CIONI, MADDALENA
 Distribuzione geografica
Continente #
NA - Nord America 1.136
EU - Europa 657
AS - Asia 113
OC - Oceania 1
Totale 1.907
Nazione #
US - Stati Uniti d'America 1.133
GB - Regno Unito 178
IE - Irlanda 167
CN - Cina 93
UA - Ucraina 87
SE - Svezia 65
DE - Germania 41
FR - Francia 38
FI - Finlandia 31
IT - Italia 22
ES - Italia 15
SG - Singapore 8
TR - Turchia 7
BE - Belgio 5
CZ - Repubblica Ceca 3
CA - Canada 2
IN - India 2
JP - Giappone 2
RU - Federazione Russa 2
AU - Australia 1
ID - Indonesia 1
IM - Isola di Man 1
LU - Lussemburgo 1
LV - Lettonia 1
PA - Panama 1
Totale 1.907
Città #
Fairfield 199
Dublin 165
Southend 162
Ashburn 104
Chandler 86
Woodbridge 85
Wilmington 82
Ann Arbor 81
Houston 78
Seattle 78
Cambridge 74
Jacksonville 68
Princeton 29
Nanjing 19
Helsinki 18
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
Singapore 5
Lancaster 4
Tianjin 4
Zhengzhou 4
Brno 3
Jiaxing 3
London 3
Milan 3
Norwalk 3
Rome 3
Somerville 3
Changsha 2
Hebei 2
Jinan 2
Kilburn 2
Moscow 2
Pune 2
Washington 2
Andover 1
Canberra 1
Changchun 1
Chicago 1
Chiswick 1
Chiyoda-ku 1
Desio 1
Duncan 1
Falkenstein 1
Florence 1
Hangzhou 1
Islington 1
Kunming 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
Totale 1.532
Nome #
Chromosome 18 aberrations and epilepsy: a review 287
3.2 Mb microdeletion in chromosome 7 bands q22.2-q22.3 associated with overgrowth and delayed bone age 161
De novo complete trisomy 5p clinical and neuroradiological findings 149
Transient neonatal hypothyroidism after gestational exposure to amiodarone: a follow-up of two cases 131
Efficacy and safety of topiramate in infants according to epilepsy syndromes 130
Pseudo-TORCH syndrome or Baraitser-Reardon syndrome: diagnostic criteria 126
EEG in assessing hydroxycobalamin therapy in neonatal methylmalonic aciduria with homocystinuria 125
Schinzel-Giedion syndrome: a further cause of West syndrome 125
HUNTER SYNDROME: FIRST ITALIAN CASE TREATED WITH ENZYME-REPLACEMENT THERAPY. TEN YEARS OF FOLLOW-UP 121
Growth hormone secretion in Prader-Willi syndrome 113
Selective mutism, speech delay, dysmorphisms, and deletion of the short arm of chromosome 18: a distinct entity? 107
Spermatogenesis in a man with complete deletion of USP9Y 101
CKAP2L mutation confirms the diagnosis of Filippi syndrome 96
Complete deletion of USP9Y gene in normospermic man: new insights into human Y AZFa gene function in spermatogenesis 82
Pontocerebellar hypoplasia type 2: further clinical characterization and evidence of positive response of dyskinesia to levodopa 70
Totale 1.924
Categoria #
all - tutte 6.202
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 6.202


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020403 51 13 27 73 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
2024/20257 7 0 0 0 0 0 0 0 0 0 0 0
Totale 1.924