IRIS
DEL GIUDICE, ENNIO
 Distribuzione geografica
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Continente #
AS - Asia 15.184
EU - Europa 12.954
NA - Nord America 11.768
SA - Sud America 1.894
AF - Africa 283
Continente sconosciuto - Info sul continente non disponibili 34
OC - Oceania 14
AN - Antartide 2
Totale 42.133
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Nazione #
US - Stati Uniti d'America 11.277
SG - Singapore 7.562
IT - Italia 5.196
RU - Federazione Russa 4.007
VN - Vietnam 2.545
CN - Cina 2.510
BR - Brasile 1.561
HK - Hong Kong 1.328
FR - Francia 936
FI - Finlandia 632
UA - Ucraina 632
DE - Germania 338
CA - Canada 290
NL - Olanda 255
GB - Regno Unito 230
IN - India 217
JP - Giappone 215
SE - Svezia 211
IE - Irlanda 193
AR - Argentina 113
MX - Messico 113
BD - Bangladesh 107
IQ - Iraq 93
PH - Filippine 82
PL - Polonia 76
TH - Thailandia 66
TR - Turchia 63
ZA - Sudafrica 61
KR - Corea 58
PK - Pakistan 51
ID - Indonesia 50
EC - Ecuador 49
TW - Taiwan 45
CO - Colombia 44
ES - Italia 42
VE - Venezuela 39
MA - Marocco 34
RO - Romania 30
CH - Svizzera 27
CI - Costa d'Avorio 26
KE - Kenya 26
CL - Cile 25
EG - Egitto 25
EU - Europa 25
AT - Austria 23
UZ - Uzbekistan 23
BE - Belgio 20
PE - Perù 20
PY - Paraguay 20
JO - Giordania 19
TN - Tunisia 17
DZ - Algeria 15
AZ - Azerbaigian 14
JM - Giamaica 13
PT - Portogallo 13
BG - Bulgaria 12
NP - Nepal 12
UY - Uruguay 12
BO - Bolivia 11
ET - Etiopia 11
IL - Israele 11
LB - Libano 11
SA - Arabia Saudita 11
CZ - Repubblica Ceca 10
IR - Iran 10
OM - Oman 10
CR - Costa Rica 9
HN - Honduras 9
AE - Emirati Arabi Uniti 8
AL - Albania 8
GT - Guatemala 8
MY - Malesia 8
TT - Trinidad e Tobago 8
DO - Repubblica Dominicana 7
GR - Grecia 7
KZ - Kazakistan 7
LT - Lituania 7
QA - Qatar 7
BA - Bosnia-Erzegovina 6
BH - Bahrain 6
CG - Congo 6
KG - Kirghizistan 6
MD - Moldavia 6
NO - Norvegia 6
SN - Senegal 6
AU - Australia 5
BF - Burkina Faso 5
LA - Repubblica Popolare Democratica del Laos 5
LC - Santa Lucia 5
NI - Nicaragua 5
NZ - Nuova Zelanda 5
AO - Angola 4
BZ - Belize 4
CV - Capo Verde 4
CW - ???statistics.table.value.countryCode.CW??? 4
DK - Danimarca 4
MN - Mongolia 4
MW - Malawi 4
SI - Slovenia 4
BY - Bielorussia 3
Totale 42.023
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Città #
Singapore 2.869
San Jose 1.728
Hong Kong 1.291
Moscow 956
Chandler 794
Ho Chi Minh City 755
Millbury 666
Ashburn 635
Princeton 588
Hanoi 569
The Dalles 540
Lauterbourg 501
Beijing 483
Santa Clara 482
Nanjing 412
Rome 288
Jacksonville 281
Los Angeles 270
Milan 253
Boston 249
Naples 242
Wilmington 229
Amsterdam 196
Tokyo 186
Buffalo 183
Redondo Beach 173
Ottawa 168
Hefei 156
Nanchang 147
Dallas 142
Woodbridge 140
Da Nang 122
Haiphong 120
São Paulo 110
New York 102
Napoli 101
Hebei 95
Norwalk 95
Falls Church 94
Houston 88
Jiaxing 84
Shenyang 81
Florence 70
Tianjin 69
Orem 66
Ann Arbor 62
Bologna 52
Seattle 52
Catania 51
Frankfurt am Main 51
Munich 49
Rio de Janeiro 47
Des Moines 45
Mexico City 45
Padova 44
Palermo 44
Bari 42
Chennai 42
Biên Hòa 41
Warsaw 41
Belo Horizonte 40
Brooklyn 39
Hải Dương 39
Toronto 38
Montreal 37
Turin 37
Changsha 36
Dearborn 35
Baghdad 34
Chicago 32
Verona 32
Denver 31
Genova 29
Helsinki 29
Can Tho 28
Curitiba 28
Johannesburg 28
Kronberg 28
Pescara 27
Brasília 26
Stockholm 26
Trieste 26
Boardman 25
Manaus 25
Nairobi 25
San Francisco 25
Washington 25
Hangzhou 24
London 24
Mumbai 24
Atlanta 23
Bangkok 23
Council Bluffs 23
Kunming 23
