IRIS
FALSAPERLA, Raffaele Giuseppe
 Distribuzione geografica
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Continente #
NA - Nord America 1.332
EU - Europa 1.023
AF - Africa 334
AS - Asia 189
SA - Sud America 9
OC - Oceania 7
Totale 2.894
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Nazione #
US - Stati Uniti d'America 1.294
IT - Italia 494
IE - Irlanda 289
CI - Costa d'Avorio 231
CN - Cina 127
SN - Senegal 75
RU - Federazione Russa 61
DE - Germania 52
UA - Ucraina 38
CA - Canada 37
VN - Vietnam 31
NG - Nigeria 27
FR - Francia 24
GB - Regno Unito 12
SE - Svezia 11
CH - Svizzera 8
GR - Grecia 8
PL - Polonia 8
SG - Singapore 8
AU - Australia 7
BR - Brasile 7
NL - Olanda 7
TR - Turchia 6
IN - India 5
LB - Libano 3
BE - Belgio 2
HK - Hong Kong 2
JP - Giappone 2
RS - Serbia 2
UZ - Uzbekistan 2
AR - Argentina 1
AT - Austria 1
CL - Cile 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
EE - Estonia 1
EG - Egitto 1
FI - Finlandia 1
ME - Montenegro 1
MM - Myanmar 1
MX - Messico 1
MY - Malesia 1
NO - Norvegia 1
SA - Arabia Saudita 1
Totale 2.894
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Città #
Chandler 484
Dublin 289
Abidjan 231
Catania 109
Cambridge 79
Lawrence 79
Andover 77
Dakar 75
Ashburn 60
Des Moines 49
Nanjing 42
Jacksonville 41
Bremen 32
Seattle 31
Abuja 26
Toronto 25
Wilmington 25
Dong Ket 23
Lago 22
Rome 21
Palermo 14
Boardman 12
Saint Petersburg 11
Shenyang 11
Campobasso 9
Hanoi 8
Milan 8
Ottawa 8
Riposto 8
Beijing 7
Bergamo 7
Hebei 7
Los Angeles 7
Nanchang 7
Falls Church 6
Moscow 6
Naples 6
San Giovanni la Punta 6
Avola 5
Den Haag 5
Gravina di Catania 4
Istanbul 4
Jiaxing 4
Santa Venerina 4
Anguillara Sabazia 3
Belo Horizonte 3
Butera 3
Canberra 3
Chicago 3
Crosia 3
Houston 3
Lipari 3
New York 3
Pelham 3
Reggio Calabria 3
Rio De Janeiro 3
San Francisco 3
San Mateo 3
Scordia 3
Sydney 3
Syracuse 3
Torino 3
Trento 3
Vittoria 3
Adrano 2
Assago 2
Belgrade 2
Bengaluru 2
Boca 2
Bodrum 2
Brussels 2
Carini 2
Castel Volturno 2
Central 2
Cepagatti 2
Changsha 2
Corsico 2
Delia 2
Florence 2
Fuzhou 2
Hangzhou 2
Hounslow 2
Jinan 2
Las Vegas 2
Leonforte 2
Mainz 2
Messina 2
Mestre 2
Monterotondo 2
Ningbo 2
Niscemi 2
Norwalk 2
Paduli 2
Porza 2
Redwood City 2
Salerno 2
San Gregorio di Catania 2
San Martino in Strada 2
Singapore 2
Tappahannock 2
Totale 2.126
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Nome #
ENT involvement and orobuccal movements' disorders in Pandas patients: assessment and rehabilitations tools 63
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 58
Array-CGH in pediatric neurology: A prospective observational study 55
Pediatria dalla A alla Z - Guida Pratica alla diagnosi e al trattamento. Neurologia, disturbi psichiatrici e comportamentali 54
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 54
Transverse cervical megapophysis as an uncommon cause of torticollis 52
GRIN2A and GRIN2B and Their Related Phenotypes 52
Aristaless-related homeobox (ARX): Epilepsy phenotypes beyond lissencephaly and brain malformations 51
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 50
SCN2A and Its Related Epileptic Phenotypes 49
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 48
Therapeutic approaches to pediatric pseudotumor cerebri: New insights from literature data. 47
E se non fossero solo incubi notturni? 45
A case of covid-19 with late-onset rash and transient loss of taste and smell in a 15-year-old boy 45
SCN1B gene: A close relative to SCN1A 44
TBC1D24 and Its Related Epileptic Encephalopathy 44
DNM1 Gene and Its Related Epileptic Phenotypes 44
Plexus Neuropathy in Infants Secondary to Arthro-Osteomyelitis: Report of 2 Cases and Review of the Literature 43
