Catalogo dei prodotti della ricerca

LEONARDI, LUCA
 Distribuzione geografica
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Continente #
NA - Nord America 1.924
EU - Europa 873
AS - Asia 408
AF - Africa 29
OC - Oceania 16
SA - Sud America 16
Totale 3.266
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Nazione #
US - Stati Uniti d'America 1.901
IT - Italia 520
SG - Singapore 157
IN - India 107
SE - Svezia 71
CN - Cina 64
GB - Regno Unito 50
FI - Finlandia 28
JP - Giappone 28
FR - Francia 25
KR - Corea 25
NL - Olanda 21
DE - Germania 20
IE - Irlanda 20
BG - Bulgaria 17
TG - Togo 17
BE - Belgio 16
CA - Canada 16
AU - Australia 15
AT - Austria 10
RO - Romania 10
HU - Ungheria 9
ES - Italia 8
UA - Ucraina 7
VN - Vietnam 7
AL - Albania 6
EE - Estonia 6
RS - Serbia 6
AR - Argentina 5
BR - Brasile 5
BA - Bosnia-Erzegovina 4
EC - Ecuador 4
MA - Marocco 4
TR - Turchia 4
ZA - Sudafrica 4
CH - Svizzera 3
CZ - Repubblica Ceca 3
GL - Groenlandia 3
GR - Grecia 3
LI - Liechtenstein 3
PK - Pakistan 3
PL - Polonia 3
SC - Seychelles 3
AE - Emirati Arabi Uniti 2
CO - Colombia 2
CR - Costa Rica 2
HK - Hong Kong 2
IR - Iran 2
IS - Islanda 2
MX - Messico 2
BT - Bhutan 1
BY - Bielorussia 1
EG - Egitto 1
GE - Georgia 1
HR - Croazia 1
ID - Indonesia 1
IL - Israele 1
JO - Giordania 1
NZ - Nuova Zelanda 1
SA - Arabia Saudita 1
UZ - Uzbekistan 1
Totale 3.266
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Città #
Fairfield 286
Chandler 178
Ashburn 174
Rome 162
Woodbridge 122
Houston 120
Singapore 120
Seattle 112
Cambridge 103
Wilmington 70
Milan 69
San Paolo di Civitate 59
Dearborn 57
Princeton 47
Lawrence 38
New York 35
Boston 25
San Diego 25
Ann Arbor 24
Santa Clara 22
Jungnang-gu 21
Plano 21
Millbury 19
Beijing 18
Dublin 17
Lomé 17
Sofia 17
Andover 13
Bengaluru 13
Norwalk 13
Fuzhou 12
Waanrode 12
Sydney 11
Helsinki 10
Boardman 9
Naples 9
Florence 8
Tokyo 8
Toronto 8
Vienna 8
Colorado Springs 7
Fasano 7
Hefei 7
Nanjing 7
Plymouth 7
Ponzano Veneto 7
Chicago 6
London 6
Los Angeles 6
Paris 6
Bremen 5
Budapest 5
Dallas 5
Edinburgh 5
Fremont 5
Hanoi 5
Nagoya 5
Palermo 5
San Mateo 5
Carol Stream 4
Federal 4
Kyoto 4
Mannheim 4
Pisa 4
Quito 4
Stockholm 4
Tallinn 4
Alghero 3
Bolzano Vicentino 3
Brent 3
Brescia 3
Buffalo 3
Cascina 3
Falls Church 3
Islamabad 3
Izmir 3
Lappeenranta 3
Madrid 3
Manchester 3
Melzo 3
Minneapolis 3
Monte Roberto 3
Montreal 3
Nanchang 3
Nuuk 3
Ottawa 3
Oxford 3
Padova 3
Sapporo 3
Stellenbosch 3
Tirana 3
Vicenza 3
Yokohama 3
Zurich 3
Amsterdam 2
Ancona 2
Barcelona 2
Bath 2
Bien Hoa 2
Birmingham 2
Totale 2.348
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Nome #
Use of dynamic movement orthoses to improve gait stability and trunk control in ataxic patients 181
Safety, efficacy, and tolerability of efgartigimod in patients with generalised myasthenia gravis (ADAPT). a multicentre, randomised, placebo-controlled, phase 3 trial 140
Early-onset optic neuropathy as initial clinical presentation in SPG7 107
Riluzole in patients with hereditary cerebellar ataxia. a randomised, double-blind, placebo-controlled trial 103
Cerebellum and neuropsychiatric disorders: Insights from ARSACS 90
Nerve high-resolution ultrasonography in peripheral nerve injuries associated with supracondylar humeral fractures in children 89
Longitudinal neurophysiological assessment of intramuscular type-A botulin toxin in healthy humans 88
GIFT-1, a phase IIa clinical trial to test the safety and efficacy of IFNγ administration in FRDA patients 86
Gait patterns in patients with hereditary spastic paraparesis 86
Multifocal motor neuropathy following treatment with adalimumab for ulcerative colitis 85
Nerve high resolution ultrasonography in Tangier disease 82
Widening the phenotypical spectrum of EGR2-related CMT: unusual phenotype for R409W mutation 82
A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias. A pilot open-labeled study 81
Pigmentary degenerative maculopathy as prominent phenotype in an Italian SPG56/CYP2U1 family 81
Acute optic neuropathy associated with a novel MFN2 mutation 81
Local stability of the trunk in patients with degenerative cerebellar ataxia during walking 80
Spinocerebellar ataxia type 3 in Italy. time to change mind 80
Changes of clinical, neurophysiological and nerve ultrasound characteristics in CIDP over time: a 3-year follow-up 80
Spinocerebellar ataxia type 10 in Peru: the missing link in the Amerindian origin of the disease 78
'When atlastin meets spastin' 78
Risk factors for chronic inflammatory demyelinating polyradiculoneuropathy (CIDP): antecedent events, lifestyle and dietary habits. Data from the Italian CIDP Database 75
Progression of gait ataxia in patients with degenerative cerebellar disorders. A 4-year follow-up study 72
Electrophysiological abnormalities in iatrogenic botulism: Two case reports and review of the literature 69
Muscle involvement in myasthenia gravis: Expanding the clinical spectrum of Myasthenia-Myositis association from a large cohort of patients 68
Sensory ataxia as a prominent clinical presentation in three families with mutations in CYP7B1 60
Attrv in lazio-italy: A high-prevalence region in a non-endemic country 58
