IRIS
DEL GIUDICE, ENNIO
 Distribuzione geografica
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Continente #
EU - Europa 12.103
AS - Asia 11.322
NA - Nord America 8.897
SA - Sud America 1.814
AF - Africa 212
Continente sconosciuto - Info sul continente non disponibili 33
OC - Oceania 13
AN - Antartide 2
Totale 34.396
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Nazione #
US - Stati Uniti d'America 8.459
SG - Singapore 7.047
IT - Italia 5.058
RU - Federazione Russa 4.006
CN - Cina 1.936
BR - Brasile 1.525
HK - Hong Kong 1.266
FI - Finlandia 630
UA - Ucraina 628
VN - Vietnam 561
FR - Francia 320
DE - Germania 302
CA - Canada 264
NL - Olanda 244
SE - Svezia 210
GB - Regno Unito 207
IE - Irlanda 187
IN - India 108
AR - Argentina 101
MX - Messico 100
PL - Polonia 75
BD - Bangladesh 62
TR - Turchia 57
ZA - Sudafrica 55
EC - Ecuador 45
ID - Indonesia 40
CO - Colombia 39
ES - Italia 38
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
PE - Perù 19
CL - Cile 18
PK - Pakistan 17
PY - Paraguay 17
UZ - Uzbekistan 16
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
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
AO - Angola 3
BY - Bielorussia 3
CD - Congo 3
CU - Cuba 3
HT - Haiti 3
MG - Madagascar 3
Totale 34.304
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Città #
Singapore 2.637
Hong Kong 1.264
Moscow 956
Chandler 794
Millbury 666
Princeton 588
Ashburn 491
Beijing 461
Santa Clara 461
Nanjing 409
Jacksonville 279
Rome 270
Boston 246
Los Angeles 246
Milan 242
Naples 230
Wilmington 228
Ho Chi Minh City 218
Amsterdam 191
Buffalo 182
Redondo Beach 173
The Dalles 172
Ottawa 167
Hefei 156
Nanchang 147
Woodbridge 140
Dallas 119
Hanoi 118
São Paulo 106
Napoli 101
Hebei 95
Norwalk 95
Falls Church 94
Jiaxing 84
Houston 80
Shenyang 80
Florence 69
Tianjin 68
Ann Arbor 62
New York 51
Bologna 50
Seattle 50
Munich 49
Catania 48
Mexico City 45
Rio de Janeiro 45
Padova 44
Palermo 44
Des Moines 43
Belo Horizonte 40
Warsaw 40
Bari 39
Turin 36
Dearborn 35
Montreal 34
Changsha 33
Brooklyn 32
Haiphong 32
Verona 32
Toronto 31
Genova 29
Curitiba 28
Kronberg 28
Tokyo 28
Helsinki 27
Pescara 27
Chicago 26
Trieste 26
Boardman 25
Brasília 25
Manaus 25
Stockholm 25
Johannesburg 24
Washington 24
Frankfurt am Main 23
Kunming 23
Perugia 23
Torino 23
Denver 22
Hangzhou 22
Orem 22
Salerno 22
Campinas 21
Chennai 21
Parma 21
Biên Hòa 20
Porto Alegre 20
London 19
Vicenza 19
Da Nang 18
Poplar 18
Redwood City 18
St Louis 18
Turku 18
Augusta 17
Guayaquil 17
Redmond 17
Manchester 16
Nuremberg 16
San Francisco 16
Totale 14.915
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Nome #
Cisti della fessura corioidea 2.280
Test Screening dello Sviluppo di Denver (DDST): sua applicazione in una popolazione di bambini di asili nido 587
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 156
Le amminoacidopatie e le organicoacidurie: approccio alla diagnosi e al trattamento 156
Displasia corticale focale benigna 143
Steroid treatment in Ataxia-Telangiectasia induces alterations of functional magnetic resonance imaging during prono-supination task. 133
Familial white matter hypoplasia agenesis of the corpus callosum, mental retardation and growth deficiency: A new distinctive syndrome. 131
Agenesia completa isolata del corpo calloso: follow up di una casistica clinica 128
Long term follow-up to evaluate the efficacy of miglustat treatment in Italian patients with Niemann-Pick disease type C 127
Epilessia parziale migrante dell'infanzia ed encefalopatia demielinizzante 125
A mobile e-Health software project for remote monitoring of children enrolled in the Carolina Curriculum. 123
A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability 119
Megalocornea and mental retardation syndrome: two new cases. 117
Diabetes mellitus in Kearns-Sayre syndrome: a case with a 10-year follow-up. 116
Approccio clinico alle macrocranie non familiari: presentazione di una casistica di 21 pazienti. 116
Disordini motori dello sfintere esofageo superiore (UES) e dell'esofago in bambini cerebropatici. 116
