Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

PIRO, Ettore
 Distribuzione geografica
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Continente #
NA - Nord America 11.127
EU - Europa 9.468
AS - Asia 5.986
SA - Sud America 1.067
AF - Africa 201
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 6
Totale 27.867
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Nazione #
US - Stati Uniti d'America 10.910
IT - Italia 3.822
SG - Singapore 2.136
RU - Federazione Russa 1.717
CN - Cina 1.488
BR - Brasile 819
UA - Ucraina 694
HK - Hong Kong 684
FI - Finlandia 617
VN - Vietnam 588
DE - Germania 552
PL - Polonia 415
FR - Francia 413
GB - Regno Unito 328
IE - Irlanda 288
JP - Giappone 240
SE - Svezia 190
BD - Bangladesh 129
IN - India 126
KR - Corea 119
AR - Argentina 95
NL - Olanda 93
CA - Canada 91
BE - Belgio 72
RO - Romania 71
MX - Messico 70
TR - Turchia 66
IQ - Iraq 65
ZA - Sudafrica 52
ES - Italia 40
AT - Austria 34
PK - Pakistan 33
CH - Svizzera 32
MY - Malesia 31
CI - Costa d'Avorio 28
CL - Cile 28
MA - Marocco 28
UZ - Uzbekistan 28
VE - Venezuela 27
CO - Colombia 26
ID - Indonesia 26
EC - Ecuador 23
SA - Arabia Saudita 23
EG - Egitto 19
PH - Filippine 18
DZ - Algeria 17
KE - Kenya 17
TN - Tunisia 17
AE - Emirati Arabi Uniti 16
AZ - Azerbaigian 16
IR - Iran 16
JO - Giordania 16
PY - Paraguay 16
PE - Perù 15
CR - Costa Rica 14
PT - Portogallo 14
UY - Uruguay 14
BH - Bahrain 13
IL - Israele 12
NP - Nepal 12
AU - Australia 11
JM - Giamaica 11
KG - Kirghizistan 11
KZ - Kazakistan 11
LT - Lituania 11
BG - Bulgaria 9
GE - Georgia 9
TW - Taiwan 9
HN - Honduras 8
LB - Libano 8
NO - Norvegia 8
AL - Albania 7
CZ - Repubblica Ceca 7
OM - Oman 7
RS - Serbia 6
ET - Etiopia 5
GR - Grecia 5
GT - Guatemala 5
TH - Thailandia 5
BN - Brunei Darussalam 4
DK - Danimarca 4
EU - Europa 4
HU - Ungheria 4
MN - Mongolia 4
SN - Senegal 4
TT - Trinidad e Tobago 4
AO - Angola 3
BO - Bolivia 3
GH - Ghana 3
IS - Islanda 3
KW - Kuwait 3
PA - Panama 3
PS - Palestinian Territory 3
AM - Armenia 2
BY - Bielorussia 2
BZ - Belize 2
DO - Repubblica Dominicana 2
EE - Estonia 2
GA - Gabon 2
HR - Croazia 2
Totale 27.835
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Città #
Singapore 1.324
Ashburn 1.264
Fairfield 819
Chandler 741
San Jose 739
Hong Kong 665
Ann Arbor 470
Wilmington 460
Woodbridge 454
Palermo 411
Zgierz 364
Houston 359
Seattle 359
Jacksonville 326
Council Bluffs 276
Dublin 275
Beijing 273
Moscow 271
Cambridge 259
Santa Clara 256
Medford 253
Des Moines 229
Tokyo 227
Ho Chi Minh City 200
Helsinki 196
Rome 178
Lauterbourg 169
Frankfurt am Main 165
Princeton 161
Hefei 157
Los Angeles 155
Milan 154
Dallas 152
Nanjing 149
New York 138
Hanoi 137
Boardman 101
Altamura 98
Tulsa 80
Dearborn 77
Buffalo 75
Chicago 74
Lawrence 74
San Diego 69
Brussels 65
São Paulo 61
Ludwigshafen am Rhein 55
Catania 52
Napoli 52
The Dalles 50
Nanchang 49
Shenyang 47
Hebei 45
London 45
Orem 45
Changsha 42
Naples 42
Seoul 41
Tianjin 37
Bologna 35
Warsaw 35
Jinan 34
Guangzhou 33
Amsterdam 32
Redwood City 32
Toronto 31
Abidjan 28
Da Nang 28
Florence 28
Verona 28
Columbus 27
Johannesburg 27
Phoenix 27
Jiaxing 26
Bari 25
San Mateo 24
Seongnam 23
Tashkent 23
Atlanta 22
Baghdad 22
Brooklyn 22
Denver 22
Haiphong 22
Messina 22
Nuremberg 22
Padova 22
Saint Petersburg 22
Aversa 20
Belfast 20
Lappeenranta 20
