ARMAROLI, Annarita
 Distribuzione geografica
Continente #
NA - Nord America 1429
EU - Europa 690
AS - Asia 155
SA - Sud America 5
Continente sconosciuto - Info sul continente non disponibili 1
Totale 2280
Nazione #
US - Stati Uniti d'America 1428
PL - Polonia 332
DE - Germania 103
CN - Cina 99
IT - Italia 77
UA - Ucraina 54
TR - Turchia 47
GB - Regno Unito 41
BE - Belgio 23
SE - Svezia 23
RU - Federazione Russa 18
FI - Finlandia 13
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
PH - Filippine 1
RO - Romania 1
Totale 2280
Città #
Warsaw 332
Fairfield 246
Woodbridge 192
Chandler 147
Ann Arbor 140
Houston 88
Cambridge 82
Ashburn 80
Wilmington 78
Jacksonville 75
Seattle 73
Ferrara 40
Beijing 34
Izmir 29
Milan 22
Bremen 21
Brussels 21
Princeton 21
Falls Church 14
Nanjing 14
Shenyang 14
Boardman 13
San Diego 12
Addison 6
Des Moines 6
Hebei 6
Changsha 5
London 5
Nanchang 5
Dearborn 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
Rome 2
Varazze 2
Waanrode 2
Almaty 1
Alpedrete 1
Andover 1
Barcelona 1
Birmingham 1
Chicago 1
Edinburgh 1
Guarda Veneta 1
Haikou 1
Hangzhou 1
Hanoi 1
Madrid 1
Manila 1
Modena 1
Mountain View 1
New York 1
Norwalk 1
Reggio Nell'emilia 1
Sabz 1
San Mateo 1
Taizhou 1
Toronto 1
Yellow Springs 1
Totale 1894
Nome #
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy 307
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression 290
Transcriptomics analysis in collagen VI myopathy: Role of circadian genes using novel fluidic card tools 144
Omics approach and novel biostatistic tools identified RPL3L as potential genetic modifier of clinical severity in female carriers of Duchenne muscle dystrophy 137
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype 135
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype 132
Paternal germline mosaicism in collagen VI related myopathies 125
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: Implications for clinical trials 119
Biochemical characterization of patients with in-frame or out-of-frame DMD deletions pertinent to exon 44 or 45 skipping. 119
Cyclosporine a in Ullrich congenital muscular dystrophy: Long-term results 111
Early corticosteroid treatment in 4 duchenne muscular dystrophy patients: 14-year follow-up 102
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation 99
Huntington's disease-like presentation in Spinocerebellar ataxia type 12 97
Genetic counseling for women referred for advanced maternal age: a telegenetic approach 95
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia 93
Becker muscular dystrophy due to an intronic splicing mutation inducing a dual dystrophin transcript 74
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies 51
Hypospadias prevalence in the Emilia Romagna Region registry: Increasing or methodology? 38
Functional characterization of two novel mutations in scn5a associated with brugada syndrome identified in Italian patients 26
Chromatin configuration, RNA and protein studies identified novel DNA elements that influence the dystrophin transcription dynamics 15
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 8
ncRNAs originating from the dystrophin gene as biomarker for assessing antisense therapy 6
TeleNEwCARe: An Italian case-control telegenetics study in patients with Hereditary NEuromuscular and CARdiac diseases 1
Totale 2324
Categoria #
all - tutte 5124
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 5124


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2017/20189 0000 00 00 0009
2018/2019432 12121212 1914 369 336399111
2019/2020570 76252980 4263 5547 44503623
2020/2021385 33382253 2348 2141 9443320
2021/2022260 192459 821 3111 12232968
2022/2023333 26441134 6531 2935 325210
Totale 2324