IRIS
PRATICO', ANDREA DOMENICO
 Distribuzione geografica
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Continente #
NA - Nord America 3.969
EU - Europa 3.171
AS - Asia 1.045
AF - Africa 410
OC - Oceania 13
SA - Sud America 11
Continente sconosciuto - Info sul continente non disponibili 2
Totale 8.621
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Nazione #
US - Stati Uniti d'America 3.829
IT - Italia 1.823
IE - Irlanda 573
CN - Cina 487
SG - Singapore 459
CI - Costa d'Avorio 283
UA - Ucraina 240
RU - Federazione Russa 143
CA - Canada 137
DE - Germania 122
SN - Senegal 119
SE - Svezia 54
FR - Francia 48
VN - Vietnam 47
GB - Regno Unito 32
PL - Polonia 22
CH - Svizzera 20
NL - Olanda 19
GR - Grecia 17
CZ - Repubblica Ceca 14
AU - Australia 12
IN - India 12
BE - Belgio 8
LB - Libano 7
NG - Nigeria 6
TR - Turchia 6
UZ - Uzbekistan 6
AT - Austria 5
BR - Brasile 5
JP - Giappone 5
ES - Italia 4
NO - Norvegia 4
RO - Romania 4
CL - Cile 3
DK - Danimarca 3
FI - Finlandia 3
IR - Iran 3
RS - Serbia 3
EU - Europa 2
HU - Ungheria 2
ID - Indonesia 2
MX - Messico 2
PE - Perù 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
AR - Argentina 1
BA - Bosnia-Erzegovina 1
BT - Bhutan 1
EE - Estonia 1
GL - Groenlandia 1
HK - Hong Kong 1
IL - Israele 1
IS - Islanda 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
LU - Lussemburgo 1
MA - Marocco 1
ME - Montenegro 1
MK - Macedonia 1
MM - Myanmar 1
MY - Malesia 1
NZ - Nuova Zelanda 1
PH - Filippine 1
TH - Thailandia 1
ZA - Sudafrica 1
Totale 8.621
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Città #
Chandler 937
Dublin 573
Chicago 445
Singapore 339
Jacksonville 287
Abidjan 283
Boardman 247
Houston 228
Catania 224
Cambridge 160
Lawrence 160
Andover 158
Nanjing 140
Ashburn 123
Dakar 119
Milan 105
Des Moines 84
Toronto 82
Rome 78
Bremen 71
Wilmington 66
Ottawa 49
Padova 46
Oakland 45
Shenyang 39
Dong Ket 37
Lago 37
Saint Petersburg 31
Nanchang 30
Palermo 28
San Mateo 28
Hebei 27
Jiaxing 26
Beijing 25
Naples 24
Tianjin 23
Seattle 22
Changsha 20
Gravina di Catania 20
Los Angeles 20
Moscow 20
Riposto 19
Brescia 18
Ferrara 18
Munich 17
Santa Clara 17
Bari 16
Falls Church 16
Florence 16
Den Haag 15
Bologna 14
Campobasso 14
Lipari 13
Washington 13
Adrano 12
Jinan 12
Norwalk 12
Castelnovo 11
Frattamaggiore 11
Turin 11
Cagliari 10
Gela 10
Hanoi 10
Milazzo 10
Priolo Gargallo 10
Ragusa 10
Redmond 10
Verona 10
Catanzaro 9
Marseille 9
Redwood City 9
Tappahannock 9
Bergamo 8
Iesi 8
Reggio Emilia 8
Vicenza 8
Ancona 7
Brno 7
Brussels 7
Edinburgh 7
San Francisco 7
San Giovanni la Punta 7
Foggia 6
Montepaone Lido 6
Ningbo 6
Warsaw 6
Augusta 5
Desio 5
Genova 5
Hangzhou 5
Kunming 5
Liberty Lake 5
London 5
Lucca 5
Missaglia 5
Napoli 5
Pozzallo 5
Scordia 5
Abuja 4
Acerra 4
Totale 6.063
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Nome #
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 625
Sindromi Neurocutanee 356
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] 199
Speckled Lentiginous Nevus Syndrome 113
Mycoplasma pneumoniae: dalla polmonite atipica primaria alle complicanze extrapolmonari 89
Blue Rubber Bleb Nevus Syndrome 81
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 81
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 79
Phacomatosis Pigmentokeratotica 79
Becker's Nevus Syndrome 78
Nevus Sebaceous Syndrome 77
Phacomatosis Pigmentovascularis 77
Anti-mog associated encephalitis: when steroid therapy is not enough 75
Isolated liver disease in a patient with a CFTR genotype F508del/12TG-5T and 470MV: A new face of an old disease 70
Congenital muscular dystrophy: from muscle to brain 70
Encefalopatia acuta da probabile deficit cerebrale di acido folico in paziente con iperfenilalaninemia da deficit di DHPR 69
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 68
Did Cro-Magnon 1 have neurofibromatosis type 2? 68
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 67
Wyburn-Mason Syndrome 65
Multiseptate Gallbladder in a Child: A Possible Cause of Poor Growth? 65
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 64
Pediatria dalla A alla Z - Guida Pratica alla diagnosi e al trattamento. Neurologia, disturbi psichiatrici e comportamentali 64
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 64
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 63
Cognitive disabilities and bioethical implications in down syndrome 63
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 62
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 62
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 61
GRIN2A and GRIN2B and Their Related Phenotypes 61
Aristaless-related homeobox (ARX): Epilepsy phenotypes beyond lissencephaly and brain malformations 60
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 59
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 59
Recurrent obstructive hydrocephalus in a 4-month-old infant 58
Ataxia in children: early recognition and clinical evaluation. 58
Cutis Tricolor 58
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 58
