Gidaro, Teresa
 Distribuzione geografica
Continente #
EU - Europa 672
NA - Nord America 540
AS - Asia 104
AF - Africa 10
Totale 1.326
Nazione #
US - Stati Uniti d'America 537
DE - Germania 258
PL - Polonia 142
SE - Svezia 98
UA - Ucraina 72
CN - Cina 68
IE - Irlanda 25
GB - Regno Unito 23
FR - Francia 18
VN - Vietnam 17
IT - Italia 15
FI - Finlandia 13
IN - India 11
CI - Costa d'Avorio 10
TR - Turchia 5
BE - Belgio 4
RU - Federazione Russa 3
MX - Messico 2
CA - Canada 1
CH - Svizzera 1
IR - Iran 1
JP - Giappone 1
SG - Singapore 1
Totale 1.326
Città #
Warsaw 142
Chandler 93
Ashburn 50
Jacksonville 42
Houston 34
San Mateo 31
Dublin 25
Fairfield 24
Nanjing 22
Ann Arbor 21
Wilmington 19
Woodbridge 19
Nürnberg 18
Bremen 13
Dearborn 13
Boston 12
Detroit 12
Lawrence 12
Nanchang 11
Abidjan 10
New York 10
Marseille 9
Seattle 9
Fremont 8
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
Munich 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
Moscow 2
Norwalk 2
Shanghai 2
Zhengzhou 2
Ardabil 1
Auburn Hills 1
Beijing 1
Dong Ket 1
Edinburgh 1
Guangzhou 1
Kilburn 1
Lancaster 1
Las Vegas 1
London 1
Mountain View 1
Phoenix 1
Phoenixville 1
Princeton 1
Redmond 1
Saint Louis 1
San Diego 1
San Jose 1
Simi Valley 1
Toronto 1
Winterthur 1
Wuhan 1
Yellow Springs 1
Totale 778
Nome #
MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle. 313
alpha-Dystroglycan does not play a major pathogenic role in autosomal recessive hereditary inclusion-body myopathy 136
Mesoangioblasts from Facioscapulohumeral Muscular Dystrophy display in vivo a variable myogenic ability predictable by their in vitro behavior. 107
An Italian family with inclusion-body myopathy and frontotemporal dementia due to mutation in the VCP gene 105
Hereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle 94
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle 89
Analysis of NCAM helps identify unusual phenotypes of hereditary inclusion-body myopathy 84
TWEAK in inclusion-body myositis muscle: possible pathogenic role of a cytokine inhibiting myogenesis 78
Hereditary inclusion-body myopathy: clues on pathogenesis and possible therapy 74
Neprilysin participates in skeletal muscle regeneration and is accumulated in abnormal muscle fibres of inclusion body myositis. 74
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). 66
Increased aging in primary muscle cultures of sporadic inclusion-body myositis. 60
Vessel-associated stem cells from skeletal muscle: From biology to future uses in cell therapy 54
Totale 1.334
Categoria #
all - tutte 3.833
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 3.833


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201950 0 0 0 0 0 0 0 0 0 0 34 16
2019/2020238 32 18 25 30 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
2023/202481 7 28 2 18 5 7 8 0 2 4 0 0
Totale 1.334