IRIS
PRATICO', ANDREA DOMENICO
 Distribuzione geografica
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Continente #
NA - Nord America 7.829
EU - Europa 4.198
AS - Asia 3.157
SA - Sud America 782
AF - Africa 666
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 3
Totale 16.648
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Nazione #
US - Stati Uniti d'America 7.611
IT - Italia 2.534
SG - Singapore 1.470
CN - Cina 1.035
BR - Brasile 675
IE - Irlanda 573
CI - Costa d'Avorio 470
UA - Ucraina 248
VN - Vietnam 189
IN - India 185
CA - Canada 177
RU - Federazione Russa 162
DE - Germania 148
SN - Senegal 121
GB - Regno Unito 86
SE - Svezia 71
KR - Corea 70
NL - Olanda 61
FR - Francia 57
FI - Finlandia 54
PL - Polonia 50
AR - Argentina 40
MX - Messico 30
JP - Giappone 29
BD - Bangladesh 28
ZA - Sudafrica 26
CH - Svizzera 25
ES - Italia 25
TR - Turchia 24
CZ - Repubblica Ceca 23
EC - Ecuador 17
GR - Grecia 17
ID - Indonesia 15
MA - Marocco 15
AT - Austria 14
CO - Colombia 14
IR - Iran 14
UZ - Uzbekistan 14
HK - Hong Kong 13
AU - Australia 12
BJ - Benin 12
IQ - Iraq 10
LB - Libano 9
SA - Arabia Saudita 9
VE - Venezuela 9
BE - Belgio 8
AE - Emirati Arabi Uniti 7
PE - Perù 7
PY - Paraguay 7
CL - Cile 6
LT - Lituania 6
NG - Nigeria 6
PK - Pakistan 6
DO - Repubblica Dominicana 5
IL - Israele 5
UY - Uruguay 5
AZ - Azerbaigian 4
DK - Danimarca 4
KE - Kenya 4
NO - Norvegia 4
OM - Oman 4
RO - Romania 4
RS - Serbia 4
BY - Bielorussia 3
EG - Egitto 3
HU - Ungheria 3
AO - Angola 2
BB - Barbados 2
BO - Bolivia 2
EU - Europa 2
GE - Georgia 2
JO - Giordania 2
MY - Malesia 2
NP - Nepal 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
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
NZ - Nuova Zelanda 1
PH - Filippine 1
Totale 16.642
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Città #
Dallas 1.594
Santa Clara 1.005
Chandler 937
Singapore 826
Dublin 573
Abidjan 470
Chicago 458
Catania 293
Jacksonville 290
Ashburn 265
Boardman 247
Houston 242
Los Angeles 212
Beijing 209
Hefei 187
Cambridge 160
Lawrence 160
Andover 158
Milan 155
Civitanova Marche 142
Nanjing 140
Rome 140
Kochi 127
Dakar 121
Toronto 89
Des Moines 85
Bremen 71
New York 70
Seoul 70
Wilmington 66
Palermo 59
São Paulo 54
Ho Chi Minh City 52
Ottawa 49
Padova 49
Oakland 45
The Dalles 45
Naples 40
Columbus 39
Shenyang 39
Dong Ket 37
Lago 37
Munich 33
Warsaw 33
Turku 32
Council Bluffs 31
Hanoi 31
Saint Petersburg 31
Brooklyn 30
Nanchang 30
Buffalo 29
San Mateo 28
Florence 27
Hebei 27
Seattle 27
Tokyo 27
Jiaxing 26
Bologna 25
Bussero 25
Bari 24
Tianjin 23
Denver 22
Phoenix 22
Brescia 21
Montreal 21
Moscow 21
Rio de Janeiro 21
Changsha 20
Gravina di Catania 20
Redondo Beach 20
Riposto 19
Ferrara 18
Poplar 18
Stockholm 18
Amsterdam 16
Belo Horizonte 16
Chennai 16
Falls Church 16
Johannesburg 16
Atlanta 15
Den Haag 15
Orem 15
San Francisco 15
Turin 15
Cagliari 14
Campobasso 14
Boston 13
Curitiba 13
Lipari 13
Ragusa 13
Washington 13
Adrano 12
Cotonou 12
Hong Kong 12
Jinan 12
Lappeenranta 12
London 12
Norwalk 12
Verona 12
Castelnovo 11
Totale 11.262
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Nome #
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 805
Sindromi Neurocutanee 614
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] 246
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 163
Speckled Lentiginous Nevus Syndrome 161
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 157
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 156
Periventricular Heterotopias: Neuroependymal Abnormalities 148
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 148
Encefalopatia acuta da probabile deficit cerebrale di acido folico in paziente con iperfenilalaninemia da deficit di DHPR 145
Becker's Nevus Syndrome 145
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 144
Anti-mog associated encephalitis: when steroid therapy is not enough 143
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 135
Phacomatosis Pigmentovascularis 134
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 133
Blue Rubber Bleb Nevus Syndrome 133
Phacomatosis Pigmentokeratotica 132
Nevus Sebaceous Syndrome 129
Mycoplasma pneumoniae: dalla polmonite atipica primaria alle complicanze extrapolmonari 128
A New Patient with Potocki-Lupski Syndrome: A Literature Review 126
Isolated liver disease in a patient with a CFTR genotype F508del/12TG-5T and 470MV: A new face of an old disease 124
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 122
Aristaless-related homeobox (ARX): Epilepsy phenotypes beyond lissencephaly and brain malformations 122
At the Origin of Brain Malformations: Embryology of the Central and Peripheral Nervous System 121
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 117
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 114
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 114
E se non fossero solo incubi notturni? 113
Megalencephaly Capillary Malformation Syndrome 113
