IRIS
MASSA, ROBERTO
 Distribuzione geografica
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Continente #
NA - Nord America 36.607
AS - Asia 4.020
EU - Europa 3.432
SA - Sud America 622
AF - Africa 45
OC - Oceania 15
Continente sconosciuto - Info sul continente non disponibili 7
Totale 44.748
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Nazione #
US - Stati Uniti d'America 36.530
SG - Singapore 2.337
CN - Cina 801
IT - Italia 683
DE - Germania 582
BR - Brasile 527
UA - Ucraina 467
IE - Irlanda 388
HK - Hong Kong 381
RU - Federazione Russa 259
GB - Regno Unito 205
PL - Polonia 199
FR - Francia 189
VN - Vietnam 143
FI - Finlandia 141
SE - Svezia 127
KR - Corea 102
NL - Olanda 61
CA - Canada 44
ID - Indonesia 41
JP - Giappone 40
AR - Argentina 39
IN - India 35
CZ - Repubblica Ceca 23
MX - Messico 22
AT - Austria 21
BE - Belgio 21
TR - Turchia 20
ES - Italia 19
ZA - Sudafrica 18
BD - Bangladesh 17
IL - Israele 17
KG - Kirghizistan 14
AU - Australia 13
EC - Ecuador 11
IQ - Iraq 11
CO - Colombia 10
IR - Iran 10
PK - Pakistan 10
PE - Perù 9
MA - Marocco 8
CH - Svizzera 7
CL - Cile 7
EU - Europa 7
PY - Paraguay 7
EG - Egitto 6
UZ - Uzbekistan 6
VE - Venezuela 5
AL - Albania 4
DK - Danimarca 4
KZ - Kazakistan 4
MY - Malesia 4
NO - Norvegia 4
PH - Filippine 4
PT - Portogallo 4
RS - Serbia 4
SA - Arabia Saudita 4
TW - Taiwan 4
BG - Bulgaria 3
BO - Bolivia 3
GR - Grecia 3
KE - Kenya 3
MK - Macedonia 3
RO - Romania 3
SN - Senegal 3
TH - Thailandia 3
TN - Tunisia 3
UY - Uruguay 3
AZ - Azerbaigian 2
CU - Cuba 2
DZ - Algeria 2
HU - Ungheria 2
MD - Moldavia 2
NZ - Nuova Zelanda 2
OM - Oman 2
PA - Panama 2
AE - Emirati Arabi Uniti 1
BN - Brunei Darussalam 1
BW - Botswana 1
CR - Costa Rica 1
CY - Cipro 1
DM - Dominica 1
DO - Repubblica Dominicana 1
ET - Etiopia 1
FK - Isole Falkland (Malvinas) 1
GD - Grenada 1
JM - Giamaica 1
JO - Giordania 1
KW - Kuwait 1
LB - Libano 1
LI - Liechtenstein 1
LK - Sri Lanka 1
LT - Lituania 1
LV - Lettonia 1
NI - Nicaragua 1
NP - Nepal 1
SK - Slovacchia (Repubblica Slovacca) 1
TT - Trinidad e Tobago 1
Totale 44.748
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Città #
Woodbridge 10.506
Wilmington 9.609
Houston 8.789
Fairfield 1.115
Singapore 941
Ann Arbor 820
Ashburn 591
Seattle 423
Jacksonville 404
Cambridge 392
Hong Kong 379
Dublin 360
Beijing 335
Chandler 314
Medford 288
Dearborn 245
Rome 194
Santa Clara 187
Kraków 174
Zhengzhou 166
New York 156
The Dalles 146
Lawrence 128
Los Angeles 103
Buffalo 80
Redwood City 77
San Diego 76
Menlo Park 71
Milan 68
Moscow 62
Ho Chi Minh City 55
Mülheim 54
São Paulo 54
Munich 52
Council Bluffs 49
Boardman 45
London 39
Dallas 35
Shanghai 35
Nuremberg 34
Helsinki 31
Norwalk 28
Jakarta 26
Atlanta 25
Hanoi 24
University Park 23
Warsaw 22
Mountain View 21
Redondo Beach 21
Brussels 19
Monte Porzio Catone 19
Falls Church 18
Palo Alto 18
Nanjing 17
Tokyo 17
Verona 17
Brasília 16
Guangzhou 16
Phoenix 16
Stockholm 16
Toronto 16
Chicago 15
Rio de Janeiro 15
Saint Petersburg 14
Ankara 12
Detroit 12
San Francisco 12
Seoul 12
Turin 12
Vienna 12
Brno 11
Brooklyn 11
Hefei 11
Bologna 10
Boston 10
Chennai 10
Columbus 10
Johannesburg 10
Marseille 10
Montreal 10
Nürnberg 10
Denver 9
Turku 9
Belo Horizonte 8
Hounslow 8
Kunming 8
Lima 8
Madrid 8
Salt Lake City 8
San Jose 8
Chengdu 7
Curitiba 7
Jinan 7
Manchester 7
Mcallen 7
Naples 7
Orem 7
Padova 7
Petah Tikva 7
San Mateo 7
Totale 38.450
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Nome #
Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases 590
Restless legs syndrome and daytime sleepiness are prominent in myotonic dystrophy type 2 565
Paucisymptomatic Marchiafava-Bignami disease with relevant diffusion-weighted MRI lesions 530
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease 510
An Age-standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome province, Italy 500
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-Tooth disease type 1A 498
Vitamin D deficiency in myotonic dystrophy type 1 497
Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2) 493
The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' muscles 479
Subacute demyelinating polyneuropathy in B-cell lymphoma with IgM antibodies against glycolipid GD1b 479
Brain MR diffusion tensor imaging in Kennedy's disease 478
Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients 467
