CRIS Current Research Information System

CORDELLI, DUCCIO MARIA
 Distribuzione geografica
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Continente #
NA - Nord America 5.926
AS - Asia 5.645
EU - Europa 5.452
SA - Sud America 443
AF - Africa 275
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 6
Totale 17.757
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Nazione #
US - Stati Uniti d'America 5.846
IT - Italia 2.392
SG - Singapore 1.777
CN - Cina 1.626
VN - Vietnam 1.024
GB - Regno Unito 723
DE - Germania 541
HK - Hong Kong 453
SE - Svezia 361
BR - Brasile 315
KR - Corea 276
IN - India 250
RU - Federazione Russa 218
FR - Francia 214
NL - Olanda 194
IE - Irlanda 185
UA - Ucraina 171
FI - Finlandia 103
CI - Costa d'Avorio 90
JP - Giappone 79
AR - Argentina 73
ZA - Sudafrica 70
PL - Polonia 56
CH - Svizzera 54
JO - Giordania 54
AT - Austria 52
SC - Seychelles 52
CA - Canada 47
EE - Estonia 46
BG - Bulgaria 45
TG - Togo 40
ID - Indonesia 36
ES - Italia 23
MX - Messico 19
BE - Belgio 17
CO - Colombia 14
EC - Ecuador 14
CZ - Repubblica Ceca 11
TR - Turchia 11
BD - Bangladesh 10
RO - Romania 9
VE - Venezuela 8
LT - Lituania 7
UZ - Uzbekistan 7
AE - Emirati Arabi Uniti 6
AU - Australia 6
CL - Cile 6
GR - Grecia 5
IQ - Iraq 5
IR - Iran 5
PY - Paraguay 5
CR - Costa Rica 4
HU - Ungheria 4
LB - Libano 4
MA - Marocco 4
MY - Malesia 4
NG - Nigeria 4
PK - Pakistan 4
PT - Portogallo 4
A2 - ???statistics.table.value.countryCode.A2??? 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
EU - Europa 3
PE - Perù 3
AL - Albania 2
BJ - Benin 2
BO - Bolivia 2
DZ - Algeria 2
HR - Croazia 2
JM - Giamaica 2
KE - Kenya 2
KZ - Kazakistan 2
LK - Sri Lanka 2
LU - Lussemburgo 2
MC - Monaco 2
NZ - Nuova Zelanda 2
PH - Filippine 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
TN - Tunisia 2
UY - Uruguay 2
ZM - Zambia 2
AZ - Azerbaigian 1
BH - Bahrain 1
BS - Bahamas 1
BW - Botswana 1
BZ - Belize 1
EG - Egitto 1
GE - Georgia 1
GH - Ghana 1
GN - Guinea 1
GT - Guatemala 1
GY - Guiana 1
HN - Honduras 1
IS - Islanda 1
KI - Kiribati 1
KW - Kuwait 1
LY - Libia 1
NI - Nicaragua 1
NO - Norvegia 1
Totale 17.752
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Città #
Singapore 1.187
Ashburn 687
Fairfield 630
Southend 615
Hefei 599
Hong Kong 451
Chandler 435
Bologna 418
Woodbridge 293
Santa Clara 284
Seoul 275
Seattle 243
Wilmington 239
Houston 234
Ho Chi Minh City 226
Beijing 207
Milan 194
Princeton 193
Cambridge 187
Dublin 183
Rome 176
New York 174
Dong Ket 173
Boardman 164
Ann Arbor 161
Hanoi 153
Dallas 125
Abidjan 90
Los Angeles 87
Helsinki 74
Tokyo 68
Turin 66
Westminster 65
Jacksonville 60
Berlin 58
Nanjing 56
Frankfurt am Main 55
Redmond 55
Amman 54
Buffalo 54
Bengaluru 51
Redondo Beach 50
São Paulo 47
Florence 46
Sofia 44
San Diego 41
Lomé 40
Naples 39
Bern 38
Padova 38
Jinan 32
Loreto Aprutino 32
Saint Petersburg 32
Nuremberg 31
Jakarta 29
Palermo 29
Vienna 27
Munich 25
Falkenstein 24
Haiphong 24
Parma 24
Shanghai 24
Falls Church 23
Yubileyny 23
Des Moines 22
Modena 22
Guangzhou 21
Shenyang 21
Tongling 21
Lappeenranta 20
Mülheim 20
The Dalles 20
Verona 20
Hải Dương 19
London 19
Mountain View 19
Thái Nguyên 19
Changsha 18
Dearborn 18
Genoa 18
Ha Long 18
Nanchang 18
Warsaw 18
Brussels 17
Chicago 17
Columbus 17
Da Nang 17
Ferrara 16
Paris 16
Phoenix 16
Toronto 16
Zhengzhou 16
Catania 15
Cesena 15
Amsterdam 14
Biên Hòa 14
Brooklyn 14
Düsseldorf 14
Tianjin 14
Hebei 13
Totale 11.193
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Nome #
Neonato e bambino: parametri normali di sviluppo; riflessi primitivi; principali tappe dello sviluppo psicomotorio 713
Risk factor analysis of posterior reversible encephalopathy syndrome after allogeneic hematopoietic SCT in children 634
EFFICACIA DEL LEVETIRACETAM IN UN CASO DI ESES SECONDARIO A DISPLASIA CORTICALE. 597
Le convulsioni associate a gastroenterite nel lattante: una entità clinica benigna 287
A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype. 275
Down Syndrome: how to communicate the diagnosis 232
Autism spectrum disorder and anorexia nervosa: an Italian prospective study 223
A comparative study of hydrocortisone versus deflazacort in drug-resistant epilepsy of childhood 215
A novel mutation in SPART gene causes a severe neurodevelopmental delay due to mitochondrial dysfunction with complex I impairments and altered pyruvate metabolism 214
COQ7 defect causes prenatal onset of mitochondrial CoQ10 deficiency with cardiomyopathy and gastrointestinal obstruction 203
Central nervous system complications in children receiving chemotherapy or hematopoietic stem cell transplantation 200
