ARMAROLI, Annarita
 Distribuzione geografica
Continente #
NA - Nord America 260
EU - Europa 105
AS - Asia 32
SA - Sud America 5
AF - Africa 3
OC - Oceania 3
Totale 408
Nazione #
US - Stati Uniti d'America 255
IT - Italia 30
DE - Germania 28
CN - Cina 20
FR - Francia 17
RU - Federazione Russa 11
GB - Regno Unito 7
CA - Canada 5
VN - Vietnam 5
PL - Polonia 4
CL - Cile 3
IN - India 3
ZA - Sudafrica 3
AR - Argentina 2
AU - Australia 2
ES - Italia 2
FI - Finlandia 2
JP - Giappone 2
SE - Svezia 2
AE - Emirati Arabi Uniti 1
CH - Svizzera 1
HU - Ungheria 1
NZ - Nuova Zelanda 1
TR - Turchia 1
Totale 408
Città #
Fairfield 32
Santa Cruz 22
Buffalo 21
Columbus 15
Houston 15
Ferrara 13
Ashburn 12
Seattle 12
Woodbridge 9
Cambridge 6
Des Moines 6
Albignasego 5
Chicago 5
Dong Ket 5
London 5
Wilmington 5
Ann Arbor 4
San Francisco 4
Warsaw 4
Boardman 3
Bremen 3
Henderson 3
Las Vegas 3
Los Angeles 3
Muizenberg 3
New York 3
Paris 3
San Diego 3
Auburn 2
Beijing 2
Bengaluru 2
Bologna 2
Buenos Aires 2
Dallas 2
Easton 2
Guangzhou 2
Helsinki 2
Herndon 2
Leawood 2
Lincoln 2
Montreal 2
Otemae 2
Phoenix 2
Rockville 2
Rome 2
Santiago 2
Shanghai 2
Stockholm 2
Wuhan 2
Austin 1
Barcelona 1
Cedar Knolls 1
Charlotte 1
Clearwater 1
Crugers 1
Edison 1
Esslingen am Neckar 1
Evanston 1
Geneve 1
Hangzhou 1
Istanbul 1
Lake Forest 1
Mainz 1
Melbourne 1
Milan 1
Montecatini Terme 1
Montréal 1
Nanjing 1
Nottingham 1
Ottawa 1
Padova 1
Pittsburg 1
Presque Isle 1
Scranton 1
Solagna 1
Toronto 1
Trebaseleghe 1
Zaragoza 1
Totale 298
Nome #
Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression, file e309ade1-7717-3969-e053-3a05fe0a2c94 171
Deep RNA profiling identified CLOCK and molecular clock genes as pathophysiological signatures in collagen VI myopathy, file e309ade0-d00c-3969-e053-3a05fe0a2c94 127
Lamin A/C Missense Mutation R216C Pinpoints Overlapping Features Between Brugada Syndrome and Laminopathies, file e309ade2-9ddb-3969-e053-3a05fe0a2c94 55
Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype, file e309ade1-3a17-3969-e053-3a05fe0a2c94 14
Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype, file e309ade0-3a91-3969-e053-3a05fe0a2c94 10
Functional characterization of two novel mutations in scn5a associated with brugada syndrome identified in Italian patients, file e309ade5-3a03-3969-e053-3a05fe0a2c94 7
Huntington's disease-like presentation in Spinocerebellar ataxia type 12, file e309ade1-3b6e-3969-e053-3a05fe0a2c94 6
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, file e309ade5-6b00-3969-e053-3a05fe0a2c94 6
Paternal germline mosaicism in collagen VI related myopathies, file e309ade0-88d5-3969-e053-3a05fe0a2c94 5
Hypospadias prevalence in the Emilia Romagna Region registry: Increasing or methodology?, file e309ade2-adef-3969-e053-3a05fe0a2c94 5
A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation, file e309ade0-41aa-3969-e053-3a05fe0a2c94 4
Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia, file e309ade1-6d4b-3969-e053-3a05fe0a2c94 3
TeleNEwCARe: An Italian case-control telegenetics study in patients with Hereditary NEuromuscular and CARdiac diseases, file 18716a30-2358-4048-995b-c3b1f0087cd3 2
Cyclosporine a in Ullrich congenital muscular dystrophy: Long-term results, file e309ade0-2fbc-3969-e053-3a05fe0a2c94 2
Omics approach and novel biostatistic tools identified RPL3L as potential genetic modifier of clinical severity in female carriers of Duchenne muscle dystrophy, file e309ade3-1e2a-3969-e053-3a05fe0a2c94 2
TeleNEwCARe: An Italian case-control telegenetics study in patients with Hereditary NEuromuscular and CARdiac diseases, file 3b39bc49-96be-4853-b3f3-4d73beba16d7 1
Dystrophin quantification and clinical correlations in Becker muscular dystrophy: Implications for clinical trials, file e309ade0-38f6-3969-e053-3a05fe0a2c94 1
Transcriptomics analysis in collagen VI myopathy: Role of circadian genes using novel fluidic card tools, file e309ade0-f00f-3969-e053-3a05fe0a2c94 1
Totale 422
Categoria #
all - tutte 1.317
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 1.317


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201915 0 0 0 0 0 0 0 0 0 0 9 6
2019/202077 6 8 8 14 5 5 9 4 7 5 2 4
2020/202156 4 7 2 6 4 4 3 5 5 3 6 7
2021/202273 1 3 2 7 13 4 2 4 2 3 23 9
2022/2023105 0 7 21 17 18 9 10 11 2 2 7 1
2023/202448 2 2 2 1 3 5 5 5 4 1 18 0
Totale 422