Hypoglossal nerve paralysis in a child after a dental procedure 112
Wyburn-Mason Syndrome 112
Congenital muscular dystrophy: from muscle to brain 111
GRIN2A and GRIN2B and Their Related Phenotypes 109
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 108
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 107
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 107
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 106
SCN1B gene: A close relative to SCN1A 105
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 104
KCNT1-Related Epilepsy: A Review 104
A child with congenital heart disease and situs viscerum inversus 103
Microcephaly-Capillary Malformation Syndrome 103
Did Cro-Magnon 1 have neurofibromatosis type 2? 102
Multiseptate Gallbladder in a Child: A Possible Cause of Poor Growth? 102
Neurocutaneous melanocytosis (melanosis) 102
Mixed Vascular Nevus Syndrome 101
Ataxia in children: early recognition and clinical evaluation 101
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 101
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 100
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 100
Allergia agli insetti 100
Cognitive disabilities and bioethical implications in down syndrome 100
Recurrent obstructive hydrocephalus in a 4-month-old infant 99
Hypomelanosis of Ito 99
Pott disease in a 14-year-old girl affected by congenital lamellar ichthyosis type 3 and diabetes mellitus 99
Cutis Tricolor 99
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 98
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 98
Pediatria dalla A alla Z - Guida Pratica alla diagnosi e al trattamento. Neurologia, disturbi psichiatrici e comportamentali 98
The immunopathogenesis of cows milk protein allergy (CMPA) 98
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 98
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 97
Tetralogy of Fallot variant with pulmonary atresia (pseudotruncus arteriosus) in a case of maternal PKU syndrome 96
DNM1 Gene and Its Related Epileptic Phenotypes 96
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 95
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 95
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa 93
Actualities on molecular pathogenesis and repairing processes of cerebral damage in perinatal hypoxic-ischemic encephalopathy 91
Gamma-aminobutyric acid type a receptor genes and their related epilepsies 91
Neuroaspergillosis as the Presenting Sign of a Chronic Granulomatous Disease 90
PCDH19-Related Epilepsies 90
Eczema herpeticum in a patient with atopic dermatitis, coxsackie B virus, and staphylococcal infection: A double skin damage 89
Graph theory in paediatric epilepsy: A systematic review 88
HyperCKemia as a biomarker for muscular diseases 88
SYNGAP1 and Its Related Epileptic Syndromes 88
Introduction to phacomatoses (neurocutaneous disorders) in childhood 88
A sudden weight gain in a child as clinical presentation of Chiari Type I malformation: a case report 87
A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: A new patient with a novel feature 87
A Retrospective Study on Standard Regimen for Vaccination in Celiac Children 87
Genotype-phenotype variable correlation in Wilson disease: clinical history of two sisters with the similar genotype 87
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles 86
COVID-19 Pandemic Outbreak and its Psychological Impact on Patients with Rare Lysosomal Diseases 86
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 86
Acquired peripheral neuropathy: a report on 20 children. 85
Epatite Autoimmune: esperienza personale e revisione della letteratura 85
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] 85
Autoimmune hepatitis: clinical findings in six pediatric patients. 84
Parossismi non epilettici: Una trappola per i pediatri 84
FOXG1 Gene and Its Related Phenotypes 84
Neurofibromatosis type 1 and infantile spasms 83
WDR45 gene and its role in pediatric epilepsies 83
Congenital generalized hypertrichosis: the skin as a clue to complex malformation Syndromes. 82
Blepharoptosis in children: Our experience at the light of literature 82
Holoprosencephaly and Recurrent Episodes of Severe Neurogenic Hypernatremia 81
Intossicazione accidentale da alcol etilico in un lattante di 30 giorni. Quadro clinico e follow-up neurologico 81
Astrocitoma gigante in un paziente affetto da Sclerosi Tuberosa 81
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 80
Cervical neurenteric cyst and Klippel-Feil syndrome: An abrupt onset of myelopathic signs in a young patient 80
Clinical spectrum of woolly hair: Indications for cerebral involvement 80
Totale 11.872
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Categoria #
all - tutte 57.066
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 57.066
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021720 0 0 0 0 199 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
2025/20264.357 571 640 1.710 686 750 0 0 0 0 0 0 0
Totale 17.004