A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright Objects. 116
Episodi ricorrenti d rabdomiolisi secondari a difetto della beta-ossidazione degli acidi grassi. 115
Acute Chorea in children: the value of Single Photon Emission Computed Tomographic Scan (SPECT) and Magnetic Resonance Imaging (MRI) findings 115
A case of 14q11.2 microdeletion with autistic features, severe obesity and facial dysmorphisms suggestive of Wolf-Hirschhorn syndrome. 115
A further contribution to the delineation of the 17q21.31 microdeletion syndrome: Central nervous involvement in two Italian patients. 113
Aminotransferases and muscular diseases: a disregarded lesson. Case reports and review of the literature 112
Congenital fiber type disproportion myopathy. Report of a case with late onset and myalgia. 111
PP-8 ESOPHAGEAL HIGH RESOLUTION MANOMETRY IN NEUROLOGICALLLY IMPAIRED CHILDREN AND GASTRO-OESOPHAGEAL REFLUX DISEASE 110
Alterazioni della motilità gastrointestinale in bambini con handicap neuromotorio 108
Clinical Description of a Patient Carrying the Smallest Reported Deletion Involving 10p14 Region 108
A Social Network Framework for the Carolina Software 108
Steroid-induced improvement of neurological signs in ataxia-telangiectasia patients. 108
Temporal lobe epilepsy in early childhood. 107
Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy 106
Vaccination against hepatitis B in preschool children with Down's syndrome 105
Long-term enzyme replacement therapy for Pompe disease with recombinant human alpha-glucosidase derived from chinese hamster ovary cells. 105
Spatial cognition in children. I. Development of drawing-related (visuospatial and constructional) abilities in preschool and early school years 104
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. 104
Miopatia congenita da sproporzione tra fibre di tipo I e di tipo II (congenital fiber type dispropotion myopathy) 104
Epilessia da deficit di PNPO: follow-up di 5 anni. 102
Sindrome di West ed errori congeniti del metabolismo 101
Low-dose amitriptyline-induced acute dystonia in a patient with metachromatic leukodystrophy. 101
A mathematical formulation for estimating age levels in the Carolina Curriculum 101
Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasia 100
Cromosoma 18 pseudoisodicentrico: Studio clinico e citogenetico di un caso 100
Brain alteration in a Nude/SCID fetus carrying FOXN1 homozygous mutation. 99
Subclinical hypothyroidism and Down's syndrome; studies on myocardial structure and function 98
Alterazioni cerebrali e sintomatologia gastroinetstinale. 98
Minimum effective betamethasone dosage on the neurological phenotype in patients with Ataxia-Telangiectasia: a multicenter observer-blind study 98
Intrafamilial variability in SPTAN1-related disorder: From benign convulsions with mild gastroenteritis to developmental encephalopathy 97
Unexplained Bilateral Occipital Calcification and Reduced Vision. 96
Absence of microcephalin gene mutations in a large cohort of non-consanguineous patients with autosomal recessive primary microcephaly. 95
Selective cognitive impairment and tall stature due to chromosome 19 supernumerary ring. 95
Approcci diagnostico-terapeutici al dolore cronico delle patologie neurodegenerative: l'esempio delle leucodistrofie. 95
Variabilità fenotipica intrafamiliare nella miotonia da mutazioni nel gene CLCN1 94
Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22 94
Mild Wolf-Hirschhorn phenotype and partial GH deficiency in a patient with a 4p terminal deletion. 93
Atypical expression of beta-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalities 93
Malattia di Tay-Sachs con elevata attività residua di esosoaminidasi A in leucociti e fibroblasti. 93
Pearls & Oy-sters: Familial epileptic encephalopathy due to methylenetetrahydrofolate reductase deficiency. 93
Calcificazioni cerebrali parietooccipitali ed epilessia associate a celiachia 92
