IRIS
PRATICO', ANDREA DOMENICO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 5.570
EU - Europa 3.957
AS - Asia 2.294
SA - Sud America 589
AF - Africa 438
OC - Oceania 13
Continente sconosciuto - Info sul continente non disponibili 2
Totale 12.863
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 5.398
IT - Italia 2.411
SG - Singapore 1.157
CN - Cina 751
IE - Irlanda 573
BR - Brasile 529
CI - Costa d'Avorio 283
UA - Ucraina 248
IN - India 166
RU - Federazione Russa 157
CA - Canada 152
DE - Germania 148
SN - Senegal 120
SE - Svezia 60
VN - Vietnam 58
GB - Regno Unito 56
FR - Francia 51
FI - Finlandia 48
NL - Olanda 47
KR - Corea 36
PL - Polonia 36
CH - Svizzera 25
CZ - Repubblica Ceca 21
TR - Turchia 21
AR - Argentina 19
GR - Grecia 17
BD - Bangladesh 15
UZ - Uzbekistan 13
AU - Australia 12
MA - Marocco 12
MX - Messico 12
AT - Austria 11
ZA - Sudafrica 11
EC - Ecuador 9
IQ - Iraq 9
JP - Giappone 9
LB - Libano 9
SA - Arabia Saudita 9
BE - Belgio 8
ES - Italia 8
VE - Venezuela 8
CL - Cile 6
CO - Colombia 6
NG - Nigeria 6
IL - Israele 5
PK - Pakistan 5
AE - Emirati Arabi Uniti 4
KE - Kenya 4
NO - Norvegia 4
PY - Paraguay 4
RO - Romania 4
RS - Serbia 4
AZ - Azerbaigian 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
HK - Hong Kong 3
IR - Iran 3
PE - Perù 3
UY - Uruguay 3
BO - Bolivia 2
EU - Europa 2
HU - Ungheria 2
ID - Indonesia 2
JO - Giordania 2
NP - Nepal 2
OM - Oman 2
PT - Portogallo 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
AL - Albania 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BG - Bulgaria 1
BT - Bhutan 1
BY - Bielorussia 1
EE - Estonia 1
GA - Gabon 1
GE - Georgia 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
MY - Malesia 1
NI - Nicaragua 1
NZ - Nuova Zelanda 1
PH - Filippine 1
PS - Palestinian Territory 1
TH - Thailandia 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
Totale 12.863
Salva come PNG Salva come JPEG
Città #
Santa Clara 993
Chandler 937
Singapore 786
Dublin 573
Chicago 453
Jacksonville 290
Abidjan 283
Catania 277
Boardman 247
Houston 231
Ashburn 162
Cambridge 160
Lawrence 160
Andover 158
Beijing 145
Milan 145
Civitanova Marche 142
Nanjing 140
Rome 130
Kochi 127
Dakar 120
Hefei 93
Des Moines 84
Toronto 83
Bremen 71
Wilmington 66
Palermo 56
Ottawa 49
Padova 49
Los Angeles 45
Oakland 45
The Dalles 45
New York 40
Columbus 39
Shenyang 39
Dong Ket 37
Lago 37
Naples 36
Seoul 36
Munich 33
Turku 32
Council Bluffs 31
Saint Petersburg 31
Nanchang 30
São Paulo 30
San Mateo 28
Hebei 27
Jiaxing 26
Bussero 25
Seattle 24
Tianjin 23
Bologna 21
Brescia 21
Bari 20
Changsha 20
Florence 20
Gravina di Catania 20
Moscow 20
Rio de Janeiro 19
Riposto 19
Warsaw 19
Ferrara 18
Brooklyn 17
Falls Church 16
Den Haag 15
San Francisco 15
Turin 15
Campobasso 14
Hanoi 14
Lipari 13
Ragusa 13
Washington 13
Adrano 12
Belo Horizonte 12
Cagliari 12
Jinan 12
Norwalk 12
Castelnovo 11
Frattamaggiore 11
Reggio Emilia 11
Curitiba 10
Gela 10
Helsinki 10
Milazzo 10
Priolo Gargallo 10
Redmond 10
Verona 10
Boston 9
Catanzaro 9
Marseille 9
Montreal 9
Phoenix 9
Redwood City 9
Tappahannock 9
Atlanta 8
Bergamo 8
Chennai 8
Dallas 8
Fortaleza 8
Iesi 8
Totale 8.585
Salva come PNG Salva come JPEG
Nome #
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 756
Sindromi Neurocutanee 563
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] 221
Speckled Lentiginous Nevus Syndrome 140
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 129
Mycoplasma pneumoniae: dalla polmonite atipica primaria alle complicanze extrapolmonari 118
Encefalopatia acuta da probabile deficit cerebrale di acido folico in paziente con iperfenilalaninemia da deficit di DHPR 115
Blue Rubber Bleb Nevus Syndrome 112
Phacomatosis Pigmentokeratotica 111
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 111
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 110
Anti-mog associated encephalitis: when steroid therapy is not enough 109
Becker's Nevus Syndrome 108
Phacomatosis Pigmentovascularis 107
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 103
Congenital muscular dystrophy: from muscle to brain 103
Nevus Sebaceous Syndrome 99
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 96
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 94
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 93
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 93
SCN1B gene: A close relative to SCN1A 93
Isolated liver disease in a patient with a CFTR genotype F508del/12TG-5T and 470MV: A new face of an old disease 92
Cognitive disabilities and bioethical implications in down syndrome 90
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 90
GRIN2A and GRIN2B and Their Related Phenotypes 90
Did Cro-Magnon 1 have neurofibromatosis type 2? 89
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 89
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 88
E se non fossero solo incubi notturni? 88
Pediatria dalla A alla Z - Guida Pratica alla diagnosi e al trattamento. Neurologia, disturbi psichiatrici e comportamentali 88
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 88