Morphological changes in the sciatic nerve of diabetic rats treated with low molecular weight heparin OP 2123/parnaparin 464
Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2 456
Sural nerve without nerve fibers in leprous neuropathy 455
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy 454
Association of HLA-DQB1∗05:02 and DRB1∗16 Alleles with Late-Onset,Nonthymomatous, AChR-Ab-Positive Myasthenia Gravis 446
Migraine-like disorder segregating with mtDNA 14484 Leber hereditary optic neuropathy mutation 445
Early subclinical cochlear dysfunction in myotonic dystrophy type 1. 444
Dopamine denervation induces neurotensin immunoreactivity in GABA-parvalbumin striatal neurons 442
Dystrophin is not essential for the integrity of the cytoskeleton 438
Randomized comparison of awake nonresectional versus nonawake resectional lung volume reduction surgery. 438
Glucocorticoids and immunosuppressants do not change the prevalence of necrosis and regeneration in mdx skeletal muscles 437
Differential features of muscle fiber atrophy in osteoporosis and osteoarthritis 437
Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1 434
Adult polyglucosan body disease: Proton magnetic resonance spectroscopy of the brain and novel mutation in the GBE1 gene 432
Neurofibromatous neuropathy: An ultrastructural study 429
Intestinal pseudobstruction as presenting event of fatal cerivastatin-induced myopathy 426
EFFICACY OF INTRAVENOUS IMMUNOGLOBULIN IN POEMS-RELATED RELAPSING AIDP 425
Identification and characterization of 5' CCG interruptions in complex DMPK expanded alleles 425
Familial inclusion body myositis among Kurdish-Iranian Jews 424
Upper motor neuron involvement in X-linked recessive bulbospinal muscular atrophy 424
Acute demyelinating sensorimotor polyneuropathy in B-cell lymphoma with IGM autoantibodies against glycolipid GD1B 424
Inverse correlation between VEGF and soluble VEGF receptor 2 in POEMS with AIDP responsive to intravenous immunoglobulin 421
Subcellular localization of the myotonic dystrophy type 2 protein ZNF9 in skeletal muscle 421
Preferential central nucleation of type 2 myofibers is an invariable feature of myotonic dystrophy type 2 420
null 419
Late-onset MNGIE without peripheral neuropathy due to incomplete loss of thymidine phosphorylase activity 415
Active muscle length reduction progressively damages soleus in hindlimb-suspended rabbits 413
Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues 411
IMMUNOCYTOCHEMICAL LOCALIZATION OF VINCULIN IN MUSCLE AND NERVE 411
Hashimoto's encephalopathy presenting with musical hallucinosis 411
Neuroelectrophysiological abnormalities are related to metabolic and advanced non-enzymatic glycation changes in prospectively evaluated diabetic Sprague-Dawley rats 410
Diagnosis, treatment and follow-up of the carpal tunnel syndrome: a review 410
NADPH DIAPHORASE ACTIVITY IS INHIBITED BY EDTA IN NEURONS BUT NOT IN CHOROID-PLEXUS EPITHELIUM 410
Correlation between clinical features and HLA genetic variability in myasthenia gravis 406
null 400
NADPH-Diaphorase neurons contacting the cerebrospinal fluid in the ventricles of rat brain 399
Protective effect of clonazepam on ischemic brain damage induced by 10-minute bilateral carotid occlusion in Mongolian gerbils. 397
Peripheral nerve extracellular matrix remodeling in Charcot-Marie-Tooth type 1 disease 396
Sleep disorders in spinal and bulbar muscular atrophy (Kennedy's disease): a controlled polysomnographic and self-reported questionnaires study 396
Transcranial unifocal stimulation in rabbit: subcutaneous and meningeal changes 395
Measuring quality of life impairment in skeletal muscle channelopathies 394
Expanded [CCTG]n repetitions are not associated with abnormal methylation at the CNBP locus in myotonic dystrophy type 2 (DM2) patients 393
Spasticity as an ictal pattern due to excitotoxic upper motor neuron damage 392
Erratum to: Increased risk of tumor in DM1 is not related to exposure to common lifestyle risk factors (J Nerol, 10.1007/s00415-015-8006-y) 391
Recommendations for anesthesia and perioperative management of patients with neuromuscular disorders. 390
EPILEPTIC ACTIVITY FOLLOWING CEREBRAL-ISCHEMIA IN MONGOLIAN GERBILS IS DEPRESSED BY CPP, A COMPETITIVE ANTAGONIST OF THE N-METHYL-D-ASPARTATE RECEPTOR 388
Partial block of glycolysis in late-onset phosphofructokinase deficiency myopathy 387
