Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

PIRO, Ettore
 Distribuzione geografica
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Continente #
NA - Nord America 11.817
EU - Europa 9.568
AS - Asia 6.135
SA - Sud America 1.085
AF - Africa 202
OC - Oceania 12
Continente sconosciuto - Info sul continente non disponibili 6
Totale 28.825
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Nazione #
US - Stati Uniti d'America 11.501
IT - Italia 3.913
SG - Singapore 2.138
RU - Federazione Russa 1.718
CN - Cina 1.494
BR - Brasile 828
UA - Ucraina 694
HK - Hong Kong 686
FI - Finlandia 617
VN - Vietnam 590
DE - Germania 553
PL - Polonia 415
FR - Francia 414
GB - Regno Unito 328
IE - Irlanda 288
BD - Bangladesh 254
JP - Giappone 240
SE - Svezia 190
CA - Canada 138
KR - Corea 130
IN - India 127
AR - Argentina 95
NL - Olanda 95
MX - Messico 74
BE - Belgio 73
RO - Romania 71
TR - Turchia 66
IQ - Iraq 65
ZA - Sudafrica 52
ES - Italia 42
AT - Austria 34
PK - Pakistan 33
CH - Svizzera 32
MY - Malesia 31
CO - Colombia 30
VE - Venezuela 29
CI - Costa d'Avorio 28
CL - Cile 28
MA - Marocco 28
UZ - Uzbekistan 28
CR - Costa Rica 26
ID - Indonesia 26
EC - Ecuador 24
JM - Giamaica 23
SA - Arabia Saudita 23
EG - Egitto 19
PH - Filippine 18
DZ - Algeria 17
KE - Kenya 17
PY - Paraguay 17
TN - Tunisia 17
AE - Emirati Arabi Uniti 16
AZ - Azerbaigian 16
IR - Iran 16
JO - Giordania 16
PE - Perù 16
PT - Portogallo 14
UY - Uruguay 14
BH - Bahrain 13
HN - Honduras 13
IL - Israele 12
NP - Nepal 12
AU - Australia 11
KG - Kirghizistan 11
KZ - Kazakistan 11
LT - Lituania 11
GT - Guatemala 10
BG - Bulgaria 9
GE - Georgia 9
TW - Taiwan 9
CZ - Repubblica Ceca 8
LB - Libano 8
NO - Norvegia 8
AL - Albania 7
OM - Oman 7
RS - Serbia 6
TT - Trinidad e Tobago 6
ET - Etiopia 5
GR - Grecia 5
PR - Porto Rico 5
TH - Thailandia 5
BB - Barbados 4
BN - Brunei Darussalam 4
DK - Danimarca 4
EU - Europa 4
HU - Ungheria 4
MN - Mongolia 4
NI - Nicaragua 4
SN - Senegal 4
AO - Angola 3
BO - Bolivia 3
DO - Repubblica Dominicana 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
Totale 28.788
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Città #
Singapore 1.324
Ashburn 1.323
San Jose 920
Fairfield 819
Chandler 741
Hong Kong 666
Ann Arbor 470
Wilmington 462
Woodbridge 454
Palermo 421
Zgierz 364
Houston 361
Seattle 361
Jacksonville 331
Council Bluffs 280
Beijing 277
Dublin 275
Moscow 271
Santa Clara 267
Cambridge 261
Medford 253
Des Moines 229
Tokyo 227
Ho Chi Minh City 200
Helsinki 196
Rome 185
Lauterbourg 169
Frankfurt am Main 165
Los Angeles 161
Princeton 161
Dallas 158
Hefei 157
Milan 157
Nanjing 149
New York 148
Hanoi 137
Boardman 126
Altamura 98
Buffalo 82
Tulsa 80
Chicago 79
Dearborn 78
Lawrence 74
San Diego 69
Brussels 65
São Paulo 61
Ludwigshafen am Rhein 55
Catania 54
Napoli 52
The Dalles 50
Nanchang 49
Naples 48
Shenyang 47
Hebei 45
London 45
Orem 45
Changsha 42
Seoul 41
Tianjin 37
Bologna 35
Toronto 35
Warsaw 35
Jinan 34
Guangzhou 33
Amsterdam 32
Redwood City 32
Phoenix 30
Florence 29
Abidjan 28
Columbus 28
Da Nang 28
Verona 28
Bari 27
Johannesburg 27
Atlanta 26
Jiaxing 26
Montreal 25
Brooklyn 24
San Mateo 24
Denver 23
Seongnam 23
Tashkent 23
Baghdad 22
Haiphong 22
Messina 22
