IRIS
MASSA, ROBERTO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 36.720
EU - Europa 2.980
AS - Asia 1.512
SA - Sud America 13
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 7
AF - Africa 3
Totale 41.246
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 36.698
SG - Singapore 817
DE - Germania 524
CN - Cina 479
UA - Ucraina 479
IT - Italia 454
IE - Irlanda 400
RU - Federazione Russa 245
PL - Polonia 199
FR - Francia 193
GB - Regno Unito 169
FI - Finlandia 116
SE - Svezia 112
KR - Corea 104
JP - Giappone 25
BE - Belgio 22
CZ - Repubblica Ceca 22
CA - Canada 17
KG - Kirghizistan 14
IN - India 12
IR - Iran 10
AU - Australia 9
IL - Israele 9
NL - Olanda 9
ES - Italia 8
TR - Turchia 8
EU - Europa 7
HK - Hong Kong 6
VN - Vietnam 6
CH - Svizzera 5
BR - Brasile 4
KZ - Kazakistan 4
MY - Malesia 4
AR - Argentina 3
CL - Cile 3
EG - Egitto 3
IQ - Iraq 3
NO - Norvegia 3
PT - Portogallo 3
RO - Romania 3
TH - Thailandia 3
TW - Taiwan 3
AT - Austria 2
BG - Bulgaria 2
CU - Cuba 2
GR - Grecia 2
HU - Ungheria 2
ID - Indonesia 2
MK - Macedonia 2
NZ - Nuova Zelanda 2
PA - Panama 2
PE - Perù 2
CY - Cipro 1
DK - Danimarca 1
DM - Dominica 1
FK - Isole Falkland (Malvinas) 1
LK - Sri Lanka 1
LV - Lettonia 1
MD - Moldavia 1
PK - Pakistan 1
SK - Slovacchia (Repubblica Slovacca) 1
Totale 41.246
Salva come PNG Salva come JPEG
Città #
Woodbridge 10.953
Wilmington 9.863
Houston 9.050
Fairfield 1.152
Ann Arbor 842
Singapore 741
Ashburn 503
Seattle 443
Jacksonville 420
Cambridge 413
Dublin 368
Chandler 336
Medford 294
Dearborn 251
Kraków 197
Santa Clara 183
Zhengzhou 178
Rome 151
Beijing 143
Lawrence 132
New York 118
San Diego 78
Redwood City 77
Menlo Park 73
Moscow 60
Mülheim 55
Milan 42
Shanghai 33
Boardman 30
London 30
Norwalk 29
University Park 23
Brussels 21
Mountain View 21
Falls Church 19
Palo Alto 19
Atlanta 18
Nanjing 16
Helsinki 15
Munich 15
Hefei 14
Saint Petersburg 14
Verona 13
Detroit 12
Brno 11
Guangzhou 11
Nürnberg 11
Marseille 10
Phoenix 10
Seoul 10
Toronto 10
Hounslow 9
Kunming 8
Los Angeles 8
Nuremberg 8
San Mateo 8
Ankara 7
Chengdu 7
Indiana 7
Jinan 7
Mcallen 7
Naples 7
Petah Tikva 7
Wuhan 7
Bari 6
Del Norte 6
Engelhard 6
Center 5
Changsha 5
Creede 5
Dong Ket 5
Kilburn 5
Madrid 5
New Delhi 5
Padova 5
Prescot 5
Salt Lake City 5
The Dalles 5
Turin 5
Wandsworth 5
Almaty 4
Ancona 4
Auburn Hills 4
Bologna 4
Chiswick 4
Council Bluffs 4
Fuzhou 4
Hong Kong 4
Mariano Comense 4
Novara 4
Redmond 4
Viterbo 4
Bonorva 3
Burlington 3
Catania 3
Chongqing 3
Columbus 3
Dusit 3
Fulham 3
Hangzhou 3
Totale 37.783
Salva come PNG Salva come JPEG
Nome #
Italian validation of INQoL, a quality of life questionnaire for adults with muscle diseases 491
Overexpression of ErbB2 and ErbB3 receptors in Schwann cells of patients with Charcot-Marie-Tooth disease type 1A 479
Vitamin D deficiency in myotonic dystrophy type 1 479
A novel LITAF/SIMPLE mutation within a family with a demyelinating form of Charcot-Marie-Tooth disease 475
An Age-standardized prevalence estimate and a sex and age distribution of myotonic dystrophy types 1 and 2 in the Rome province, Italy 459
Subacute demyelinating polyneuropathy in B-cell lymphoma with IgM antibodies against glycolipid GD1b 456
Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2) 451
The myotonic dystrophy type 2 (DM2) gene product zinc finger protein 9 (ZNF9) is associated with sarcomeres and normally localized in DM2 patients' muscles 449
Risk prediction for clinical phenotype in myotonic dystrophy type 1: data from 2,650 patients 443
Sural nerve without nerve fibers in leprous neuropathy 439
Brain MR diffusion tensor imaging in Kennedy's disease 439
Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2 436
Morphological changes in the sciatic nerve of diabetic rats treated with low molecular weight heparin OP 2123/parnaparin 434
Dystrophin is not essential for the integrity of the cytoskeleton 424
Complete loss of the DNAJB6 G/F domain and novel missense mutations cause distal-onset DNAJB6 myopathy 424
Migraine-like disorder segregating with mtDNA 14484 Leber hereditary optic neuropathy mutation 423
Dopamine denervation induces neurotensin immunoreactivity in GABA-parvalbumin striatal neurons 421