Neurodevelopmental Correlates of Brain Magnetic Resonance Imaging Abnormalities in Extremely Low-birth-weight Infants 188
FA2H-related disorders: a novel c.270+3A>T splice-site mutation leads to a complex neurodegenerative phenotype. 181
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle East 176
Cytogenetic and molecular characterization of a recombinant X chromosome in a family with a severe neurologic phenotype and macular degeneration 174
Acute diplopia in the pediatric Emergency Department. A cohort multicenter Italian study 172
Psichiatria e neurologia nell'encefalite limbica curabile da anticorpi anti NMDAR: una sfida diagnostico-terapeutico-assistenziale tra ospedale e territorio. 166
Bi-allelic mutations in TRAPPC2L result in a neurodevelopmental disorder and have an impact on RAB11 in fibroblasts 164
Juvenile dermatomyositis: A report of three cases 163
Efficacy and safety of levetiracetam: An add-on trial in children with refractory epilepsy. 162
Pediatric epilepsies misdiagnosed as gastrointestinal disorders 160
Bathing epilepsy: report of two Caucasian cases. 160
Gait performance in toddlers born preterm: A sensor based quantitative characterization 159
VNS in drug resistant epilepsy: preliminary report on a small group of patients 159
Cerebral Ischemic Involvement in Vogt-Koyanagi-Harada Disease 158
Teaching NeuroImages: Neurovascular features of suspected antenatal-onset Sturge-Weber syndrome without skin involvement 154
Myoclonic epilepsy with photosensitivity in infants with Pallister-Killian Syndrome 153
Eating disorders in young patients with neurofibromatosis type 1 152
Fever as a seizure precipitant factor in Panayiotopoulos syndrome: A clinical and genetic study 152
Life-threatening complications of posterior reversible encephalopathy syndrome in children 150
PRES in children undergoing hematopoietic stem cell or solid organ transplantation 150
Cannabidiol in the acute phase of febrile infection-related epilepsy syndrome (FIRES) 149
New patients with Temple syndrome caused by 14q32 deletion: Genotype-phenotype correlations and risk of thyroid cancer 149
Acute ataxia in paediatric emergency departments: A multicentre Italian study 149
Infantile TK2 Deficiency Causing Mitochondrial Encephalomyopathy With Migrating Focal Seizures 148
Phenotype and genotype of 87 patients with Mowat–Wilson syndrome and recommendations for care 148
Ultrastructural and Immunohistochemical Diagnosis of a Neonatal Herpes Simplex Virus Infection Presenting as Fulminant Hepatitis: A Case Report 148
Progressive cerebral white matter involvement in a patient with Congenital Cataracts Facial Dysmorphisms Neuropathy (CCFDN). 146
Prospective study on long-term treatment with oxcarbazepine in pediatric epilepsy. 145
Clinical characterization of status epilepticus in childhood: a retrospective study in 124 patients 144
Efficacy and safety of levetiracetam in infants and young children with refractory epilepsy 143
Computed Tomography in Acute Severe Central Nervous System Complications in Children Treated for Cancer: Still a Useful Diagnostic Tool in the Emergency Setting 143
A new PLA2G6 mutation in a family with infantile neuroaxonal dystrophy 142
Status epilepticus as a main manifestation of posterior reversible encephalopathy syndrome after pediatric hematopoietic stem cell transplantation 141
Diagnosis of congenital myasthenic syndrome with mutation of the RAPSN gene after general anaesthesia 140
Epilepsy in Mowat-Wilson syndrome: is it a matter of GABA? 139
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts 139
Neuroimaging findings in Mowat-Wilson syndrome: A study of 54 patients 138
Epilepsy after acute central nervous system complications of pediatric hematopoietic cell transplantation: A retrospective, multicenter study 136
Analgesic effect of watching TV during venipuncture 136
Expanding the Clinical Spectrum of UBTF-Related Neurodevelopmental Disorder 135
Sleep in Mowat-Wilson Syndrome: a clinical and video-polysomnographic study 133
Anti-Inflammatory and Immunomodulatory Effect of High-Dose Immunoglobulins in Children: From Approved Indications to Off-Label Use 132
Community-onset pediatric status epilepticus: Barriers to care and outcomes in a real-world setting 132
Early Immunotherapy and Longer Corticosteroid Treatment Are Associated With Lower Risk of Relapsing Disease Course in Pediatric MOGAD 131
Psychopathological Impact in Patients with History of Rheumatic Fever with or without Sydenham's Chorea: A Multicenter Prospective Study 130
Status Epilepticus in Chromosomal Disorders Associated with Epilepsy: A Systematic Review 128
Mowat-Wilson syndrome: Growth charts 128
