Gidaro, Teresa
 Distribuzione geografica
Continente #
EU - Europa 691
NA - Nord America 547
AS - Asia 171
AF - Africa 10
SA - Sud America 1
Totale 1.420
Nazione #
US - Stati Uniti d'America 544
DE - Germania 263
PL - Polonia 143
SE - Svezia 98
CN - Cina 79
UA - Ucraina 72
SG - Singapore 40
IE - Irlanda 25
GB - Regno Unito 23
FR - Francia 18
VN - Vietnam 17
IT - Italia 15
RU - Federazione Russa 14
FI - Finlandia 13
ID - Indonesia 13
IN - India 11
CI - Costa d'Avorio 10
TR - Turchia 5
BE - Belgio 4
CH - Svizzera 2
KR - Corea 2
MX - Messico 2
CA - Canada 1
EC - Ecuador 1
HU - Ungheria 1
IR - Iran 1
JP - Giappone 1
LK - Sri Lanka 1
UZ - Uzbekistan 1
Totale 1.420
Città #
Warsaw 143
Chandler 93
Ashburn 51
Jacksonville 42
Houston 34
San Mateo 31
Singapore 30
Dublin 25
Fairfield 24
Nanjing 22
Ann Arbor 21
Wilmington 19
Woodbridge 19
Nürnberg 18
Bremen 13
Dearborn 13
Jakarta 13
Boston 12
Detroit 12
Lawrence 12
Moscow 12
Nanchang 11
Abidjan 10
New York 10
Marseille 9
Seattle 9
Fremont 8
Munich 7
Redwood City 7
Leawood 6
Cambridge 5
Hebei 5
Izmir 5
Brussels 4
Philadelphia 4
Chicago 3
Falls Church 3
Hounslow 3
Jiaxing 3
Jinan 3
Kunming 3
Lanzhou 3
Milan 3
Shanghai 3
Shenyang 3
Tianjin 3
University Park 3
Anagni 2
Anguillara Sabazia 2
Boardman 2
Bonn 2
Cattolica 2
Changsha 2
Hangzhou 2
Indiana 2
Norwalk 2
Seoul 2
Zhengzhou 2
Ardabil 1
Auburn Hills 1
Beijing 1
Colombo 1
Dong Ket 1
Edinburgh 1
Guangzhou 1
Guayaquil 1
Kilburn 1
Lancaster 1
Las Vegas 1
London 1
Los Angeles 1
Mountain View 1
Phoenix 1
Phoenixville 1
Princeton 1
Redmond 1
Saint Louis 1
San Diego 1
San Jose 1
Simi Valley 1
Sopron 1
Tashkent 1
Toronto 1
Winterthur 1
Wuhan 1
Yellow Springs 1
Zurich 1
Totale 846
Nome #
MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle. 319
alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy 143
Mesoangioblasts from Facioscapulohumeral Muscular Dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior. 115
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene 113
Hereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle 103
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle 98
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 88
TWEAK in inclusion-body myositis muscle: possible pathogenic role of a cytokine inhibiting myogenesis 84
Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis. 83
Hereditary inclusion-body myopathy: clues on pathogenesis and possible therapy 81
Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2). 74
Increased aging in primary muscle cultures of sporadic inclusion-body myositis. 67
Vessel-associated stem cells from skeletal muscle: From biology to future uses in cell therapy 60
Totale 1.428
Categoria #
all - tutte 4.846
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 4.846


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020133 0 0 0 0 14 17 22 16 10 10 23 21
2020/2021158 3 18 2 17 22 10 19 3 17 7 37 3
2021/2022157 13 19 5 22 8 10 4 17 14 3 18 24
2022/2023269 15 30 26 38 36 33 22 16 42 0 6 5
2023/2024109 7 28 2 18 5 7 8 0 2 4 19 9
2024/202566 9 4 20 11 22 0 0 0 0 0 0 0
Totale 1.428