ARMAROLI, Annarita
 Distribuzione geografica
Continente #
NA - Nord America 1.531
EU - Europa 731
AS - Asia 166
SA - Sud America 5
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2.434
Nazione #
US - Stati Uniti d'America 1.530
PL - Polonia 332
CN - Cina 108
DE - Germania 107
IT - Italia 86
UA - Ucraina 54
GB - Regno Unito 47
TR - Turchia 47
BE - Belgio 37
SE - Svezia 23
FI - Finlandia 21
RU - Federazione Russa 18
BR - Brasile 4
VN - Vietnam 4
ES - Italia 3
NL - Olanda 2
AE - Emirati Arabi Uniti 1
CA - Canada 1
CL - Cile 1
EU - Europa 1
IN - India 1
IR - Iran 1
KZ - Kazakistan 1
MY - Malesia 1
PH - Filippine 1
RO - Romania 1
SG - Singapore 1
Totale 2.434
Città #
Warsaw 332
Fairfield 246
Woodbridge 192
Chandler 147
Ann Arbor 140
Ashburn 102
Houston 88
Cambridge 82
Wilmington 78
Jacksonville 75
Seattle 74
Ferrara 42
Brussels 35
Beijing 34
Izmir 29
New York 29
Milan 22
Bremen 21
Princeton 21
Falls Church 14
Nanjing 14
Shenyang 14
Boardman 13
San Diego 12
Helsinki 8
Shanghai 8
London 7
Addison 6
Des Moines 6
Hebei 6
Changsha 5
Nanchang 5
Cagliari 4
Dearborn 4
Rome 4
São Paulo 4
Trebaseleghe 4
Dong Ket 3
Jinan 3
Ningbo 3
Redwood City 3
Tianjin 3
Zhengzhou 3
Jiaxing 2
Kunming 2
Lanzhou 2
Monmouth Junction 2
Orange 2
Phoenix 2
Redmond 2
Varazze 2
Waanrode 2
Almaty 1
Alpedrete 1
Andover 1
Barcelona 1
Birmingham 1
Bologna 1
Chicago 1
Edinburgh 1
George Town 1
Guarda Veneta 1
Haikou 1
Hangzhou 1
Hanoi 1
Kilburn 1
Madrid 1
Manila 1
Modena 1
Mountain View 1
Norwalk 1
Palm Bay 1
Prescot 1
Reggio Nell'emilia 1
Sabz 1
San Mateo 1
Taizhou 1
Toronto 1
Wandsworth 1
Yellow Springs 1
Totale 1.991
Nome #
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 322
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression 295
Transcriptomics analysis in collagen VI myopathy: Role of circadian genes using novel fluidic card tools 149
Omics approach and novel biostatistic tools identified RPL3L as potential genetic modifier of clinical severity in female carriers of Duchenne muscle dystrophy 146
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 141
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype 138
Paternal germline mosaicism in collagen VI related myopathies 132
Biochemical characterization of patients with in-frame or out-of-frame DMD deletions pertinent to exon 44 or 45 skipping. 124
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: Implications for clinical trials 122
Cyclosporine a in Ullrich congenital muscular dystrophy: Long-term results 115
Early corticosteroid treatment in 4 duchenne muscular dystrophy patients: 14-year follow-up 107
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia 105
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 104
Huntington's disease-like presentation in Spinocerebellar ataxia type 12 103
Genetic counseling for women referred for advanced maternal age: a telegenetic approach 100
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript 77
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies 58
Hypospadias prevalence in the Emilia Romagna Region registry: Increasing or methodology? 44
Functional characterization of two novel mutations in scn5a associated with brugada syndrome identified in Italian patients 34
Chromatin configuration, RNA and protein studies identified novel DNA elements that influence the dystrophin transcription dynamics 22
ncRNAs originating from the dystrophin gene as biomarker for assessing antisense therapy 16
TRANSCRIPTIONAL PROFILING IN DUCHENNE MUSCULAR DYSTROPHY REVEALED A PROFOUND DEREGULATION OF BOTH CIRCADIAN RHYTHM GENES AND GENES INVOLVED IN MUSCLE REGENERATIVE PROCESS AS POSSIBLE NEW DISEASE BIOMARKERS 16
TeleNEwCARe: An Italian case-control telegenetics study in patients with Hereditary NEuromuscular and CARdiac diseases 10
Totale 2.480
Categoria #
all - tutte 8.418
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 8.418


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019315 0 0 0 0 0 0 0 9 33 63 99 111
2019/2020570 76 25 29 80 42 63 55 47 44 50 36 23
2020/2021385 33 38 22 53 23 48 21 41 9 44 33 20
2021/2022260 19 24 5 9 8 21 31 11 12 23 29 68
2022/2023344 26 44 11 34 65 31 29 35 32 5 21 11
2023/2024145 17 19 18 6 16 51 4 14 0 0 0 0
Totale 2.480