IRIS
DEL GIUDICE, ENNIO
 Distribuzione geografica
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Continente #
EU - Europa 12.121
AS - Asia 11.652
NA - Nord America 9.002
SA - Sud America 1.820
AF - Africa 213
Continente sconosciuto - Info sul continente non disponibili 33
OC - Oceania 13
AN - Antartide 2
Totale 34.856
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Nazione #
US - Stati Uniti d'America 8.563
SG - Singapore 7.330
IT - Italia 5.061
RU - Federazione Russa 4.006
CN - Cina 1.953
BR - Brasile 1.529
HK - Hong Kong 1.266
FI - Finlandia 630
UA - Ucraina 628
VN - Vietnam 579
FR - Francia 323
DE - Germania 302
CA - Canada 265
NL - Olanda 246
GB - Regno Unito 211
SE - Svezia 211
IE - Irlanda 188
IN - India 113
AR - Argentina 102
MX - Messico 100
PL - Polonia 76
BD - Bangladesh 65
TR - Turchia 60
ZA - Sudafrica 55
EC - Ecuador 45
ES - Italia 41
ID - Indonesia 40
CO - Colombia 39
IQ - Iraq 36
VE - Venezuela 31
RO - Romania 30
JP - Giappone 29
MA - Marocco 29
CH - Svizzera 26
CI - Costa d'Avorio 26
EU - Europa 25
AT - Austria 23
BE - Belgio 20
CL - Cile 19
PE - Perù 19
PK - Pakistan 17
PY - Paraguay 17
UZ - Uzbekistan 17
KE - Kenya 13
KR - Corea 13
PT - Portogallo 13
UY - Uruguay 12
AZ - Azerbaigian 11
DZ - Algeria 11
SA - Arabia Saudita 11
TN - Tunisia 11
BG - Bulgaria 10
CZ - Repubblica Ceca 10
IR - Iran 10
JO - Giordania 10
HN - Honduras 9
AE - Emirati Arabi Uniti 8
EG - Egitto 8
GT - Guatemala 8
IL - Israele 8
AL - Albania 7
BO - Bolivia 7
DO - Repubblica Dominicana 7
LB - Libano 7
TW - Taiwan 7
BA - Bosnia-Erzegovina 6
GR - Grecia 6
KG - Kirghizistan 6
KZ - Kazakistan 6
LT - Lituania 6
MD - Moldavia 6
NO - Norvegia 6
QA - Qatar 6
TT - Trinidad e Tobago 6
BF - Burkina Faso 5
CR - Costa Rica 5
JM - Giamaica 5
LA - Repubblica Popolare Democratica del Laos 5
LC - Santa Lucia 5
NI - Nicaragua 5
NP - Nepal 5
NZ - Nuova Zelanda 5
OM - Oman 5
AO - Angola 4
AU - Australia 4
BH - Bahrain 4
BZ - Belize 4
CV - Capo Verde 4
CW - ???statistics.table.value.countryCode.CW??? 4
DK - Danimarca 4
ET - Etiopia 4
MW - Malawi 4
MY - Malesia 4
PH - Filippine 4
SI - Slovenia 4
BY - Bielorussia 3
CD - Congo 3
CU - Cuba 3
HT - Haiti 3
MG - Madagascar 3
Totale 34.764
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Città #
Singapore 2.678
Hong Kong 1.264
Moscow 956
Chandler 794
Millbury 666
Princeton 588
Ashburn 507
Beijing 464
Santa Clara 461
Nanjing 409
Jacksonville 279
Rome 270
Los Angeles 250
Boston 246
Milan 243
Naples 230
Wilmington 228
Ho Chi Minh City 225
Amsterdam 192
Buffalo 182
Redondo Beach 173
The Dalles 172
Ottawa 167
Hefei 156
Nanchang 147
Woodbridge 140
Hanoi 123
Dallas 119
São Paulo 106
Napoli 101
Hebei 95
Norwalk 95
Falls Church 94
Jiaxing 84
Houston 81
Shenyang 80
Florence 69
Tianjin 68
Ann Arbor 62
New York 56
San Jose 55
Bologna 50
Seattle 50
Munich 49
Catania 48
Rio de Janeiro 46
Mexico City 45
Padova 44
Palermo 44
Des Moines 43
Warsaw 41
Belo Horizonte 40
Bari 39
Turin 36
Dearborn 35
Montreal 35
Brooklyn 33
Changsha 33
Haiphong 32
Verona 32
Toronto 31
Genova 29
Curitiba 28
Kronberg 28
Tokyo 28
Chicago 27
Helsinki 27
Pescara 27
Orem 26
Stockholm 26
Trieste 26
Boardman 25
Brasília 25
Manaus 25
Denver 24
Johannesburg 24
Washington 24
Frankfurt am Main 23
Kunming 23
Perugia 23
Torino 23
Hangzhou 22
Poplar 22
Salerno 22
Campinas 21
Chennai 21
Parma 21
Biên Hòa 20
Porto Alegre 20
London 19
Vicenza 19
Da Nang 18
Redwood City 18
St Louis 18
Turku 18
Augusta 17
Guayaquil 17
Redmond 17
Ankara 16
Manchester 16
Totale 15.054
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Nome #
Cisti della fessura corioidea 2.282
Test Screening dello Sviluppo di Denver (DDST): sua applicazione in una popolazione di bambini di asili nido 588
Effetti collaterali a lungo termine dei farmaci antiepilettici: studio di una casistica pediatrica. 400
Epilessia frontale con bisincronismo secondario in encefalopatia perinatale 389
Sindrome plurimalformativa caratterizzata da: ritardp psicomotorio, microcefalia, atrofia ottica,eterotopie neuronali, anomalie cardiovascolari 249
Ipernatriemia neuroendocrina: diabete insipido e oloprosencefalia 157
Le amminoacidopatie e le organicoacidurie: approccio alla diagnosi e al trattamento 156
Displasia corticale focale benigna 144
Steroid treatment in Ataxia-Telangiectasia induces alterations of functional magnetic resonance imaging during prono-supination task. 136
Familial white matter hypoplasia agenesis of the corpus callosum, mental retardation and growth deficiency: A new distinctive syndrome. 131
