IRIS
GENTILE, Luca
 Distribuzione geografica
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Continente #
EU - Europa 1.445
NA - Nord America 1.300
AS - Asia 519
SA - Sud America 5
AF - Africa 3
Continente sconosciuto - Info sul continente non disponibili 3
Totale 3.275
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Nazione #
US - Stati Uniti d'America 1.295
IE - Irlanda 485
IT - Italia 355
SE - Svezia 282
SG - Singapore 237
CN - Cina 193
PL - Polonia 119
IN - India 55
FR - Francia 52
DE - Germania 42
FI - Finlandia 37
GB - Regno Unito 22
BE - Belgio 19
ID - Indonesia 10
VN - Vietnam 9
NL - Olanda 8
HK - Hong Kong 7
RU - Federazione Russa 5
AT - Austria 4
CA - Canada 4
RO - Romania 4
UA - Ucraina 4
CL - Cile 3
EU - Europa 3
BR - Brasile 2
LT - Lituania 2
PH - Filippine 2
RS - Serbia 2
TR - Turchia 2
UG - Uganda 2
AE - Emirati Arabi Uniti 1
CZ - Repubblica Ceca 1
ES - Italia 1
GR - Grecia 1
JP - Giappone 1
LK - Sri Lanka 1
MX - Messico 1
PK - Pakistan 1
TG - Togo 1
Totale 3.275
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Città #
Dublin 484
Chandler 320
Nyköping 217
Singapore 204
Warsaw 118
Ashburn 114
Messina 105
Princeton 73
Beijing 67
Medford 64
Ann Arbor 50
Des Moines 47
Jacksonville 36
Pune 29
Wilmington 29
Bremen 24
Dearborn 24
Hyderabad 20
Cambridge 19
Helsinki 17
Brussels 15
Los Angeles 15
Boardman 14
Jinan 14
Redwood City 14
Rome 13
Duncan 12
Falls Church 12
Seattle 11
Zhengzhou 10
New York 9
Catania 8
Dong Ket 8
Houston 8
Jakarta 8
Ningbo 8
Shenyang 8
Haikou 7
Lappeenranta 7
Livorno 7
Milan 7
Nanjing 7
San Mateo 7
Taizhou 7
Changsha 6
Chicago 6
London 6
Palermo 6
Tianjin 6
Woodbridge 6
Bagheria 5
Collegeville 5
Hangzhou 5
Hebei 5
Munich 5
North Brunswick 5
Padova 5
Piazza Armerina 5
Aci Sant'antonio 4
Fuzhou 4
San Gregorio di Catania 4
Santa Clara 4
Shanghai 4
Taiyuan 4
Vienna 4
Waanrode 4
Como 3
Guangzhou 3
Hamburg 3
Hong Kong 3
Kemerovo 3
Lancaster 3
Nanchang 3
Sector 3 3
Sortino 3
Amsterdam 2
Baoding 2
Belgrade 2
Cordenons 2
Cosenza 2
Fiumefreddo Di Sicilia 2
Gravina di Catania 2
Inverigo 2
Kampala 2
Lanzhou 2
Lucca 2
Mabalacat 2
Norwalk 2
Nuremberg 2
Pescara 2
Springfield 2
Torino 2
Villacidro 2
Woodbine 2
Albuquerque 1
Avezzano 1
Bend 1
Bengkulu 1
Bologna 1
Bracknell 1
Totale 2.476
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Nome #
6MWT performance correlates with peripheral neuropathy but not with cardiac involvement in patients with hereditary transthyretin amyloidosis (hATTR) 143
HATTR italian registry: preliminary data from the collaborative network of telethon GUP 15010 study 128
Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP): A Single-Center Experience in Sicily, an Italian Endemic Area 118
Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area 115
Diagnostic utility of Sudoscan for detecting Bortezomib-induced painful neuropathy 113
Circulating microRNAs Profile in Patients With Transthyretin Variant Amyloidosis 81
A NOVEL SERUM MICRORNA SIGNATURE TO SCREEN TRANSTHYRETIN-RELATED FAMILIAL AMYLOID POLYNEUROPATHY 79
Serial scanning with 99mTc-3, 3-diphosphono-1, 2-propanodicarboxylic acid (99mTc-DPD) for early detection of cardiac amyloid deposition and prediction of clinical worsening in subjects carrying a transthyretin gene mutation 73
A Nouvel serum MicroRNA signature to screen ATTR 71
Novel outcome measures for Charcot-Marie-Tooth disease: Validation and reliability of the 6-min walk test and StepWatch™ Activity Monitor and identification of the walking features related to higher quality of life 70
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family 68
Phenotypic variability of TTR Val122Ile mutation: a Caucasian patient with axonal neuropathy and normal heart 68
ATTRv amyloidosis Italian Registry: clinical and epidemiological data 67
Advances in Treatment of ATTRv Amyloidosis: State of the Art and Future Prospects 66
Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study 61
Genetic neuromuscular disorders: living the era of a therapeutic revolution. Part 1: peripheral neuropathies 60
Prevalence and diagnostic value of extra-left ventricle echocardiographic findings in transthyretin-related cardiac amyloidosis 60
Subcutaneous immunoglobulin in CIDP and MMN: a different long-term clinical response? 58
Cardiac 99mTc-DPD uptake in subjects with Glu89Gln transthyretin gene mutation: is it the earliest sign of disease development? 57
null 54
Considerable post-partum worsening in a patient with CMT2E 53
Monitoring safety and effectiveness of tafamidis in transthyretin amyloidosis in italy. A 3-year longitudinal multicenter study in a non-endemic area. 52