Nuremberg 22
Padova 22
Saint Petersburg 22
Rio de Janeiro 21
Aversa 20
Belfast 20
Lappeenranta 20
Orange 20
Turin 20
Belo Horizonte 19
Hangzhou 19
Belpasso 18
Boston 18
Chennai 18
Latina 18
Totale 15.940
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Nome #
LO SCREENING DI SVILUPPO 533
Arteria ombelicale unica (AOU): un marker di anomalie congenite 452
POTENZIALI EVOCATI VISIVI (PEV) IN NEONATI DA GRAVIDANZA PLURIMA: RELAZIONE CON LA DISCORDANZA IN PESO (AGA VS SGA) 450
Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcome 342
Autostima,sensation seeking e impulsività nell'uso problematico delle nuove tecnologie in adolescenza 328
A Case of Cardiomyopathy Due to Premature Ductus Arteriosus Closure: The Flip Side of Paracetamol 313
16P11.2 MICRODELETION/MICRODUPLICATION SYNDROME: FURTHER CHARACTERIZATION OF A CRITICAL REGION FOR NEUROPSYCHIATRIC DEVELOPMENT 298
Congenital hepatic mesenchymal hamartoma associated with mesenchymal stem villous hyperplasia of the placenta: case report 294
Clinical and molecular characterization of 112 single-center patients with Neurofibromatosis type 1 291
Sindrome di Down da duplicazione della regione critica 21q22.2-q22.3 290
LONG GAP ESOPHAGEAL ATRESIA AND ASSOCIATED ANOMALIES ATRESIA ESOFAGEA “LONG GAP” ED ANOMALIE ASSOCIATE 267
DIABETE INSIPIDO E PANIPOPITUITARISMO IN IDROCEFALO CONGENITO: DESCRIZIONE DI UN CASO 266
Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: Case report of an Italian patient 259
Dilated azygos arch mimicking an aortic arch anomaly during thoracic surgery 241
DIAGNOSIS AND FOLLOW-UP OF COMPLEX CONGENITAL MALFORMATIONS/MENTAL RETARDATION (MRA/MR) 239
Artrogriposi multipla congenita da lesione del II motoneurone, descrizione di un caso e considerazioni clinico-diagnostiche. 238
10qter deletion: A new case 236
SINDROME DA ASTINENZA NEONATALE 236
Transitional hemodynamics in infants of diabetic mothers by targeted neonatal echocardiography, electrocardiography and peripheral flow study 235
Etiological heterogeneity and clinical variability in newborns with esophageal atresia 235
Predictive Factors of Abdominal Compartment Syndrome in Neonatal Age 229
A novel mutation in KCNQ3-related benign familial neonatal epilepsy: electroclinical features and neurodevelopmental outcome 229
An acute headache due a nodulary swell- ing of the skull 228
General Movements (GMs): assessment and predictive value 227
INTERNET OUT OF CONTROL: THE ROLE OF SELF-ESTEEM AND PERSONALITY TRAITS IN PATHOLOGICAL INTERNET USE 226
A premature infant with Costello syndrome due to a rare G13C HRAS mutation 225
Clinical cardiac assessment in newborns with prenatally diagnosed intrathoracic masses 222
Management of multiple pregnancy with an affected twin 214
Microvillous Inclusion Disease in a newborn with positive family history of intractable diarrhoea 213
Patologia cromosomica rara:47,XXX / 48 XXXX. 211
Dyke-Davidoff-Masson syndrome: case report of fetal unilateral ventriculomegaly and hypoplastic left middle cerebral artery 211
Diabete insipido centrale da idrocefalo congenito in un neonato di genitori immigrati 208
Prematurity and twinning 207
Intrauterine growth pattern and birthweight discordance in twin pregnancies: a retrospective study 207
