SORARU', GIANNI
 Distribuzione geografica
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Continente #
NA - Nord America 10.555
EU - Europa 1.235
AS - Asia 594
Continente sconosciuto - Info sul continente non disponibili 4
AF - Africa 2
SA - Sud America 2
OC - Oceania 1
Totale 12.393
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Nazione #
US - Stati Uniti d'America 10.543
CN - Cina 446
IT - Italia 386
FI - Finlandia 230
SE - Svezia 205
GB - Regno Unito 111
UA - Ucraina 108
DE - Germania 96
VN - Vietnam 92
FR - Francia 35
HK - Hong Kong 22
IN - India 19
IE - Irlanda 15
NL - Olanda 13
CA - Canada 11
RO - Romania 7
BG - Bulgaria 5
RU - Federazione Russa 5
TR - Turchia 4
ES - Italia 3
EU - Europa 3
GR - Grecia 3
ID - Indonesia 3
SG - Singapore 3
BE - Belgio 2
BR - Brasile 2
CH - Svizzera 2
CZ - Repubblica Ceca 2
KR - Corea 2
NO - Norvegia 2
PL - Polonia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AT - Austria 1
AU - Australia 1
EG - Egitto 1
HU - Ungheria 1
IL - Israele 1
IR - Iran 1
KZ - Kazakistan 1
PA - Panama 1
SI - Slovenia 1
ZA - Sudafrica 1
Totale 12.393
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Città #
Fairfield 1.774
Woodbridge 1.308
Houston 1.148
Ann Arbor 935
Ashburn 803
Seattle 730
Wilmington 634
Chandler 625
Cambridge 594
Jacksonville 316
San Diego 180
Princeton 177
Padova 175
Beijing 133
Medford 113
Des Moines 98
Roxbury 97
Dong Ket 92
Helsinki 89
Nanjing 86
Boardman 68
New York 34
Milan 28
Norwalk 27
Shenyang 27
Guangzhou 22
Detroit 21
Hebei 21
London 20
Jinan 17
Lappeenranta 17
Hong Kong 16
Kharkiv 16
Nanchang 16
Dearborn 15
Dublin 15
Washington 15
Jiaxing 13
Paris 11
Tianjin 11
Treviso 11
Changsha 10
Los Angeles 10
Ogden 10
Phoenix 10
Redwood City 10
Auburn Hills 9
Hefei 9
Kunming 9
Zhengzhou 9
Aprilia 8
Shanghai 8
Borås 7
Chicago 6
Ovada 6
Prescot 6
Timisoara 6
Brescia 5
Chiswick 5
Indiana 5
Ningbo 5
Rome 5
Sofia 5
Tappahannock 5
Trento 5
Venice 5
Atlanta 4
Florence 4
Kilburn 4
Rockville 4
St Louis 4
Toronto 4
Cumming 3
Eastleigh 3
Falls Church 3
Hangzhou 3
Montegrosso d'Asti 3
Montréal 3
Palermo 3
Redmond 3
Southwark 3
Taiyuan 3
Verona 3
Vicenza 3
Yellow Springs 3
Apice 2
Baotou 2
Berlin 2
Brugherio 2
Buffalo 2
Chengdu 2
Collegno 2
Dalmine 2
Diyarbakır 2
Este 2
Fuzhou 2
Groningen 2
Haikou 2
Kālva 2
Munich 2
Totale 10.819
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Nome #
Onset Manifestations of Spinal and Bulbar Muscular Atrophy (Kennedy’s Disease) 488
Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat diet 184
Specific numerical processing impairment in ALS patients 183
Non-neural phenotype of spinal and bulbar muscular atrophy: Results from a large cohort of Italian patients 177
null 171
SPP1 genotype and glucocorticoid treatment modify osteopontin expression in Duchenne muscular dystrophy cells 162
Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat diet 157
Female gender doubles executive dysfunction risk in ALS: a case-control study in 165 patients. 151
Increased mitophagy in the skeletal muscle of spinal and bulbar muscular atrophy patients 151
Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants. 149
Parkinson-like features in ALS with predominant upper motor neuron involvement 145
Unimpaired Neuropsychological Performance and Enhanced Memory Recall in Patients with Sbma: A Large Sample Comparative Study. 142
Analysis of hnRNPA1, A2/B1, and A3 genes in patients with amyotrophic lateral sclerosis. 140
Progress in enzyme replacement therapy in glycogen storage disease type II 136
Functional changes in Becker muscular dystrophy: Implications for clinical trials in dystrophinopathies 134
210th ENMC International Workshop: Research and clinical management of patients with spinal and bulbar muscular atrophy, 27-29 March, 2015, Naarden, The Netherlands 132
ALS risk but not phenotype is affected by ataxin-2 intermediate length polyglutamine expansion 130
