Catalogo dei prodotti della ricerca

NICITA, Francesco
 Distribuzione geografica
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Continente #
NA - Nord America 4.248
EU - Europa 1.199
AS - Asia 571
AF - Africa 33
SA - Sud America 19
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 6.073
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Nazione #
US - Stati Uniti d'America 4.224
IT - Italia 537
SG - Singapore 227
SE - Svezia 200
IN - India 167
CN - Cina 162
UA - Ucraina 150
FI - Finlandia 92
GB - Regno Unito 46
IE - Irlanda 36
TG - Togo 31
DE - Germania 26
BG - Bulgaria 23
CA - Canada 22
FR - Francia 21
BE - Belgio 18
RO - Romania 17
AR - Argentina 15
NL - Olanda 12
ID - Indonesia 7
CZ - Repubblica Ceca 4
ES - Italia 3
JP - Giappone 3
PT - Portogallo 3
BD - Bangladesh 2
CL - Cile 2
HU - Ungheria 2
MX - Messico 2
PE - Perù 2
RU - Federazione Russa 2
AL - Albania 1
AU - Australia 1
CH - Svizzera 1
DK - Danimarca 1
EG - Egitto 1
EU - Europa 1
HR - Croazia 1
IL - Israele 1
LV - Lettonia 1
MY - Malesia 1
NZ - Nuova Zelanda 1
PL - Polonia 1
RS - Serbia 1
SC - Seychelles 1
TJ - Tagikistan 1
Totale 6.073
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Città #
Fairfield 779
Woodbridge 387
Ashburn 332
Houston 304
Seattle 285
Cambridge 274
Chandler 246
Wilmington 224
Ann Arbor 168
Singapore 157
Rome 122
Beijing 108
Princeton 105
Plano 83
San Paolo di Civitate 58
Dearborn 57
Lawrence 52
Jacksonville 49
Millbury 48
San Diego 40
Santa Clara 39
Dublin 36
Boston 33
Fremont 31
Lomé 31
Andover 30
Norwalk 29
Sofia 23
Helsinki 22
New York 17
Boardman 15
Federal 15
Toronto 12
Brussels 11
Milan 10
Bologna 9
Des Moines 9
Mannheim 9
Auburn Hills 8
Florence 8
Los Angeles 8
San Mateo 8
Jakarta 7
Turin 7
Waanrode 7
Bari 6
Falls Church 6
Ottawa 6
Palermo 6
Redwood City 6
Falkenstein 5
Fasano 5
Genoa 5
Kunming 5
London 5
Verbania 5
Brisighella 4
Brno 4
Bühl 4
Nanjing 4
Naples 4
Redmond 4
Southend 4
Abbiategrasso 3
Barcelona 3
Bassano del Grappa 3
Catania 3
Chicago 3
Guangzhou 3
Hebei 3
Hefei 3
Messina 3
Padova 3
Phoenix 3
Provo 3
Sant'Elena 3
Torre del Greco 3
Altamura 2
Anzio 2
Baotou 2
Bisceglie 2
Bremen 2
Buffalo 2
Bussolengo 2
Cento 2
Changchun 2
Frankfurt am Main 2
Guidonia Montecelio 2
Indiana 2
Kilburn 2
Marmirolo 2
Menlo Park 2
Mexico City 2
Monserrato 2
Monte San Giusto 2
Nanchang 2
Novara 2
Olevano Romano 2
Paganica 2
Palhaca 2
Totale 4.488
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Nome #
Epilessia rolandica e malformazione di Arnold Chiari tipo I in due fratelli: link genetico? 268
Epilessia rolandica e malformazione di Arnold Chiari tipo I in due fratelli: link genetico 114
Acute necrotizing encephalopathy during novel influenza A (H1N1) virus infection 113
Efficacy of verapamil as an adjunctive treatment in children with drug-resistant epilepsy. A pilot study 107
Clinical and Pharmacological Aspects of Inflammatory Demyelinating Diseases in Childhood. An Update 103
Developmental anomalies of the medial septal area. possible implication for limbic epileptogenesis 101
The possible use of the L-type calcium channel antagonist verapamil in drug-resistant epilepsy 101
Unilateral lisch nodules in a 47-year-old woman without other stigmata of neurofibromatosis type I: An example of segmental neurofibromatosis? 99
Evaluation and management of nonsyndromic craniosynostosis 99
Usefulness of diffusion tensor imaging and fiber tractography in neurological and neurosurgical pediatric diseases 96
Reply to “post-surgical mutism and catatonia” 96
Four-year follow-up study in a NF1 Boy with a focal pontine hamartoma 96
Genotype-phenotype correlations in a group of 15 SCN1A-mutated italian patients with GEFS+ spectrum (seizures plus, classical and borderline severe myoclonic epilepsy of infancy) 95
Correlazione clinica, genetica e neuroradiologica nei difetti di migrazione neuronale: presentazione di una casistica. 93