Nuremberg 23
Perugia 23
Torino 23
Parma 22
Poplar 22
Salerno 22
Totale 19.706
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Nome #
Cisti della fessura corioidea 2.335
Test Screening dello Sviluppo di Denver (DDST): sua applicazione in una popolazione di bambini di asili nido 614
Epilessia frontale con bisincronismo secondario in encefalopatia perinatale 419
Effetti collaterali a lungo termine dei farmaci antiepilettici: studio di una casistica pediatrica. 415
Sindrome plurimalformativa caratterizzata da: ritardp psicomotorio, microcefalia, atrofia ottica,eterotopie neuronali, anomalie cardiovascolari 262
Ipernatriemia neuroendocrina: diabete insipido e oloprosencefalia 164
Le amminoacidopatie e le organicoacidurie: approccio alla diagnosi e al trattamento 161
Displasia corticale focale benigna 158
A mobile e-Health software project for remote monitoring of children enrolled in the Carolina Curriculum. 155
Steroid treatment in Ataxia-Telangiectasia induces alterations of functional magnetic resonance imaging during prono-supination task. 154
Long term follow-up to evaluate the efficacy of miglustat treatment in Italian patients with Niemann-Pick disease type C 147
Familial white matter hypoplasia agenesis of the corpus callosum, mental retardation and growth deficiency: A new distinctive syndrome. 142
A Social Network Framework for the Carolina Software 140
Acute Chorea in children: the value of Single Photon Emission Computed Tomographic Scan (SPECT) and Magnetic Resonance Imaging (MRI) findings 139
A novel SHANK3 interstitial microdeletion in a family with intellectual disability and brain MRI abnormalities resembling Unidentified Bright Objects. 139
Agenesia completa isolata del corpo calloso: follow up di una casistica clinica 137
A case of 14q11.2 microdeletion with autistic features, severe obesity and facial dysmorphisms suggestive of Wolf-Hirschhorn syndrome. 137
A small 7q11.23 microduplication involving GTF2I in a family with intellectual disability 137
Approccio clinico alle macrocranie non familiari: presentazione di una casistica di 21 pazienti. 136
PP-8 ESOPHAGEAL HIGH RESOLUTION MANOMETRY IN NEUROLOGICALLLY IMPAIRED CHILDREN AND GASTRO-OESOPHAGEAL REFLUX DISEASE 136
Epilessia parziale migrante dell'infanzia ed encefalopatia demielinizzante 135
Episodi ricorrenti d rabdomiolisi secondari a difetto della beta-ossidazione degli acidi grassi. 135
Megalocornea and mental retardation syndrome: two new cases. 133
A further contribution to the delineation of the 17q21.31 microdeletion syndrome: Central nervous involvement in two Italian patients. 133
A mathematical formulation for estimating age levels in the Carolina Curriculum 132
Clinical Description of a Patient Carrying the Smallest Reported Deletion Involving 10p14 Region 130
Aminotransferases and muscular diseases: a disregarded lesson. Case reports and review of the literature 129
Disordini motori dello sfintere esofageo superiore (UES) e dell'esofago in bambini cerebropatici. 129
Alterazioni cerebrali e sintomatologia gastroinetstinale. 126
Early onset Charcot-Marie-Tooth neuropathy type 2A and severe developmental delay: expanding the clinical phenotype of MFN2-related neuropathy 126
Congenital fiber type disproportion myopathy. Report of a case with late onset and myalgia. 125
Alterazioni della motilità gastrointestinale in bambini affetti da distrofia muscolare progressiva. 125
Steroid-induced improvement of neurological signs in ataxia-telangiectasia patients. 125
