Archivio istituzionale della ricerca dell'Università degli Studi di Palermo

SERRA, Gregorio
 Distribuzione geografica
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Continente #
NA - Nord America 2.374
EU - Europa 959
AS - Asia 294
AF - Africa 11
SA - Sud America 7
Continente sconosciuto - Info sul continente non disponibili 4
OC - Oceania 2
Totale 3.651
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Nazione #
US - Stati Uniti d'America 2.367
IT - Italia 580
SG - Singapore 169
DE - Germania 67
CN - Cina 66
GB - Regno Unito 49
IE - Irlanda 45
SE - Svezia 44
FI - Finlandia 34
RO - Romania 26
UA - Ucraina 24
RU - Federazione Russa 21
IR - Iran 16
IN - India 13
BE - Belgio 12
FR - Francia 12
NL - Olanda 10
CH - Svizzera 9
HK - Hong Kong 9
ES - Italia 8
CI - Costa d'Avorio 6
AT - Austria 5
CA - Canada 4
EU - Europa 4
ID - Indonesia 4
PL - Polonia 4
JP - Giappone 3
NO - Norvegia 3
PE - Perù 3
PH - Filippine 3
TH - Thailandia 3
CZ - Repubblica Ceca 2
KR - Corea 2
MA - Marocco 2
NZ - Nuova Zelanda 2
RS - Serbia 2
AE - Emirati Arabi Uniti 1
AR - Argentina 1
BR - Brasile 1
CO - Colombia 1
EG - Egitto 1
GH - Ghana 1
GL - Groenlandia 1
HR - Croazia 1
IL - Israele 1
IQ - Iraq 1
KZ - Kazakistan 1
LT - Lituania 1
MX - Messico 1
MY - Malesia 1
NG - Nigeria 1
PR - Porto Rico 1
UY - Uruguay 1
VN - Vietnam 1
Totale 3.651
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Città #
Fairfield 299
Chandler 261
Ashburn 231
Woodbridge 173
Houston 164
Seattle 152
Singapore 146
Ann Arbor 130
Wilmington 121
Palermo 107
Cambridge 105
Medford 61
Altamura 49
Dublin 40
Princeton 39
Santa Clara 38
Rome 36
Lawrence 33
San Diego 32
Des Moines 31
Milan 29
Ludwigshafen am Rhein 26
New York 22
London 21
San Paolo di Civitate 13
Bologna 12
Jacksonville 12
Nanjing 12
Boardman 11
Brussels 11
Helsinki 11
Beijing 9
Columbus 8
Naples 8
Pune 8
Bremen 7
Central 7
Dearborn 7
Falls Church 7
Jiaxing 7
Lappeenranta 7
Abidjan 6
Lentini 6
Redwood City 6
Kilburn 5
Monreale 5
Mountain View 5
Munich 5
Udine 5
Cedar Knolls 4
Latina 4
Paris 4
Phoenix 4
Pozzuoli 4
Saint Petersburg 4
Trapani 4
Tulsa 4
Washington 4
Albignasego 3
Angri 3
Cagliari 3
Castelnuovo Rangone 3
Chennai 3
Council Bluffs 3
Florence 3
Frankfurt am Main 3
Guangzhou 3
Incisa 3
Minneapolis 3
Nanchang 3
Ningbo 3
Oslo 3
Parma 3
Paternò 3
Salemi 3
San Francisco 3
Santa Lucia Di Piave 3
Santa Marinella 3
Sassari 3
Shenyang 3
Taranto 3
Tehran 3
Telde 3
Tokyo 3
Worcester 3
Zhengzhou 3
Agadir 2
Arequipa 2
Atlanta 2
Aversa 2
Bangkok 2
Bari 2
Belgrade 2
Belpasso 2
Berlin 2
Brescia 2
Bucharest 2
Castrolibero 2
Chicago 2
Dallas 2
Totale 2.694
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Nome #
Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcome 220
Novel LRPPRC compound heterozygous mutation in a child with early-onset Leigh syndrome French-Canadian type: Case report of an Italian patient 209
Clinical and molecular characterization of 112 single-center patients with Neurofibromatosis type 1 205
The vaccinaTion & Hpv Knowledge (THinK) questionnaire: a reliability and validity study on a sample of women living in Sicily (southern-Italy) 194
Antimicrobial therapy in neonatal intensive care unit 150
NF1 microdeletion syndrome: Case report of two new patients 145
14q13.1-21.1 Deletion Encompassing the HPE8 Locus in an Adolescent With Intellectual Disability and Bilateral Microphthalmia, But Without Holoprosencephaly 131
Portal Vein Thrombosis in a Preterm Newborn with Mutation of the MTHFR and PAI-1 Genes and Sepsis by Candida parapsilosis 128
ADOLESCENTE CON DATTILITE DELLE MANI DA INFEZIONE DA HELICOBACTER PYLORI 109
Standard and Specialized Infant Formulas in Europe: Making, Marketing, and Health Outcomes 103
MALFORMATIONS OF CENTRAL NERVOUS SYSTEM: GENERAL ISSUES 102
Neonatal hyperinsulinemic hypoglycemia: Case report of kabuki syndrome due to a novel KMT2D splicing-site mutation 99
Growth patterns and associated risk factors of congenital malformations in twins 90
MACROCEPHALY FROM A NORMAL VARIANT TO A THREATENING CONDITION. A SINGLE CENTER RETROSPECTIVE STUDY ON 189 SUBJECTS 86
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 86
Neonatal ten-year retrospective study on neural tube defects in a second level University Hospital 83
LARGE FOR GESTATIONAL AGE, MACROSOMIA, OVERGROWTH: AN UPDATE ON DEFINITIONS AND DETERMINANTS 77
Il neonato che “sa di sale” 76
A new mutation in EDA gene in X-linked hypohidrotic ectodermal dysplasia associated with keratoconus. 75
Smartphone use and addiction during the coronavirus disease 2019 (COVID-19) pandemic: cohort study on 184 Italian children and adolescents 72
Infant developmental profile of Crisponi syndrome due to compound heterozygosity for CRLF1 deletion 68
Fetal growth restriction: A growth pattern with fetal, neonatal and long-term consequences 66
The child with overgrowth between clinical variability and genetic heterogeneity 66
