IRIS
FALSAPERLA, Raffaele Giuseppe
 Distribuzione geografica
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Continente #
NA - Nord America 5.490
AS - Asia 3.352
EU - Europa 2.000
SA - Sud America 722
AF - Africa 617
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 3
Totale 12.194
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Nazione #
US - Stati Uniti d'America 5.359
SG - Singapore 1.667
CN - Cina 909
IT - Italia 888
BR - Brasile 634
CI - Costa d'Avorio 425
IE - Irlanda 287
VN - Vietnam 214
RU - Federazione Russa 204
DE - Germania 188
IN - India 183
KR - Corea 167
FI - Finlandia 88
CA - Canada 84
SN - Senegal 77
GB - Regno Unito 64
NL - Olanda 48
PL - Polonia 46
UA - Ucraina 46
AR - Argentina 41
JP - Giappone 35
MX - Messico 35
FR - Francia 33
ZA - Sudafrica 30
SE - Svezia 29
BD - Bangladesh 27
BJ - Benin 27
NG - Nigeria 27
TR - Turchia 25
HK - Hong Kong 24
ES - Italia 19
EC - Ecuador 17
IQ - Iraq 14
UZ - Uzbekistan 14
IR - Iran 13
ID - Indonesia 12
CO - Colombia 11
MA - Marocco 11
LT - Lituania 10
CH - Svizzera 9
PK - Pakistan 9
AE - Emirati Arabi Uniti 8
AT - Austria 8
AU - Australia 8
GR - Grecia 8
KE - Kenya 8
CZ - Repubblica Ceca 7
DZ - Algeria 5
EG - Egitto 5
SA - Arabia Saudita 5
VE - Venezuela 5
AZ - Azerbaigian 4
LB - Libano 4
CL - Cile 3
DO - Repubblica Dominicana 3
GD - Grenada 3
IL - Israele 3
JO - Giordania 3
KZ - Kazakistan 3
PE - Perù 3
PT - Portogallo 3
PY - Paraguay 3
UY - Uruguay 3
XK - ???statistics.table.value.countryCode.XK??? 3
BE - Belgio 2
BG - Bulgaria 2
CR - Costa Rica 2
DK - Danimarca 2
MY - Malesia 2
NI - Nicaragua 2
PW - Palau 2
RS - Serbia 2
SI - Slovenia 2
AO - Angola 1
BO - Bolivia 1
BY - Bielorussia 1
EE - Estonia 1
GE - Georgia 1
GY - Guiana 1
JM - Giamaica 1
LY - Libia 1
ME - Montenegro 1
MM - Myanmar 1
NO - Norvegia 1
NP - Nepal 1
PH - Filippine 1
PS - Palestinian Territory 1
QA - Qatar 1
RO - Romania 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
Totale 12.194
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Città #
Dallas 1.459
Singapore 1.054
Santa Clara 868
Chandler 481
Abidjan 425
Chicago 391
Hefei 340
Dublin 287
Ashburn 233
Los Angeles 220
Beijing 169
Seoul 167
Catania 166
Civitanova Marche 147
Boardman 140
Munich 131
Kochi 124
Ho Chi Minh City 93
New York 80
Cambridge 78
Lawrence 78
Dakar 77
Andover 76
Moscow 70
São Paulo 68
Des Moines 48
Helsinki 48
Buffalo 47
Jacksonville 43
Nanjing 42
Hanoi 39
Warsaw 39
Seattle 38
Brooklyn 34
Rome 33
Tokyo 33
Bremen 31
Palermo 30
Toronto 30
Amsterdam 29
Chennai 27
Cotonou 27
Abuja 26
Belo Horizonte 26
Phoenix 26
Bussero 25
Wilmington 25
Milan 24
Dong Ket 23
Johannesburg 23
Hong Kong 22
Houston 22
Turku 22
Lago 21
Council Bluffs 20
Montreal 20
Denver 19
Rio de Janeiro 18
Boston 17
Stockholm 17
The Dalles 17
Lappeenranta 16
Orem 16
Poplar 16
Curitiba 15
Tehran 13
Atlanta 12
Bari 12
Mexico City 12
Naples 12
San Francisco 12
Charlotte 11
London 11
Shenyang 11
Campinas 10
Columbus 10
Manchester 10
Messina 10
Ottawa 10
Redondo Beach 10
Saint Petersburg 10
Tashkent 10
Brasília 9
Campobasso 9
Querétaro 9
Istanbul 8
Nairobi 8
Raleigh 8
Riposto 8
Ankara 7
Bergamo 7
Bologna 7
Da Nang 7
Dhaka 7
Goiânia 7
Hebei 7
Nanchang 7
Ribeirão Preto 7
Salvador 7
San Giovanni la Punta 7
Totale 8.838
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Nome #
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 401
Acute Glomerulonephritis in a Child with Chlamydia pneumoniae Infection: A Case Report 244
Periventricular Heterotopias: Neuroependymal Abnormalities 151
ENT involvement and orobuccal movements' disorders in Pandas patients: assessment and rehabilitations tools 148
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 144
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 138
TBC1D24 and Its Related Epileptic Encephalopathy 137
A New Patient with Potocki-Lupski Syndrome: A Literature Review 134