Clinical spectrum of woolly hair: Indications for cerebral involvement 43
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 43
WDR45 gene and its role in pediatric epilepsies 43
Cervical neurenteric cyst and Klippel-Feil syndrome: An abrupt onset of myelopathic signs in a young patient 41
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 41
SARS-CoV-2 related Paediatric Acute-onset Neuropsychiatric Syndrome 41
KCNT1-Related Epilepsy: A Review 41
SYNGAP1 and Its Related Epileptic Syndromes 40
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 40
SCN1A and its related epileptic phenotypes 40
The spectrum of DEPDC5-related epilepsy 37
Cyclic Vomiting Syndrome in Children 37
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 36
Otorhinolaryngologic Findings in Pediatric Patients with Pandas 36
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 36
MECP2-related disorders and epilepsy phenotypes 36
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 35
Giant melanocytic nevi and soft tissue undergrowth in the left leg: Pathogenetic hypothesis 34
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 34
A New Patient with Potocki-Lupski Syndrome: A Literature Review 33
A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: A new patient with a novel feature 33
HyperCKemia as a biomarker for muscular diseases 33
Clinicoradiographic data and management of children with Chiari malformation type 1 and 1.5: an Italian case series 33
PCDH19-Related Epilepsies 33
Early Motor Delay: An Outstanding, Initial Sign of Osteogenesis Imperfecta Type 1 32
Could electrical needle stimulation reduce diagnostic errors in electromyography? 32
Paternally inherited 17q12 microduplication: similar pattern of neurological signs and features in the father and his children 32
CDKL5 gene: Beyond rett syndrome 32
FOXG1 Gene and Its Related Phenotypes 32
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 31
ALDH7A1 Gene and Its Related Pyridoxine-Dependent Epilepsy 31
Calcium Channels Genes and Their Epilepsy Phenotypes 31
Resuming the obsolete term "small head": when microcephaly occurs without cognitive impairment 30
7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature review 30
Malformations of cortical development, cognitive involvement and epilepsy: A single institution experience in 19 young patients 30
Slc25a22 and its related epileptic encephalopathies 30
PRRT2 Related Epilepsies: A Gene Review 30
West syndrome: a comprehensive review 30
Cerebral Palsy and Epilepsy in Children: Clinical Perspectives on a Common Comorbidity 29
Intronic Variant in CNTNAP2 Gene in a Boy With Remarkable Conduct Disorder, Minor Facial Features, Mild Intellectual Disability, and Seizures 29
PRRT2 gene variant in a child with dysmorphic features, congenital microcephaly, and severe epileptic seizures: genotype-phenotype correlation? 28
Gamma-aminobutyric acid type a receptor genes and their related epilepsies 28
Hypomelanosis of Ito: a round on the frequency and type of epileptic complications. 27
Otorrhea in Kawasaki disease diagnosis complicated by an EBV infection: coincidental disease or a true association 27
Ketogenic diet for infants with epilepsy: A literature review 27
Primary headache in childhood associated with psychiatric disturbances: An update 27
Non-Epileptic Paroxysmal Events: Clinical features and diagnostic differences with epileptic seizures. A Single Tertiary Centre Study 27
Oxidative stress in preterm infants: Overview of current evidence and future prospects 27
Syntaxin binding protein 1 related epilepsies 26
Neurodevelopmental outcomes of neonatal non-epileptic paroxysmal events: a prospective study 25
