Rossi, Salvatore
 Distribuzione geografica
Continente #
NA - Nord America 610
EU - Europa 452
AS - Asia 196
OC - Oceania 3
AF - Africa 2
SA - Sud America 2
Totale 1.265
Nazione #
US - Stati Uniti d'America 605
SE - Svezia 131
IT - Italia 104
SG - Singapore 77
CN - Cina 52
DE - Germania 44
IE - Irlanda 32
PL - Polonia 30
FI - Finlandia 25
ID - Indonesia 24
FR - Francia 23
GB - Regno Unito 20
IN - India 20
RU - Federazione Russa 17
BE - Belgio 9
HK - Hong Kong 6
UA - Ucraina 6
CA - Canada 5
IR - Iran 5
VN - Vietnam 4
CH - Svizzera 3
TR - Turchia 3
AT - Austria 2
AU - Australia 2
KR - Corea 2
LK - Sri Lanka 2
NL - Olanda 2
BR - Brasile 1
CI - Costa d'Avorio 1
ES - Italia 1
JP - Giappone 1
LT - Lituania 1
NZ - Nuova Zelanda 1
PE - Perù 1
RO - Romania 1
RS - Serbia 1
SC - Seychelles 1
Totale 1.265
Città #
Chandler 152
Singapore 58
Ashburn 55
New York 42
Rome 34
Dublin 32
Ann Arbor 31
Warsaw 30
Jakarta 24
Fairfield 21
Houston 20
Wilmington 19
Helsinki 18
Moscow 15
Princeton 14
San Mateo 13
Woodbridge 13
Marseille 12
Beijing 11
Jacksonville 11
Milan 11
Nanjing 10
Boston 9
Brussels 8
London 8
Seattle 8
Pune 7
Bremen 6
Dearborn 6
Detroit 6
Hong Kong 6
Lappeenranta 6
Busto Arsizio 5
San Diego 5
Cambridge 4
Cattolica 3
Dong Ket 3
Frankfurt am Main 3
Hebei 3
Lancaster 3
Los Angeles 3
Munich 3
Paris 3
Washington 3
Zurich 3
Ankara 2
Aurangabad 2
Boardman 2
Campobasso 2
Casalgrande 2
Catania 2
Colombo 2
Meppel 2
Monza 2
Nanchang 2
Norwalk 2
Novara 2
Phoenix 2
Redwood City 2
Santa Clara 2
Seoul 2
Toronto 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
Cormano 1
Dallas 1
Edinburgh 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
Nova Iguaçu 1
Nuremberg 1
Nürnberg 1
Ottawa 1
Parma 1
Totale 833
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 143
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) 117
Reader response: High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2 88
Response to "Autosomal recessive axonal neuropathy caused by HINT1 mutation: New association of a psychiatric disorder to the neurological phenotype" 83
Application of a Clinical Workflow May Lead to Increased Diagnostic Precision in Hereditary Spastic Paraplegias and Cerebellar Ataxias: A Single Center Experience 79
Clinical characteristics of metabolic associated fatty liver disease (MAFLD) in subjects with myotonic dystrophy type 1 (DM1) 77
Next Generation Molecular Diagnosis of Hereditary Spastic Paraplegias: An Italian Cross-Sectional Study 69
Pathological findings in chronic inflammatory demyelinating polyradiculoneuropathy: A single-center experience 63
Dysautonomia as Onset Symptom of Myotonic Dystrophy Type 2 62
A next generation sequencing-based analysis of a large cohort of ataxic patients refines the clinical spectrum associated with spinocerebellar ataxia 21 55
Elevated serum Neurofilament Light chain (NfL) as a potential biomarker of neurological involvement in Myotonic Dystrophy type 1 (DM1) 51
Neurofilament light chain as a disease severity biomarker in ATTRv: data from a single-centre experience 49
Clarification on Uveal Melanoma Associated With Myotonic Dystrophy 48
Clinical-Genetic Features Influencing Disability in Spastic Paraplegia Type 4: A Cross-sectional Study by the Italian DAISY Network 48
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 47
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 45
Ngs in hereditary ataxia: When rare becomes frequent 34
Clinical Reasoning: A Young Man With Subacute Onset of Spastic Paraparesis 33
Fluid Biomarkers of Central Nervous System (CNS) Involvement in Myotonic Dystrophy Type 1 (DM1) 23
Power of NGS-based tests in HSP diagnosis: analysis of massively parallel sequencing in clinical practice 22
Neurological Erdheim-Chester Disease Manifesting with Subacute or Progressive Cerebellar Ataxia: Novel Case Series and Review of the Literature 21
Role of the repeat expansion size in predicting age of onset and severity in RFC1 disease 21
Spinocerebellar ataxia 27B: a frequent and slowly progressive autosomal-dominant cerebellar ataxia—experience from an Italian cohort 9
Hereditary spastic paraparesis type 46 (SPG46): new GBA2 variants in a large Italian case series and review of the literature 9
Totale 1.296
Categoria #
all - tutte 7.690
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 7.690


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202058 0 0 0 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
2024/2025125 16 12 46 22 29 0 0 0 0 0 0 0
Totale 1.296