Rossi, Salvatore
 Distribuzione geografica
Continente #
NA - Nord America 597
EU - Europa 433
AS - Asia 115
OC - Oceania 3
AF - Africa 2
SA - Sud America 2
Totale 1.152
Nazione #
US - Stati Uniti d'America 595
SE - Svezia 131
IT - Italia 98
CN - Cina 51
DE - Germania 40
IE - Irlanda 32
PL - Polonia 30
SG - Singapore 24
FI - Finlandia 23
FR - Francia 22
IN - India 18
GB - Regno Unito 17
RU - Federazione Russa 17
BE - Belgio 8
HK - Hong Kong 6
UA - Ucraina 6
IR - Iran 5
CH - Svizzera 3
TR - Turchia 3
VN - Vietnam 3
AT - Austria 2
AU - Australia 2
CA - Canada 2
KR - Corea 2
LK - Sri Lanka 2
NL - Olanda 2
BR - Brasile 1
CI - Costa d'Avorio 1
JP - Giappone 1
NZ - Nuova Zelanda 1
PE - Perù 1
RO - Romania 1
RS - Serbia 1
SC - Seychelles 1
Totale 1.152
Città #
Chandler 152
Ashburn 54
New York 42
Rome 34
Dublin 32
Ann Arbor 31
Warsaw 30
Fairfield 21
Houston 20
Wilmington 19
Helsinki 17
Moscow 15
Princeton 14
San Mateo 13
Singapore 13
Woodbridge 13
Marseille 12
Beijing 11
Jacksonville 11
Milan 11
Nanjing 10
Boston 9
Seattle 8
Brussels 7
Pune 7
Bremen 6
Dearborn 6
Detroit 6
Hong Kong 6
London 6
Busto Arsizio 5
Lappeenranta 5
San Diego 5
Cambridge 4
Cattolica 3
Dong Ket 3
Hebei 3
Lancaster 3
Los Angeles 3
Washington 3
Zurich 3
Ankara 2
Boardman 2
Campobasso 2
Casalgrande 2
Catania 2
Colombo 2
Meppel 2
Monza 2
Nanchang 2
Norwalk 2
Novara 2
Paris 2
Phoenix 2
Redwood City 2
Seoul 2
Valence 2
Abidjan 1
Ardea 1
Auburn Hills 1
Auckland 1
Brisbane 1
Bristol 1
Buffalo 1
Chiavenna 1
Chicago 1
Chiswick 1
Clearwater 1
Dallas 1
Edinburgh 1
Frankfurt am Main 1
Gurgaon 1
Haikou 1
Hangzhou 1
Hefei 1
Hounslow 1
Jinan 1
Kensington 1
Kish 1
Kunming 1
Lawrence 1
Leawood 1
Liedekerke 1
Lima 1
Limbiate 1
Livorno 1
Melbourne 1
Miami 1
Monmouth Junction 1
Munich 1
Nova Iguaçu 1
Nuremberg 1
Nürnberg 1
Pioltello 1
Pomezia 1
Portland 1
Sacrofano 1
San Jose 1
Shanghai 1
Stockholm 1
Totale 751
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 136
Expansion size and presence of CCG/CTC/CGG sequence interruptions in the expanded CTG array are independently associated to hypermethylation at the DMPK locus in myotonic dystrophy type 1 (DM1) 113
Reader response: High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2 82
Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype" 77
Application of a Clinical Workflow May Lead to Increased Diagnostic Precision in Hereditary Spastic Paraplegias and Cerebellar Ataxias: A Single Center Experience 75
Clinical characteristics of metabolic associated fatty liver disease (MAFLD) in subjects with myotonic dystrophy type 1 (DM1) 69
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 66
Pathological findings in chronic inflammatory demyelinating polyradiculoneuropathy: A single-center experience 58
Dysautonomia as Onset Symptom of Myotonic Dystrophy Type 2 57
A next generation sequencing-based analysis of a large cohort of ataxic patients refines the clinical spectrum associated with spinocerebellar ataxia 21 53
Elevated serum Neurofilament Light chain (NfL) as a potential biomarker of neurological involvement in Myotonic Dystrophy type 1 (DM1) 47
Clarification on Uveal Melanoma Associated With Myotonic Dystrophy 46
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 45
Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experience 44
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network 42
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 41
Ngs in hereditary ataxia: When rare becomes frequent 33
Clinical Reasoning: A Young Man With Subacute Onset of Spastic Paraparesis 28
Fluid Biomarkers of Central Nervous System (CNS) Involvement in Myotonic Dystrophy Type 1 (DM1) 17
Neurological Erdheim-Chester Disease Manifesting with Subacute or Progressive Cerebellar Ataxia: Novel Case Series and Review of the Literature 16
Power of NGS-based tests in HSP diagnosis: analysis of massively parallel sequencing in clinical practice 16
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease 16
Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literature 5
Totale 1.182
Categoria #
all - tutte 6.503
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 6.503


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202075 13 2 2 0 6 2 5 2 10 9 20 4
2020/2021120 6 5 7 8 14 4 12 4 17 14 22 7
2021/2022180 14 11 3 33 6 9 6 24 8 15 22 29
2022/2023445 49 47 23 65 31 51 18 36 71 12 29 13
2023/2024299 11 50 11 22 6 62 31 3 15 11 47 30
2024/202511 11 0 0 0 0 0 0 0 0 0 0 0
Totale 1.182