aEEG vs cEEG's sensivity for seizure detection in the setting of neonatal intensive care units: A systematic review and meta-analysis 24
Recurrent Hopkin's syndrome: A case report and review of the literature 24
Monogenic epilepsies: Channelopathies, synaptopathies, mtorpathies, and otheropathies 24
Is benign familial neonatal KCNQ2-related epilepsy always familially benign? J pediatric neonatal individualized medicine 23
SCN8A and Its Related Epileptic Phenotypes 22
Ptosis in childhood: A clinical sign of several disorders: Case series reports and literature review 21
The spectrum of KCNQ2- And KCNQ3-related epilepsy 21
Short Efficacy Evaluation of External Ventricular Drains Versus Ventriculosubgaleal Shunt in the Management of Neonatal Posthemorrhagic Hydrocephalus: A Retrospective Single-Center Cohort Study 19
SARS-CoV-2: The Impact of Co-Infections with Particular Reference to Mycoplasma pneumonia-A Clinical Review 19
Chilblains-like lesions and SARS-CoV-2 in children: An overview in therapeutic approach 18
Syringomyelia and Bone Malformations in the Setting of Hypertrichosis Cubiti (Hairy Elbow Syndrome) 18
Ocular Motor Paroxysmal Events in Neonates and Infants: A Review of the Literature 18
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 17
PANS/PANDAS: Clinical Experience in IVIG Treatment and State of the Art in Rehabilitation Approaches 16
Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review 16
Cerebral White Matter Lesions and Dysmorphisms: Signs Suggestive of 6p25 Deletion Syndrome-Literature Review 16
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 15
Primary Microcephaly with Novel Variant of MCPH1 Gene in Twins: Both Manifesting in Childhood at the Same Time with Hashimoto's Thyroiditis 14
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 13
Is SARSCoV-2 nasopharyngeal swab still a gold standard in children? 13
Impressive efficacy of the ketogenic diet in a KCNQ2 encephalopathy infant: a case report and exhaustive literature review 12
Acute Glomerulonephritis in a Child with Chlamydia pneumoniae Infection: A Case Report 12
Microcephaly/trigonocephaly, intellectual disability, autism spectrum disorder, and atypical dysmorphic features in a boy with Xp22.31 duplication 11
SARS-CoV-2 and Swabs: Disease Severity and the Numbers of Cycles of Gene Amplification, Single Center Experience 9
Neonatal seizures as onset of Inborn Errors of Metabolism (IEMs): from diagnosis to treatment. A systematic review 9
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 8
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 8
Pathogenic correlation between mosaic variegated aneuploidy 1 (MVA1) and a novel BUB1B variant: a reappraisal of a severe syndrome 8
From Neonatal Intensive Care to Neurocritical Care: Is It Still a Mirage? The Sicilian Multicenter Project 7
Neonates Born to COVID-19 Mother and Risk in Management within 4 Weeks of Life: A Single-Center Experience, Systematic Review, and Meta-Analysis 7
Sutures ultrasound: useful diagnostic screening for posterior plagiocephaly 7
Alternating hemiplegia of childhood: a distinct clinical entity and ATP1A3-related disorders: A narrative review 7
Totale 3.033
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Categoria #
all - tutte 13.732
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 13.732
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20197 0 0 0 0 0 0 0 0 0 0 2 5
2019/2020123 55 19 3 0 2 5 9 3 3 8 3 13
2020/2021227 2 5 9 11 44 10 16 5 27 10 53 35
2021/2022678 23 86 72 8 106 6 126 24 18 17 15 177
2022/20231.326 94 122 18 131 110 207 11 253 248 19 56 57
2023/2024673 33 138 102 44 37 209 9 75 10 16 0 0
Totale 3.109