricular heterotopia in fragile X sindrome. 43
The phenotype of SCN8A developmental and epileptic encephalopathy 43
CDKL5 deficiency disorder in males: Five new variants and review of the literature 43
Mioclonic-astatic epilepsy (MAE): Longitudinal electroclinical study of 25 subjects,Epilessia Mioclono-Astatica (EMA): Studio elettroclinico longitudinale di 25 soggetti 43
Familial Ohtahara syndrome due to a novel ARX gene mutation 42
Electroclinical findings in four patients with karyotype 47,XYY 42
Remote Teamwork Management of NORSE During the COVID-19 Lockdown 42
Basal Ganglia Dysmorphism in Patients With Aicardi Syndrome 39
EEG features in Encephalopathy related to Status Epilepticus during slow Sleep 38
Ring chromosome 20 syndrome: Report of 3 cases,Cromosoma 20 ad anello: Studio elettroclinico di 3 osservazioni personali 38
Sociodemographic and clinical changes in pediatric in-patient admissions for mental health emergencies during the COVID-19 pandemic: March 2020 to June 2021 38
Efficacy and safety of Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: A real-world study 37
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) 37
Early Treatment with Quinidine in 2 Patients with Epilepsy of Infancy with Migrating Focal Seizures (EIMFS) Due to Gain-of-Function KCNT1 Mutations: Functional Studies, Clinical Responses, and Critical Issues for Personalized Therapy 34
Epilepsy features in ARID1B-related Coffin-Siris syndrome 34
Adaptive behaviour in adolescents and adults with Dravet syndrome 31
Totale 6.470
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Categoria #
all - tutte 23.944
article - articoli 21.328
book - libri 0
conference - conferenze 460
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 2.156
Totale 47.888
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020839 126 35 12 68 69 79 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
2024/20258 8 0 0 0 0 0 0 0 0 0 0 0
Totale 6.983