BERARDI, ROSARIO
 Distribuzione geografica
Continente #
NA - Nord America 1.427
EU - Europa 813
AS - Asia 137
OC - Oceania 3
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
SA - Sud America 1
Totale 2.383
Nazione #
US - Stati Uniti d'America 1.425
IE - Irlanda 231
GB - Regno Unito 203
CN - Cina 132
UA - Ucraina 125
SE - Svezia 72
DE - Germania 46
FR - Francia 46
FI - Finlandia 44
ES - Italia 22
IT - Italia 16
AU - Australia 3
TR - Turchia 3
BE - Belgio 2
CA - Canada 2
NL - Olanda 2
AT - Austria 1
CL - Cile 1
EE - Estonia 1
EU - Europa 1
HK - Hong Kong 1
ID - Indonesia 1
NG - Nigeria 1
PL - Polonia 1
RO - Romania 1
Totale 2.383
Città #
Fairfield 247
Dublin 230
Southend 183
Ashburn 126
Chandler 112
Woodbridge 108
Wilmington 106
Jacksonville 103
Seattle 103
Cambridge 88
Houston 86
Ann Arbor 58
Princeton 42
Nanjing 36
Helsinki 23
Málaga 21
New York 20
San Diego 19
Beijing 16
Boardman 16
Norwalk 11
Shanghai 10
San Mateo 9
Tianjin 9
Nanchang 8
Changsha 7
Shenyang 7
Zhengzhou 6
Hebei 5
Jiaxing 5
Jinan 5
London 4
Siena 4
Izmir 3
Kunming 3
Ningbo 3
Taizhou 3
Washington 3
Andover 2
Chiswick 2
Falkenstein 2
Guangzhou 2
Hangzhou 2
Lanzhou 2
Melbourne 2
Venezia 2
Waanrode 2
Abuja 1
Bonndorf 1
Canberra 1
Central 1
Changchun 1
Chicago 1
Duncan 1
Düsseldorf 1
Florence 1
Gdynia 1
Islington 1
Kilburn 1
Lancaster 1
Los Angeles 1
Markham 1
Menlo Park 1
Paris 1
Philadelphia 1
San Francisco 1
Tallinn 1
Tappahannock 1
Valencia 1
Vienna 1
Winnipeg 1
Totale 1.890
Nome #
Precocious puberty with trisomy X syndrome 156
A 3 Mb deletion in 14q12 causes severe mental retardation, mild facial dysmorphisms and Rett-like features 147
Posterior knee pain: primary symptom of a small non-occlusive venous clot. 135
Transient neonatal hypothyroidism after gestational exposure to amiodarone: a follow-up of two cases 130
Efficacy and safety of topiramate in infants according to epilepsy syndromes 129
Craniofacial dyssynostosis: case report and review 124
Post-ictal circulating levels of allopregnanolone in children with partial or generalized seizures 123
Familial Axenfeld-Rieger anomaly, cardiac malformations, and sensorineural hearing loss a provisionally unique genetic syndrome 122
Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation 121
Central precocious puberty and abnormal chromosomal patterns 118
Facial hemangioma and malformation of the cortical development: a broadening of the PHACE spectrum or a new entity? 115
Efficacy and safety of felbamate in children under 4 years of age: a retrospective chart review 114
Late-onset childhood occipital epilepsy(Gastaut type): a family study 114
Multiple neuroendocrine disorder in Salla disease 113
Growth hormone secretion in Prader-Willi syndrome 111
A comparative study of hydrocortisone versus deflazacort in drug-resistant epilepsy of childhood 107
Elettroencephalographic and epileptic patterns in x chromosome anomalies 96
Recurrent torticollis caused by dissecting vertebral artery aneurysm in a pediatric patient results of endovascular treatment by use of coil embolization case report 93
Ethylmalonic encephalopathy: further clinical and neuroradiological characterization 82
GM2 gangliosidosis variant B1 neuroradiological findings 73
Medial temporal lobe dysgenesis in Muenke sindrome and hypochondrolplasia 67
Best practices for the management of thymic epithelial tumors: A position paper by the Italian collaborative group for ThYmic MalignanciEs (TYME) 9
Totale 2.399
Categoria #
all - tutte 8.535
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 8.535


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019181 0 0 0 0 0 0 0 0 0 0 84 97
2019/2020579 76 20 48 102 44 44 43 76 52 32 14 28
2020/2021385 10 87 8 44 7 32 13 63 22 29 54 16
2021/2022235 11 28 9 7 2 9 11 43 11 13 20 71
2022/2023399 23 36 48 52 21 85 7 34 53 22 13 5
2023/2024309 14 5 26 21 7 92 132 8 1 3 0 0
Totale 2.399