CATALOGO DEI PRODOTTI DELLA RICERCA

RIZZUTO, Nicolo'
 Distribuzione geografica
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Continente #
NA - Nord America 12.695
EU - Europa 12.081
AS - Asia 7.103
SA - Sud America 946
AF - Africa 79
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 14
Totale 32.942
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Nazione #
US - Stati Uniti d'America 12.565
GB - Regno Unito 3.612
RU - Federazione Russa 3.349
SG - Singapore 2.965
CN - Cina 2.606
SE - Svezia 1.027
FR - Francia 892
BR - Brasile 796
IT - Italia 756
FI - Finlandia 688
HK - Hong Kong 659
DE - Germania 642
IE - Irlanda 561
VN - Vietnam 282
UA - Ucraina 273
KR - Corea 233
TR - Turchia 67
AR - Argentina 65
CA - Canada 65
IN - India 54
NL - Olanda 54
BE - Belgio 46
MX - Messico 37
BD - Bangladesh 36
PL - Polonia 34
JP - Giappone 32
ES - Italia 31
ID - Indonesia 26
ZA - Sudafrica 26
CL - Cile 22
AU - Australia 21
CO - Colombia 19
IQ - Iraq 19
EC - Ecuador 17
IL - Israele 17
IR - Iran 15
LT - Lituania 15
AT - Austria 14
CH - Svizzera 12
EU - Europa 11
KE - Kenya 11
AZ - Azerbaigian 10
RO - Romania 10
EG - Egitto 8
HU - Ungheria 8
NP - Nepal 8
SA - Arabia Saudita 8
TN - Tunisia 8
BG - Bulgaria 7
LB - Libano 7
LV - Lettonia 7
PK - Pakistan 7
AL - Albania 6
DO - Repubblica Dominicana 6
DZ - Algeria 6
KG - Kirghizistan 6
MA - Marocco 6
UY - Uruguay 6
UZ - Uzbekistan 6
VE - Venezuela 6
BO - Bolivia 5
GR - Grecia 5
KZ - Kazakistan 5
NO - Norvegia 5
PE - Perù 5
PY - Paraguay 5
AE - Emirati Arabi Uniti 4
CR - Costa Rica 4
CZ - Repubblica Ceca 4
DK - Danimarca 4
EE - Estonia 4
OM - Oman 4
PA - Panama 4
AM - Armenia 3
HR - Croazia 3
JO - Giordania 3
LK - Sri Lanka 3
PT - Portogallo 3
TH - Thailandia 3
TT - Trinidad e Tobago 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BB - Barbados 2
BW - Botswana 2
CI - Costa d'Avorio 2
HN - Honduras 2
JM - Giamaica 2
MN - Mongolia 2
MU - Mauritius 2
MY - Malesia 2
PH - Filippine 2
SN - Senegal 2
TW - Taiwan 2
AF - Afghanistan, Repubblica islamica di 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BJ - Benin 1
BY - Bielorussia 1
CD - Congo 1
CW - ???statistics.table.value.countryCode.CW??? 1
DJ - Gibuti 1
Totale 32.919
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Città #
Southend 3.143
Jacksonville 2.352
Chandler 1.466
Singapore 1.304
Woodbridge 1.163
Dallas 1.115
Moscow 997
Ann Arbor 742
Ashburn 713
Hong Kong 655
Houston 629
Dublin 560
Beijing 316
Wilmington 276
New York 267
Lawrence 263
Princeton 263
Los Angeles 259
Nanjing 252
Jinan 233
Shenyang 189
Buffalo 174
Sindelfingen 157
Verona 155
Hebei 139
Tianjin 122
Helsinki 109
Ho Chi Minh City 109
Boardman 104
The Dalles 99
Munich 98
Milan 96
Nanchang 91
Changsha 85
Ningbo 85
Zhengzhou 79
Hangzhou 77
Columbus 74
Haikou 72
Taizhou 71
Philadelphia 69
São Paulo 65
Guangzhou 64
Jiaxing 64
Hanoi 62
Santa Clara 62
Redondo Beach 59
Lancaster 58
Taiyuan 53
Council Bluffs 50
Turku 49
Seattle 47
San Francisco 44
Chicago 42
Brussels 41
Auburn Hills 40
Rio de Janeiro 39
Fuzhou 37
Seoul 36
Lanzhou 33
London 33
Brooklyn 31
Falls Church 31
Warsaw 31
Norwalk 30
Fairfield 29
Detroit 28
Istanbul 27
Dearborn 26
Denver 26
Tokyo 24
Washington 22
Rome 21
Toronto 21
Curitiba 20
Stockholm 20
Belo Horizonte 19
Frankfurt am Main 19
Kent 19
Redwood City 19
Atlanta 18
Boston 18
Cambridge 17
Montreal 17
Clearwater 16
Brasília 14
Chennai 14
Redmond 14
Da Nang 13
Riva 13
Biên Hòa 12
Edinburgh 12
Johannesburg 12
Orem 12
Phoenix 12
Bologna 11
Kemerovo 11
Mumbai 11
Poplar 11
Salvador 11
Totale 20.932
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Nome #
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 251
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 249
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 244
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 241
Complement-mediated demyelination in patients with IgM monoclonal gammopathy and polyneuropathy 223
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 211
Un caso di sclerosi multipla con esordio "tumor-like" e decorso benigno 204
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 200
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 196
AZT-induced mitochondrial myopathy 195
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 194
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 191
A 49-year-old man with neuropsychiatric symptoms followed by progressive cognitive decline. 189
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 187
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 184
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 184
Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton. 183
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence study. 182
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 180
Acute reversible paralysis in critically ill patients 180
Lesione bilaterale della corteccia cingolata anteriore: studio polisonnografico ad autonomico di un caso. 180
[Hypertrophic neuropathies beginning in infancy: a study of 3 cases (author's transl)] 177
[Myopathy with lipid accumulation and type-II glutaric aciduria] 176
Binding of monoclonal anti-myelin-associated glycoprotein antibodies to human foetal peripheral neurons in culture 174
[Electromyographic study of 2 cases of nystagmus-myoclonus of the velum palatinum] 172
Cytoskeletal changes in cultured human fibroblasts following exposure to 2,5-hexanedione 171
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 171
A case of multifocal CIS with unusual MRI features suggestive of Balo's concentric sclerosis 170
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 169
Congenital hypomyelination neuropathy with a novel mutation of PMP22 168
Potenziali evocati acustici troncoencefalici e rilievi anatomo-patologici in un caso di sindrome di Wallenberg 168
