FALSAPERLA, Raffaele Giuseppe
 Distribuzione geografica
Continente #
NA - Nord America 6.950
AS - Asia 4.377
EU - Europa 4.170
SA - Sud America 836
AF - Africa 754
OC - Oceania 16
Continente sconosciuto - Info sul continente non disponibili 3
Totale 17.106
Nazione #
US - Stati Uniti d'America 6.723
SG - Singapore 2.027
RU - Federazione Russa 1.866
CN - Cina 1.055
IT - Italia 1.012
BR - Brasile 713
CI - Costa d'Avorio 427
VN - Vietnam 417
IE - Irlanda 290
KR - Corea 221
DE - Germania 212
IN - India 211
FR - Francia 194
CA - Canada 143
BD - Bangladesh 121
NG - Nigeria 109
FI - Finlandia 106
GB - Regno Unito 103
SE - Svezia 89
SN - Senegal 79
UA - Ucraina 61
HK - Hong Kong 59
NL - Olanda 57
PL - Polonia 53
AR - Argentina 50
MX - Messico 48
JP - Giappone 47
ZA - Sudafrica 47
TR - Turchia 43
IQ - Iraq 33
BJ - Benin 27
ES - Italia 27
ID - Indonesia 21
EC - Ecuador 19
PK - Pakistan 19
KE - Kenya 17
MA - Marocco 17
UZ - Uzbekistan 16
CO - Colombia 15
LT - Lituania 15
AU - Australia 14
CH - Svizzera 14
EG - Egitto 14
IR - Iran 13
AT - Austria 12
CZ - Repubblica Ceca 11
DZ - Algeria 11
AE - Emirati Arabi Uniti 9
CL - Cile 9
GR - Grecia 9
SA - Arabia Saudita 9
VE - Venezuela 9
JM - Giamaica 8
GT - Guatemala 7
JO - Giordania 7
UY - Uruguay 7
IL - Israele 6
AZ - Azerbaigian 5
CR - Costa Rica 5
KZ - Kazakistan 5
LB - Libano 5
MY - Malesia 5
PY - Paraguay 5
BE - Belgio 4
DO - Repubblica Dominicana 4
PH - Filippine 4
PT - Portogallo 4
RS - Serbia 4
BO - Bolivia 3
ET - Etiopia 3
GD - Grenada 3
MT - Malta 3
PE - Perù 3
RO - Romania 3
SI - Slovenia 3
SY - Repubblica araba siriana 3
TT - Trinidad e Tobago 3
XK - ???statistics.table.value.countryCode.XK??? 3
AL - Albania 2
AO - Angola 2
BG - Bulgaria 2
BY - Bielorussia 2
DK - Danimarca 2
HR - Croazia 2
HU - Ungheria 2
KH - Cambogia 2
MM - Myanmar 2
NI - Nicaragua 2
NP - Nepal 2
PS - Palestinian Territory 2
PW - Palau 2
SR - Suriname 2
SV - El Salvador 2
TH - Thailandia 2
CY - Cipro 1
EE - Estonia 1
GE - Georgia 1
GY - Guiana 1
IM - Isola di Man 1
KG - Kirghizistan 1
Totale 17.096
Città #
Dallas 1.475
Singapore 1.342
Santa Clara 906
Moscow 878
San Jose 537
Chandler 481
Abidjan 426
Chicago 396
Ashburn 376
Hefei 341
Dublin 290
Los Angeles 276
Seoul 220
Beijing 186
Catania 179
Ho Chi Minh City 162
Civitanova Marche 147
Boardman 140
Lauterbourg 139
New York 133
Munich 131
Kochi 124
São Paulo 88
Hanoi 83
Dakar 79
Cambridge 78
Lawrence 78
Andover 76
Council Bluffs 76
Buffalo 71
Lagos 61
Hong Kong 51
Montreal 51
Des Moines 49
Helsinki 49
Orem 49
Jacksonville 45
Warsaw 45
Tokyo 44
Abuja 42
Brooklyn 42
Nanjing 42
Seattle 41
Toronto 39
Amsterdam 38
Milan 38
Rome 38
Johannesburg 35
Palermo 34
Chennai 33
Lappeenranta 33
Phoenix 32
Bremen 31
Cotonou 27
Atlanta 26
Belo Horizonte 26
Houston 26
Wilmington 26
Bussero 25
Denver 25
London 24
Stockholm 24
Dong Ket 23
Poplar 23
Turku 22
Lago 21
Da Nang 20
Rio de Janeiro 20
The Dalles 20
Boston 19
Frankfurt am Main 19
Mexico City 18
San Francisco 18
Curitiba 17
Messina 17
Naples 16
Charlotte 14
Bari 13
Istanbul 13
Nairobi 13
Tehran 13
Ankara 12
Baghdad 12
Kyiv 12
Manchester 12
Paris 12
Tashkent 12
Bologna 11
Haiphong 11
Shenyang 11
Brasília 10
Campinas 10
Columbus 10
Mumbai 10
Ottawa 10
Querétaro 10
Redondo Beach 10
Saint Petersburg 10
Biên Hòa 9
Cairo 9
Totale 11.647
Nome #
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 445
Acute Glomerulonephritis in a Child with Chlamydia pneumoniae Infection: A Case Report 292
Gamma-aminobutyric acid type a receptor genes and their related epilepsies 189
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 186
A New Patient with Potocki-Lupski Syndrome: A Literature Review 180
ENT involvement and orobuccal movements' disorders in Pandas patients: assessment and rehabilitations tools 179
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 176
TBC1D24 and Its Related Epileptic Encephalopathy 175
Periventricular Heterotopias: Neuroependymal Abnormalities 171
Aristaless-related homeobox (ARX): Epilepsy phenotypes beyond lissencephaly and brain malformations 166