Skin biopsy and quantitative sensory assessment in an Italian cohort of ATTRv patients with polyneuropathy and asymptomatic carriers: possible evidence of early non-length dependent denervation 55
Gender effect on cardiac involvement in myotonic dystrophy type 1 54
null 53
Quantitative sensory testing and skin biopsy findings in late‐onset ATTRv pre‐symptomatic carriers: relationships with predicted time of disease onset (PADO) 52
Muscle magnetic resonance imaging in myotonic dystrophy type 1 (DM1): Refining muscle involvement and implications for clinical trials 52
Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark cores 51
Impact of environmental factors and physical activity on disability and quality of life in CIDP 48
ATTRv amyloidosis Italian Registry: clinical and epidemiological data 48
Chronic inflammatory demyelinating polyradiculoneuropathy: can we make a diagnosis in patients not fulfilling electrodiagnostic criteria? 47
Muscle MRI in immune-mediated necrotizing myopathy (IMNM). implications for clinical management and treatment strategies 44
Functional and morphometric assessment of small-fibre damage in late-onset hereditary transthyretin amyloidosis with polyneuropathy: the controversial relation between small-fibre-related symptoms and diagnostic test findings 44
Psychosocial burden and professional and social support in patients with hereditary transthyretin amyloidosis (ATTRv) and their relatives in Italy 40
Nerve ultrasonography findings as possible pitfall in differential diagnosis between hereditary transthyretin amyloidosis with polyneuropathy and chronic inflammatory demyelinating polyneuropathy 38
The neurophysiological lesson from the Italian CIDP database 38
Comparison of quantitative muscle ultrasound and whole-body muscle MRI in facioscapulohumeral muscular dystrophy type 1 patients 37
Frequency of diabetes and other comorbidities in chronic inflammatory demyelinating polyradiculoneuropathy and their impact on clinical presentation and response to therapy 36
Relevance of diagnostic investigations in chronic inflammatory demyelinating poliradiculoneuropathy. Data from the Italian CIDP database 36
High-resolution ultrasound of peripheral nerves in late-onset hereditary transthyretin amyloidosis with polyneuropathy: similarities and differences with CIDP 36
Real-life experience with inotersen in hereditary transthyretin amyloidosis with late-onset phenotype: data from an early- access program in Italy 35
Prolonged distal motor latency of median nerve does not improve diagnostic accuracy for CIDP 34
Distal upper limb involvement in myasthenia-myositis association 31
Prominent mitochondrial pathology in a case of refractory dermatomyositis: coincidence or concause? 31
Risk of disease relapse, safety and tolerability of SARS-CoV-2 vaccination in patients with chronic inflammatory neuropathies 29
Neuropathic pain experience in symptomatic and presymptomatic subjects carrying a transthyretin gene mutation 29
Unclassified clinical presentations of chronic inflammatory demyelinating polyradiculoneuropathy 27
Skin amyloid deposits and nerve fiber loss as markers of neuropathy onset and progression in hereditary transthyretin amyloidosis 23
Muscle MRI as a biomarker of disease activity and progression in myotonic dystrophy type 1: a longitudinal study 22
Serum neurofilament light chain levels correlate with small fiber related parameters in patients with hereditary transthyretin amyloidosis with polyneuropathy (ATTRv-PN) 22
Italian Real-Life Experience of Patients with Hereditary Transthyretin Amyloidosis Treated with Patisiran 21
Impact of 2021 European Academy of Neurology/Peripheral Nerve Society diagnostic criteria on diagnosis and therapy of chronic inflammatory demyelinating polyradiculoneuropathy variants 20
Nerve high-resolution ultrasound in a 2-years follow-up of radial nerve palsy related to humeral shaft fractures 19
Eculizumab for myasthenic exacerbation during treatment with immune-checkpoint inhibitors 17
De novo mutations in SPG3A: a challenge in differential diagnosis and genetic counselling 14
Assessment of diagnostic criteria for multifocal motor neuropathy in patients included in the Italian database 12
Muscle hypertrophy following acquired neurogenic injury: systematic review and analysis of existing literature 11
Detailed clinical, physiological and pathological phenotyping can impact access to disease-modifying treatments in ATTR carriers 10
Serum neurofilament light chain: a promising early diagnostic biomarker for hereditary transthyretin amyloidosis? 10
null 4
Long-term treatment of hereditary transthyretin amyloidosis with patisiran: multicentre, real-world experience in Italy 3
Totale 3.493
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Categoria #
all - tutte 11.523
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 11.523
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020470 0 0 6 36 61 91 88 58 53 31 23 23
2020/2021280 17 22 10 29 16 10 19 15 32 55 29 26
2021/2022632 64 25 45 30 73 26 24 48 39 29 143 86
2022/2023758 96 136 18 86 90 85 30 47 72 25 49 24
2023/2024685 21 57 25 44 42 85 61 72 19 100 89 70
2024/2025221 49 172 0 0 0 0 0 0 0 0 0 0
Totale 3.493