Orange 20
Rio de Janeiro 20
Belo Horizonte 19
Hangzhou 19
Montreal 19
Belpasso 18
Chennai 18
Latina 18
Paris 18
Boston 17
Totale 15.551
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Nome #
LO SCREENING DI SVILUPPO 529
Arteria ombelicale unica (AOU): un marker di anomalie congenite 448
POTENZIALI EVOCATI VISIVI (PEV) IN NEONATI DA GRAVIDANZA PLURIMA: RELAZIONE CON LA DISCORDANZA IN PESO (AGA VS SGA) 418
Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcome 339
Autostima,sensation seeking e impulsività nell'uso problematico delle nuove tecnologie in adolescenza 323
A Case of Cardiomyopathy Due to Premature Ductus Arteriosus Closure: The Flip Side of Paracetamol 311
Congenital hepatic mesenchymal hamartoma associated with mesenchymal stem villous hyperplasia of the placenta: case report 289
Clinical and molecular characterization of 112 single-center patients with Neurofibromatosis type 1 287
Sindrome di Down da duplicazione della regione critica 21q22.2-q22.3 285
16P11.2 MICRODELETION/MICRODUPLICATION SYNDROME: FURTHER CHARACTERIZATION OF A CRITICAL REGION FOR NEUROPSYCHIATRIC DEVELOPMENT 284
DIABETE INSIPIDO E PANIPOPITUITARISMO IN IDROCEFALO CONGENITO: DESCRIZIONE DI UN CASO 262
LONG GAP ESOPHAGEAL ATRESIA AND ASSOCIATED ANOMALIES ATRESIA ESOFAGEA “LONG GAP” ED ANOMALIE ASSOCIATE 261
Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: Case report of an Italian patient 252
Dilated azygos arch mimicking an aortic arch anomaly during thoracic surgery 237
10qter deletion: A new case 235
SINDROME DA ASTINENZA NEONATALE 234
DIAGNOSIS AND FOLLOW-UP OF COMPLEX CONGENITAL MALFORMATIONS/MENTAL RETARDATION (MRA/MR) 233
Transitional hemodynamics in infants of diabetic mothers by targeted neonatal echocardiography, electrocardiography and peripheral flow study 233
Artrogriposi multipla congenita da lesione del II motoneurone, descrizione di un caso e considerazioni clinico-diagnostiche. 231
Etiological heterogeneity and clinical variability in newborns with esophageal atresia 229
Predictive Factors of Abdominal Compartment Syndrome in Neonatal Age 226
A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome 225
A premature infant with Costello syndrome due to a rare G13C HRAS mutation 221
INTERNET OUT OF CONTROL: THE ROLE OF SELF-ESTEEM AND PERSONALITY TRAITS IN PATHOLOGICAL INTERNET USE 221
Clinical cardiac assessment in newborns with prenatally diagnosed intrathoracic masses 220
An acute headache due a nodulary swell- ing of the skull 219
General Movements (GMs): assessment and predictive value 218
Management of multiple pregnancy with an affected twin 210
Microvillous Inclusion Disease in a newborn with positive family history of intractable diarrhoea 209
Diabete insipido centrale da idrocefalo congenito in un neonato di genitori immigrati 205
Patologia cromosomica rara:47,XXX / 48 XXXX. 202
Prematurity and twinning 202
Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral artery 202
Intrauterine growth pattern and birthweight discordance in twin pregnancies: a retrospective study 202
MACROCEPHALY FROM A NORMAL VARIANT TO A THREATENING CONDITION. A SINGLE CENTER RETROSPECTIVE STUDY ON 189 SUBJECTS 201
NF1 microdeletion syndrome: Case report of two new patients 200
Intrauterine growth restriction and congenital malformations: a retrospective epidemiological study 195