A case of covid-19 with late-onset rash and transient loss of taste and smell in a 15-year-old boy 163
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 159
GRIN2A and GRIN2B and Their Related Phenotypes 156
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 153
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 150
Array-CGH in pediatric neurology: A prospective observational study 149
Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four-member family and an unrelated boy 148
PANS/PANDAS: Clinical Experience in IVIG Treatment and State of the Art in Rehabilitation Approaches 145
Short Efficacy Evaluation of External Ventricular Drains Versus Ventriculosubgaleal Shunt in the Management of Neonatal Posthemorrhagic Hydrocephalus: A Retrospective Single-Center Cohort Study 145
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 145
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 144
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 144
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 143
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 143
SCN1B gene: A close relative to SCN1A 143
E se non fossero solo incubi notturni? 141
KCNT1-Related Epilepsy: A Review 138
DNM1 Gene and Its Related Epileptic Phenotypes 136
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 135
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 135
Malformations of cortical development, cognitive involvement and epilepsy: A single institution experience in 19 young patients 135
ALDH7A1 Gene and Its Related Pyridoxine-Dependent Epilepsy 135
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature 134
Non-Epileptic Paroxysmal Events: Clinical features and diagnostic differences with epileptic seizures. A Single Tertiary Centre Study 134
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 133
The spectrum of DEPDC5-related epilepsy 133
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 132
Therapeutic approaches to pediatric pseudotumor cerebri: New insights from literature data. 132
7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature review 131
Chilblains-like lesions and SARS-CoV-2 in children: An overview in therapeutic approach 130
Pediatria dalla A alla Z - Guida Pratica alla diagnosi e al trattamento. Neurologia, disturbi psichiatrici e comportamentali 130
Otorhinolaryngologic Findings in Pediatric Patients with Pandas 129
aEEG vs cEEG's sensivity for seizure detection in the setting of neonatal intensive care units: A systematic review and meta-analysis 128
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 128
Drug resistant epilepsies: A multicentre case series of steroid therapy 126
A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: A new patient with a novel feature 126
Clinicoradiographic data and management of children with Chiari malformation type 1 and 1.5: an Italian case series 126
PCDH19-Related Epilepsies 126
GLUT-1DS resistant to ketogenic diet: from clinical feature to in silico analysis. An exemplificative case report with a literature review 124
Molecular Dynamic Simulations to Determine Individualized Therapy: Tetrabenazine for the GNAO1 Encephalopathy E246K Variant 124
SYNGAP1 and Its Related Epileptic Syndromes 124
WDR45 Gene and Its Role in Pediatric Epilepsies 124
HyperCKemia as a biomarker for muscular diseases 123
Cerebral Palsy and Epilepsy in Children: Clinical Perspectives on a Common Comorbidity 122
Plexus Neuropathy in Infants Secondary to Arthro-Osteomyelitis: Report of 2 Cases and Review of the Literature 121
Giant melanocytic nevi and soft tissue undergrowth in the left leg: Pathogenetic hypothesis 120
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 120
Near-infrared spectroscopy (NIRS) as a tool to prevent cerebral desaturation in newborns with bradycardia events: A systematic review 119
From Neonatal Intensive Care to Neurocritical Care: Is It Still a Mirage? The Sicilian Multicenter Project 118
Impressive efficacy of the ketogenic diet in a KCNQ2 encephalopathy infant: a case report and exhaustive literature review 118
