IRIS
PRATICO', ANDREA DOMENICO
 Distribuzione geografica
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Continente #
NA - Nord America 8.019
EU - Europa 5.921
AS - Asia 3.801
SA - Sud America 808
AF - Africa 675
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 3
Totale 19.240
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Nazione #
US - Stati Uniti d'America 7.786
IT - Italia 2.568
SG - Singapore 2.049
RU - Federazione Russa 1.826
CN - Cina 1.050
BR - Brasile 693
IE - Irlanda 573
CI - Costa d'Avorio 470
UA - Ucraina 248
VN - Vietnam 210
IN - India 194
CA - Canada 187
DE - Germania 149
SN - Senegal 121
GB - Regno Unito 91
SE - Svezia 73
KR - Corea 71
NL - Olanda 66
FR - Francia 57
PL - Polonia 55
FI - Finlandia 54
AR - Argentina 42
MX - Messico 34
JP - Giappone 32
BD - Bangladesh 30
ZA - Sudafrica 29
ES - Italia 27
TR - Turchia 27
CH - Svizzera 25
CZ - Repubblica Ceca 23
EC - Ecuador 19
GR - Grecia 17
HK - Hong Kong 16
ID - Indonesia 15
MA - Marocco 15
UZ - Uzbekistan 15
AT - Austria 14
CO - Colombia 14
IR - Iran 14
IQ - Iraq 13
AU - Australia 12
BJ - Benin 12
VE - Venezuela 11
LB - Libano 9
LT - Lituania 9
SA - Arabia Saudita 9
AE - Emirati Arabi Uniti 8
BE - Belgio 8
KE - Kenya 7
PE - Perù 7
PY - Paraguay 7
CL - Cile 6
IL - Israele 6
NG - Nigeria 6
PK - Pakistan 6
UY - Uruguay 6
DK - Danimarca 5
DO - Repubblica Dominicana 5
AZ - Azerbaigian 4
EG - Egitto 4
HU - Ungheria 4
NO - Norvegia 4
OM - Oman 4
RO - Romania 4
RS - Serbia 4
BO - Bolivia 3
BY - Bielorussia 3
JO - Giordania 3
NP - Nepal 3
AO - Angola 2
BB - Barbados 2
ET - Etiopia 2
EU - Europa 2
GE - Georgia 2
MY - Malesia 2
PT - Portogallo 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
TN - Tunisia 2
AL - Albania 1
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BT - Bhutan 1
DZ - Algeria 1
EE - Estonia 1
GA - Gabon 1
GL - Groenlandia 1
GT - Guatemala 1
IS - Islanda 1
JM - Giamaica 1
KH - Cambogia 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
LU - Lussemburgo 1
ME - Montenegro 1
MK - Macedonia 1
MM - Myanmar 1
NE - Niger 1
NI - Nicaragua 1
Totale 19.232
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Città #
Dallas 1.599
Singapore 1.301
Santa Clara 1.008
Chandler 937
Moscow 839
Dublin 573
Abidjan 470
Chicago 459
Ashburn 310
Catania 293
Jacksonville 290
Boardman 247
Houston 247
Los Angeles 229
Beijing 209
Hefei 187
Milan 163
Cambridge 160
Lawrence 160
Andover 158
Rome 144
Civitanova Marche 142
Nanjing 140
Kochi 127
Dakar 121
Toronto 91
Des Moines 85
New York 73
Bremen 71
Seoul 70
Wilmington 66
Ho Chi Minh City 61
Palermo 59
São Paulo 58
Ottawa 49
Padova 49
The Dalles 47
Buffalo 45
Oakland 45
Naples 41
Columbus 39
Shenyang 39
Warsaw 38
Dong Ket 37
Lago 37
Brooklyn 35
Hanoi 33
Munich 33
Council Bluffs 32
Turku 32
Saint Petersburg 31
Nanchang 30
Tokyo 30
Denver 29
San Mateo 28
Seattle 28
Florence 27
Hebei 27
Jiaxing 26
Bari 25
Bologna 25
Bussero 25
Montreal 24
Orem 24
Phoenix 24
Tianjin 23
Rio de Janeiro 22
Brescia 21
Chennai 21
Changsha 20
Gravina di Catania 20
Redondo Beach 20
Stockholm 20
Johannesburg 19
Poplar 19
Riposto 19
Atlanta 18
Ferrara 18
San Jose 18
Amsterdam 16
Belo Horizonte 16
Cagliari 16
Falls Church 16
Boston 15
Den Haag 15
Hong Kong 15
San Francisco 15
Turin 15
Campobasso 14
Curitiba 14
London 14
Lipari 13
Ragusa 13
Washington 13
Adrano 12
Cotonou 12
Dhaka 12
Jinan 12
Lappeenranta 12
Norwalk 12
Totale 12.751
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Nome #
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 848
Sindromi Neurocutanee 637
Childhood neurofibromatosis type 2 (NF2) and related disorders: From bench to bedside and biologically targeted therapies [Neurofibromatosi tipo 2 (NF2) e sindromi correlate in età infantile: dalla biologia molecolare alla pratica clinica e nuove terapie con farmaci biologici] 266
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 187
Speckled Lentiginous Nevus Syndrome 182
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 181
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 178
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 173
Becker's Nevus Syndrome 169
Anti-mog associated encephalitis: when steroid therapy is not enough 168
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 166
Encefalopatia acuta da probabile deficit cerebrale di acido folico in paziente con iperfenilalaninemia da deficit di DHPR 165
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 164
Nevus Sebaceous Syndrome 155
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 154
A New Patient with Potocki-Lupski Syndrome: A Literature Review 153
Periventricular Heterotopias: Neuroependymal Abnormalities 152
Blue Rubber Bleb Nevus Syndrome 152
Phacomatosis Pigmentovascularis 152
Phacomatosis Pigmentokeratotica 150
Aristaless-related homeobox (ARX): Epilepsy phenotypes beyond lissencephaly and brain malformations 148
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 144
At the Origin of Brain Malformations: Embryology of the Central and Peripheral Nervous System 143
Isolated liver disease in a patient with a CFTR genotype F508del/12TG-5T and 470MV: A new face of an old disease 143
Hypoglossal nerve paralysis in a child after a dental procedure 141
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 141
Mycoplasma pneumoniae: dalla polmonite atipica primaria alle complicanze extrapolmonari 138
GRIN2A and GRIN2B and Their Related Phenotypes 137
Megalencephaly Capillary Malformation Syndrome 136
Wyburn-Mason Syndrome 134
