BUONI, SABRINA
 Distribuzione geografica
Continente #
NA - Nord America 1.638
EU - Europa 1.055
AS - Asia 157
SA - Sud America 2
OC - Oceania 1
Totale 2.853
Nazione #
US - Stati Uniti d'America 1.634
IE - Irlanda 289
GB - Regno Unito 275
CN - Cina 146
UA - Ucraina 125
SE - Svezia 118
FR - Francia 62
IT - Italia 55
DE - Germania 53
FI - Finlandia 38
BE - Belgio 15
NL - Olanda 9
ES - Italia 8
CA - Canada 4
PL - Polonia 4
AM - Armenia 2
SG - Singapore 2
TR - Turchia 2
AR - Argentina 1
AU - Australia 1
CZ - Repubblica Ceca 1
EC - Ecuador 1
HK - Hong Kong 1
IR - Iran 1
KR - Corea 1
LA - Repubblica Popolare Democratica del Laos 1
LT - Lituania 1
MN - Mongolia 1
RO - Romania 1
RU - Federazione Russa 1
Totale 2.853
Città #
Dublin 284
Fairfield 252
Southend 234
Ashburn 158
Chandler 152
Woodbridge 129
Houston 117
Ann Arbor 104
Jacksonville 102
Seattle 97
Cambridge 94
Wilmington 92
Princeton 39
Nanjing 34
New York 27
Beijing 24
Lancaster 22
Siena 20
Helsinki 17
Menlo Park 16
Nanchang 15
San Diego 15
Boardman 13
Shanghai 12
Brussels 11
San Mateo 10
Changsha 8
London 8
Málaga 8
Hebei 7
Norwalk 7
Hangzhou 5
Jiaxing 5
Jinan 5
Shenyang 5
Tianjin 5
Zhengzhou 5
Redwood City 4
Sesto Fiorentino 4
Toronto 4
Waanrode 4
Changchun 3
Gdynia 3
Kunming 3
Los Angeles 3
Lucca 3
Milan 3
Rome 3
Venezia 3
Washington 3
Berlin 2
Bologna 2
Cagnes-sur-mer 2
Chicago 2
Dearborn 2
Düsseldorf 2
Guangzhou 2
Izmir 2
Ningbo 2
Singapore 2
Tappahannock 2
Yerevan 2
Amsterdam 1
Bonndorf 1
Buenos Aires 1
Canberra 1
Castiglione D'orcia 1
Chiswick 1
Dottingen 1
Edinburg 1
Edinburgh 1
Frankfurt am Main 1
Fremont 1
Kilburn 1
Lanzhou 1
Montgomery Village 1
Philadelphia 1
Phoenix 1
Prague 1
Providence 1
Quito 1
Sacramento 1
Saint Petersburg 1
San Jose 1
Shaoxing 1
St Louis 1
Udine 1
Ulan Bator 1
Waco 1
Xian 1
Zanjan 1
Totale 2.254
Nome #
Attention-deficit/hyperactivity disorder (ADHD) and variable clinical expression of Aarskog-Scott syndrome due to a novel FGD1 gene mutation (R408Q) 204
Novel PTEN mutations in neurodevelopmental disorders and macrocephaly 195
SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy 177
Late-onset Lennox-Gastaut syndrome in a patient with 15q11.2-q13.1 duplication 165
Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies 148
Segregation analysis in typical absence epilepsy 134
Homocystinuria with transverse sinus thrombosis 132
Drug-resistant epilepsy and epileptic phenotype-EEG association in MECP2 mutated Rett syndrome 131
Hypertelorism, ptosis and myopia associated with drug-resistanr epilepsy, mental delay, growth deficiency, ectodermal defects, and osteopenia. 130
Occipital intermittent rhythmic delta activity only following eye closure in atypical CNS Salmonellosis 129
Myoclonic ecephalopathy in the CDKL5 gene mutation 124
Vagus nerve stimulation for drug-resistant epilepsy in children and young adults. 123
Selenium status, birth weight, and breast-feeding: pattern in the first month 119
Lamotrigine in typical absence epilepsy 118
Epilepsy in Mowat-Wilson syndrome: Delineation of the electroclinical phenotype. 116
Blood pressure in the small-for-date newborn 112
Growth hormone secretion in Prader-Willi syndrome 111
Diagnosis of Angelman syndrome: clinical and EEG criteria 109
null 102
Surgery removes EEG abnormalities in patient with Chiari type I malformation and poor CSF flow 102
Risultati preliminari sulla incidenza nei bambini in età scolare del disturbo da deficit di attenzione ed iperattività 90
Natural history of KBG syndrome in a large European cohort 59
Bone marrow failure and developmental delay caused by mutations in poly(A)-specific ribonuclease (PARN) 37
Totale 2.867
Categoria #
all - tutte 9.053
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 9.053


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019200 0 0 0 0 0 0 0 0 0 0 99 101
2019/2020677 78 31 60 110 52 56 55 83 65 41 12 34
2020/2021408 26 46 6 37 42 36 21 61 43 28 44 18
2021/2022263 17 35 13 11 10 7 14 29 8 20 24 75
2022/2023526 26 55 71 60 58 112 9 40 61 9 12 13
2023/2024375 15 2 25 28 12 125 157 7 3 1 0 0
Totale 2.867