Posterior Reversible Encephalopathy Syndrome in infants and young children 127
Structural brain abnormalities in Pallister-Killian syndrome: a neuroimaging study of 31 children 126
Is the ABC pain scale reliable for premature babies? 126
Lo stroke in età pediatrica 126
Deoxyguanosine kinase deficiency: natural history and liver transplant outcome 125
Psychotic episode during steroid therapy in hashimoto encephalopathy 125
Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype. 124
CDKL5 deficiency-related neurodevelopmental disorders: a multi-center cohort study in Italy 121
Symmetric polymicrogyria and pachygyria associated with TUBB2B gene mutations 121
KETASER01 protocol: What went right and what went wrong 120
A nationwide study on Sydenham's chorea: Clinical features, treatment and prognostic factors 120
Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients 118
Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes 117
Conventional magnetic resonance imaging and diffusion tensor imaging studies in children with novel GPR56 mutations: Further delineation of a cobblestone-like phenotype 116
Characteristics of acute nystagmus in the pediatric emergency department 114
Post-traumatic stress, anxiety, and depressive symptoms in caregivers of children tested for COVID-19 in the acute phase of the Italian outbreak 114
Sleep in Children With Pallister Killian Syndrome: A Prospective Clinical and Videopolysomnographic Study 114
Expanding Phenotype of Poirier-Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients 113
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus 113
Extended Glasgow Outcome Scale to Evaluate the Functional Impairment of Patients With Subcortical Band Heterotopia: A Multicentric Cross-sectional Study 112
Inflammatory disease of the central nervous system induced by anti-GD2 monoclonal antibody in a patient with high risk neuroblastoma. 112
Etiology, characteristics and outcome of seizures after pediatric hematopoietic stem cell transplantation 111
Caratteristiche cliniche ed outcome dell’encafalopatia posteriore reversibile (PRES) in età pediatrica: studio multicentrico italiano su 78 pazienti. 111
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review. 110
Post-Traumatic Headache in Children after Minor Head Trauma: Incidence, Phenotypes, and Risk Factors 108
Expanding the therapeutic role of highly purified cannabidiol in monogenic epilepsies: A multicenter real-world study 108
Early onset absence epilepsy with onset in the first year of life: A multicenter cohort study 108
Inter-observer reliability of two pain scales for newborns 108
Early vagus nerve stimulator implantation as a main predictor of positive outcome in pediatric patients with epileptic encephalopathy 108
Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort 106
Sleep disorders reveal distress among children and adolescents during the Covid-19 first wave: results of a large web-based Italian survey 106
The "eye-of-the-tiger" sign may be absent in the early stages of classic pantothenate kinase associated neurodegeneration 105
Efficacy and Safety of Pulse Intravenous Methylprednisolone in Pediatric Epileptic Encephalopathies: Timing and Networks Consideration 104
Leukoencephalopathy with calcifications and cysts: A purely neurological disorder distinct from coats plus 104
Long-term effects of antepartum bed rest on offspring 103
The pandemic within the pandemic: the surge of neuropsychological disorders in Italian children during the COVID-19 era 103
Pediatric Headache in Primary Care and Emergency Departments: Consensus with RAND/UCLA Method 102
Is an excessive number of prenatal echographies a risk for fetal growth? 102
Identification of the DNA methylation signature of Mowat-Wilson syndrome 101
Relationship between Sensory Alterations and Repetitive Behaviours in Children with Autism Spectrum Disorders: A Parents' Questionnaire Based Study 101
Ritardo mentale ed epilessia nella distrofia muscolare facio-scapolo-omerale: manifestazioni extramuscolari della patologia o associazione casuale? 99
Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures 96
Totale 15.526
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Categoria #
all - tutte 51.601
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 51.601
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021919 0 0 0 0 0 74 104 76 97 72 102 394
2021/20221.819 136 62 81 101 148 117 73 190 79 101 439 292
2022/20232.174 225 240 123 235 163 167 84 114 411 82 195 135
2023/20241.346 50 167 92 135 113 279 70 105 80 121 76 58
2024/20253.910 157 433 386 296 468 202 294 166 122 287 340 759
2025/20264.783 782 1.440 786 718 842 215 0 0 0 0 0 0
Totale 18.151