RIZZUTO, Nicolo'
 Distribuzione geografica
Continente #
NA - Nord America 9.792
EU - Europa 8.683
AS - Asia 2.877
SA - Sud America 29
OC - Oceania 21
Continente sconosciuto - Info sul continente non disponibili 13
AF - Africa 6
Totale 21.421
Nazione #
US - Stati Uniti d'America 9.768
GB - Regno Unito 3.523
CN - Cina 2.142
SE - Svezia 1.008
FR - Francia 867
IT - Italia 700
FI - Finlandia 628
SG - Singapore 580
IE - Irlanda 557
DE - Germania 492
RU - Federazione Russa 470
UA - Ucraina 262
BE - Belgio 45
NL - Olanda 42
KR - Corea 34
TR - Turchia 29
AU - Australia 20
IN - India 17
IR - Iran 15
ES - Italia 13
IL - Israele 13
BR - Brasile 12
CA - Canada 12
CL - Cile 12
JP - Giappone 12
EU - Europa 11
RO - Romania 10
MX - Messico 9
CH - Svizzera 7
LV - Lettonia 7
BG - Bulgaria 5
NO - Norvegia 5
AL - Albania 4
BD - Bangladesh 4
CZ - Repubblica Ceca 4
DK - Danimarca 4
GR - Grecia 4
HU - Ungheria 4
KG - Kirghizistan 4
AT - Austria 3
EE - Estonia 3
EG - Egitto 3
PK - Pakistan 3
SA - Arabia Saudita 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AM - Armenia 2
AZ - Azerbaigian 2
CO - Colombia 2
HK - Hong Kong 2
HR - Croazia 2
LT - Lituania 2
PA - Panama 2
PL - Polonia 2
PT - Portogallo 2
TW - Taiwan 2
AE - Emirati Arabi Uniti 1
BA - Bosnia-Erzegovina 1
BO - Bolivia 1
CR - Costa Rica 1
DZ - Algeria 1
ID - Indonesia 1
IM - Isola di Man 1
IQ - Iraq 1
IS - Islanda 1
KH - Cambogia 1
KW - Kuwait 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
MA - Marocco 1
MD - Moldavia 1
ME - Montenegro 1
MK - Macedonia 1
MN - Mongolia 1
MO - Macao, regione amministrativa speciale della Cina 1
MY - Malesia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PE - Perù 1
PH - Filippine 1
RS - Serbia 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
VE - Venezuela 1
ZA - Sudafrica 1
Totale 21.421
Città #
Southend 3.143
Jacksonville 2.352
Chandler 1.466
Woodbridge 1.163
Ann Arbor 742
Houston 618
Dublin 557
Ashburn 470
Singapore 433
Wilmington 276
Lawrence 263
Princeton 263
Nanjing 250
Jinan 231
Beijing 200
New York 194
Shenyang 186
Sindelfingen 157
Verona 152
Hebei 139
Tianjin 116
Boardman 104
Helsinki 98
Nanchang 90
Milan 84
Ningbo 84
Changsha 77
Hangzhou 74
Zhengzhou 74
Haikou 72
Taizhou 69
Philadelphia 67
Jiaxing 64
Lancaster 58
Guangzhou 55
Taiyuan 53
Auburn Hills 40
Brussels 40
Seattle 39
Fuzhou 37
Los Angeles 36
Lanzhou 32
Falls Church 31
Norwalk 30
Fairfield 29
Chicago 27
Detroit 27
Dearborn 26
San Francisco 26
Dallas 25
Seoul 25
Washington 20
Kent 19
Redwood City 19
Cambridge 17
Clearwater 16
Rome 15
Redmond 14
Riva 13
Edinburgh 12
Kemerovo 11
San Mateo 11
Bologna 10
Moscow 10
Leawood 9
Curitiba 8
Andover 7
Bolzano 7
London 7
Melbourne 7
Palermo 7
Santa Clara 7
Tokyo 7
Toronto 7
Arco 6
Ardabil 6
Augusta 6
Düsseldorf 6
Las Vegas 6
Naples 6
Novokuznetsk 6
Romola 6
Tappahannock 6
Canberra 5
Gangdong-gu 5
Madrid 5
Mehlingen 5
Monmouth Junction 5
Riga 5
Sacramento 5
San Diego 5
Bishkek 4
Boston 4
Buk-gu 4
Dalian 4
Durango 4
Florence 4
Frankfurt am Main 4
Lappeenranta 4
Napoli 4
Totale 15.354
Nome #
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 227
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 220
Un caso di sclerosi multipla con esordio "tumor-like" e decorso benigno 173
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 153
Complement-mediated demyelination in patients with IgM monoclonal gammopathy and polyneuropathy 144
Potenziali evocati acustici troncoencefalici e rilievi anatomo-patologici in un caso di sindrome di Wallenberg 144
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 143
Lesione bilaterale della corteccia cingolata anteriore: studio polisonnografico ad autonomico di un caso. 138
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 136
Binding of monoclonal anti-myelin-associated glycoprotein antibodies to human foetal peripheral neurons in culture 116
Lower-limb lengthening in short stature. An electrophysiological and clinical assessment of peripheral nerve function 115
Acute reversible paralysis in critically ill patients 115
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 114
Cytoskeletal changes in cultured human fibroblasts following exposure to 2,5-hexanedione 113
Three-dimensional Structure of the Transthyretin (TTR) Phe64Leu Variant 112
AZT-induced mitochondrial myopathy 112
A case of multifocal CIS with unusual MRI features suggestive of Balo's concentric sclerosis 112
Splicing mutation causes infantile Sandhoff disease 111
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 111
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 110
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 110
Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton. 110
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 109
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 108
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 107
Phosphorylated 14-3-3zeta protein in the CSF of neuroleptic-treated patients 106
Prosopagnosia. Report of four cases 105
Gene dosage sensitivity of a novel mutation in the intracellular domain of P0 associated with Charcot-Marie-Tooth disease type 1B 105
Cytoskeletal pathology in ataxia-telangiectasia. 104
T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathy 103
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 103
Congenital hypomyelination neuropathy with a novel mutation of PMP22 102
A 49-year-old man with neuropsychiatric symptoms followed by progressive cognitive decline. 102
Human skeletal muscle as a target organ of trichloroethylene toxicity. 102
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 102
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 102
Clinical features of Kleine-Levin syndrome with localized encephalitis 101