Sleep disorders in spinal and bulbar muscular atrophy (Kennedy's disease): a controlled polysomnographic and self-reported questionnaires study. 409
Association of HLA-DQB1∗05:02 and DRB1∗16 Alleles with Late-Onset,Nonthymomatous, AChR-Ab-Positive Myasthenia Gravis 405
Randomized comparison of awake nonresectional versus nonawake resectional lung volume reduction surgery. 404
Familial inclusion body myositis among Kurdish-Iranian Jews 403
Upper motor neuron involvement in X-linked recessive bulbospinal muscular atrophy 403
Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1 403
Preferential central nucleation of type 2 myofibers is an invariable feature of myotonic dystrophy type 2 402
Intestinal pseudobstruction as presenting event of fatal cerivastatin-induced myopathy 401
Adult polyglucosan body disease: Proton magnetic resonance spectroscopy of the brain and novel mutation in the GBE1 gene 400
Association of HLA-DQB1*05:02 with Myasthenia gravis in Italian patients 400
EFFICACY OF INTRAVENOUS IMMUNOGLOBULIN IN POEMS-RELATED RELAPSING AIDP 399
Subcellular localization of the myotonic dystrophy type 2 protein ZNF9 in skeletal muscle 398
IMMUNOCYTOCHEMICAL LOCALIZATION OF VINCULIN IN MUSCLE AND NERVE 398
Sleep disorders in myotonic dystrophy type 2: a controlled polysomnographic study and self-reported questionnaires 398
Identification and characterization of 5' CCG interruptions in complex DMPK expanded alleles 397
Glucocorticoids and immunosuppressants do not change the prevalence of necrosis and regeneration in mdx skeletal muscles 396
Hashimoto's encephalopathy presenting with musical hallucinosis 396
Diagnosis, treatment and follow-up of the carpal tunnel syndrome: a review 394
NADPH DIAPHORASE ACTIVITY IS INHIBITED BY EDTA IN NEURONS BUT NOT IN CHOROID-PLEXUS EPITHELIUM 394
Differential features of muscle fiber atrophy in osteoporosis and osteoarthritis 393
Neurofibromatous neuropathy: An ultrastructural study 392
Acute demyelinating sensorimotor polyneuropathy in B-cell lymphoma with IGM autoantibodies against glycolipid GD1B 392
Neuroelectrophysiological abnormalities are related to metabolic and advanced non-enzymatic glycation changes in prospectively evaluated diabetic Sprague-Dawley rats 387
Correlation between clinical features and HLA genetic variability in myasthenia gravis 385
Late-onset MNGIE without peripheral neuropathy due to incomplete loss of thymidine phosphorylase activity 385
Early subclinical cochlear dysfunction in myotonic dystrophy type 1. 384
NADPH-Diaphorase neurons contacting the cerebrospinal fluid in the ventricles of rat brain 383
Transcranial unifocal stimulation in rabbit: subcutaneous and meningeal changes 381
Inverse correlation between VEGF and soluble VEGF receptor 2 in POEMS with AIDP responsive to intravenous immunoglobulin 379
Restless legs syndrome and daytime sleepiness are prominent in myotonic dystrophy type 2 379
Protective effect of clonazepam on ischemic brain damage induced by 10-minute bilateral carotid occlusion in Mongolian gerbils. 378
Cutaneous features of myotonic dystrophy types 1 and 2: implication of premature aging and vitamin d homeostasis 375
Active muscle length reduction progressively damages soleus in hindlimb-suspended rabbits 372
EPILEPTIC ACTIVITY FOLLOWING CEREBRAL-ISCHEMIA IN MONGOLIAN GERBILS IS DEPRESSED BY CPP, A COMPETITIVE ANTAGONIST OF THE N-METHYL-D-ASPARTATE RECEPTOR 371
Partial block of glycolysis in late-onset phosphofructokinase deficiency myopathy 370
Aberrant splicing and expression of the non muscle myosin heavy-chain gene MYH14 in DM1 muscle tissues 369
Delayed focal involvement of upper motor neurons in the Madras pattern of motor neuron disease 369
Measuring quality of life impairment in skeletal muscle channelopathies 368
Peripheral nerve extracellular matrix remodeling in Charcot-Marie-Tooth type 1 disease 367
Peripheral nerve extracellular matrix remodeling in Charcot-Marie- Tooth type I disease. 365
ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease 365
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 364
Recommendations for anesthesia and perioperative management of patients with neuromuscular disorders. 364