Lacune neonatali: l’aplasia cutis congenita 194
Diastematomelia:descrizione di un caso con quadro clinico peculiare 188
INTELLECTUAL DISABILITY, EPILEPSY AND MILD DYSMORPHISMS DUE 22q11.2 DISTAL DUPLICATION: CLINICAL AND MOLECULAR CHARACTERIZATION OF A 0.5 Mb MINIMAL CRITICAL REGION 188
Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletion 188
Sindrome di Smith Magenis da delezione 17 q 11.2: descrizione di un caso ad elevata espressività clinica 187
La neurofibromatosi 1 in età evolutiva: contributo casistico e revisione clinica 184
SINDROME DI APERT, SVILUPPO NEUROPSICOMOTORIO E FUNZIONE VISIVA: FATTORI DI RISCHIO PROGNOSTICO IN TRE PAZIENTI 180
Grave ipotonia neonatale con artrogriposi: descrizione di un caso clinico e problematiche diagnostiche 176
Assessment of Cardiac funcionality in term newborns born to diabetic mothers 175
COPY NUMBER VARIATIONS IN THE ETIOLOGY OF AUTISM SPECTRUM DISORDERS 173
Array CGH identifies a 823 kb Microduplication at 22q 11.22 encompassing the Rab36 gene in a Child with Autism Spectrum Disorder and Mild Dysmorphism 172
The world of twins: an update 170
EDEME GENERALIZZATO, IPOTONIA E IPERECCITABILITA' ALLA NASCITA IN NEONATO A TERMINE CON GALATTOSIALIDOSI:APPROCCIO CLINICO E DIAGNOSTICO 169
PESCHIAMO NELLA RETE: ORPHANET 168
Displasia setto-ottica: descrizione di un caso con progressivo deterioramento dei PEV 167
High Resolution CT Angiography in Detection of an Aneurysm of the Vein of Galen as a Source of Intracranial Haemorrhage in a Newborn 167
Perlman sindrome: Clinical report and nine-year follow-up 166
Rara aneuploidia cromosomica, trisomia parziale 14 (q24.3_ter) de novo 164
Aspetti neuroevolutivi 164
2q13 microdeletion syndrome: Report on a newborn with additional features expanding the phenotype 164
Sindrome di Rett da ampia delezione del gene MeCP2 163
Congenital pelvic skeletal anomalies: Clinical and radiographic evaluation of newborns with gastrointestinal malformation 163
Novel missense mutation of the TP63 gene in a newborn with Hay-Wells/Ankyloblepharon-Ectodermal defects-Cleft lip/palate (AEC) syndrome: clinical report and follow-up 163
Osservazioni cliniche su due coppie di gemelli monozigotici discordanti per la presenza di anencefalia 162
MALFORMATIONS OF CENTRAL NERVOUS SYSTEM: GENERAL ISSUES 161
Riarrangiamento cromosomico subtelomerico Del 10Q25: descrizione di un caso con elevata espressività clinica. 160
ASFISSIA PERINATALE:VALUTAZIONE CLINICO-EPIDEMIOLOGICA IN UN CAMPIONE DI NEONATI DI ≥ 34 SEG 160
Methemoglobinemia Associated with Late-Onset Neonatal Sepsis: A Single-Center Experience 160
Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event? 160
IX SINDROME DI RETT DA AMPIA DELEZIONE DEL GENE MeCP2. 159
Macrocefalia: analisi dei fattori predittivi di compromissione dello sviluppo neuropsicomotorio in un campione selezionato di 22 casi. 159
Oriental facial features, growth impairment, mental retardation, hypotonia, severe scoliosis, and precocious thelarche in females. 158
Dysmorphic face, precociously senile appearance, microcephaly, growth retardation and neuropsychomotor delay 158
Marker cromosomico soprannumerario: iso 18p 158
Six patients with Pro250Arg mutation in FGFR3 in a family with coronal craniosynostosis: intrafamilial variability and clinical management 157