Long term follow-up to evaluate the efficacy of miglustat treatment in Italian patients with Niemann-Pick disease type C 129
Agenesia completa isolata del corpo calloso: follow up di una casistica clinica 128
Epilessia parziale migrante dell'infanzia ed encefalopatia demielinizzante 126
A mobile e-Health software project for remote monitoring of children enrolled in the Carolina Curriculum. 126
A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability 121
Megalocornea and mental retardation syndrome: two new cases. 119
Diabetes mellitus in Kearns-Sayre syndrome: a case with a 10-year follow-up. 118
Disordini motori dello sfintere esofageo superiore (UES) e dell'esofago in bambini cerebropatici. 118
Approccio clinico alle macrocranie non familiari: presentazione di una casistica di 21 pazienti. 117
A further contribution to the delineation of the 17q21.31 microdeletion syndrome: Central nervous involvement in two Italian patients. 117
Episodi ricorrenti d rabdomiolisi secondari a difetto della beta-ossidazione degli acidi grassi. 117
Acute Chorea in children: the value of Single Photon Emission Computed Tomographic Scan (SPECT) and Magnetic Resonance Imaging (MRI) findings 117
A case of 14q11.2 microdeletion with autistic features, severe obesity and facial dysmorphisms suggestive of Wolf-Hirschhorn syndrome. 117
A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright Objects. 117
Aminotransferases and muscular diseases: a disregarded lesson. Case reports and review of the literature 115
Congenital fiber type disproportion myopathy. Report of a case with late onset and myalgia. 112
Clinical Description of a Patient Carrying the Smallest Reported Deletion Involving 10p14 Region 112
PP-8 ESOPHAGEAL HIGH RESOLUTION MANOMETRY IN NEUROLOGICALLLY IMPAIRED CHILDREN AND GASTRO-OESOPHAGEAL REFLUX DISEASE 111
A Social Network Framework for the Carolina Software 109
Steroid-induced improvement of neurological signs in ataxia-telangiectasia patients. 109
Temporal lobe epilepsy in early childhood. 108
Alterazioni della motilità gastrointestinale in bambini con handicap neuromotorio 108
Long-term enzyme replacement therapy for Pompe disease with recombinant human alpha-glucosidase derived from chinese hamster ovary cells. 108
Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy 108
Vaccination against hepatitis B in preschool children with Down's syndrome 106
Disturbi da deficit dell'attenzione, percettivi e motori in età scolare. II. Risultati di uno studio effettuato su una popolazione di bambini della scuola elementare. 106
A mathematical formulation for estimating age levels in the Carolina Curriculum 106
Miopatia congenita da sproporzione tra fibre di tipo I e di tipo II (congenital fiber type dispropotion myopathy) 105
Spatial cognition in children. I. Development of drawing-related (visuospatial and constructional) abilities in preschool and early school years 104
Epilessia da deficit di PNPO: follow-up di 5 anni. 104
Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasia 103
Low-dose amitriptyline-induced acute dystonia in a patient with metachromatic leukodystrophy. 102
Sindrome di West ed errori congeniti del metabolismo 101
Alterazioni cerebrali e sintomatologia gastroinetstinale. 101
Cromosoma 18 pseudoisodicentrico: Studio clinico e citogenetico di un caso 100
Subclinical hypothyroidism and Down's syndrome; studies on myocardial structure and function 99
Brain alteration in a Nude/SCID fetus carrying FOXN1 homozygous mutation. 99
Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22 99
Minimum effective betamethasone dosage on the neurological phenotype in patients with Ataxia-Telangiectasia: a multicenter observer-blind study 99
Intrafamilial variability in SPTAN1-related disorder: From benign convulsions with mild gastroenteritis to developmental encephalopathy 99
Absence of microcephalin gene mutations in a large cohort of non-consanguineous patients with autosomal recessive primary microcephaly. 97
Unexplained Bilateral Occipital Calcification and Reduced Vision. 96
Selective cognitive impairment and tall stature due to chromosome 19 supernumerary ring. 96
Approcci diagnostico-terapeutici al dolore cronico delle patologie neurodegenerative: l'esempio delle leucodistrofie. 96
Mild Wolf-Hirschhorn phenotype and partial GH deficiency in a patient with a 4p terminal deletion. 95
Malattia di Tay-Sachs con elevata attività residua di esosoaminidasi A in leucociti e fibroblasti. 95
Alterazioni della motilità gastrointestinale in bambini affetti da distrofia muscolare progressiva. 95
Variabilità fenotipica intrafamiliare nella miotonia da mutazioni nel gene CLCN1 95
