Pietrobono, Roberta
 Distribuzione geografica
Continente #
EU - Europa 604
NA - Nord America 557
AS - Asia 113
AF - Africa 2
SA - Sud America 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 1.279
Nazione #
US - Stati Uniti d'America 550
DE - Germania 214
PL - Polonia 143
CN - Cina 86
SE - Svezia 76
UA - Ucraina 52
IT - Italia 48
FR - Francia 20
IE - Irlanda 17
FI - Finlandia 12
GB - Regno Unito 11
IN - India 8
TR - Turchia 6
NL - Olanda 5
BZ - Belize 4
HK - Hong Kong 4
IR - Iran 3
VN - Vietnam 3
BE - Belgio 2
CI - Costa d'Avorio 2
CL - Cile 2
JP - Giappone 2
MX - Messico 2
AE - Emirati Arabi Uniti 1
BG - Bulgaria 1
CA - Canada 1
CH - Svizzera 1
CZ - Repubblica Ceca 1
EU - Europa 1
RU - Federazione Russa 1
Totale 1.279
Città #
Warsaw 142
Chandler 112
Ashburn 37
Fairfield 32
Jacksonville 32
Woodbridge 32
Ann Arbor 29
Nanjing 24
Wilmington 23
San Mateo 21
Dublin 17
Houston 17
Seattle 17
Nürnberg 15
Beijing 13
Boston 10
Lawrence 10
Nanchang 8
New York 8
Redwood City 7
Shenyang 7
Zhengzhou 7
Cambridge 6
Cattolica 6
Chicago 6
Dearborn 6
Falls Church 6
Hangzhou 6
Milan 6
Fremont 5
Izmir 5
Belize City 4
Boardman 4
Kunming 4
Marseille 4
Norwalk 4
Cava de' Tirreni 3
Las Vegas 3
Munich 3
University Park 3
Abidjan 2
Augusta 2
Brussels 2
Cerro Maggiore 2
Changsha 2
Guangzhou 2
Hanoi 2
Hebei 2
Helsinki 2
Hong Kong 2
Jiaxing 2
Jinan 2
Kinde 2
Leawood 2
London 2
Milwaukee 2
Monmouth Junction 2
Mountain View 2
Rome 2
San Francisco 2
San Jose 2
Tianjin 2
Acquaviva Delle Fonti 1
Amsterdam 1
Ardabil 1
Austin 1
Bremen 1
Buffalo 1
Busto Arsizio 1
Costa Mesa 1
Dong Ket 1
Dordrecht 1
Dubai 1
Eden Prairie 1
Geneve 1
Genova 1
Groningen 1
Istanbul 1
Kish 1
Köln 1
Lancaster 1
Lanzhou 1
Magenta 1
Montréal 1
Ningbo 1
Pars 1
Phoenix 1
Phoenixville 1
Princeton 1
Pune 1
Reggio Nell'emilia 1
Saint Louis 1
Segrate 1
Shanghai 1
Simi Valley 1
Sofia 1
Urbana 1
Xian 1
Totale 784
Nome #
Molecular, clinical, and muscle studies in myotonic dystrophy type 1 (DM1) associated with novel variant CCG expansions 357
Mild beckwith-wiedemann and severe long-QT syndrome due to deletion of the imprinting center 2 on chromosome 11p. 198
A unique case of reversion to normal size of a maternal premutation FMR1 allele in a normal boy 116
A premature infant with Costello syndrome due to a rare G13C HRAS mutation 96
The Simpson-Golabi-Behmel syndrome: a clinical case and a detective story 90
Simpson–Golabi–Behmel syndrome in a female: A case report and an unsolved issue 86
Rare missense variants in the ALPK1 gene may predispose to periodic fever, aphthous stomatitis, pharyngitis and adenitis (PFAPA) syndrome. 82
Simpson-Golabi-Behmel syndrome type 1 in a 27-week macrosomic preterm newborn: the diagnostic value of rib malformations and index nail and finger hypoplasia. 71
Quantitative analysis of DNA demethylation and transcriptional reactivation of the FMR1gene in fragile X cells treated with 5-aza-deoxycitidine 66
Unexpected finding of paternal premutation of the fragile X FMR1 gene in a female fetus of a premutation carrier mother 65
A premature infant with Costello syndrome due to a rare G13C HRAS mutation. 63
Totale 1.290
Categoria #
all - tutte 3.389
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 3.389


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201954 0 0 0 0 0 0 0 0 0 15 19 20
2019/2020244 45 9 17 31 16 27 16 8 20 15 28 12
2020/2021149 6 17 10 15 22 5 26 1 18 10 16 3
2021/2022148 21 15 2 6 12 8 7 22 8 9 15 23
2022/2023277 40 50 26 48 15 34 10 20 26 0 5 3
2023/202473 9 30 3 7 2 11 4 2 4 1 0 0
Totale 1.290