IRIS
DI LEO, RITA
 Distribuzione geografica
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Continente #
NA - Nord America 978
EU - Europa 868
AS - Asia 189
Continente sconosciuto - Info sul continente non disponibili 2
SA - Sud America 1
Totale 2.038
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Nazione #
US - Stati Uniti d'America 977
IE - Irlanda 276
SE - Svezia 191
CN - Cina 145
IT - Italia 94
UA - Ucraina 86
DE - Germania 77
FI - Finlandia 53
PL - Polonia 31
GB - Regno Unito 28
SG - Singapore 26
IN - India 11
FR - Francia 9
BE - Belgio 7
RU - Federazione Russa 7
NL - Olanda 6
IR - Iran 3
VN - Vietnam 3
EU - Europa 2
CA - Canada 1
CL - Cile 1
CZ - Repubblica Ceca 1
DK - Danimarca 1
IL - Israele 1
NO - Norvegia 1
Totale 2.038
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Città #
Dublin 276
Chandler 222
Jacksonville 183
Nyköping 115
Beijing 73
Cambridge 47
Princeton 47
Dearborn 37
Des Moines 37
Medford 37
Ann Arbor 34
Messina 33
Ashburn 31
Warsaw 30
Boardman 21
Bremen 21
San Mateo 17
Lancaster 14
Wilmington 13
New York 12
Singapore 12
Woodbridge 12
Jinan 9
Ningbo 8
Helsinki 7
Hyderabad 6
Waanrode 6
Hangzhou 5
Haikou 4
Monmouth Junction 4
Nanjing 4
Shenyang 4
Taizhou 4
Tianjin 4
Zhengzhou 4
Augusta 3
Cagliari 3
Changsha 3
Dong Ket 3
Fuzhou 3
Houston 3
Leawood 3
Los Angeles 3
Nanchang 3
Wheaton 3
Ardabil 2
Clearwater 2
Guangzhou 2
Hebei 2
Jiaxing 2
London 2
Milan 2
Mumbai 2
Norwalk 2
Reston 2
Saint Petersburg 2
Washington 2
Atlanta 1
Auburn Hills 1
Brno 1
Brussels 1
Clifton 1
Copenhagen 1
Dallas 1
Fiesole 1
Florence 1
Gela 1
Hefei 1
Jeffries 1
Kemerovo 1
Klyuchik 1
Kunming 1
Leninsk-kuznetskiy 1
Lille 1
Montreal 1
Mountain View 1
Nashville 1
Porto 1
Pune 1
Redmond 1
Rende 1
Riva 1
Sabz 1
Santa Clara 1
Seattle 1
Tel Aviv 1
Xian 1
Totale 1.477
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Nome #
Increase in synchronization of autonomic rhythms between individuals when listening to music 74
Community-acquired enterococcal meningitis caused by Enterococcus casseliflavus: first case report 73
TRANSTHYRETIN AMYLOIDOSIS IN SOUTHERN ITALY POPULATION: DESCRIPTION OF A COHORT OF PATIENTS WITH PHE64LEU MUTATION AND LATE ONSET 66
Charcot-Marie-Tooth 2F: phenotypic presentation of the Arg136Leu HSP27 mutation in a multigenerational family 65
Cardiac longitudinal and radial strain is impaired in TTR-FAP: a magnetic resonance and 2-dimensional strain echocardiography study 64
A multicenter, randomized, double-blind, placebo-controlled trial of long-term ascorbic acid treatment in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL): the study protocol 62
Cardiovascular autonomic control in Becker muscular dystrophy 61
Cardiac longitudinal and radial strain is impaired in TTR-FAP: a magnetic resonance and 2-dimensional strain echocardiography study. 59
Central and peripheral autonomic failure in cold induced sweating syndrome type 1 58
Upper body venous thrombosis associated with ovarian stimulation: Case report and review of the literature 57
A standardized clinical evaluation of patients affected by facioscapulohumeralmuscular dystrophy: The FSHD clinical score. 55
Autonomic nervous system function in mitochondrial disorders 54
null 54
Cardiac involvement in transthyretin familial amyloid polyneuropathy - comparison between 99mTc-DPD SPECT and magnetic resonance imaging 53
Enterococcal meningitis caused by Enterococcus casseliflavus. First case report. 52