MACROCEPHALY FROM A NORMAL VARIANT TO A THREATENING CONDITION. A SINGLE CENTER RETROSPECTIVE STUDY ON 189 SUBJECTS 206
NF1 microdeletion syndrome: Case report of two new patients 203
Lacune neonatali: l’aplasia cutis congenita 201
Intrauterine growth restriction and congenital malformations: a retrospective epidemiological study 198
Diastematomelia:descrizione di un caso con quadro clinico peculiare 193
INTELLECTUAL DISABILITY, EPILEPSY AND MILD DYSMORPHISMS DUE 22q11.2 DISTAL DUPLICATION: CLINICAL AND MOLECULAR CHARACTERIZATION OF A 0.5 Mb MINIMAL CRITICAL REGION 193
Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletion 192
Sindrome di Smith Magenis da delezione 17 q 11.2: descrizione di un caso ad elevata espressività clinica 190
La neurofibromatosi 1 in età evolutiva: contributo casistico e revisione clinica 187
SINDROME DI APERT, SVILUPPO NEUROPSICOMOTORIO E FUNZIONE VISIVA: FATTORI DI RISCHIO PROGNOSTICO IN TRE PAZIENTI 187
Assessment of Cardiac funcionality in term newborns born to diabetic mothers 186
Hypertrophic pyloric stenosis masked by kidney failure in a male infant with a contiguous gene deletion syndrome at Xp22.31 involving the steroid sulfatase gene: case report 182
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 181
COPY NUMBER VARIATIONS IN THE ETIOLOGY OF AUTISM SPECTRUM DISORDERS 179
Grave ipotonia neonatale con artrogriposi: descrizione di un caso clinico e problematiche diagnostiche 178
EDEME GENERALIZZATO, IPOTONIA E IPERECCITABILITA' ALLA NASCITA IN NEONATO A TERMINE CON GALATTOSIALIDOSI:APPROCCIO CLINICO E DIAGNOSTICO 175
The world of twins: an update 174
Rara aneuploidia cromosomica, trisomia parziale 14 (q24.3_ter) de novo 172
PESCHIAMO NELLA RETE: ORPHANET 171
High Resolution CT Angiography in Detection of an Aneurysm of the Vein of Galen as a Source of Intracranial Haemorrhage in a Newborn 171
Congenital pelvic skeletal anomalies: Clinical and radiographic evaluation of newborns with gastrointestinal malformation 171
Displasia setto-ottica: descrizione di un caso con progressivo deterioramento dei PEV 170
2q13 microdeletion syndrome: Report on a newborn with additional features expanding the phenotype 170
Sindrome di Rett da ampia delezione del gene MeCP2 169
Perlman sindrome: Clinical report and nine-year follow-up 168
Aspetti neuroevolutivi 168
MALFORMATIONS OF CENTRAL NERVOUS SYSTEM: GENERAL ISSUES 167
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 167
Osservazioni cliniche su due coppie di gemelli monozigotici discordanti per la presenza di anencefalia 166
Marker cromosomico soprannumerario: iso 18p 165
IPOGLICEMIA NEONATALE: RILIEVI EPIDEMIOLOGICI IN UN CAMPIONE DI NEONATI RICOVERATI (2012-2017) 165
ASFISSIA PERINATALE:VALUTAZIONE CLINICO-EPIDEMIOLOGICA IN UN CAMPIONE DI NEONATI DI ≥ 34 SEG 164
Fetal growth restriction: A growth pattern with fetal, neonatal and long-term consequences 164
Benign familial infantile epilepsy associated with KCNQ3 mutation: a rare occurrence or an underestimated event? 164
Riarrangiamento cromosomico subtelomerico Del 10Q25: descrizione di un caso con elevata espressività clinica. 163