Aristaless-related homeobox (ARX): Epilepsy phenotypes beyond lissencephaly and brain malformations 129
A case of covid-19 with late-onset rash and transient loss of taste and smell in a 15-year-old boy 124
E se non fossero solo incubi notturni? 119
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 117
Array-CGH in pediatric neurology: A prospective observational study 116
GRIN2A and GRIN2B and Their Related Phenotypes 116
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 115
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 112
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 112
PANS/PANDAS: Clinical Experience in IVIG Treatment and State of the Art in Rehabilitation Approaches 111
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 110
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 109
SCN1B gene: A close relative to SCN1A 109
KCNT1-Related Epilepsy: A Review 109
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 105
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 105
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 104
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 104
Pediatria dalla A alla Z - Guida Pratica alla diagnosi e al trattamento. Neurologia, disturbi psichiatrici e comportamentali 103
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 102
Therapeutic approaches to pediatric pseudotumor cerebri: New insights from literature data. 101
The spectrum of DEPDC5-related epilepsy 101
DNM1 Gene and Its Related Epileptic Phenotypes 101
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 100
Plexus Neuropathy in Infants Secondary to Arthro-Osteomyelitis: Report of 2 Cases and Review of the Literature 100
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 98
PCDH19-Related Epilepsies 96
Gamma-aminobutyric acid type a receptor genes and their related epilepsies 95
Short Efficacy Evaluation of External Ventricular Drains Versus Ventriculosubgaleal Shunt in the Management of Neonatal Posthemorrhagic Hydrocephalus: A Retrospective Single-Center Cohort Study 94
HyperCKemia as a biomarker for muscular diseases 94
Non-Epileptic Paroxysmal Events: Clinical features and diagnostic differences with epileptic seizures. A Single Tertiary Centre Study 94
Neurodevelopmental outcomes of neonatal non-epileptic paroxysmal events: a prospective study 94
aEEG vs cEEG's sensivity for seizure detection in the setting of neonatal intensive care units: A systematic review and meta-analysis 93
A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: A new patient with a novel feature 93
Otorhinolaryngologic Findings in Pediatric Patients with Pandas 93
SYNGAP1 and Its Related Epileptic Syndromes 93
ALDH7A1 Gene and Its Related Pyridoxine-Dependent Epilepsy 93
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 93
Clinicoradiographic data and management of children with Chiari malformation type 1 and 1.5: an Italian case series 91
Drug resistant epilepsies: A multicentre case series of steroid therapy 90
7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature review 90
Malformations of cortical development, cognitive involvement and epilepsy: A single institution experience in 19 young patients 90
Oxidative stress in preterm infants: Overview of current evidence and future prospects 89
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 88
Transverse cervical megapophysis as an uncommon cause of torticollis 88
Cervical neurenteric cyst and Klippel-Feil syndrome: An abrupt onset of myelopathic signs in a young patient 87
FOXG1 Gene and Its Related Phenotypes 87
WDR45 gene and its role in pediatric epilepsies 87
Chilblains-like lesions and SARS-CoV-2 in children: An overview in therapeutic approach 86
Clinical spectrum of woolly hair: Indications for cerebral involvement 86
Giant melanocytic nevi and soft tissue undergrowth in the left leg: Pathogenetic hypothesis 86
