NIKOLIC, ANA
 Distribuzione geografica
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Continente #
NA - Nord America 758
EU - Europa 248
AS - Asia 95
Continente sconosciuto - Info sul continente non disponibili 1
OC - Oceania 1
Totale 1.103
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Nazione #
US - Stati Uniti d'America 755
GB - Regno Unito 91
IT - Italia 47
SE - Svezia 33
CN - Cina 29
SG - Singapore 22
DE - Germania 19
HK - Hong Kong 16
TR - Turchia 16
UA - Ucraina 12
FI - Finlandia 9
FR - Francia 9
BE - Belgio 7
BG - Bulgaria 5
ES - Italia 5
CZ - Repubblica Ceca 4
ID - Indonesia 3
IR - Iran 3
NL - Olanda 3
VN - Vietnam 2
AU - Australia 1
AZ - Azerbaigian 1
BZ - Belize 1
CA - Canada 1
EU - Europa 1
IE - Irlanda 1
JP - Giappone 1
KG - Kirghizistan 1
LT - Lituania 1
MY - Malesia 1
PA - Panama 1
PL - Polonia 1
RU - Federazione Russa 1
Totale 1.103
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Città #
Fairfield 137
Houston 84
Southend 75
Ashburn 72
Woodbridge 60
Seattle 49
Ann Arbor 42
Chandler 41
Cambridge 34
Wilmington 33
Dearborn 25
Santa Clara 25
Modena 23
Nyköping 21
Hong Kong 16
Jacksonville 14
Singapore 14
Izmir 11
Boardman 9
Fremont 9
Princeton 8
Beijing 7
Brussels 7
Eugene 6
Falls Church 6
New York 6
Bremen 5
Helsinki 5
San Diego 5
San Jose 5
Shanghai 5
Sofia 5
Brno 4
El Espinar 3
Jakarta 3
London 3
Munich 3
Phoenix 3
Amsterdam 2
Dong Ket 2
Hebei 2
Mountain View 2
Napoli 2
Acton 1
Alessandria 1
Ardabil 1
Augusta 1
Baku 1
Belize City 1
Bishkek 1
Bologna 1
Chiswick 1
Dublin 1
Fiorano Modenese 1
Frankfurt am Main 1
Guangzhou 1
Hefei 1
Indiana 1
Istanbul 1
Kilburn 1
Kish 1
Lask 1
Leiden 1
Leninsk-kuznetskiy 1
Madrid 1
Milan 1
Nanchang 1
Norwalk 1
Padova 1
Panama City 1
Prescot 1
Redwood City 1
Reggio Emilia 1
Saint Louis 1
San Francisco 1
San Mateo 1
Santiago De Compostela 1
Shenyang 1
Southwark 1
Suzhou 1
Sydney 1
Tokyo 1
Toronto 1
Turin 1
Wandsworth 1
Yiwu 1
Totale 936
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Nome #
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes 314
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry 246
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient data 213
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy. 199
D4Z4 reduced allele in myopathic subjects with no FSHD phenotype: why inconsistency between molecular and clinical data should prompt us to further investigations. 140
Totale 1.112
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Categoria #
all - tutte 3.735
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 3.735
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020174 0 0 0 0 23 38 37 26 18 11 16 5
2020/2021258 20 1 16 21 34 41 13 26 12 35 32 7
2021/2022161 12 13 28 5 6 10 10 13 18 6 29 11
2022/2023136 14 18 10 11 25 10 2 13 18 0 9 6
2023/202495 3 7 6 8 18 2 10 12 1 0 4 24
2024/202556 8 7 1 14 26 0 0 0 0 0 0 0
Totale 1.112