Perna, Alessia
 Distribuzione geografica
Continente #
NA - Nord America 786
EU - Europa 551
AS - Asia 187
AF - Africa 3
OC - Oceania 2
SA - Sud America 2
Totale 1.531
Nazione #
US - Stati Uniti d'America 784
SE - Svezia 169
IT - Italia 121
CN - Cina 73
SG - Singapore 58
PL - Polonia 56
DE - Germania 45
IE - Irlanda 40
FR - Francia 35
IN - India 27
GB - Regno Unito 19
TR - Turchia 15
FI - Finlandia 13
RU - Federazione Russa 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
ES - Italia 2
RO - Romania 2
SC - Seychelles 2
AT - Austria 1
AU - Australia 1
BR - Brasile 1
CI - Costa d'Avorio 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
KR - Corea 1
KZ - Kazakistan 1
LU - Lussemburgo 1
NZ - Nuova Zelanda 1
PE - Perù 1
RS - Serbia 1
Totale 1.531
Città #
Chandler 183
Ashburn 93
Warsaw 56
Ann Arbor 51
Singapore 43
Dublin 40
New York 31
Fairfield 29
Wilmington 26
Marseille 24
Chicago 21
Jacksonville 20
San Mateo 19
Beijing 18
Princeton 18
Rome 18
Milan 17
Houston 14
Woodbridge 14
Redwood City 13
Boston 12
Brussels 10
Moscow 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
Frattamaggiore 4
Hong Kong 4
Los Angeles 4
Zurich 4
Leawood 3
Amsterdam 2
Bari 2
Catania 2
Dallas 2
Edinburgh 2
Groningen 2
Istanbul 2
Jiaxing 2
Kunming 2
Lappeenranta 2
Meppel 2
Monza 2
Mountain View 2
Novara 2
Qingdao 2
Timisoara 2
Valence 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
Brno 1
Campobasso 1
Carol Stream 1
Chandigarh 1
Changchun 1
Cormano 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
Totale 985
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 137
Abnormal Cortical Thickness Is Associated With Deficits in Social Cognition in Patients With Myotonic Dystrophy Type 1 114
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 97
Reader response: High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2 84
Hereditary spastic paraplegia: Novel mutations and expansion of the phenotype variability in SPG56 81
Case of postpartum Parsonage-Turner syndrome 80
Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype" 79
Application of a Clinical Workflow May Lead to Increased Diagnostic Precision in Hereditary Spastic Paraplegias and Cerebellar Ataxias: A Single Center Experience 77
Clinical characteristics of metabolic associated fatty liver disease (MAFLD) in subjects with myotonic dystrophy type 1 (DM1) 71
Severe 5,10-methylenetetrahydrofolate reductase deficiency: A rare, treatable cause of complicated hereditary spastic paraplegia 68
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 68
Clinical use of bioelectrical impedance analysis in patients affected by myotonic dystrophy type 1: A cross-sectional study. 65
Spectral domain optical coherence tomography findings in myotonic dystrophy 63
Resveratrol corrects aberrant splicing of RYR1 pre-mRNA and Ca2+ signal in myotonic dystrophy type 1 myotubes 63
A novel nonsense EIF1AX mutation identified in a thyroid nodule histologically diagnosed as oncocytic carcinoma 61
A Clinical and Epidemiological Prevalence Study on Friedreich's Ataxia in Latium, Italy 55
Elevated serum Neurofilament Light chain (NfL) as a potential biomarker of neurological involvement in Myotonic Dystrophy type 1 (DM1) 48
Unusual case of long survival patient with leptomeningeal carcinomatosis from breast cancer 46
Surgical Decision-Making in Spinal Instability in Facioscapulohumeral Muscular Dystrophy Related with a Spinal Muscle Atrophy 45
Translational control of polyamine metabolism by cnbp is required for drosophila locomotor function 45
An Italian Neurology Outpatient Clinic Facing SARS-CoV-2 Pandemic: Data From 2,167 Patients 44
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 42
Neurological Erdheim-Chester Disease Manifesting with Subacute or Progressive Cerebellar Ataxia: Novel Case Series and Review of the Literature 17
Creutzfeldt-Jakob disease in a man surviving COVID-19: disentangling a casual or causal association by neuropathology 9
Familial childhood onset, slowly progressive myopathy plus cardiomyopathy expands the phenotype related to variants in the TTN gene 8
Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia—experience from an Italian cohort 6
Totale 1.573
Categoria #
all - tutte 7.725
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 7.725


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020133 0 0 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
2023/2024322 22 64 13 16 14 61 40 8 4 12 46 22
2024/202562 9 24 29 0 0 0 0 0 0 0 0 0
Totale 1.573