IRIS Institutional Research Information System - AIR Archivio Istituzionale della Ricerca

BRESOLIN, NEREO
 Distribuzione geografica
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Continente #
EU - Europa 62.220
NA - Nord America 54.641
AS - Asia 49.397
SA - Sud America 4.536
AF - Africa 1.032
OC - Oceania 457
Continente sconosciuto - Info sul continente non disponibili 65
Totale 172.348
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Nazione #
US - Stati Uniti d'America 51.595
GB - Regno Unito 19.737
CN - Cina 15.516
SG - Singapore 13.069
IT - Italia 9.371
DE - Germania 8.876
SE - Svezia 5.477
RU - Federazione Russa 4.251
VN - Vietnam 3.642
HK - Hong Kong 3.633
BD - Bangladesh 3.428
FR - Francia 3.114
BR - Brasile 3.012
IN - India 2.962
CA - Canada 2.388
UA - Ucraina 2.343
NL - Olanda 1.886
TR - Turchia 1.829
KR - Corea 1.697
IE - Irlanda 1.562
FI - Finlandia 1.534
JP - Giappone 1.235
EU - Europa 1.030
ES - Italia 703
PL - Polonia 688
CO - Colombia 669
ID - Indonesia 491
GR - Grecia 478
BE - Belgio 447
AU - Australia 399
DK - Danimarca 392
CI - Costa d'Avorio 364
AR - Argentina 323
MX - Messico 320
CH - Svizzera 205
TW - Taiwan 202
PT - Portogallo 183
IQ - Iraq 182
ZA - Sudafrica 174
AT - Austria 173
RO - Romania 159
PK - Pakistan 152
IR - Iran 140
PH - Filippine 133
CL - Cile 131
SA - Arabia Saudita 124
EC - Ecuador 122
UZ - Uzbekistan 116
NO - Norvegia 114
CZ - Repubblica Ceca 109
MY - Malesia 103
IL - Israele 99
MA - Marocco 89
VE - Venezuela 88
EG - Egitto 79
AE - Emirati Arabi Uniti 74
PE - Perù 71
TH - Thailandia 69
JO - Giordania 58
CR - Costa Rica 54
DZ - Algeria 54
NZ - Nuova Zelanda 53
NP - Nepal 51
HU - Ungheria 50
KE - Kenya 50
AZ - Azerbaigian 48
PY - Paraguay 48
LT - Lituania 43
TN - Tunisia 43
JM - Giamaica 42
BG - Bulgaria 39
KZ - Kazakistan 39
UY - Uruguay 37
SI - Slovenia 36
PR - Porto Rico 35
DO - Repubblica Dominicana 33
BO - Bolivia 29
CY - Cipro 29
HR - Croazia 29
KG - Kirghizistan 29
LB - Libano 29
LU - Lussemburgo 28
LK - Sri Lanka 27
PA - Panama 26
LV - Lettonia 25
OM - Oman 25
PS - Palestinian Territory 25
ET - Etiopia 24
SC - Seychelles 24
TT - Trinidad e Tobago 24
HN - Honduras 23
RS - Serbia 23
AL - Albania 22
AM - Armenia 20
GT - Guatemala 20
GE - Georgia 19
BA - Bosnia-Erzegovina 18
BY - Bielorussia 18
EE - Estonia 17
SK - Slovacchia (Repubblica Slovacca) 16
Totale 172.934
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Città #
Southend 16.658
Singapore 7.671
Ashburn 4.898
Chandler 3.977
Hong Kong 3.293
Beijing 3.105
Seattle 2.645
Milan 2.513
San Jose 2.466
Princeton 1.923
Jacksonville 1.844
Wilmington 1.844
Frankfurt am Main 1.668
Santa Clara 1.571
Dublin 1.507
Dallas 1.455
Council Bluffs 1.431
Fairfield 1.419
Ann Arbor 1.319
Los Angeles 1.232
Bengaluru 1.126
New York 1.123
Toronto 1.092
Woodbridge 1.009
Ho Chi Minh City 998
Nanjing 988
Redmond 945
Hanoi 894
Houston 892
Boardman 832
Munich 810
Mountain View 781
Lauterbourg 768
Dearborn 676
Buffalo 653
Redwood City 644
Des Moines 641
Shanghai 640
Guangzhou 611
Sakarya 607
Moscow 604
Serra 599
Cambridge 590
Helsinki 584
Andover 558
Warsaw 558
Bogotá 555
Tokyo 551
Somerville 467
Jinan 441
Hefei 419
Rome 411
Montréal 387
Phoenix 387
Berlin 385
Shenyang 379
Athens 376
Ottawa 375
Mcallen 371
Abidjan 363
Tianjin 336
Changsha 320
The Dalles 309
Columbus 304
Cangzhou 291
São Paulo 291
Nanchang 286
Jakarta 282
Brussels 263
Hanover 260
Hangzhou 252
Grafing 240
Fuzhou 236
Hebei 234
Istanbul 227
Zhengzhou 209
Chicago 208
London 208
Medford 201
Bitonto 196
Naples 190
Kent 183
Kiez 182
Seoul 180
Da Nang 179
Turin 161
Margão 157
Shenzhen 157
Atlanta 155
San Diego 155
Dong Ket 149
Mumbai 144
Haiphong 140
Paris 140
Jiaxing 134
Nürnberg 134
Wuhan 133
Madrid 132
Kunming 127
Eitensheim 126