TGFB2R but not SPP1 genotype modulates osteopontin expression in Duchenne muscular dystrophy muscle. 130
Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy. 125
No association of DPP6 with amyotrophic lateral sclerosis in an Italian population. 122
Hypnosis-based psychodynamic treatment in ALS: a longitudinal study on patients and their caregivers 122
SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy 121
C9ORF72 repeat expansion in a large Italian ALS cohort: Evidence of a founder effect 120
TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations 119
Abnormal free radical homeostasis and oxphos activity in ALS muscle 118
Brain involvement in myotonic dystrophies: neuroimaging and neuropsychological comparative study in DM1 and DM2 118
Genetic modifiers of Duchenne muscular dystrophy and dilated cardiomyopathy 115
Survival and quality of life after tracheostomy for acute respiratory failure in patients with amyotrophic lateral sclerosis 115
Theory of mind, empathy and neuropsychological functioning in X-linked Spinal and Bulbar Muscular Atrophy: a controlled study of 20 patients 111
Clinical and molecular characterization of limb girdle muscular dystrophy due to LAMA2 mutations. 110
Polyglutamine-Expanded Androgen Receptor Alteration of Skeletal Muscle Homeostasis and Myonuclear Aggregation Are Affected by Sex, Age and Muscle Metabolism 109
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways. 105
Activities of mitochondrial complexes correlate with nNOS amount in muscle from ALS patients 105
Enhanced neural empathic responses in patients with Spino-Bulbar Muscular Atrophy: An electrophysiological study 104
New FIG4 gene mutations causing aggressive ALS 103
Safety and efficacy of edaravone compared to historical controls in patients with amyotrophic lateral sclerosis from North-Eastern Italy 103
Muscle MRI and functional outcome measures in Becker muscular dystrophy 102
Mitochondrial implications in bulbospinal muscular atrophy (Kennedy disease) 101
Epidemiology of ALS in Padova district, Italy, from 1992 to 2005 100
Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia 99
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutations 99
Activities of mitochondrial complexes correlate with nNOS amount in muscle from ALS patients. 98
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis 98
The MITOS system predicts long-term survival in amyotrophic lateral sclerosis 98
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations 98
Androgen-dependent impairment of myogenesis in spinal and bulbar muscular atrophy. 97
Spinal and bulbar muscular atrophy: skeletal muscle pathology in male patients and heterozygous females. 97
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis 94
Quality of life and motor impairment in ALS: Italian validation of ALSAQ 94
No association of DPP6 with amyotrophic lateral sclerosis in an Italian population 94
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease 94
CAG repeat length in androgen receptor gene is not associated with amyotrophic lateral sclerosis. 93
Human skeletal muscle atrophy in amyotrophic lateral sclerosis reveals a reduction in Akt and an increase in atrogin-1 92
Diagnostic and Prognostic Biomarkers in Amyotrophic Lateral Sclerosis: Neurofilament Light Chain Levels in Definite Subtypes of Disease 92
The role of AR polyQ tract in male breast carcinoma: lesson from an SBMA case 92
Genetic variation in KIFAP3 is associated with an upper motor neuron-predominant phenotype in amyotrophic lateral sclerosis 91
Efficacy of Hypnosis-Based Treatment in Amyotrophic Lateral Sclerosis: A Pilot Study 91
Assessment of patients with idiopathic inflammatory myopathies and isolated creatin-kinase elevation 91
Lithium carbonate in amyotrophic lateral sclerosis Lack of efficacy in a dose-finding trial 91
Validation of the Italian version of the SBMA Functional Rating Scale as outcome measure 91