Impressive efficacy of the ketogenic diet in a KCNQ2 encephalopathy infant: a case report and exhaustive literature review 85
From Neonatal Intensive Care to Neurocritical Care: Is It Still a Mirage? The Sicilian Multicenter Project 84
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 84
Molecular Dynamic Simulations to Determine Individualized Therapy: Tetrabenazine for the GNAO1 Encephalopathy E246K Variant 84
Ketogenic diet for infants with epilepsy: A literature review 84
The spectrum of KCNQ2- And KCNQ3-related epilepsy 84
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature 83
Treatment Options for Cyclic Vomiting Syndrome: A Real‐World, Single‐Center Experience with Systematic Literature Review and Meta‐Analysis 83
CDKL5 gene: Beyond rett syndrome 83
PRRT2 Related Epilepsies: A Gene Review 83
Cerebral Palsy and Epilepsy in Children: Clinical Perspectives on a Common Comorbidity 83
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 83
SARS-CoV-2 related Paediatric Acute-onset Neuropsychiatric Syndrome 82
SCN1A and its related epileptic phenotypes 82
Slc25a22 and its related epileptic encephalopathies 82
Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review 81
Otorrhea in Kawasaki disease diagnosis complicated by an EBV infection: coincidental disease or a true association 81
Case report: A gain-of-function of hamartin may lead to a distinct "inverse TSC1-hamartin" phenotype characterized by reduced cell growth 80
Calcium Channels Genes and Their Epilepsy Phenotypes 80
MECP2-related disorders and epilepsy phenotypes 80
PYRIDOXINE-dependent epilepsy (PDE): An observational study of neonatal cases on the role of pyridoxine in patients treated with standard anti-seizure medications 79
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review 79
Magnetic Resonance Imaging in Preterm Infant: A Systematic Review on Clinical Procedure Safety 78
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? 77
Cyclic Vomiting Syndrome in Children 77
Epileptic spasms in infants: can video-EEG reveal the disease’s etiology? A retrospective study and literature review 76
Comment on: “Steps to Improve Precision Medicine in Epilepsy”: Are we all Agreed on the Definition? 75
Clinical features and long-term outcomes in pediatric cyclic vomiting syndrome: A 9-year experience at three tertiary academic centers 74
Neonatal seizures as onset of Inborn Errors of Metabolism (IEMs): from diagnosis to treatment. A systematic review 74
Syntaxin binding protein 1 related epilepsies 74
SCN8A and Its Related Epileptic Phenotypes 74
Neonates Born to COVID-19 Mother and Risk in Management within 4 Weeks of Life: A Single-Center Experience, Systematic Review, and Meta-Analysis 73
SARS-CoV-2 and Swabs: Disease Severity and the Numbers of Cycles of Gene Amplification, Single Center Experience 72
Could electrical needle stimulation reduce diagnostic errors in electromyography? 71
Human herpes 6 encephalitis in co-infection with Covid-19 69
Pediatric RSV infection and respiratory coinfections: Is a link related to clinical severity? Single center retrospective study 69
Isolated ictal apnea in neonatal age: Clinical features and treatment options. A systematic review 69
Fever-Associated Seizures or Epilepsy: An Overview of Old and Recent Literature Acquisitions 68
Early Motor Delay: An Outstanding, Initial Sign of Osteogenesis Imperfecta Type 1 68
Primary headache in childhood associated with psychiatric disturbances: An update 68
West syndrome: a comprehensive review 68
Totale 9.782
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Categoria #
all - tutte 44.050
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 44.050
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021150 0 0 0 0 0 10 16 5 25 9 50 35
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
2025/20265.243 526 829 1.675 769 1.313 131 0 0 0 0 0 0
Totale 12.441