Unilateral hyperhidrosis as persistently isolated feature of syringomyelia and Arnold Chiari type 1 51
Predicting needlestick and sharps injuries in nursing students: Development of the SNNIP scale 51
HATTR : Neurotrophic factors expression in schwann cell line after MIR-150 transfection. 50
CMT subtypes in a cohort of italian patients enrolled at Messina neuromuscular centre since 1994 to 2014. 49
Safety and tolerability of orally administered tafamidis meglumine in TTR FAP: preliminary data at 3-month follow-up 49
Description of a large cohort of Caucasian patients with V122I ATTRv amyloidosis: neurological and cardiological features 49
Diagnosis of cardiac amyloid transthyretin (ATTR) amyloidosis by early (soft tissue) phase [99mTc]Tc-DPD whole body scan: comparison with late (bone) phase imaging 47
"It is not what it seems." Ultrasound findings in a case of unusual iatrogenic ulnar nerve damage. 46
Patients' and physicians' interpretation of chemotherapy-induced peripheral neurotoxicity 45
The THAOS: record of patients from our site. 43
Chronic inflammatory demyelinating polyradiculoneuropathy: can a diagnosis be made in patients not fulfilling electrodiagnostic criteria? 43
Early detection of cardiac amyloid deposition in patients with transthyretin-related familial amyloid polyneuropathy by 99mTc-diphosphonate scintigraphy 42
A multicentre study on epidemiology and prevention of needle stick injuries among students of nursing schools 42
Use of the International Classification of Functioning, Disability and Health Generic-30 Set for the characterization of outpatients: Italian Society of physical and rehabilitative medicine residents section project 41
hATTR Pathology: Nerve Biopsy Results from Italian Referral Centers 40
Early detection of cardiac amyloid deposition in subjects with transthyretin gene mutation by 99mTc-disphosphonate scintigraphy 39
Patisiran in hATTR Amyloidosis: Six-Month Latency Period before Efficacy 37
Transthyretin-related familial amyloidotic polyneuropathy: description of a cohort of patients with Leu64 mutation and late onset. 36
Erratum to: Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area (Journal of Neurology, DOI: 10.1007/s00415-016-8064-9) 35
Efficacy and quality of life in patients with multifocal motor neuropathy treated by subcutaneous immunoglobulin. 34
Anxiety and depression in Charcot-Marie-Tooth disease: data from the Italian CMT national registry 34
Neurological data collection protocol on tafamidis meglumine treatment for familial amyloid polyneuropathy: preliminary data on patients enrolled by the italian network 33
Frequency of diabetes and other comorbidities in chronic inflammatory demyelinating polyradiculoneuropathy and their impact on clinical presentation and response to therapy 32
Quantitative comparison between amyloid deposition detected by 99mTc-diphosphonate imaging and myocardial deformation evaluated by strain echocardiography in transthyretin related cardiac amyloidosis 31
Long-term treatment with subcutaneous immunoglobulin in patients with chronic inflammatory demyelinating polyradiculoneuropathy: a follow-up period up to 7 years 31
Relevance of diagnostic investigations in chronic inflammatory demyelinating poliradiculoneuropathy: Data from the Italian CIDP database 31
Pregnancy in Charcot-Marie-Tooth disease: Data from the Italian CMT national registry 31
A Cyst Compressing the Ulnar Nerve Motor Branch: Ultrasonographic Diagnosis of a Tricking Neuropathy. 31
null 30
From a misdiagnosis of anorexia nervosa to a dramatic patisiran-induced improvement in a patient with ATTRE89Q amyloidosis 30
TTR-FAP: a single-center experience in Sicily, an Italian endemic area 29
Charcot-Marie-Tooth disease: experience from a large Italian tertiary neuromuscular center 29
Very Early Onset of ATTRE89Q Amyloidosis in a Homozygous Patient 29
Correction to: Diagnosis of cardiac amyloid transthyretin (ATTR) amyloidosis by early (soft tissue) phase [99mTc]Tc-DPD whole body scan: comparison with late (bone) phase imaging 27
Subcutaneous immunoglobulin in CIDP and MMN: a short-term nationwide study 27
"Seeing Through the Wall": Ultrasound Application for the Diagnosis and Treatment of Abdominal Pain. 27
"Who seeks finds, who compares discovers". Usefulness of ultrasound to assess small nerve branches. 27
Comparison of the diagnostic accuracy of the 2021 EAN/PNS and 2010 EFNS/PNS diagnostic criteria for chronic inflammatory demyelinating polyradiculoneuropathy 26