Macrocefalia: analisi dei fattori predittivi di compromissione dello sviluppo neuropsicomotorio in un campione selezionato di 22 casi. 163
IX SINDROME DI RETT DA AMPIA DELEZIONE DEL GENE MeCP2. 162
Methemoglobinemia Associated with Late-Onset Neonatal Sepsis: A Single-Center Experience 162
Parenting Stress Profile and Children Behaviour in Patients with Congenital Hypothyroidism 162
Oriental facial features, growth impairment, mental retardation, hypotonia, severe scoliosis, and precocious thelarche in females. 161
Dysmorphic face, precociously senile appearance, microcephaly, growth retardation and neuropsychomotor delay 161
Six patients with Pro250Arg mutation in FGFR3 in a family with coronal craniosynostosis: intrafamilial variability and clinical management 161
SINDROME DA MICRODELEZIONE 17q21.31: DESCRIZIONE DI UN CASO CON ELEVATA ESPRESSIVITA' CLINICA 160
Spontaneous Resorption of an Occipital Meningocele: Computed Tomography and Magnetic Resonance Imaging Evaluation 160
Characterization of a complex rearrangement involving chromosomes 1, 4 and 8 by FISH and array-CGH 159
The impact of genetic diseases on neonatal and pediatric care 159
Recognizable neonatal clinical features of aplasia cutis congenita 159
Oloprosencefalia semilobare: aspetti elettroencefalografici 157
Congenital heart defects in newborns with apparently isolated single gastrointestinal malformation: A retrospective study 157
Microcephaly and macrocephaly. A study on anthropometric and clinical data from 308 subjects 155
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 154
Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcome 153
WIDENING THE SCOPE OF THE 15q13.3 MICRODUPLICATION SYNDROME. PATIENT REPORT AND GENOTYPE-PHENOTYPE CORRELATION. 152
COPY NUMBER VARIATIONS IN THE ETIOLOGY OF EPILEPSY 151
Newborn screening of inherited metabolic disorders by tandem mass spectrometry: past, present and future 151
Screening ecografico cerebrale nel neonato sano:descrizione di 3 casi di cisti aracnoidea 150
Mild twin–twin transfusion syndrome: Clinical report. 150
Interstitial deletion of chromosome 2p15-16.1: report of two patients and critical review of current genotype-phenotype correlation. 150
TYPE AND COUNTER-TYPE FROM SPECIFIC CHROMOSOMAL REGIONS 149
Neonatal hyperinsulinemic hypoglycemia: Case report of kabuki syndrome due to a novel KMT2D splicing-site mutation 149
Esophageal atresia and Beckwith–Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first report 149
Consensus protocol for EEG and amplitude-integrated EEG assessment and monitoring in neonates 148
Oxidative stress in preterm infants: Overview of current evidence and future prospects 148
NEUROFIBROMATOSI TIPO 1 E TUMORI INFANTILI OSSERVAZIONI SU 9 CASI 146
KANGAROO MOTHER CARE UNA GUIDA PRATICA 146
Congenital cytomegalovirus infection and brain injury in a newborn following maternal non-primary infection: case report of an unexpected diagnosis 145
Totale 20.109
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Categoria #
all - tutte 98.273
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 98.273
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/202611.216 754 339 698 917 940 1.569 1.587 1.167 714 1.541 538 452
2026/2027416 416 0 0 0 0 0 0 0 0 0 0 0
Totale 29.639