IPOGLICEMIA NEONATALE: RILIEVI EPIDEMIOLOGICI IN UN CAMPIONE DI NEONATI RICOVERATI (2012-2017) 64
Perinatal and newborn care in a two years retrospective study in a first level peripheral hospital in Sicily (Italy) 63
2q13 microdeletion syndrome: Report on a newborn with additional features expanding the phenotype 62
Jacobsen syndrome and neonatal bleeding: report on two unrelated patients 55
Cardio-facio-cutaneous syndrome and gastrointestinal defects: report on a newborn with 19p13.3 deletion including the MAP 2K2 gene 54
Lesioni cutanee stellate e simmetriche in un gemello “rimasto solo” 52
Neonatal osteomyelitis of the talus due to methicillin-resistant Staphylococcus epidermidis 48
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 47
La Bioetica sul campo: una sfida per il neonatologo e il pediatra 45
Acute pancreatitis in children and rotavirus infection. Description of a case and minireview 45
Interstitial deletions of chromosome 1p: novel 1p31.3p22.2 microdeletion in a newborn with craniosynostosis, coloboma and cleft palate, and review of the genomic and phenotypic profiles 43
Recommendations for neonatologists and pediatricians working in first level birthing centers on the first communication of genetic disease and malformation syndrome diagnosis: consensus issued by 6 Italian scientific societies and 4 parents’ associations 40
Esophageal atresia and Beckwith–Wiedemann syndrome in one of the naturally conceived discordant newborn twins: first report 40
Manifestazioni cutanee anulari e lupus eritematoso neonatale 40
Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis 39
Quality of life improving after propranolol treatment in patients with Infantile Hemangiomas 38
Necrotizing enterocolitis in the preterm: newborns medical and nutritional Management in a Single-Center Study 38
Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small town 38
Follow-Up to Ensure Continuity of Care and Support Preventive Care 36
Distal Arthrogryposis type 5 in an Italian family due to an autosomal dominant gain-of-function mutation of the PIEZO2 gene 34
Cutis verticis gyrata and Noonan syndrome: report of two cases with pathogenetic variant in SOS1 gene 32
Congenital syphilis in a preterm newborn with gastrointestinal disorders and postnatal growth restriction 32
Lo spettro dei disordini feto-alcolici: una guida per il pediatra 31
Quando l’amnios si rompe troppo presto e… da solo 31
New insights on partial trisomy 3q syndrome: de novo 3q27.1-q29 duplication in a newborn with pre and postnatal overgrowth and assisted reproductive conception 30
Safety of Rotavirus Vaccination in Preterm Infants Admitted in Neonatal Intensive Care Units in Sicily, Italy: A Multicenter Observational Study 29
Useless and limits of Postmortem CT (PMCT) in a complex case of preterm infant murder 29
Congenital hypopituitarism and multiple midline defects in a newborn with non-familial Cat Eye syndrome 26
THE “SALT-TASTING” NEWBORN 24
The social role of pediatrics in the past and present times 24
Novel de novo missense mutation in the interferon regulatory factor 6 gene in an Italian infant with IRF6-related disorder 20
Intestinal malrotation in a female newborn affected by Osteopathia Striata with Cranial Sclerosis due to a de novo heterozygous nonsense mutation of the AMER1 gene 20
Penile Length Assessment of Children Treated for Primary Buried Penis: Can Satisfying Penile Growth Always Be Achieved? 19
Intraoperative ultrasound-assisted endoscopic treatment of primary intermediate and high-grade vesicoureteral reflux in children in a long-term follow-up 17
Group B streptococcus colonization in pregnancy and neonatal outcomes: a three-year monocentric retrospective study during and after the COVID-19 pandemic 15
Penile Length Assessment of Children Treated for Primary Buried Penis: Can Satisfying Penile Growth Always Be Achieved? 14
Carnitine palmitoyltransferase II (CPT II) deficiency responsible for refractory cardiac arrhythmias, acute multiorgan failure and early fatal outcome 13
Increased adherence to influenza vaccination among Palermo family pediatricians: a study on safety and compliance of qLAIV vaccination 12
Report and follow-up on two new patients with congenital mesoblastic nephroma 10
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Encefalopatia neonatale e disfunzione multiorgano, considerazioni eziologiche e correlati clinici. Valutazione di una casistica 1
Totale 3.994
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Categoria #
all - tutte 20.286
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 20.286
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020301 0 0 0 0 36 57 42 30 42 20 34 40
2020/2021784 38 33 46 117 191 55 91 56 29 50 33 45
2021/2022687 63 84 30 26 21 41 37 45 85 89 72 94
2022/2023872 88 169 37 94 69 110 36 77 77 36 51 28
2023/2024569 29 63 42 52 53 120 58 26 18 21 20 67
2024/2025422 39 120 110 123 30 0 0 0 0 0 0 0
Totale 3.994