Totale 98.740
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Nome #
Silence superoxide dismutase 1 (SOD1): a promising therapeutic target for amyotrophic lateral sclerosis (ALS) 4.758
Monogenic disorders related to ischemic stroke: a clinical approach 2.058
The Italian limb girdle muscular dystrophy registry : relative frequency, clinical features, and differential diagnosis 1.570
Variants in KIF1A gene in dominant and sporadic forms of hereditary spastic paraparesis 1.086
Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis 910
R-Loops in Motor Neuron Diseases 803
Development of Therapeutics for C9ORF72 ALS/FTD-related disorders 786
Insights into disease mechanisms and potential therapeutics for C9orf72-related amyotrophic lateral sclerosis/frontotemporal dementia 693
Current understanding of and emerging treatment options for spinal muscular atrophy with respiratory distress type 1 (SMARD1) 669
Assessing mental health in boys with Duchenne muscular dystrophy: Emotional, behavioural and neurodevelopmental profile in an Italian clinical sample 648
Cryptogenic Epileptic Syndromes Related to SCN1A Twelve Novel Mutations Identified 585
A de novo C19orf12 heterozygous mutation in a patient with MPAN 583
Functional analysis of novel KCNQ2 and KCNQ3 gene variants found in a large pedigree with benign familial neonatal convulsions (BFNC) 556
Mental health and coping strategies in families of children and young adults with muscular dystrophies 547
Subclinical leukodystrophy and infertility in a man with a novel homozygous CLCN2 mutation 545
Noncoding RNAs in Duchenne and Becker muscular dystrophies: role in pathogenesis and future prognostic and therapeutic perspectives 537
Loss of the nucleoporin Aladin in central nervous system and fibroblasts of Allgrove Syndrome 528
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy 520
Decline of ALS-FRS and Norris scale scores in a group of patients affected by ALS and treated with lithium 509
Anti-sulfatide reactivity in patients with celiac disease 476
Clinical studies in stem cells transplantation for stroke: a review 464
Effect of human skin-derived stem cells on vessel architecture, tumor growth, and tumor invasion in brain tumor animal models 463
Preconditioning and Cellular Engineering to Increase the Survival of Transplanted Neural Stem Cells for Motor Neuron Disease Therapy 458
Advances, Challenges, and Perspectives in Translational Stem Cell Therapy for Amyotrophic Lateral Sclerosis 448
SLC25A46 mutations in patients with Parkinson's Disease and optic atrophy 448
Key role of SMN/SYNCRIP and RNA-Motif 7 in spinal muscular atrophy: RNA-Seq and motif analysis of human motor neurons 440
Minimally invasive transplantation of iPSC-derived ALDHhiSSCloVLA4+ neural stem cells effectively improves the phenotype of an amyotrophic lateral sclerosis model 424
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 424
Molecular Approaches for the Treatment of Pompe Disease 403
Beta-lactam antibiotic offers neuroprotection in a spinal muscular atrophy model by multiple mechanisms 394
La canalopatia del cloro : diagnosi clinica differenziale 389
Spinal muscular atrophy phenotype is ameliorated in human motor neurons by SMN increase via different novel RNA therapeutic approaches 384
Clinical reasoning: a 75-year-old man with parkinsonism, mood depression, and weight loss 376
Expanding the genotypic and phenotypic spectrum of Beta-propeller-associated neurodegeneration (BPAN) 375
Gene therapy rescues disease phenotype in a spinal muscular atrophy with respiratory distress type 1 (SMARD1) mouse model 369
Herpes Simplex virus type 2 myeloradiculitis with a pure motor presentationin a liver transplant recipient 366