Stroke and migraine is there a possible comorbidity? 92
Tension-type headache in paediatric age 91
Defining the clinical-genetic and neuroradiological features in SPG54: description of eight additional cases and nine novel DDHD2 variants 91
Refractory absence seizures. An Italian multicenter retrospective study 89
Metabolic epilepsy, an update 87
WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features 87
"Headache and epilepsy" - How are they connected? 85
Migraine treatment in developmental age: guidelines update 85
Evaluation of the basal ganglia in neurofibromatosis type 1 84
Effectiveness and tolerability of perampanel in children and adolescents with refractory epilepsies-An Italian observational multicenter study 83
Early-onset absence epilepsy. SLC2A1 gene analysis and treatment evolution 83
Fiber tractography assessment in double cortex syndrome 82
Novel homozygous GBA2 mutation in a patient with complicated spastic paraplegia 80
Correlazione clinica, genetica e neuroradiologica nei difetti di migrazione neuronale: presentazione di una casistica. 79
Severe early onset ethylmalonic encephalopathy with west syndrome 79
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 79
Mean platelet volume, Vitamin D and C reactive protein levels in normal weight children with primary snoring and obstructive sleep apnea syndrome 78
Teaching NeuroImages: Schizencephaly in fetal alcohol syndrome 75
Early add-on immunoglobulin administration in Rasmussen encephalitis: The hypothesis of neuroimmunomodulation 74
Electroclinical features and long-term outcome of cryptogenic epilepsy in children with down syndrome 74
The genetics of monogenic idiopathic epilepsies and epileptic encephalopathies 73
Seizures and epilepsy in Sotos syndrome. analysis of 19 Caucasian patients with long-term follow-up 73
Neuronal migration disorders: clinical, neuroradiological and genetics aspects 73
Bilateral middle cerebral artery thromboembolic occlusion. Could maternal hyperthermia be a detrimental factor? 73
Sudden benzodiazepine-induced resolution of post-operative pediatric cerebellar mutism syndrome: a clinical-SPECT study 72
Spinal neurofibromatosis in a family with classical neurofibromatosis type 1 and a novel NF1 gene mutation 72
Epileptic nystagmus: description of a pediatric case with EEG correlation and SPECT findings. 70
SINCOPI IN ETA’ PEDIATRICA: LA NOSTRA ESPERIENZA CLINICA 69
Spinal neurofibromatosis in children 69
Childhood-onset ATP1A3-related conditions: Report of two new cases of phenotypic spectrum 69
Complex malformation (Ruggieri-Happle) phenotype with "cutis tricolor" in a 10-year-old girl 68
Displasia corticale focale versus encefalite di Rasmussen: long term follow up 66
null 66
Spinal neurofibromatosis with central nervous system involvement in a set of twin girls and a boy: further expansion of the phenotype 65
LA SINDROME DI OHTAHARA: NUOVE ACQUISIZIONI EZIOPATOGENETICHE 64
Novel mutations in the glycine receptor alpha subunit gene in two sisters with hyperekplexia 64
Recent understanding on diagnosis and management of central nervous system vasculitis in children 64
Seizures in fetal alcohol spectrum disorders: evaluation of clinical, electroencephalographic, and neuroradiologic features in a pediatric case series 64
Macrocephaly-capillary malformation syndrome: Description of a case and review of clinical diagnostic criteria 63
The natural history of Spinal Neurofibromatosis: a critical review of clinical and genetic features 63
Immunotherapy in Rasmussen's encephalitis: When should it be taken into account? 61
Neurological features of 14q24-q32 interstitial deletion: report of a new case 60
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Long-term prognosis of patients with Ehlers-Danlos syndrome and epilepsy 60