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 167
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 167
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 167
Lower-limb lengthening in short stature. An electrophysiological and clinical assessment of peripheral nerve function 166
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 165
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 165
[Oculo-facio-cervical dystonia syndrome revealed by plurisystematized degeneration of the central nervous system with pallidoreticular pigmentary condition] 162
[Seitelberger's infantile neuroaxonal dystrophy: anatomoclinical study of a sibling group] 162
Gene dosage sensitivity of a novel mutation in the intracellular domain of P0 associated with Charcot-Marie-Tooth disease type 1B 162
[Alzheimer's disease. Histopathological and ultrastructural study of 6 cases (author's transl)] 159
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 158
T-cell cytotoxicity of human Schwann cells: TNFalpha promotes fasL-mediated apoptosis and IFN gamma perforin-mediated lysis 157
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 155
Botulinum toxin for the treatment of genital pain syndromes 155
Cerebral amyloidoses: molecular pathways and therapeutic challenges 155
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 155
[On a peculiar form of Creutzfeldt-Jakob disease, with anatomo-clinical dissociation] 153
pH-dependent prion protein conformation in classical Creutzfeldt-Jakob disease 153
BAEP and autopsy findings in Wallenberg syndrome 152
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 152
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 152
Dysmyelinating neuropathies of infancy: defined and undefined forms 152
Amyotrophy in Shy-Drager syndrome. 151
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 151
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 150
[Histopathologic and ultrastructural study of various amputation neuromas] 149
An unusual case of meningeal gliomatosis 148
Three-dimensional Structure of the Transthyretin (TTR) Phe64Leu Variant 148
Blood lymphocytes in neuronal ceroid lipofuscinosis 147
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 147
Prosopagnosia. Report of four cases 146
Hepatitis C virus infection of peripheral nerves in type II cryoglobulinaemia 146
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 146
Glial cell and macrophage reactions in rat spinal ganglion after peripheral nerve lesions: an immuno-cytochemical and morphometric study 146
A novel missense mutation in the L1CAM gene in a boy with L1-disease. 146
Clinical features of Kleine-Levin syndrome with localized encephalitis 145
[4 cases of Jakob-Creutzfeldt's disease] 145
[Hereditary sensory neuropathies with acrodystrophic lesions. Nosographic considerations] 145
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 145
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 144
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 144
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 144
[Spino-olivo-cerebello-nigral degeneration. Study of a case begining in infancy] 143
Congenital toxoplasmosis: histological and ultrastructural study 143
Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes. 143
[Diffuse sclerosis. Anatomo-clinical study of a subacute case with a striated demyelination] 142
Splicing mutation causes infantile Sandhoff disease 142
T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathy 142
Cytoskeletal pathology in ataxia-telangiectasia. 141
The role of muscle biopsy in investigating isolated muscle pain 141
Eclamptic encephalopathy: imaging and pathogenetic considerations 140
Brain metastases from post-radiation malignant peripheral nerve sheath tumour 139
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 139
T-cell anti-apoptotic mechanisms in inflammatory myopathies 139
Gonosomal mosaicism of a novel heterozygous mutation of P0 causes Charcot-Marie-Tooth neuropathy type 1B with apparent autosomal recessive inheritance 138
Satellite cells and interstitial macrophages activation in rat dorsal root ganglia following peripheral nerve lesions 138
Adhesion molecules expression on the vascular endothelium of peripheral nerve in HIV-associated Distal Sensory Polyneuropathy 138
Friedreich's ataxia. A light- and electron microscopic study of peripheral nerve biopsies 137
[Myoclonic form of Hallervorden-Spatz disease. Clinical aspect simulating a subacute spongiform encephalitis] 137
Human skeletal muscle as a target organ of trichloroethylene toxicity. 137
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 137
Impaired heteronymous somatosensory motor cortical inhibition in dystonia 136
Charcot-Marie-Tooth disease with giant axons:a clinicopathological and genetic study 135
Effetti della luce laser He-Ne sulla rigenerazione assonale del nervo safeno di ratto sottoposto a neurotmesi e neurorrafia. 135
Cytoskeletal changes induced by 2,5-hexanedione on developing human neurons in vitro 134
PMP22 related congenital hypomyelination neuropathy 134
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 134
Atypical Alzheimer's disease: a case report. 134
Inherited neuroaxonal dystrophy in C6 deficient rabbits 133
Totale 16.119
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Categoria #
all - tutte 107.615
article - articoli 94.507
book - libri 0
conference - conferenze 7.613
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 5.495
Totale 215.230
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.627 0 0 0 0 221 334 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
2024/20254.852 335 375 99 795 248 78 222 192 775 294 394 1.045
2025/20267.636 1.078 817 1.136 2.047 2.558 0 0 0 0 0 0 0
Totale 33.098