Sleep disorders in spinal and bulbar muscular atrophy (Kennedy's disease): a controlled polysomnographic and self-reported questionnaires study 364
Spasticity as an ictal pattern due to excitotoxic upper motor neuron damage 363
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) 363
Early diagnosis and early treatment in LOPD: when asymptomatic patients should be treated 360
Vulnerability of globus pallidus to Mn2+ may be dependent on preferential Mn2+ accumulation in pallidal neurons' nucleoli 357
Expanded [CCTG]n repetitions are not associated with abnormal methylation at the CNBP locus in myotonic dystrophy type 2 (DM2) patients 355
Myofibrillar disruption in the rabbit soleus muscle after one-week hindlimb suspension 354
Periodic acid-Schiff staining on resin muscle sections: improvement in the histological diagnosis of late-onset Pompe disease 354
Muscle phosphofructokinase deficiency 353
Late-onset MNGIE without peripheral neuropathy due to incomplete loss of thymidine phosphorylase activity 350
Long-term outcome of thoracoscopic extended thymectomy for nonthymomatous myasthenia gravis 347
Bilateral carotid occlusion in normotensive rats: olds facts and new observations 347
Screening of ARHSP-TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion 346
SPATACSIN mutations cause autosomal recessive juvenile amyotrophic lateral sclerosis 346
Long-term outcome of thoracoscopic extended thymectomy for nonthymomatous myasthenia gravis 346
Subclinical autonomic dysfunction in spinobulbar muscular atrophy (Kennedy disease) 345
Paucisymptomatic Marchiafava-Bignami disease with relevant diffusion-weighted MRI lesions 343
Epileptic activity following 10 minute cerebral ischemia in Mongolian gerbils: an electrophysiological study 339
Zinc distribution in various tissues, (brain, eye, skin, muscle and blood) of rat during hindlimb suspension 339
Intracellular localization and isoform expression of the voltage-dependent anion channel (VDAC) in normal and dystrophic skeletal muscle 338
Loss and renewal of thick myofilaments in glucocorticoid-treated rat soleus after denervation and reinnervation 336
Sudomotor skin responses to brain stimulation do not depend on nerve sensory fiber functionality 335
FUNCTIONAL, MORPHOLOGICAL AND BIOCHEMICAL-ALTERATIONS OF CENTRAL-NERVOUS-SYSTEM IN EXPERIMENTAL DIABETES 330
Sleep disorders in adult-onset myotonic dystrophy type 1: a controlled polysomnographic study 327
LITAF/SIMPLE MUTATION ANALYSIS IN DOMINANT DEMYELINATING CHARCOT- MARIE-TOOTH DISEASE: A NOVEL MUTATION 320
Corticobulbar And Corticospinal Tract Involvement In Kennedy's Disease 320
Relapsing aidp responsive to intravenous immunoglobulin in poems syndrome 318
Corticobulbar And Corticospinal Tract Involvement In Kennedy's Disease 318
Nodular morphea in a patient with Steinert disease 318
Myotonic dystrophy unlinked to DM1 and DM2 mutations in three siblings 315
Searching modifier genes in the LHON 14484T > C mtDNA mutation associated with migraine-like disorder 312
Histopathology and Immunoanalysis of Muscle 312
Recurrent hyperCKemia with normal muscle biopsy in a pediatric patient with neuromyelitis optica. 305
Adrenomyeloneuropathy partially responsive to steroid pulse therapy 293
Novel HLA II associations in myasthenia gravis 288
Muscle regeneration in mdx mice: Resistance to repeated necrosis is compatible with myofiber maturity 287
Sleep-wake cycle in the Kennedy's disease: a controlled polysomnographic study and self-reported questionnaires 285
Modelli sperimentali di miopatie 283
Hereditary spastic paraplegia:A novel mutation and expansion of the phenotype variability in SPG10 274
Minimalist thoracoscopic resection of thymoma associated with myasthenia gravis 268
Totale 37.412
Salva come PNG Salva come JPEG
Categoria #
all - tutte 84.162
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 84.162
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20207.113 0 0 0 0 884 1.136 978 958 897 817 662 781
2020/20217.129 608 732 656 726 1.450 777 852 759 119 165 229 56
2021/20221.389 108 138 40 102 42 120 64 53 98 138 77 409
2022/20231.337 173 86 33 114 99 334 170 70 93 24 123 18
2023/2024633 52 36 32 6 63 149 25 26 24 32 45 143
2024/20251.622 107 805 466 189 55 0 0 0 0 0 0 0
Totale 41.760