TRABANELLI, Cecilia
 Distribuzione geografica
Continente #
NA - Nord America 105
EU - Europa 54
AS - Asia 13
AF - Africa 1
Totale 173
Nazione #
US - Stati Uniti d'America 105
IT - Italia 25
FR - Francia 16
CN - Cina 6
DE - Germania 5
SE - Svezia 4
IN - India 3
FI - Finlandia 2
VN - Vietnam 2
AT - Austria 1
JP - Giappone 1
RU - Federazione Russa 1
TW - Taiwan 1
ZA - Sudafrica 1
Totale 173
Città #
Columbus 14
Santa Cruz 14
Ferrara 13
Ashburn 8
Fairfield 5
Des Moines 4
San Diego 4
Seattle 4
Stockholm 4
Bremen 3
Chicago 3
Houston 3
Woodbridge 3
Albignasego 2
Boardman 2
Cambridge 2
Delhi 2
Dong Ket 2
Los Angeles 2
New York 2
Paris 2
Rockville 2
Auburn 1
Charlotte 1
Clearwater 1
Dehradun 1
Edison 1
Esslingen am Neckar 1
Ferrara di Monte Baldo 1
Helsinki 1
Lappeenranta 1
Las Vegas 1
Mainz 1
Milan 1
Montecatini Terme 1
Muizenberg 1
New Orleans 1
Padova 1
Presque Isle 1
Provo 1
Saint Petersburg 1
San Francisco 1
San Jose 1
Shanghai 1
Solagna 1
Taipei 1
Tokyo 1
Vienna 1
Totale 126
Nome #
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries, file e309ade3-3b50-3969-e053-3a05fe0a2c94 62
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies, file e309ade2-9ddb-3969-e053-3a05fe0a2c94 55
The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study, file e309ade2-c0a5-3969-e053-3a05fe0a2c94 12
A novel custom high density-comparative genomic hybridization array detects common rearrangements as well as deep intronic mutations in dystrophinopathies, file e309ade0-29cf-3969-e053-3a05fe0a2c94 11
DMD gene molecular genetic characterization in Eastern Europe and non European countries, file e309ade2-61c0-3969-e053-3a05fe0a2c94 7
Reactivation of infectious simian virus 40 from normal human tissues, file e309ade0-2454-3969-e053-3a05fe0a2c94 5
Paternal germline mosaicism in collagen VI related myopathies, file e309ade0-88d5-3969-e053-3a05fe0a2c94 5
Left ventricular myocardial noncompaction with advanced atrioventricular conduction disorder and ventricular arrhythmias in a young patient: Role of MIB1 gene, file 62d9c485-10cf-498f-bdf1-bca1010b1ce3 4
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation, file e309ade0-41aa-3969-e053-3a05fe0a2c94 4
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies, file e309ade2-5900-3969-e053-3a05fe0a2c94 4
Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report, file e309ade0-4575-3969-e053-3a05fe0a2c94 2
Exon skipping-mediated dystrophin reading frame restoration for small mutations, file e309ade0-3387-3969-e053-3a05fe0a2c94 1
International-DMD (IDMD): a PTC Therapeutics-supported diagnostic project to widely identify Dystrophin mutations by NGS technologies, file e309ade2-c1b3-3969-e053-3a05fe0a2c94 1
Totale 173
Categoria #
all - tutte 1.007
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 1.007


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20207 0 0 0 0 0 3 4 0 0 0 0 0
2020/202111 0 0 0 1 0 0 0 0 2 0 1 7
2021/202247 0 5 1 7 3 3 1 3 1 2 16 5
2022/202362 1 1 11 13 7 7 7 8 1 3 3 0
2023/202446 1 0 1 1 2 6 5 7 5 2 16 0
Totale 173