Aristaless-related homeobox (ARX): Epilepsy phenotypes beyond lissencephaly and brain malformations 87
Wyburn-Mason Syndrome 86
Mixed Vascular Nevus Syndrome 85
Recurrent obstructive hydrocephalus in a 4-month-old infant 84
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 83
Hypoglossal nerve paralysis in a child after a dental procedure 83
Microcephaly-Capillary Malformation Syndrome 83
Multiseptate Gallbladder in a Child: A Possible Cause of Poor Growth? 83
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 83
Ataxia in children: early recognition and clinical evaluation 82
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 82
Cutis Tricolor 81
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 80
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 80
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 80
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 79
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 79
Hypomelanosis of Ito 78
KCNT1-Related Epilepsy: A Review 78
Pott disease in a 14-year-old girl affected by congenital lamellar ichthyosis type 3 and diabetes mellitus 77
DNM1 Gene and Its Related Epileptic Phenotypes 77
Neuroaspergillosis as the Presenting Sign of a Chronic Granulomatous Disease 76
Congenital generalized hypertrichosis: the skin as a clue to complex malformation Syndromes. 75
Parossismi non epilettici: Una trappola per i pediatri 75
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 75
At the Origin of Brain Malformations: Embryology of the Central and Peripheral Nervous System 74
A New Patient with Potocki-Lupski Syndrome: A Literature Review 74
Megalencephaly Capillary Malformation Syndrome 74
Clinical spectrum of woolly hair: Indications for cerebral involvement 74
Reconstructive Surgery in Children with Down's Syndrome: Bioethical Implications 74
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 74
Cervical neurenteric cyst and Klippel-Feil syndrome: An abrupt onset of myelopathic signs in a young patient 73
Blepharoptosis in children: Our experience at the light of literature 73
SYNGAP1 and Its Related Epileptic Syndromes 73
PCDH19-Related Epilepsies 73
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 72
Genotype-phenotype variable correlation in Wilson disease: clinical history of two sisters with the similar genotype 72
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 71
Congenital myasthenic syndromes: Clinical and molecular report on 7 Sicilian patients 71
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa 71
WDR45 gene and its role in pediatric epilepsies 71
Holoprosencephaly and Recurrent Episodes of Severe Neurogenic Hypernatremia 70
The immunopathogenesis of cows milk protein allergy (CMPA) 70
Allergia agli insetti 70
Eczema herpeticum in a patient with atopic dermatitis, coxsackie B virus, and staphylococcal infection: A double skin damage 70
The multiple faces of artwork diagnoses. 70
Neurofibromatosis type 1 and infantile spasms 69
Autoimmune hepatitis: clinical findings in six pediatric patients. 69
SCN1A and its related epileptic phenotypes 69
Rediagnosing one of Smith's patients (John McCann) with "neuromas tumours" (1849). 68
Astrocitoma gigante in un paziente affetto da Sclerosi Tuberosa 68
Epatite Autoimmune: esperienza personale e revisione della letteratura 68
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] 68
Prognostic challenges of SCN1A genetic mutations: report of two children with mild features 67
Biochemical Insights into Merlin/NF2 Pathophysiology and Biologically Targeted Therapies in Childhood NF2 and Related Forms 67
Una febbre “strana” nel lattante 67
Tetralogy of Fallot variant with pulmonary atresia (pseudotruncus arteriosus) in a case of maternal PKU syndrome 67
A Retrospective Study on Standard Regimen for Vaccination in Celiac Children 67
Encefalomielite acuta demielinizzante ricorrente: dalla clinica alla diagnosi. 67
Giant melanocytic nevi and soft tissue undergrowth in the left leg: Pathogenetic hypothesis 67
A child with congenital heart disease and situs viscerum inversus 66
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles 66
Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardation 65
Intossicazione accidentale da alcol etilico in un lattante di 30 giorni. Quadro clinico e follow-up neurologico 65
Sindrome di Sturge Weber: presentazione atipica con malformazione capillare cerebrale 65
A mild phenotype associated with a de novo microdeletion 10q23.1-q23.2: A new patient with a novel feature 65
Neurocutaneous melanocytosis (melanosis) 65
Erratum: Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports (Medicine 95:10 (e2705)) (2016) Medicine (United States), 95 (15) 65
Totale 9.471
Salva come PNG Salva come JPEG
Categoria #
all - tutte 47.678
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 47.678
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021893 25 50 85 13 199 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
2025/2026569 569 0 0 0 0 0 0 0 0 0 0 0
Totale 13.216