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion 364
Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature 356
Nusinersen treatment and cerebrospinal fluid neurofilaments : An explorative study on Spinal Muscular Atrophy type 3 patients 356
Clinical features and disease course of patients with acute ischaemic stroke just before the Italian index case: Was COVID-19 already there? 356
Parasites represent a major selective force for interleukin genes and shape the genetic predisposition to autoimmune conditions 351
Mitochondrial Dysregulation and Impaired Autophagy in iPSC-Derived Dopaminergic Neurons of Multiple System Atrophy 350
Neural stem cell transplantation for neurodegenerative diseases 346
Central nervous system involvement in common variable immunodeficiency: A case of acute unilateral optic neuritis in a 26 -year-old Italian Patient 337
A functional variant in ERAP1 predisposes to multiple sclerosis 334
A novel homozygous VPS11 variant may cause generalized dystonia 334
Lactate detection in the brain of growth-restricted fetuses with magnetic resonance spectroscopy 332
Ophthalmoplegia due to Miller Fisher syndrome in a patient with myasthenia gravis 330
Influence of the Glu298Asp polymorphism of NOS3 on age at aonset and homocysteine levels in AD patients 329
Impairment of brain and muscle energy metabolism detected by magnetic resonance spectroscopy in hereditary spastic paraparesis type 28 patients with DDHD1 mutations 328
Outcome measures validation study for mesoangioblasts transplantation in children affected by Duchenne Muscular Dystrophy 326
Mutations in TMEM230 are rare in autosomal dominant Parkinson's disease 326
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of Andersen Disease associated with a new mutation in GBE1 gene 325
Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing 321
Human induced pluripotent stem cell models for the study and treatment of Duchenne and Becker muscular dystrophies 320
Limb girdle muscular dystrophy due to LAMA2 gene mutations: new mutations expand the clinical spectrum of a still challenging diagnosis 317
Rs5848 Variant Influences GRN mRNA Levels in Brain and Peripheral Mononuclear Cells in Patients with Alzheimer’s Disease 316
Induction of neurotrophin expression via human adult mesenchymal stem cells : implication for cell therapy in neurodegenerative diseases 313
The mitochondrial disulfide relay system protein GFER is mutated in autosomal recessive myopathy with congenital cataract and COX deficiency. 312
ISPD mutations account for a small proportion of Italian Limb Girdle Muscular Dystrophy cases 312
A case report of late-onset cerebellar ataxia associated with a rare p.R342W TGM6 (SCA35) mutation 309
The Role of Mitochondria in Neurodegenerative Diseases: the Lesson from Alzheimer’s Disease and Parkinson’s Disease 308
Paroxysmal Nocturnal Hemoglobinuria (Pnh) : Brain Mri Ischemic Lesions in Neurologically Asymtomatic Patients 305
Management of patients with neuromuscular disorders at the time of the SARS-CoV-2 pandemic 302
The T-786C NOS3 polymorphism in Alzheimer's disease : association and influence on gene expression 299
Brain mitochondria, aging, and Parkinson’s disease 299
Usefulness of multi-parametric MRI for the investigation of posterior cortical atrophy 299
Diverse evolutionary histories for beta-adrenoreceptor genes in humans 298
Progranulin gene variability and plasma levels in bipolar disorder and schizophrenia 298
Myotonia congenita : novel mutations in CLCN1 gene and functional characterizations in Italian patients 297
Effects of rituximab in two patients with dysferlin-deficient muscular dystrophy 296
Hyperacute extensive spinal cord infarction and negative spine magnetic resonance imaging: a case report and review of the literature 296