Diabetes mellitus in Kearns-Sayre syndrome: a case with a 10-year follow-up. 123
Alterazioni della motilità gastrointestinale in bambini con handicap neuromotorio 123
Efficacy of very-low-dose betamethasone on neurological symptoms in ataxia-telangiectasia 123
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. 123
Mental retardation, congenital heart malformation, and myelodysplasia in a patient with a complex chromosomal rearrangement involving the critical region 21q22 123
Spatial cognition in children. I. Development of drawing-related (visuospatial and constructional) abilities in preschool and early school years 122
Long-term enzyme replacement therapy for Pompe disease with recombinant human alpha-glucosidase derived from chinese hamster ovary cells. 122
Epilessia da deficit di PNPO: follow-up di 5 anni. 122
Approcci diagnostico-terapeutici al dolore cronico delle patologie neurodegenerative: l'esempio delle leucodistrofie. 120
Low-dose amitriptyline-induced acute dystonia in a patient with metachromatic leukodystrophy. 120
Sindrome di West ed errori congeniti del metabolismo 119
Temporal lobe epilepsy in early childhood. 118
Subclinical hypothyroidism and Down's syndrome; studies on myocardial structure and function 118
Developmental delay, epilepsy and brain atrophy of different severity in two first cousins with methylenetetrahydrofolate reductase deficiency. 117
Minimum effective betamethasone dosage on the neurological phenotype in patients with Ataxia-Telangiectasia: a multicenter observer-blind study 117
Mild Wolf-Hirschhorn phenotype and partial GH deficiency in a patient with a 4p terminal deletion. 115
Vaccination against hepatitis B in preschool children with Down's syndrome 115
Absence of microcephalin gene mutations in a large cohort of non-consanguineous patients with autosomal recessive primary microcephaly. 115
Intrafamilial variability in SPTAN1-related disorder: From benign convulsions with mild gastroenteritis to developmental encephalopathy 115
Unexplained Bilateral Occipital Calcification and Reduced Vision. 114
Brain alteration in a Nude/SCID fetus carrying FOXN1 homozygous mutation. 114
Selective cognitive impairment and tall stature due to chromosome 19 supernumerary ring. 114
Miopatia congenita da sproporzione tra fibre di tipo I e di tipo II (congenital fiber type dispropotion myopathy) 114
Microdeletion of pseudogene chr14.232.a affects LRFN5 expression in cells of a patient with autism spectrum disorder 112
Cromosoma 18 pseudoisodicentrico: Studio clinico e citogenetico di un caso 111
Pearls & Oy-sters: Familial epileptic encephalopathy due to methylenetetrahydrofolate reductase deficiency. 111
Sindrome di Miller-Dieker: osservazione di un caso con studio tomografico computerizzato. 110
Disturbi da deficit dell'attenzione, percettivi e motori in età scolare. I. Aspetti della procedura di screening. 110
The administration of methotrexate in patients with Still's disease, “real-life” findings from AIDA Network Still Disease Registry 109
Alterazioni della motilità gastrointestinale in bambini affetti da distrofia muscolare progressiva 108
Malattia di Tay-Sachs con elevata attività residua di esosoaminidasi A in leucociti e fibroblasti. 108
Targeting oxidative stress improves disease outcomes in a rat model of acquired epilepsy 107
Variabilità fenotipica intrafamiliare nella miotonia da mutazioni nel gene CLCN1 106