Nerve ultrasound in hereditary transthyretin amyloidosis: red flags and possible progression biomarkers 26
Psychosocial burden and professional and social support in patients with hereditary transthyretin amyloidosis (ATTRv) and their relatives in Italy 26
Diagnostic utility of Sudoscan for detecting bortezomib-induced painful neuropathy: a study on 18 patients with multiple myeloma 25
Long-term treatment with subcutaneous immunoglobulin in multifocal motor neuropathy 23
Use of Drugs for ATTRv Amyloidosis in the Real World: How Therapy Is Changing Survival in a Non-Endemic Area 22
null 21
Impact of environmental factors and physical activity on disability and quality of life in CIDP 21
Use of drugs for ATTRv amyloidosis in the real world: How therapy is changing survival in a non-endemic area 21
Shear wave elastography of median nerve at wrist and forearm. Heterogeneity of normative values. 18
Rare among rare: Phenotypes of uncommon CMT genotypes 18
Clinical spectrum and frequency of Charcot-Marie-Tooth disease in Italy: data from the national CMT registry 15
Progressive brachial plexus enlargement in hereditary transthyretin amyloidosis 14
Ultrasound guidance increases diagnostic yield of needle EMG in plegic muscle. 13
Prolonged distal motor latency of median nerve does not improve diagnostic accuracy for CIDP 12
A multicentric study of the disease risks and first manifestations in Hereditary transthyretin amyloidosis (ATTRv): insights for an earlier diagnosis 11
Phenotypic Differences of Glu89Gln Genotype in ATTR Amyloidosis From Endemic Loci: Update From THAOS 10
Frequency, entity and determinants of fatigue in Charcot-Marie-Tooth disease 8
Unclassified clinical presentations of chronic inflammatory demyelinating polyradiculoneuropathy 8
Phenotypic characteristics of F64L, I68L, I107V, and S77Y ATTRv genotypes from the Transthyretin Amyloidosis Outcomes Survey (THAOS) 6
Long-term efficacy and safety of inotersen for hereditary transthyretin amyloidosis: NEURO-TTR open-label extension 3-year update 6
Italian Real-Life Experience of Patients with Hereditary Transthyretin Amyloidosis Treated with Patisiran 5
Assessment of diagnostic criteria for multifocal motor neuropathy in patients included in the Italian database 5
TRPA1 rare variants in chronic neuropathic and nociplastic pain patients 4
A 15-year consolidated overview of data in over 6000 patients from the Transthyretin Amyloidosis Outcomes Survey (THAOS) 4
Risk of disease relapse, safety and tolerability of SARS-CoV-2 vaccination in patients with chronic inflammatory neuropathies 4
Neuropathic pain experience in symptomatic and presymptomatic subjects carrying a transthyretin gene mutation 4
Use, tolerability, benefits and side effects of orthotic devices in Charcot-Marie-Tooth disease 4
Real-life experience with inotersen in hereditary transthyretin amyloidosis with late-onset phenotype: Data from an early-access program in Italy 4
Clinical and Genotype Characteristics and Symptom Migration in Patients With Mixed Phenotype Transthyretin Amyloidosis from the Transthyretin Amyloidosis Outcomes Survey 3
Impact of 2021 European Academy of Neurology/Peripheral Nerve Society diagnostic criteria on diagnosis and therapy of chronic inflammatory demyelinating polyradiculoneuropathy variants 3
Daytime sleepiness and sleep quality in Charcot-Marie-Tooth disease 3
Phenotypic spectrum of myelin protein zero-related neuropathies: a large cohort study from five mutation clusters across Italy 3
Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in Italy 3
Comparison of the diagnostic accuracy of the 2010 European Federation of Neurological Societies/Peripheral Nerve Society and American Association of Electrodiagnostic Medicine diagnostic criteria for multifocal motor neuropathy 2
Machine Learning for Early Diagnosis of ATTRv Amyloidosis in Non-Endemic Areas: A Multicenter Study from Italy 2
Serum neurofilament light chain: a promising early diagnostic biomarker for hereditary transthyretin amyloidosis? 2
The neurophysiological lesson from the Italian CIDP database 2
Totale 3.500
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Categoria #
all - tutte 16.989
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 16.989
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020348 0 0 0 0 6 38 29 52 26 97 40 60
2020/2021442 21 21 70 21 88 27 42 18 23 74 21 16
2021/2022474 14 48 3 16 40 11 48 28 16 22 31 197
2022/20231.280 106 115 78 76 86 114 19 61 570 13 27 15
2023/2024395 27 56 21 27 32 108 16 32 5 25 6 40
2024/2025413 72 22 42 141 136 0 0 0 0 0 0 0
Totale 3.500