[Myopathy with lipid accumulation and type-II glutaric aciduria] 101
Gonosomal mosaicism of a novel heterozygous mutation of P0 causes Charcot-Marie-Tooth neuropathy type 1B with apparent autosomal recessive inheritance 101
PMP22 related congenital hypomyelination neuropathy 101
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 101
Remitting infratentorial leukoencephalopathy in a patient with HIV infection. 100
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 99
T-cell anti-apoptotic mechanisms in inflammatory myopathies 99
Peripheral nerve vasculitis: a clinico-pathological study 99
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene 98
Cytoskeletal changes induced by 2,5-hexanedione on developing human neurons in vitro 97
Friedreich's ataxia. A light- and electron microscopic study of peripheral nerve biopsies 97
Cerebral amyloidoses: molecular pathways and therapeutic challenges 97
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 97
Demyelinating polyradiculoneuritis following Coxiella burnetti infection (Q fever) 96
Satellite cells and interstitial macrophages activation in rat dorsal root ganglia following peripheral nerve lesions 96
Botulinum toxin for the treatment of genital pain syndromes 96
T-cell cytotoxicity of human Schwann cells: TNFalpha promotes fasL-mediated apoptosis and IFN gamma perforin-mediated lysis 96
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence study. 96
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 96
[Hypertrophic neuropathies beginning in infancy: a study of 3 cases (author's transl)] 95
An unusual case of meningeal gliomatosis 95
Glial cell and macrophage reactions in rat spinal ganglion after peripheral nerve lesions: an immuno-cytochemical and morphometric study 95
Neuropsychological and neuroimaging correlates in corticobasal degeneration 95
Dysmyelinating neuropathies of infancy: defined and undefined forms 95
The role of muscle biopsy in investigating isolated muscle pain 95
[Alzheimer's disease. Histopathological and ultrastructural study of 6 cases (author's transl)] 94
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 94
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 94
pH-dependent prion protein conformation in classical Creutzfeldt-Jakob disease 94
Clinical and pathological correlations in Charcot-Marie-Tooth neuropathy type 1A with the 17p11.2p12 duplication: a cross-sectional morphometric and immunohistochemical study in twenty cases 93
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 93
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 93
Human peripheral nerve macrophages in normal and pathological conditions 92
BAEP and autopsy findings in Wallenberg syndrome 92
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 92
Epilessia ed imaging 92
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 92
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 92
Inherited neuroaxonal dystrophy in C6 deficient rabbits 91
Hepatitis C virus infection of peripheral nerves in type II cryoglobulinaemia 91
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 91
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 91
Molecular genetic characterization of two metachromatic leukodystrophy patients who carry the T799G mutation acid show different phenotypes; description of a novel null-type mutation (Human Genetics (1998) 102 (459-463)) 90
MELAS: clinical phenotypes and morphological brain abnormalities 90
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mithocondrial diseases 90
HIV-associated PML presenting as epilepsia partialis continua 90
[Oculo-facio-cervical dystonia syndrome revealed by plurisystematized degeneration of the central nervous system with pallidoreticular pigmentary condition] 89
[Seitelberger's infantile neuroaxonal dystrophy: anatomoclinical study of a sibling group] 89
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 89
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 89
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. 89
Motor neuron disease with pyramidal tract dysfunction involves the cortical generators of the early somatosensory evoked potential to tibial nerve stimulation 89
Complement neoantigen and vitronectin are components of plaques in amyloid AL neuropathy 88
[Thrombosis of the extracranial carotid caused by traumatic lesions of the soft palate in childhood] 88
[On a peculiar form of Creutzfeldt-Jakob disease, with anatomo-clinical dissociation] 88
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy. 88
Effetti della luce laser He-Ne sulla rigenerazione assonale del nervo safeno di ratto sottoposto a neurotmesi e neurorrafia. 88
Expression and regulation of glial-cell-line-derived neurotrophic factor (GDNF) mRNA in human astrocytes in vitro 87
Multicystic encephalomalacia associated with symmetrical necrotizing brain stem lesions in an infant: a case report 87
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 87
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 87
Congenital toxoplasmosis: histological and ultrastructural study 87
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 87
Totale 10.360
Categoria #
all - tutte 67.836
article - articoli 59.398
book - libri 0
conference - conferenze 4.912
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 3.526
Totale 135.672


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.615 0 0 0 282 316 406 353 292 109 309 84 464
2020/20212.636 265 357 188 199 221 334 34 264 241 34 394 105
2021/20222.484 251 850 19 233 56 106 23 142 72 58 209 465
2022/20234.351 345 379 443 737 454 1.002 38 304 449 21 114 65
2023/20241.667 91 174 122 276 198 282 40 66 11 63 216 128
2024/2025967 335 375 99 158 0 0 0 0 0 0 0 0
Totale 21.577