NOS3 Glu298Asp polymorphism is a risk factor for frontotemporal lobar degeneration 295
Charcot-Marie-Tooth disease type 2F associated with biallelic HSPB1 mutations 295
IPSC-derived neural stem cells act via kinase inhibition to exert neuroprotective effects in spinal muscular atrophy with respiratory distress type 1 294
Optic neuritis as isolated manifestation of leptomeningeal carcinomatosis : a case report and systematic review of ocular manifestations of neoplastic meningitis 292
Direct reprogramming of adult somatic cells into other lineages: past evidence and future perspectives 289
Role of hnRNP-A1 and miR-590-3p in neuronal death : genetics and expression analysis in patients with Alzheimer’s disease and frontotemporal lobar degeneration 288
The mitochondrial disulfide relay system protein GFER is mutated in sutosomal-tecessive myopathy with vataract and vombined respiratory-chain deficiency 285
Progranulin gene mutation scanning in Alzheimer's disease and frontotemporal lobar degeneration: functional and phenotypic correlations. 284
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study 284
A cortically blind patient with preserved visual imagery 284
Morpholino-mediated SOD1 reduction ameliorates an amyotrophic lateral sclerosis disease phenotype 283
A complex selection signature at the human AVPR1B gene 281
Clinical factors associated with statins prescription in acute ischemic stroke patients : findings from the Lombardia Stroke Registry 280
Glial cells involvement in spinal muscular atrophy: Could SMA be a neuroinflammatory disease? 279
Balancing selection is common in the extended MHC region but most alleles with opposite risk profile for autoimmune diseases are neutrally evolving 278
CSF transplantation of a specific iPSC-derived neural stem cell subpopulation ameliorates the disease phenotype in a mouse model of spinal muscular atrophy with respiratory distress type 1 278
Widespread balancing selection and pathogen-driven selection at blood group antigen genes 276
Animal Models of CMT2A: State-of-art and Therapeutic Implications 276
Transplanted ALDH(hi)SSC(lo) neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1 275
Amyotrophic lateral sclerosis linked to a novel SOD1 mutation with muscle mitochondrial dysfunction 275
P-selectin glycoprotein ligand-1 variable number of tandem repeats (VNTR) polymorphism in patients with multiple sclerosis 273
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency 273
Hereditary hemorrhagic telangiectasia associated with cortical development malformation due to a start loss mutation in ENG 273
Evaluation of Morpholino oligomers therapeutic efficacy in C9orf72 ALS iPSC-derived lines 272
Expanding the clinical spectrum of the mitochondrial mutation A13084T in the ND5 gene 271
New molecular findings in congenital myopathies due to selenoprotein N gene mutations 269
The landscape of human genes involved in the immune response to parasitic worms 268
Unravelling Genetic Factors Underlying Corticobasal Syndrome: A Systematic Review 268
Totale 45.427
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Categoria #
all - tutte 458.508
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 458.508
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.154 0 0 0 0 0 0 0 0 0 0 0 1.154
2021/202212.649 968 696 568 843 814 844 1.085 747 1.683 1.118 1.032 2.251
2022/202315.282 2.033 1.589 1.180 1.675 1.785 2.741 405 977 1.604 287 627 379
2023/202411.010 427 784 774 715 2.619 671 661 762 394 740 1.057 1.406
2024/202522.668 1.086 2.097 705 2.575 1.808 839 764 2.298 1.323 2.138 2.029 5.006
2025/202646.679 4.480 2.485 4.273 3.346 4.123 3.031 5.372 2.408 4.476 3.793 5.211 3.681
Totale 180.355