Expansion of the phenotype of lateral meningocele syndrome 106
Atypical expression of beta-galactosidase deficiency in a child with Hurler-like features but without neurological abnormalities 105
Oral Betamethasone improves neurological symptoms in Ataxia-Teleangiectasia. 105
EEG findings in West syndrome a follow-up of 20 patients. 105
Calcificazioni cerebrali parietooccipitali ed epilessia associate a celiachia 105
Impact of malnutrition on gastrointestinal disorders and gross motor abilities in children with cerebral palsy. 105
Electroencephalographic findings in ATRX syndrome: A new case series and review of literature 105
Estimate the minimum therpeutically effective dosage of short-term therapy with Betamethasone on neurologicaal symptoms in patients affected with Ataxia-Telangectasia 104
Epilepsy in Rett syndrome: can seizures play an encephalopathic effect in this disorder? 104
Brain migration disorder and T-cell activation deficiency associated with abnormal signaling through TCR/CD3 complex and hyperactivity of Fyn tyrosine kinase. 102
A preterm neonate with seizures unresponsive to conventional treatment 102
Hormonal and neuropsychological evaluation of two 47, XYY patients with pituitary anormalities. 101
La sindrome dell'X fragile. 101
Induzione enzimatica ed epatopatie da farmaci anticonvulsivanti. Studio retrospettivo su 20 bambini. 101
Alterazioni cerebrali e sintomatologia gastrointestinale 100
Sindromi coreiche in età pediatrica. 99
Malattia di Tay-Sachs con elevata affinità residua di esosaminidasi A in leucociti e fibroblasti 99
Constitutive activation of the 42 kDa MAPK in a patient with immunodeficiency and severe encephalopathy 99
L'eterozigosità per fenilchetonuria può essere responsabile di ritardo mentale aspecifico? 98
Epilessia strutturale e malformazione corticale complessa 98
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations 96
Primary cerebral neuroblastomas. 96
Factor Analysis of the Italian Version of the Alabama Parenting Questionnaire in a Community Sample 96
Acute chorea in children: the value of Single Photon Emission Computed Tomography Scan (SPECT) and Magnetic Resonance Imaging (MRI) findings 95
Spatial cognition in children. II. Visuospatial and constructional skills in developmental reading disability. 94
Cisapride in neurologically impaired children with chronic constipation 94
Cerebral palsy and gut functions. 93
Disturbi da deficit d'attenzione, percettivi e motori in età scolare. III. Aspetti neuroevolutivi. 93
Gastrointestinal motility in children with muscular dystrophy 93
Studio multicentrico della microcefalia vera. Rete clinico-genetica ed analisi sperimentale funzionale del prodotto del gene ASPM. 93
Partial cerebellar hypoplasia in a patient with Prader-Willi syndrome. 92
Taylor-type focal cortical dysplasia: is the epilepsy always resistant to medical treatment? 92
Effect of different starting dose of l-thyroxine on intellectual outcame at 8 years of age in congenital hypothyroidism. 92
Le alterazioni scheletriche dell'omocistinuria in età pediatrica. 92
Totale 15.083
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Categoria #
all - tutte 130.487
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 130.487
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021258 0 0 0 0 0 0 0 0 0 0 168 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
2025/202617.281 2.116 1.260 1.518 1.319 3.040 690 1.727 1.421 2.901 934 355 0
Totale 42.458