Insights into the genetic epidemiology of SBMA: prevalence estimation and multiple founder haplotypes in the Veneto Italian region. 90
TDP-43 in skeletal muscle of patients affected with amyotrophic lateral sclerosis 89
Memory deficits and retrieval processes in ALS 89
Retrospective study on PET-SPECT imaging in a large cohort of myotonic dystrophy type 1 patients 89
Impact on children of a parent with ALS: a case-control study 89
Skeletal muscle satellite cells in amyotrophic lateral sclerosis 89
Pilot trial of clenbuterol in spinal and bulbar muscular atrophy. 89
Beyond motor neurons: expanding the clinical spectrum in Kennedy's disease 89
TDP-43 in skeletal muscle of patients affected with amyotrophic lateral sclerosis 87
Right hemisphere dysfunction and emotional processing in ALS: an fMRI study 87
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS. 86
The Role of Motor System in Mental Rotation: New Insights from Myotonic Dystrophy Type 1 86
Clinical and electrophysiological correlations in a three-generation-HNPP pedigree. 85
A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. 84
Disruption of skeletal muscle mitochondrial network genes and miRNAs in amyotrophic lateral sclerosis 84
Correlation of quality of life and motor impairment in amyotrophic lateral sclerosis 83
Unilateral calf hypertrophy due to S1-radiculopathy 83
Factors predicting survival in ALS: a multicenter Italian study 82
Cardiac function in types II and III spinal muscular atrophy: Should we change standards of care? 82
Spinal and bulbar muscular atrophy: Skeletal muscle pathology in male patients and heterozygous females. 81
The clinical spectrum of CASQ1-related myopathy 81
Diagnostica e prevenzione delle malattie neuromuscolari 80
No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype 80
Screening of the PFN1 gene in sporadic amyotrophic lateral sclerosis and in frontotemporal dementia 79
Emotional lability in MND: relationship to cognition and psychopathology and impact on caregivers 79
Erythropoietin in amyotrophic lateral sclerosis: A multicentre, randomised, double blind, placebo controlled, phase III study 78
Genetic epidemiology of muscular dystrophies resulting from sarcoglycan gene mutations 77
A pilot trial with clenbuterol in amyotrophic lateral sclerosis 77
Psychopathological features and suicidal ideation in amyotrophic lateral sclerosis patients 73
Natural history of upper motor neuron-dominant ALS 73
Association of a locus in the CAMTA1 gene with survival in patients with sporadic amyotrophic lateral sclerosis 73
Intraspinal stem cell transplantation for amyotrophic lateral sclerosis: Ready for efficacy clinical trials? 72
Towards a European Registry and Biorepository for Patients with Spinal and Bulbar Muscular Atrophy 72
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis 72
Natural history of upper motor neuron-dominant ALS 71
Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy. 71
Emotional Lability in MND: Relationship to cognition and psychopathology and impact on caregivers. 70
Mutational analysis of VCP gene in familial amyotrophic lateral sclerosis 70
A pilot trial with clenbuterol in amiotrophic lateral sclerosis (ALS) 68
Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 67
Totale 10.600
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Categoria #
all - tutte 37.728
article - articoli 33.838
book - libri 85
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 133
Totale 71.784
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019743 0 0 0 0 0 0 0 0 0 0 409 334
2019/20202.365 324 110 46 159 250 185 272 268 271 230 140 110
2020/20212.694 76 146 83 745 124 190 101 172 301 315 257 184
2021/20222.116 157 235 316 148 69 113 168 184 53 49 228 396
2022/20231.482 287 111 17 174 257 184 2 143 189 19 79 20
2023/2024640 21 98 101 66 68 105 54 62 28 36 1 0
Totale 12.647