E se non fossero solo incubi notturni? 57
Mixed Vascular Nevus Syndrome 57
Autoimmune hepatitis: clinical findings in six pediatric patients. 56
Hypoglossal nerve paralysis in a child after a dental procedure 56
DNM1 Gene and Its Related Epileptic Phenotypes 56
Neurofibromatosis type 1 and infantile spasms 55
Reconstructive Surgery in Children with Down's Syndrome: Bioethical Implications 55
WDR45 gene and its role in pediatric epilepsies 55
Microcephaly-Capillary Malformation Syndrome 54
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 54
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) 54
Prognostic challenges of SCN1A genetic mutations: report of two children with mild features 53
Congenital generalized hypertrichosis: the skin as a clue to complex malformation Syndromes. 53
Clinical spectrum of woolly hair: Indications for cerebral involvement 53
Hypomelanosis of Ito 53
Parossismi non epilettici: Una trappola per i pediatri 53
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 53
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 53
SCN1B gene: A close relative to SCN1A 53
Biochemical Insights into Merlin/NF2 Pathophysiology and Biologically Targeted Therapies in Childhood NF2 and Related Forms 52
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 52
Congenital myasthenic syndromes: Clinical and molecular report on 7 Sicilian patients 52
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 52
Rediagnosing one of Smith's patients (John McCann) with "neuromas tumours" (1849). 51
Spine and brain malformations in a patient obligate carrier of MTHFR with autism and mental retardation 51
Neuroaspergillosis as the Presenting Sign of a Chronic Granulomatous Disease 51
The multiple faces of artwork diagnoses. 51
KCNT1-Related Epilepsy: A Review 51
Holoprosencephaly and Recurrent Episodes of Severe Neurogenic Hypernatremia 50
Early history of neurofibromatosis type 2 and related forms: earliest descriptions of acoustic neuromas, medical curiosities, misconceptions, landmarks and the pioneers behind the eponyms 50
Eczema herpeticum in a patient with atopic dermatitis, coxsackie B virus, and staphylococcal infection: A double skin damage 50
SYNGAP1 and Its Related Epileptic Syndromes 50
PCDH19-Related Epilepsies 50
Voluntary selective big toe dorsal flection: pseudo-Babinski phenomenon? 49
A child with congenital heart disease and situs viscerum inversus 49
Pott disease in a 14-year-old girl affected by congenital lamellar ichthyosis type 3 and diabetes mellitus 49
Previously Unreported COL7A1 Mutation in a Somali Patient with Dystrophic Epidermolysis Bullosa 49
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 49
Cervical neurenteric cyst and Klippel-Feil syndrome: An abrupt onset of myelopathic signs in a young patient 48
Una febbre “strana” nel lattante 48
Megalencephaly Capillary Malformation Syndrome 48
Tetralogy of Fallot variant with pulmonary atresia (pseudotruncus arteriosus) in a case of maternal PKU syndrome 48
Sindrome di Sturge Weber: presentazione atipica con malformazione capillare cerebrale 48
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 48
Genotype-phenotype variable correlation in Wilson disease: clinical history of two sisters with the similar genotype 48
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 48
SCN1A and its related epileptic phenotypes 48
Hepatitis B vaccine in celiac disease: yesterday, today and tomorrow. 47
Autonomic dysfunction manifesting with asymmetric face flushing and paroxysmal nonconvulsive episodes 47
Hydranencephaly: cerebral spinal fluid instead of cerebral mantles 47
The immunopathogenesis of cows milk protein allergy (CMPA) 47
Diagnosis, management and new therapeutic options in childhood neurofibromatosis type 2 and related disorders 47
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 47
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 46
A sudden weight gain in a child as clinical presentation of Chiari Type I malformation: a case report 46
Allergia agli insetti 46
Epatite Autoimmune: esperienza personale e revisione della letteratura 46
Encefalomielite acuta demielinizzante ricorrente: dalla clinica alla diagnosi. 46
Gelastic seizures due to hypothalamic hamartoma: Rapid resolution after endoscopic tumor disconnection. 44
Hemihydranencephaly: living with half brain dysfunction. 44
Intossicazione accidentale da alcol etilico in un lattante di 30 giorni. Quadro clinico e follow-up neurologico 44
Mycoplasma Pneumoniae: non solo polmonite atipica primaria. Esperienza personale e revisione della letteratura. 43
A New Patient with Potocki-Lupski Syndrome: A Literature Review 43
Totale 6.678
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Categoria #
all - tutte 30.215
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 30.215
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020565 0 0 75 79 64 46 88 6 58 32 45 72
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
2024/20251.145 117 755 273 0 0 0 0 0 0 0 0 0
Totale 8.965