IPOGLICEMIA NEONATALE: RILIEVI EPIDEMIOLOGICI IN UN CAMPIONE DI NEONATI RICOVERATI (2012-2017) 157
Characterization of a complex rearrangement involving chromosomes 1, 4 and 8 by FISH and array-CGH 156
Fetal growth restriction: A growth pattern with fetal, neonatal and long-term consequences 156
Recognizable neonatal clinical features of aplasia cutis congenita 156
Congenital heart defects in newborns with apparently isolated single gastrointestinal malformation: A retrospective study 155
Oloprosencefalia semilobare: aspetti elettroencefalografici 154
Spontaneous Resorption of an Occipital Meningocele: Computed Tomography and Magnetic Resonance Imaging Evaluation 153
The impact of genetic diseases on neonatal and pediatric care 151
SINDROME DA MICRODELEZIONE 17q21.31: DESCRIZIONE DI UN CASO CON ELEVATA ESPRESSIVITA' CLINICA 150
Rare chromosomal abnormalities: a mosaic of four cellular lines with two rings involving the chromosomes X and 21. First report in a male newborn patient 149
Interstitial deletion of chromosome 2p15-16.1: report of two patients and critical review of current genotype-phenotype correlation. 148
COPY NUMBER VARIATIONS IN THE ETIOLOGY OF EPILEPSY 147
Newborn screening of inherited metabolic disorders by tandem mass spectrometry: past, present and future 147
Neonatal hyperinsulinemic hypoglycemia: Case report of kabuki syndrome due to a novel KMT2D splicing-site mutation 147
Mild twin–twin transfusion syndrome: Clinical report. 146
Oxidative stress in preterm infants: Overview of current evidence and future prospects 145
Screening ecografico cerebrale nel neonato sano:descrizione di 3 casi di cisti aracnoidea 144
KANGAROO MOTHER CARE UNA GUIDA PRATICA 144
Microcephaly and macrocephaly. A study on anthropometric and clinical data from 308 subjects 144
WIDENING THE SCOPE OF THE 15q13.3 MICRODUPLICATION SYNDROME. PATIENT REPORT AND GENOTYPE-PHENOTYPE CORRELATION. 143
Paternal uniparental disomy chromosome 14-like syndrome due a maternal de novo 160kb deletion at the 14q32.2 region not encompassing the IG- and the MEG3-DMRs: Patient report and genotype-phenotype correlation 142
NEUROFIBROMATOSI TIPO 1 E TUMORI INFANTILI OSSERVAZIONI SU 9 CASI 141
Infarto cerebrale in nato a termine:esiti a 12 mesi 140
Esophageal atresia and Beckwith–Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first report 140
TYPE AND COUNTER-TYPE FROM SPECIFIC CHROMOSOMAL REGIONS 139
Parenting Stress Profile and Children Behaviour in Patients with Congenital Hypothyroidism 139
SINDROME DI PALLISTER KILLIAN. DESCRIZIONE DI UN CASO E CORRELAZIONE CLINICO GENETICA 138
ENCEFALOPATIA NEONATALE. IL RUOLO DELLA INFEZIONE. ANALISI DI UN CAMPIONE DI 1107 NEONATI RICOVERATI IN UTIN E TERAPIA SEMINTENSIVA 138
Totale 19.512
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Categoria #
all - tutte 93.991
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 93.991
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021445 0 0 0 0 0 0 0 0 0 0 210 235
2021/20222.151 129 411 73 124 53 77 96 122 290 248 154 374
2022/20232.543 275 344 84 264 315 352 194 173 261 78 139 64
2023/20241.251 77 166 63 118 74 235 116 56 40 99 46 161
2024/20253.564 93 231 357 316 119 95 218 242 343 431 364 755
2025/202610.674 754 339 698 917 940 1.569 1.587 1.167 714 1.541 448 0
Totale 28.681