IRIS
PRATICO', ANDREA DOMENICO
 Distribuzione geografica
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Continente #
NA - Nord America 9.031
EU - Europa 6.440
AS - Asia 4.526
SA - Sud America 940
AF - Africa 795
OC - Oceania 19
Continente sconosciuto - Info sul continente non disponibili 3
Totale 21.754
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Nazione #
US - Stati Uniti d'America 8.742
IT - Italia 2.727
SG - Singapore 2.245
RU - Federazione Russa 1.827
CN - Cina 1.118
BR - Brasile 774
IE - Irlanda 576
CI - Costa d'Avorio 471
VN - Vietnam 423
UA - Ucraina 261
FR - Francia 241
IN - India 221
CA - Canada 219
DE - Germania 169
GB - Regno Unito 128
KR - Corea 125
SN - Senegal 123
NL - Olanda 83
NG - Nigeria 78
SE - Svezia 76
FI - Finlandia 64
PL - Polonia 63
BD - Bangladesh 55
AR - Argentina 54
MX - Messico 52
ZA - Sudafrica 48
JP - Giappone 46
HK - Hong Kong 39
TR - Turchia 39
ES - Italia 36
IQ - Iraq 36
CH - Svizzera 30
CZ - Repubblica Ceca 26
CO - Colombia 24
ID - Indonesia 24
EC - Ecuador 23
AT - Austria 21
GR - Grecia 21
VE - Venezuela 20
MA - Marocco 19
UZ - Uzbekistan 19
AU - Australia 18
LT - Lituania 16
PK - Pakistan 16
CL - Cile 14
IR - Iran 14
SA - Arabia Saudita 14
BJ - Benin 12
KE - Kenya 11
BE - Belgio 10
EG - Egitto 10
LB - Libano 10
PY - Paraguay 10
AE - Emirati Arabi Uniti 9
PE - Perù 9
HU - Ungheria 8
JO - Giordania 8
MY - Malesia 8
UY - Uruguay 8
ET - Etiopia 7
PH - Filippine 7
RO - Romania 7
DK - Danimarca 6
DO - Repubblica Dominicana 6
IL - Israele 6
NP - Nepal 6
DZ - Algeria 5
PS - Palestinian Territory 5
RS - Serbia 5
AL - Albania 4
AO - Angola 4
AZ - Azerbaigian 4
BO - Bolivia 4
BY - Bielorussia 4
CR - Costa Rica 4
KZ - Kazakistan 4
NO - Norvegia 4
OM - Oman 4
PT - Portogallo 4
SI - Slovenia 4
SK - Slovacchia (Repubblica Slovacca) 4
TH - Thailandia 4
GE - Georgia 3
MT - Malta 3
TN - Tunisia 3
BB - Barbados 2
BG - Bulgaria 2
CY - Cipro 2
EU - Europa 2
HR - Croazia 2
JM - Giamaica 2
KH - Cambogia 2
LV - Lettonia 2
MN - Mongolia 2
SY - Repubblica araba siriana 2
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BT - Bhutan 1
EE - Estonia 1
GA - Gabon 1
Totale 21.737
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Città #
Dallas 1.605
Singapore 1.464
Santa Clara 1.028
Chandler 937
Moscow 840
Dublin 576
San Jose 484
Abidjan 471
Chicago 460
Ashburn 447
Catania 300
Jacksonville 290
Los Angeles 263
Houston 252
Boardman 247
Beijing 220
Hefei 187
Milan 174
Lauterbourg 163
Cambridge 160
Lawrence 160
Andover 158
Rome 152
Civitanova Marche 142
Nanjing 140
Ho Chi Minh City 134
Kochi 127
Seoul 124
Dakar 123
Toronto 99
New York 98
Hanoi 89
Des Moines 86
Council Bluffs 75
Bremen 71
Palermo 71
São Paulo 68
Wilmington 66
Buffalo 51
Ottawa 49
Padova 49
The Dalles 49
Oakland 45
Naples 44
Warsaw 44
Tokyo 41
Orem 40
Brooklyn 39
Columbus 39
Lagos 39
Shenyang 39
Dong Ket 37
Lago 37
Denver 33
Montreal 33
Munich 33
Hong Kong 32
Seattle 32
Turku 32
Florence 31
Johannesburg 31
Saint Petersburg 31
Bari 30
Nanchang 30
Abuja 29
Bologna 28
Chennai 28
London 28
Phoenix 28
Rio de Janeiro 28
San Mateo 28
Hebei 27
Atlanta 26
Jiaxing 26
Bussero 25
Poplar 24
Brescia 23
Stockholm 23
Tianjin 23
Amsterdam 22
Frankfurt am Main 22
Cagliari 21
Changsha 20
Gravina di Catania 20
Redondo Beach 20
Riposto 19
Ferrara 18
Belo Horizonte 17
Paris 17
Curitiba 16
Falls Church 16
Helsinki 16
Lappeenranta 16
San Francisco 16
Turin 16
Boston 15
Campobasso 15
Den Haag 15
Haiphong 15
Mexico City 15
Totale 14.302
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Nome #
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 910
Sindromi Neurocutanee 698
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] 281
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 204
Speckled Lentiginous Nevus Syndrome 200
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 197
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 196
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 194
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 193
Becker's Nevus Syndrome 193
Anti-mog associated encephalitis: when steroid therapy is not enough 190
Encefalopatia acuta da probabile deficit cerebrale di acido folico in paziente con iperfenilalaninemia da deficit di DHPR 187
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 182
A New Patient with Potocki-Lupski Syndrome: A Literature Review 176
Blue Rubber Bleb Nevus Syndrome 174
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 172
Nevus Sebaceous Syndrome 172
At the Origin of Brain Malformations: Embryology of the Central and Peripheral Nervous System 169
Phacomatosis Pigmentovascularis 169
Phacomatosis Pigmentokeratotica 169
Periventricular Heterotopias: Neuroependymal Abnormalities 164
Aristaless-related homeobox (ARX): Epilepsy phenotypes beyond lissencephaly and brain malformations 164
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 159
Isolated liver disease in a patient with a CFTR genotype F508del/12TG-5T and 470MV: A new face of an old disease 158
Hypoglossal nerve paralysis in a child after a dental procedure 158
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 158
GRIN2A and GRIN2B and Their Related Phenotypes 155
Wyburn-Mason Syndrome 152
Mycoplasma pneumoniae: dalla polmonite atipica primaria alle complicanze extrapolmonari 149