Expanding the clinical phenotype of CAPN1-associated mutations: A new case with congenital-onset pure spastic paraplegia 60
null 59
Epileptic encephalopathy of infancy and childhood: electro-clinical pictures and recent understandings 58
The role of cytomegalovirus in schizencephaly 58
Natural history of neurofibromatosis type 2 with onset before the age of 1 year 57
Clinical dissection of early onset absence epilepsy in children and prognostic implications 57
Macrocephaly capillari malformation syndrome: descrizione di un caso clinico e criteri diagnostici 56
Pediatric cerebellar stroke associated with elevated titer of antibodies to β2-glycoprotein. 55
DISORDINI NEUROLOGICI E INFEZIONI STREPTOCOCCICHE IN ETA' PEDIATRICA: PRESENTAZIONE DI UNA CASISTICA 53
Posterior fossa malformations and sex chromosomes anomalies. Report of a case with XYY syndrome and overview of known associations 53
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Pediatric idiopathic intracranial hypertension and the underlying endocrine-metabolic dysfunction: A pilot study 53
RUOLO DELLA DTI NELLA DEFINIZIONE DELLE PATOLOGIE EPILETTICHE 52
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Severe early onset ethylmalonic encephalopathy with West syndrome 50
Long-term outcome of epilepsy in Kabuki syndrome 48
Novel missense mutation (L1917P) involving sac-domain of NSD1 gene in a patient with Sotos syndrome 47
STROKE IN CHILDREN AND ACQUIRED FACTORS AND AGE-RELATED VARIATIONS IN THE PRESENTATION OF 48 PEDIATRIC PATIENTS 44
Sindrome di Williams: studio della funzione cardiaca e dell'efficienza cardiorespiratoria 42
Macrocephaly capillari malformation syndrome: descrizione di un caso clinico e criteri diagnostici 41
CORRELAZIONE CLINICA GENETICA E NEURORADIOLOGICA NEI DIFETTI DI MIGRAZIONE NEURONALE: PRESENTAZIONE DI UNA CASISTICA 40
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network 40
The sodium channel a1 subunit (SCN1A)-related epileptic phenotypes 39
Extreme phenotypic heterogeneity in non-expansion spinocerebellar ataxias 36
I NUMEROSI VOLTI DELLA PHACE: PRESNTAZIONE DI UN CASO CLINICO 31
Encefalite da EBV associata a infezione da CMV 29
Pediatric autoimmune neuropsychiatric disorder associated with group a streptococcal infection: the role of surgical treatment 29
Could Rolandic spikes be a prognostic factor of the neurocognitive outcome of children with BECTS? 28
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Stroke in età pediatrica: nuova emergenza neurologica. 14
Early myoclonic encephalopathy in 9q33-q34 deletion encompassing STXBP1 and SPTAN1 14
Beverage consumption and paediatric NAFLD 13
Epilepsy phenotypes across the different age-ranges in IQSEC2-related encephalopathy: An Italian multicentre retrospective cohort study 10
Congenital-onset spastic paraplegia in a patient with TUBB4A mutation and mild hypomyelination 10
Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region 10
Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomy 8
BCL11B-Related Dystonia: Further Evidence of an Emerging Cause of Childhood-Onset Generalized Dystonia 6
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Spectrum of ERCC6-Related Cockayne Syndrome (Type B): From Mild to Severe Forms 1
Prestatus and status dystonicus in children and adolescents 1
Totale 6.280
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Categoria #
all - tutte 15.730
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 15.730
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.327 0 0 0 0 220 232 200 217 183 139 95 41
2020/2021538 62 82 76 34 10 73 9 27 56 62 35 12
2021/2022949 17 60 95 30 120 24 14 110 74 70 157 178
2022/2023979 188 189 61 112 110 77 59 45 71 21 33 13
2023/2024452 23 52 17 53 43 50 15 37 4 61 54 43
2024/2025259 47 59 58 34 61 0 0 0 0 0 0 0
Totale 6.280