The spectrum of KCNQ2- And KCNQ3-related epilepsy 118
FOXG1 Gene and Its Related Phenotypes 118
Treatment Options for Cyclic Vomiting Syndrome: A Real‐World, Single‐Center Experience with Systematic Literature Review and Meta‐Analysis 117
Oxidative stress in preterm infants: Overview of current evidence and future prospects 117
Neurodevelopmental outcomes of neonatal non-epileptic paroxysmal events: a prospective study 116
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 116
PRRT2 Related Epilepsies: A Gene Review 115
Epileptic spasms in infants: can video-EEG reveal the disease’s etiology? A retrospective study and literature review 114
Magnetic Resonance Imaging in Preterm Infant: A Systematic Review on Clinical Procedure Safety 114
Slc25a22 and its related epileptic encephalopathies 113
Calcium Channels Genes and Their Epilepsy Phenotypes 113
MECP2-related disorders and epilepsy phenotypes 113
CDKL5 gene: Beyond rett syndrome 112
SCN8A and Its Related Epileptic Phenotypes 112
Neonatal seizures as onset of Inborn Errors of Metabolism (IEMs): from diagnosis to treatment. A systematic review 111
PYRIDOXINE-dependent epilepsy (PDE): An observational study of neonatal cases on the role of pyridoxine in patients treated with standard anti-seizure medications 111
Ketogenic diet for infants with epilepsy: A literature review 111
Pediatric RSV infection and respiratory coinfections: Is a link related to clinical severity? Single center retrospective study 110
Neonates Born to COVID-19 Mother and Risk in Management within 4 Weeks of Life: A Single-Center Experience, Systematic Review, and Meta-Analysis 110
Syntaxin binding protein 1 related epilepsies 110
Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review 109
Comment on: “Steps to Improve Precision Medicine in Epilepsy”: Are we all Agreed on the Definition? 109
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review 109
SCN1A and its related epileptic phenotypes 109
Cervical neurenteric cyst and Klippel-Feil syndrome: An abrupt onset of myelopathic signs in a young patient 108
Transverse cervical megapophysis as an uncommon cause of torticollis 108
Case report: A gain-of-function of hamartin may lead to a distinct "inverse TSC1-hamartin" phenotype characterized by reduced cell growth 107
Molecular Dynamics as a Precision Therapy: A Perspective on Epileptic Encephalopathies 105
SARS-CoV-2 parental vaccination and risk of multisystem inflammatory syndrome in children: a single-center retrospective study 105
SARS-CoV-2 related Paediatric Acute-onset Neuropsychiatric Syndrome 104
SARS-CoV-2 and Swabs: Disease Severity and the Numbers of Cycles of Gene Amplification, Single Center Experience 103
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 103
Clinical features and long-term outcomes in pediatric cyclic vomiting syndrome: A 9-year experience at three tertiary academic centers 102
Clinical spectrum of woolly hair: Indications for cerebral involvement 102
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 101
Influence of the cerebellum in paediatric epilepsy: A comprehensive systematic literature review focusing on neurodevelopmental/neuropsychological implications 99
Isolated ictal apnea in neonatal age: Clinical features and treatment options. A systematic review 99
Neonatal ischemic limb lesions: From etiology to topical nitroglycerine. A case series analysis 99
Primary headache in childhood associated with psychiatric disturbances: An update 99
Cranial ultrasonographic findings in newborns exposed to SARS-CoV-2: a single-centre cross-sectional analysis 98
Totale 13.228
Categoria #
all - tutte 55.288
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 55.288


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022658 22 85 69 8 104 6 124 24 18 17 10 171
2022/20231.314 93 121 17 130 110 205 11 251 245 19 55 57
2023/2024907 32 136 90 43 33 206 9 72 10 16 134 126
2024/20253.893 69 580 176 303 628 499 216 132 306 276 427 281
2025/202610.085 526 829 1.675 769 1.313 2.155 811 181 585 549 391 301
2026/202777 77 0 0 0 0 0 0 0 0 0 0 0
Totale 17.360