Cutaneous features of myotonic dystrophy types 1 and 2: implication of premature aging and vitamin d homeostasis 387
Peripheral nerve extracellular matrix remodeling in Charcot-Marie- Tooth type I disease. 386
Early diagnosis and early treatment in LOPD: when asymptomatic patients should be treated 386
Delayed focal involvement of upper motor neurons in the Madras pattern of motor neuron disease 381
Late-onset MNGIE without peripheral neuropathy due to incomplete loss of thymidine phosphorylase activity 377
Nitrergic neurons make synapses on dual-input dendritic spines of neurons in the cerebral cortex and the striatum of the rat: Implication for a postsynaptic action of nitric oxide 376
Periodic acid-Schiff staining on resin muscle sections: improvement in the histological diagnosis of late-onset Pompe disease 375
Muscle phosphofructokinase deficiency 374
Vulnerability of globus pallidus to Mn2+ may be dependent on preferential Mn2+ accumulation in pallidal neurons' nucleoli 374
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis 373
Bilateral carotid occlusion in normotensive rats: olds facts and new observations 372
Myofibrillar disruption in the rabbit soleus muscle after one-week hindlimb suspension 372
Subclinical autonomic dysfunction in spinobulbar muscular atrophy (Kennedy disease) 369
Intracellular localization and isoform expression of the voltage-dependent anion channel (VDAC) in normal and dystrophic skeletal muscle 369
Long-term outcome of thoracoscopic extended thymectomy for nonthymomatous myasthenia gravis 368
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion 367
Loss and renewal of thick myofilaments in glucocorticoid-treated rat soleus after denervation and reinnervation 357
Zinc distribution in various tissues, (brain, eye, skin, muscle and blood) of rat during hindlimb suspension 357
FUNCTIONAL, MORPHOLOGICAL AND BIOCHEMICAL-ALTERATIONS OF CENTRAL-NERVOUS-SYSTEM IN EXPERIMENTAL DIABETES 357
Epileptic activity following 10 minute cerebral ischemia in Mongolian gerbils: an electrophysiological study 356
Sudomotor skin responses to brain stimulation do not depend on nerve sensory fiber functionality 356
LITAF/SIMPLE MUTATION ANALYSIS IN DOMINANT DEMYELINATING CHARCOT- MARIE-TOOTH DISEASE: A NOVEL MUTATION 352
Corticobulbar And Corticospinal Tract Involvement In Kennedy's Disease 348
Sleep disorders in adult-onset myotonic dystrophy type 1: a controlled polysomnographic study 342
Muscle regeneration in mdx mice: Resistance to repeated necrosis is compatible with myofiber maturity 342
Relapsing aidp responsive to intravenous immunoglobulin in poems syndrome 341
Nodular morphea in a patient with Steinert disease 341
Adrenomyeloneuropathy partially responsive to steroid pulse therapy 338
Corticobulbar And Corticospinal Tract Involvement In Kennedy's Disease 338
Myotonic dystrophy unlinked to DM1 and DM2 mutations in three siblings 336
Histopathology and Immunoanalysis of Muscle 335
Recurrent hyperCKemia with normal muscle biopsy in a pediatric patient with neuromyelitis optica. 333
Searching modifier genes in the LHON 14484T > C mtDNA mutation associated with migraine-like disorder 333
Sleep-wake cycle in the Kennedy's disease: a controlled polysomnographic study and self-reported questionnaires 326
Modelli sperimentali di miopatie 312
Thymomatous myasthenia gravis: novel association with HLA DQB1*05:01 and strengthened evidence of high clinical and serological severity 306
Novel HLA II associations in myasthenia gravis 302
Minimalist thoracoscopic resection of thymoma associated with myasthenia gravis 291
Generation and Neuronal Differentiation of hiPSCs From Patients With Myotonic Dystrophy Type 2 277
A case of fulminant subacute sclerosing panencephalitis presenting with acute myoclonic-astatic epilepsy 270
Comparative Sleep Disturbances in Myotonic Dystrophy Types 1 and 2 269
Totale 40.002
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Categoria #
all - tutte 104.123
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 104.123
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.896 0 0 0 0 0 767 839 747 113 161 215 54
2021/20221.334 103 134 37 101 41 117 54 52 96 132 75 392
2022/20231.266 167 81 28 108 94 323 155 65 88 22 120 15
2023/2024606 47 32 29 5 60 143 25 25 24 32 45 139
2024/20254.102 103 770 454 184 73 402 158 231 376 364 490 497
2025/20262.465 451 233 693 445 488 155 0 0 0 0 0 0
Totale 45.322