Megalencephaly Capillary Malformation Syndrome 149
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 148
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 148
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 147
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 146
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 145
Microcephaly-Capillary Malformation Syndrome 143
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 142
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 142
SCN1B gene: A close relative to SCN1A 142
A child with congenital heart disease and situs viscerum inversus 139
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 139
E se non fossero solo incubi notturni? 139
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 136
Gamma-aminobutyric acid type a receptor genes and their related epilepsies 136
KCNT1-Related Epilepsy: A Review 136
Allergia agli insetti 135
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 135
Hypomelanosis of Ito 134
DNM1 Gene and Its Related Epileptic Phenotypes 134
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 133
The immunopathogenesis of cows milk protein allergy (CMPA) 132
Multiseptate Gallbladder in a Child: A Possible Cause of Poor Growth? 132
Actualities on molecular pathogenesis and repairing processes of cerebral damage in perinatal hypoxic-ischemic encephalopathy 132
Did Cro-Magnon 1 have neurofibromatosis type 2? 131
Cutis Tricolor 130
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 130
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 129
A Retrospective Study on Standard Regimen for Vaccination in Celiac Children 129
Pediatria dalla A alla Z - Guida Pratica alla diagnosi e al trattamento. Neurologia, disturbi psichiatrici e comportamentali 128
Pott disease in a 14-year-old girl affected by congenital lamellar ichthyosis type 3 and diabetes mellitus 128
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature 127
Congenital muscular dystrophy: from muscle to brain 127
Tetralogy of Fallot variant with pulmonary atresia (pseudotruncus arteriosus) in a case of maternal PKU syndrome 127
Genotype–Phenotype Correlation in a Large Cohort of Eastern Sicilian Patients Affected by Phenylketonuria: Newborn Screening Program, Clinical Features, and Follow-Up 126
Recurrent obstructive hydrocephalus in a 4-month-old infant 126
Mixed Vascular Nevus Syndrome 126
Neurocutaneous melanocytosis (melanosis) 126
A sudden weight gain in a child as clinical presentation of Chiari Type I malformation: a case report 125
Ataxia in children: early recognition and clinical evaluation 125
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 125
Cognitive disabilities and bioethical implications in down syndrome 124
PCDH19-Related Epilepsies 124
A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: A new patient with a novel feature 122
HyperCKemia as a biomarker for muscular diseases 121
Neuroaspergillosis as the Presenting Sign of a Chronic Granulomatous Disease 121
SYNGAP1 and Its Related Epileptic Syndromes 121
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa 120
COVID-19 Pandemic Outbreak and its Psychological Impact on Patients with Rare Lysosomal Diseases 120
Blepharoptosis in children: Our experience at the light of literature 119
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] 119
WDR45 Gene and Its Role in Pediatric Epilepsies 119
Pediatric Lemierre’s Syndrome: A Comprehensive Literature Review 118
Genotype-phenotype variable correlation in Wilson disease: clinical history of two sisters with the similar genotype 117
Graph theory in paediatric epilepsy: A systematic review 116
Introduction to phacomatoses (neurocutaneous disorders) in childhood 116
The spectrum of KCNQ2- And KCNQ3-related epilepsy 116
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 116
Acquired peripheral neuropathy: a report on 20 children. 115
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 114
Encefalomielite acuta demielinizzante ricorrente: dalla clinica alla diagnosi. 113
Giant melanocytic nevi and soft tissue undergrowth in the left leg: Pathogenetic hypothesis 113
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles 112
Magnetic Resonance Imaging of Central Nervous System Manifestations of Type 1 Neurofibromatosis: Pictorial Review and Retrospective Study of Their Frequency in a Cohort of Patients 111
Subacute sclerosing panencephalitis: A case report 111
Eczema herpeticum in a patient with atopic dermatitis, coxsackie B virus, and staphylococcal infection: A double skin damage 111
FOXG1 Gene and Its Related Phenotypes 111
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 109
CDKL5 gene: Beyond rett syndrome 109
Neonatal seizures as onset of Inborn Errors of Metabolism (IEMs): from diagnosis to treatment. A systematic review 108
Syntaxin binding protein 1 related epilepsies 108
Totale 15.426
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Categoria #
all - tutte 65.678
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 65.678
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021305 0 0 0 0 0 0 0 0 0 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
2025/20269.464 571 640 1.710 686 1.406 2.131 969 226 576 549 0 0
Totale 22.111