Targeting oxidative stress improves disease outcomes in a rat model of acquired epilepsy 95
Pearls & Oy-sters: Familial epileptic encephalopathy due to methylenetetrahydrofolate reductase deficiency. 94
Atypical expression of beta-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalities 93
Sindromi coreiche in età pediatrica. 93
Developmental delay, epilepsy and brain atrophy of different severity in two first cousins with methylenetetrahydrofolate reductase deficiency. 93
Calcificazioni cerebrali parietooccipitali ed epilessia associate a celiachia 92
EEG findings in West syndrome a follow-up of 20 patients. 91
Alterazioni della motilità gastrointestinale in bambini affetti da distrofia muscolare progressiva 91
A preterm neonate with seizures unresponsive to conventional treatment 91
Epilepsy in Rett syndrome: can seizures play an encephalopathic effect in this disorder? 91
The administration of methotrexate in patients with Still's disease, “real-life” findings from AIDA Network Still Disease Registry 90
Sindrome di Miller-Dieker: osservazione di un caso con studio tomografico computerizzato. 90
Disturbi da deficit dell'attenzione, percettivi e motori in età scolare. I. Aspetti della procedura di screening. 90
Malattia di Tay-Sachs con elevata affinità residua di esosaminidasi A in leucociti e fibroblasti 90
Taylor-type focal cortical dysplasia: is the epilepsy always resistant to medical treatment? 89
Spatial cognition in children. II. Visuospatial and constructional skills in developmental reading disability. 89
Brain migration disorder and T-cell activation deficiency associated with abnormal signaling through TCR/CD3 complex and hyperactivity of Fyn tyrosine kinase. 89
Oral Betamethasone improves neurological symptoms in Ataxia-Teleangiectasia. 89
Primary cerebral neuroblastomas. 88
Impact of malnutrition on gastrointestinal disorders and gross motor abilities in children with cerebral palsy. 87
Induzione enzimatica ed epatopatie da farmaci anticonvulsivanti. Studio retrospettivo su 20 bambini. 85
L'eterozigosità per fenilchetonuria può essere responsabile di ritardo mentale aspecifico? 85
Constitutive activation of the 42 kDa MAPK in a patient with immunodeficiency and severe encephalopathy 85
Alterazioni cerebrali e sintomatologia gastrointestinale 85
Hormonal and neuropsychological evaluation of two 47, XYY patients with pituitary anormalities. 84
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations 84
La sindrome dell'X fragile. 83
Factor Analysis of the Italian Version of the Alabama Parenting Questionnaire in a Community Sample 83
Microdeletion of pseudogene chr14.232.a affects LRFN5 expression in cells of a patient with autism spectrum disorder 83
Cerebellar agenesis 82
Estimate the minimum therpeutically effective dosage of short-term therapy with Betamethasone on neurologicaal symptoms in patients affected with Ataxia-Telangectasia 82
Expansion of the phenotype of lateral meningocele syndrome 82
Electroencephalographic findings in ATRX syndrome: A new case series and review of literature 82
Studio multicentrico della microcefalia vera. Rete clinico-genetica ed analisi sperimentale funzionale del prodotto del gene ASPM. 81
Le basi neurobiologiche dello sviluppo relazionale. 81
Carolina Curriculum per bambini con bisogni educativi speciali (0-3 anni). Un modello di intervento precoce centrato sulla famiglia per bambini con disabilità dello sviluppo. 80
Cerebral palsy and gut functions. 79
Disturbi da deficit d'attenzione, percettivi e motori in età scolare. III. Aspetti neuroevolutivi. 79
Modalità di approccio abilitativo alla patologia centrale motoria della prima infanzia 79
Partial cerebellar hypoplasia in a patient with Prader-Willi syndrome. 78
A two-year-old patient with an atypical expression of GM1-beta-galactosidase deficiency: biochemical, immunological and cell genetic studies 78
Cisapride in neurologically impaired children with chronic constipation 78
Totale 13.430
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Categoria #
all - tutte 114.416
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 114.416
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021818 0 0 0 0 0 0 147 89 190 134 168 90
2021/20222.419 45 33 57 77 18 58 42 135 233 94 252 1.375
2022/20232.577 625 163 74 195 296 236 29 232 330 239 112 46
2023/20242.232 97 217 256 139 146 175 105 167 87 86 527 230
2024/202510.539 857 890 93 125 233 312 840 575 1.675 1.126 2.766 1.047
2025/202610.004 2.116 1.260 1.518 1.319 3.040 690 61 0 0 0 0 0
Totale 35.181