Alterazioni della motilità gastrointestinale in bambini affetti da distrofia muscolare progressiva. 92
Targeting oxidative stress improves disease outcomes in a rat model of acquired epilepsy 92
Sindromi coreiche in età pediatrica. 91
Developmental delay, epilepsy and brain atrophy of different severity in two first cousins with methylenetetrahydrofolate reductase deficiency. 91
EEG findings in West syndrome a follow-up of 20 patients. 90
Epilepsy in Rett syndrome: can seizures play an encephalopathic effect in this disorder? 90
The administration of methotrexate in patients with Still's disease, “real-life” findings from AIDA Network Still Disease Registry 89
Spatial cognition in children. II. Visuospatial and constructional skills in developmental reading disability. 89
Oral Betamethasone improves neurological symptoms in Ataxia-Teleangiectasia. 89
Sindrome di Miller-Dieker: osservazione di un caso con studio tomografico computerizzato. 89
Disturbi da deficit dell'attenzione, percettivi e motori in età scolare. I. Aspetti della procedura di screening. 89
Malattia di Tay-Sachs con elevata affinità residua di esosaminidasi A in leucociti e fibroblasti 89
A preterm neonate with seizures unresponsive to conventional treatment 89
Taylor-type focal cortical dysplasia: is the epilepsy always resistant to medical treatment? 88
Brain migration disorder and T-cell activation deficiency associated with abnormal signaling through TCR/CD3 complex and hyperactivity of Fyn tyrosine kinase. 88
Alterazioni della motilità gastrointestinale in bambini affetti da distrofia muscolare progressiva 88
Primary cerebral neuroblastomas. 86
L'eterozigosità per fenilchetonuria può essere responsabile di ritardo mentale aspecifico? 85
Hormonal and neuropsychological evaluation of two 47, XYY patients with pituitary anormalities. 84
Induzione enzimatica ed epatopatie da farmaci anticonvulsivanti. Studio retrospettivo su 20 bambini. 84
Alterazioni cerebrali e sintomatologia gastrointestinale 84
Impact of malnutrition on gastrointestinal disorders and gross motor abilities in children with cerebral palsy. 84
Factor Analysis of the Italian Version of the Alabama Parenting Questionnaire in a Community Sample 83
Estimate the minimum therpeutically effective dosage of short-term therapy with Betamethasone on neurologicaal symptoms in patients affected with Ataxia-Telangectasia 82
La sindrome dell'X fragile. 82
Constitutive activation of the 42 kDa MAPK in a patient with immunodeficiency and severe encephalopathy 82
Microdeletion of pseudogene chr14.232.a affects LRFN5 expression in cells of a patient with autism spectrum disorder 82
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations 81
Cerebellar agenesis 80
Studio multicentrico della microcefalia vera. Rete clinico-genetica ed analisi sperimentale funzionale del prodotto del gene ASPM. 80
Expansion of the phenotype of lateral meningocele syndrome 80
Electroencephalographic findings in ATRX syndrome: A new case series and review of literature 80
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. 79
A two-year-old patient with an atypical expression of GM1-beta-galactosidase deficiency: biochemical, immunological and cell genetic studies 78
Cerebral palsy and gut functions. 78
Disturbi da deficit d'attenzione, percettivi e motori in età scolare. III. Aspetti neuroevolutivi. 78
Modalità di approccio abilitativo alla patologia centrale motoria della prima infanzia 78
Le basi neurobiologiche dello sviluppo relazionale. 78
Partial cerebellar hypoplasia in a patient with Prader-Willi syndrome. 77
Cisapride in neurologically impaired children with chronic constipation 77
Totale 13.288
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Categoria #
all - tutte 112.178
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 112.178
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.119 0 0 0 0 0 301 147 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
2025/20269.544 2.116 1.260 1.518 1.319 3.040 291 0 0 0 0 0 0
Totale 34.721