CIONI, MADDALENA
 Distribuzione geografica
Continente #
NA - Nord America 1.175
EU - Europa 719
AS - Asia 144
AF - Africa 1
OC - Oceania 1
SA - Sud America 1
Totale 2.041
Nazione #
US - Stati Uniti d'America 1.172
GB - Regno Unito 180
IE - Irlanda 168
CN - Cina 96
UA - Ucraina 87
SE - Svezia 65
RU - Federazione Russa 60
DE - Germania 41
FR - Francia 38
SG - Singapore 35
FI - Finlandia 32
IT - Italia 22
ES - Italia 15
TR - Turchia 7
BE - Belgio 5
CZ - Repubblica Ceca 3
IN - India 3
CA - Canada 2
JP - Giappone 2
AU - Australia 1
BO - Bolivia 1
CI - Costa d'Avorio 1
ID - Indonesia 1
IM - Isola di Man 1
LU - Lussemburgo 1
LV - Lettonia 1
PA - Panama 1
Totale 2.041
Città #
Fairfield 199
Dublin 166
Southend 162
Ashburn 104
Chandler 86
Woodbridge 85
Wilmington 82
Ann Arbor 81
Houston 78
Seattle 78
Cambridge 74
Jacksonville 68
Singapore 31
Santa Clara 30
Princeton 29
Helsinki 19
Nanjing 19
Beijing 17
Málaga 15
Shanghai 14
Boardman 12
New York 10
Shenyang 10
Nanchang 9
San Diego 9
Siena 9
Izmir 7
San Mateo 7
Brussels 5
Lancaster 4
Tianjin 4
Zhengzhou 4
Brno 3
Jiaxing 3
London 3
Los Angeles 3
Milan 3
Norwalk 3
Rome 3
Somerville 3
Changsha 2
Hebei 2
Jinan 2
Kilburn 2
Moscow 2
Pune 2
Washington 2
Abidjan 1
Andover 1
Canberra 1
Changchun 1
Chicago 1
Chiswick 1
Chiyoda-ku 1
Dallas 1
Delhi 1
Desio 1
Duncan 1
Falkenstein 1
Florence 1
Hangzhou 1
Islington 1
Kunming 1
La Paz 1
Leawood 1
Luxembourg 1
Monmouth Junction 1
Munich 1
Ningbo 1
Oxford 1
Philadelphia 1
Redwood City 1
Riga 1
Rivne 1
Setagaya-ku 1
Spoleto 1
Taizhou 1
Toronto 1
Weston 1
Xi'an 1
Totale 1.598
Nome #
Chromosome 18 aberrations and epilepsy: a review 297
3.2 Mb microdeletion in chromosome 7 bands q22.2-q22.3 associated with overgrowth and delayed bone age 172
De novo complete trisomy 5p clinical and neuroradiological findings 158
Efficacy and safety of topiramate in infants according to epilepsy syndromes 141
Transient neonatal hypothyroidism after gestational exposure to amiodarone: a follow-up of two cases 139
EEG in assessing hydroxycobalamin therapy in neonatal methylmalonic aciduria with homocystinuria 136
Schinzel-Giedion syndrome: a further cause of West syndrome 135
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria 134
HUNTER SYNDROME: FIRST ITALIAN CASE TREATED WITH ENZYME-REPLACEMENT THERAPY. TEN YEARS OF FOLLOW-UP 130
Growth hormone secretion in Prader-Willi syndrome 122
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity? 115
Spermatogenesis in a man with complete deletion of USP9Y 110
CKAP2L mutation confirms the diagnosis of Filippi syndrome 101
Complete deletion of USP9Y gene in normospermic man: new insights into human Y AZFa gene function in spermatogenesis 89
Pontocerebellar hypoplasia type 2: further clinical characterization and evidence of positive response of dyskinesia to levodopa 79
Totale 2.058
Categoria #
all - tutte 6.870
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 6.870


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020239 0 0 0 0 32 25 28 49 43 31 6 25
2020/2021404 13 55 88 68 13 25 6 47 21 26 36 6
2021/2022170 14 17 9 8 3 9 7 23 4 17 20 39
2022/2023314 16 29 46 34 28 60 6 30 36 18 8 3
2023/2024246 7 2 26 13 19 71 90 3 2 0 4 9
2024/2025141 7 21 50 28 35 0 0 0 0 0 0 0
Totale 2.058