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 134
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 133
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 131
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 131
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 130
E se non fossero solo incubi notturni? 128
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 127
SCN1B gene: A close relative to SCN1A 125
A child with congenital heart disease and situs viscerum inversus 124
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 124
KCNT1-Related Epilepsy: A Review 124
Microcephaly-Capillary Malformation Syndrome 123
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 122
Allergia agli insetti 122
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 122
Hypomelanosis of Ito 121
Multiseptate Gallbladder in a Child: A Possible Cause of Poor Growth? 121
The immunopathogenesis of cows milk protein allergy (CMPA) 119
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 118
DNM1 Gene and Its Related Epileptic Phenotypes 118
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 117
Did Cro-Magnon 1 have neurofibromatosis type 2? 117
Congenital muscular dystrophy: from muscle to brain 117
Pott disease in a 14-year-old girl affected by congenital lamellar ichthyosis type 3 and diabetes mellitus 117
Cutis Tricolor 117
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 117
Ataxia in children: early recognition and clinical evaluation 116
Tetralogy of Fallot variant with pulmonary atresia (pseudotruncus arteriosus) in a case of maternal PKU syndrome 115
Recurrent obstructive hydrocephalus in a 4-month-old infant 114
Mixed Vascular Nevus Syndrome 114
Pediatria dalla A alla Z - Guida Pratica alla diagnosi e al trattamento. Neurologia, disturbi psichiatrici e comportamentali 114
Neurocutaneous melanocytosis (melanosis) 114
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 113
Gamma-aminobutyric acid type a receptor genes and their related epilepsies 113
Actualities on molecular pathogenesis and repairing processes of cerebral damage in perinatal hypoxic-ischemic encephalopathy 112
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 111
PCDH19-Related Epilepsies 111
A Retrospective Study on Standard Regimen for Vaccination in Celiac Children 110
A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: A new patient with a novel feature 109
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa 109
Neuroaspergillosis as the Presenting Sign of a Chronic Granulomatous Disease 109
A sudden weight gain in a child as clinical presentation of Chiari Type I malformation: a case report 108
SYNGAP1 and Its Related Epileptic Syndromes 108
Cognitive disabilities and bioethical implications in down syndrome 107
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 106
HyperCKemia as a biomarker for muscular diseases 106
Graph theory in paediatric epilepsy: A systematic review 105
Blepharoptosis in children: Our experience at the light of literature 105
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature 104
Zespół padaczkowy z drgawkami połowiczymi i porażeniem połowiczym. Wyniki badania za pomocaogonek rezonansu magnetycznego u trzyletniego chłopca [Hemiconvulsion-hemiplegia-epilepsy syndrome. Magnetic resonance findings in a 3-year-old boy] 104
Introduction to phacomatoses (neurocutaneous disorders) in childhood 104
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 103
Acquired peripheral neuropathy: a report on 20 children. 103
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 103
Eczema herpeticum in a patient with atopic dermatitis, coxsackie B virus, and staphylococcal infection: A double skin damage 102
FOXG1 Gene and Its Related Phenotypes 102
WDR45 gene and its role in pediatric epilepsies 102
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles 100
Parossismi non epilettici: Una trappola per i pediatri 100
Genotype-phenotype variable correlation in Wilson disease: clinical history of two sisters with the similar genotype 100
The spectrum of KCNQ2- And KCNQ3-related epilepsy 100
COVID-19 Pandemic Outbreak and its Psychological Impact on Patients with Rare Lysosomal Diseases 99
Encefalomielite acuta demielinizzante ricorrente: dalla clinica alla diagnosi. 98
Genotype–Phenotype Correlation in a Large Cohort of Eastern Sicilian Patients Affected by Phenylketonuria: Newborn Screening Program, Clinical Features, and Follow-Up 97
Intossicazione accidentale da alcol etilico in un lattante di 30 giorni. Quadro clinico e follow-up neurologico 96
Astrocitoma gigante in un paziente affetto da Sclerosi Tuberosa 96
Giant melanocytic nevi and soft tissue undergrowth in the left leg: Pathogenetic hypothesis 95
CDKL5 gene: Beyond rett syndrome 95
Efficacy of the anti-seizure medications in acute symptomatic neonatal seizures caused by stroke. A systematic review 94
Subacute sclerosing panencephalitis: A case report 94
Totale 13.776
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Categoria #
all - tutte 61.031
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 61.031
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021521 0 0 0 0 0 21 86 45 64 95 140 70
2021/20221.474 82 175 84 52 208 45 233 64 87 25 34 385
2022/20232.794 196 191 48 315 264 444 45 467 509 82 140 93
2023/20241.421 69 235 66 103 65 267 69 106 40 43 231 127
2024/20254.827 117 755 321 399 812 524 182 161 300 408 541 307
2025/20266.950 571 640 1.710 686 1.406 1.937 0 0 0 0 0 0
Totale 19.597