An unusual association of dominant optic atrophy with OPA1 mutations and parkinsonian syndrome. 52
Charcot-Marie-Tooth type X: unusual phenotype of a novel CX32 mutation 50
Cardiac longitudinal and radial strain is impaired in TTR-FAP: a magnetic resonance and 2-dimensional strain echocardiography study. 50
Autonomic function in elderly uremics studied by spectral analysis of heart rate 47
Hypokalemic myopathy secondary to aldosteronoma 46
Evidence of cardiovascular autonomic impairment in mitochondrial disorders 46
Acquired idiopathic generalized anhidrosis: a case report. 46
Disautonomia acuta dopo somministrazione di Iopamidolo. 44
Acquired idiopathic generalized anhidrosis: a case report. 44
Ascorbic acid in Charcot-Marie-Tooth disease type 1A (CMT-TRIAAL and CMT-TRAUK): a double-blind randomised trial 43
CMT-X DISEASE: CLINICAL AND ELECTROPHYSIOLOGICAL STUDY OF TWO NOVEL CX-32 MUTATIONS. 41
Recurrent syncope as persistently isolated feature of transthyretin amyloidotic polyneuropathy - Case report 39
Acquired idiopathic generalized anhidrosis: a case report. 39
Peripheral neuropathy as the presenting feature of multiple system atrophy 38
Hypokalemic myopathy secondary to aldosteronoma 38
Predictive role of NCAM in the identification of patients with HIBM due to GNE mutations with atypical clinical phenotype 38
Oxidative stress in myotonic dystrophy type 1 38
AUTONOMIC DYSFUNCTION AND HEART INVOLVEMENT IN TRANSTHYRETIN FAMILIAL AMYLOIDOTIC POLYNEUROPATHY 36
Is there a relationship between somatic and autonomic neuropathies in chronic alcoholics ? 34
Le neuropatie autonomiche: dal sintomo alla causa. 34
Transthyretin-related familial amyloidotic polyneuropathy: description of a cohort of patients with Leu64 mutation and late onset. 34
Endocardial and Epicardial Deformations in Cardiac Amyloidosis and Hypertrophic Cardiomyopathy-2-D Feature Strain Echocardiography 30
CMT-X disease: clinical and electrophysiological study of two novel CX-32 mutations. 29
TRANSTHYRETIN AMYLOIDOSIS IN SOUTHERN ITALY POPULATION: DESCRIPTION OF A COHORT OF PATIENTS WITH PHE64LEU MUTATION AND LATE ONSET 28
CMT-X disease: clinical and electrophysiological study of two novel CX-32 mutations. 28
Multineuropathy in autoimmune polyglandular disease (APECED): a case report. 27
COLD PAINFUL NEUROPATHY: A PECULIAR PHENOTYPE OF NEUROPATHIC PAIN 27
null 25
Recurrent sincope as the persistently isolated sympthomatology of familial amyloid polyneuropathy 23
Transthyretin amyloidosis in Southern Italy population: description of a cohort of patients with Phe64Leu mutation and late onset 20
Subacute inflammatory demyelinating polyneuropathy disclosed by massive nerve root enhancement in CMT1A. 17
CMT2: clinical and electrophysiological features of a novel mutation in the mitofusin 2 gene. 15
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy. 13
PMP22 messenger RNA levels in skin biopsies: testing the effectiveness of a Charcot-Marie-Tooth 1A biomarker 9
Totale 2.075
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Categoria #
all - tutte 8.679
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 8.679
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020328 0 20 1 26 3 45 46 58 2 55 58 14
2020/2021262 27 5 66 10 29 27 4 23 2 26 31 12
2021/2022252 2 35 3 16 11 0 14 11 7 24 37 92
2022/2023779 66 74 25 66 71 72 9 58 321 2 12 3
2023/2024141 16 32 11 8 14 21 1 7 0 11 3 17
2024/202514 12 2 0 0 0 0 0 0 0 0 0 0
Totale 2.075