IRIS PubliCatt

Perna, Alessia
 Distribuzione geografica
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Continente #
NA - Nord America 777
EU - Europa 516
AS - Asia 103
AF - Africa 3
OC - Oceania 2
SA - Sud America 2
Totale 1.403
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Nazione #
US - Stati Uniti d'America 775
SE - Svezia 169
IT - Italia 103
PL - Polonia 56
CN - Cina 47
DE - Germania 44
IE - Irlanda 40
FR - Francia 33
IN - India 27
GB - Regno Unito 19
TR - Turchia 14
FI - Finlandia 13
BE - Belgio 12
NL - Olanda 8
UA - Ucraina 7
CH - Svizzera 4
HK - Hong Kong 4
IR - Iran 4
VN - Vietnam 4
CA - Canada 2
RO - Romania 2
RU - Federazione Russa 2
SC - Seychelles 2
AT - Austria 1
AU - Australia 1
BR - Brasile 1
CI - Costa d'Avorio 1
DK - Danimarca 1
ES - Italia 1
KR - Corea 1
KZ - Kazakistan 1
NZ - Nuova Zelanda 1
PE - Perù 1
RS - Serbia 1
SG - Singapore 1
Totale 1.403
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Città #
Chandler 183
Ashburn 89
Warsaw 56
Ann Arbor 51
Dublin 40
New York 31
Fairfield 29
Wilmington 26
Marseille 24
Chicago 21
Jacksonville 20
San Mateo 19
Beijing 18
Princeton 18
Milan 17
Houston 14
Rome 14
Woodbridge 14
Redwood City 13
Boston 12
Brussels 10
Seattle 10
Dearborn 9
Helsinki 9
Nanjing 9
London 7
Pune 7
Bremen 6
Izmir 6
Norwalk 6
Busto Arsizio 5
Cambridge 5
Cattolica 5
Falls Church 5
Kocaeli 5
Nanchang 5
San Diego 5
Washington 5
Dong Ket 4
Hong Kong 4
Zurich 4
Leawood 3
Amsterdam 2
Bari 2
Dallas 2
Edinburgh 2
Groningen 2
Istanbul 2
Jiaxing 2
Kunming 2
Lappeenranta 2
Los Angeles 2
Meppel 2
Monza 2
Mountain View 2
Novara 2
Qingdao 2
Timisoara 2
Waanrode 2
Winnipeg 2
Abidjan 1
Almaty 1
Andover 1
Ankara 1
Ardabil 1
Ardea 1
Atlanta 1
Auckland 1
Augusta 1
Berlin 1
Boardman 1
Brisbane 1
Bristol 1
Campobasso 1
Carol Stream 1
Chandigarh 1
Changchun 1
Cupertino 1
Dresden 1
Frankfurt am Main 1
Fuzhou 1
Gurgaon 1
Hangzhou 1
Hanover 1
Hebei 1
Hefei 1
Hounslow 1
Irvine 1
Jinan 1
Kashan 1
Kensington 1
Kish 1
Lawrence 1
Leipzig 1
Lima 1
Livorno 1
Miami 1
Monmouth Junction 1
Nagold 1
Nova Iguaçu 1
Totale 919
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Nome #
Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional study 130
Abnormal Cortical Thickness Is Associated With Deficits in Social Cognition in Patients With Myotonic Dystrophy Type 1 111
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 90
Hereditary spastic paraplegia: Novel mutations and expansion of the phenotype variability in SPG56 78
Case of postpartum Parsonage-Turner syndrome 77
Reader response: High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2 77
Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype" 75
Application of a Clinical Workflow May Lead to Increased Diagnostic Precision in Hereditary Spastic Paraplegias and Cerebellar Ataxias: A Single Center Experience 70
Clinical characteristics of metabolic associated fatty liver disease (MAFLD) in subjects with myotonic dystrophy type 1 (DM1) 68
Severe 5,10-methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia 65
Nuclear Factor Erythroid 2-Related Factor 2 Activation Might Mitigate Clinical Symptoms in Friedreich’s Ataxia: Clues of an “Out-Brain Origin” of the Disease From a Family Study 64
Clinical use of bioelectrical impedance analysis in patients affected by myotonic dystrophy type 1: A cross-sectional study. 63
Resveratrol corrects aberrant splicing of RYR1 pre-mRNA and Ca2+ signal in myotonic dystrophy type 1 myotubes 59
A novel nonsense EIF1AX mutation identified in a thyroid nodule histologically diagnosed as oncocytic carcinoma 58
Spectral domain optical coherence tomography findings in myotonic dystrophy 57
A Clinical and Epidemiological Prevalence Study on Friedreich's Ataxia in Latium, Italy 51
Unusual case of long survival patient with leptomeningeal carcinomatosis from breast cancer 42
Surgical Decision-Making in Spinal Instability in Facioscapulohumeral Muscular Dystrophy Related with a Spinal Muscle Atrophy 40
Translational control of polyamine metabolism by cnbp is required for drosophila locomotor function 40
Elevated serum Neurofilament Light chain (NfL) as a potential biomarker of neurological involvement in Myotonic Dystrophy type 1 (DM1) 39
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 38
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 37
Neurological Erdheim-Chester Disease Manifesting with Subacute or Progressive Cerebellar Ataxia: Novel Case Series and Review of the Literature 13
Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene 1
Totale 1.443
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Categoria #
all - tutte 6.351
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 6.351
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/20199 0 0 0 0 0 0 0 0 0 0 7 2
2019/2020149 13 3 7 2 8 4 11 9 11 36 34 11
2020/2021214 14 12 8 14 28 20 15 9 20 25 34 15
2021/2022244 17 12 5 48 14 16 3 34 18 16 27 34
2022/2023538 65 68 33 82 28 64 31 43 71 24 26 3
2023/2024254 22 64 13 16 14 61 40 8 4 12 0 0
Totale 1.443