CATALOGO DEI PRODOTTI DELLA RICERCA

RIZZUTO, Nicolo'
 Distribuzione geografica
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Continente #
NA - Nord America 18.425
EU - Europa 13.544
AS - Asia 8.878
SA - Sud America 1.099
Continente sconosciuto - Info sul continente non disponibili 194
AF - Africa 180
OC - Oceania 28
Totale 42.348
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Nazione #
US - Stati Uniti d'America 17.983
RU - Federazione Russa 4.157
SG - Singapore 3.861
GB - Regno Unito 3.670
CN - Cina 2.801
IT - Italia 1.220
SE - Svezia 1.031
FR - Francia 912
BR - Brasile 896
FI - Finlandia 693
HK - Hong Kong 693
DE - Germania 668
VN - Vietnam 617
IE - Irlanda 565
KR - Corea 307
UA - Ucraina 286
CA - Canada 214
BD - Bangladesh 96
IN - India 94
TR - Turchia 79
AR - Argentina 73
NL - Olanda 64
MX - Messico 59
JP - Giappone 49
BE - Belgio 46
NG - Nigeria 45
ES - Italia 43
PL - Polonia 41
ZA - Sudafrica 38
CR - Costa Rica 34
IQ - Iraq 34
IL - Israele 33
ID - Indonesia 31
CO - Colombia 28
CL - Cile 26
EC - Ecuador 25
AU - Australia 24
CW - ???statistics.table.value.countryCode.CW??? 23
SV - El Salvador 23
GT - Guatemala 21
LT - Lituania 20
AT - Austria 19
PK - Pakistan 19
NI - Nicaragua 18
SA - Arabia Saudita 17
VE - Venezuela 16
IR - Iran 15
KE - Kenya 15
PR - Porto Rico 15
AZ - Azerbaigian 13
PH - Filippine 13
UZ - Uzbekistan 13
CH - Svizzera 12
EG - Egitto 12
MA - Marocco 12
NP - Nepal 12
EU - Europa 11
RO - Romania 11
AL - Albania 10
HN - Honduras 10
JO - Giordania 10
LB - Libano 10
SC - Seychelles 10
TN - Tunisia 10
BG - Bulgaria 9
BO - Bolivia 9
DZ - Algeria 9
PE - Perù 9
DO - Repubblica Dominicana 8
GR - Grecia 8
HU - Ungheria 8
JM - Giamaica 8
MY - Malesia 8
PY - Paraguay 8
UY - Uruguay 8
KG - Kirghizistan 7
KZ - Kazakistan 7
LV - Lettonia 7
OM - Oman 7
TT - Trinidad e Tobago 7
AE - Emirati Arabi Uniti 6
CZ - Repubblica Ceca 6
GP - Guadalupe 6
PA - Panama 6
SN - Senegal 6
CI - Costa d'Avorio 5
DK - Danimarca 5
EE - Estonia 5
HR - Croazia 5
NO - Norvegia 5
PT - Portogallo 5
TH - Thailandia 4
AM - Armenia 3
BB - Barbados 3
ET - Etiopia 3
LK - Sri Lanka 3
TW - Taiwan 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BS - Bahamas 2
BW - Botswana 2
Totale 42.138
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Città #
Southend 3.143
Jacksonville 2.359
Ashburn 2.261
Singapore 2.110
San Jose 1.579
Chandler 1.466
Moscow 1.237
Woodbridge 1.164
Dallas 1.153
Ann Arbor 742
Hong Kong 687
Houston 644
Dublin 564
Verona 426
Council Bluffs 394
The Dalles 357
Beijing 328
New York 312
Los Angeles 308
Wilmington 276
Lawrence 263
Princeton 263
Nanjing 252
Jinan 233
Ho Chi Minh City 221
Buffalo 189
Shenyang 189
Sindelfingen 157
Hanoi 142
Hebei 139
Santa Clara 130
Tianjin 124
Milan 119
Helsinki 114
Annandale 105
Boardman 104
Munich 99
São Paulo 97
Nanchang 91
Changsha 85
Ningbo 85
Zhengzhou 80
Hangzhou 77
Columbus 75
Philadelphia 75
Haikou 72
Taizhou 71
Guangzhou 69
Jiaxing 64
San Francisco 62
Las Vegas 61
Orem 60
Redondo Beach 59
Lancaster 58
Chicago 54
Rome 53
Taiyuan 53
Seattle 50
Turku 49
Montreal 48
Toronto 47
Brooklyn 45
London 43
Abuja 42
Rio de Janeiro 42
Brussels 41
Auburn Hills 40
Denver 40
Tokyo 40
Fuzhou 37
Seoul 36
Warsaw 36
Frankfurt am Main 35
Atlanta 33
Chennai 33
Da Nang 33
Lanzhou 33
Norwalk 32
Providence 32
Detroit 31
Falls Church 31
Istanbul 30
Fairfield 29
Phoenix 29
Dearborn 27
Washington 25
Stockholm 23
Willemstad 23
Belo Horizonte 22
Boston 21
Carrboro 21
Haiphong 21
North Bergen 21
San José 21
Curitiba 20
Johannesburg 20
Kent 20
Naples 20
Redwood City 19
Amsterdam 17
Totale 27.112
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Nome #
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 294
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 288
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 282
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 279
Complement-mediated demyelination in patients with IgM monoclonal gammopathy and polyneuropathy 274
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 267
AZT-induced mitochondrial myopathy 252
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 246
Acute reversible paralysis in critically ill patients 245
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 243
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 242
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 237
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 236
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 231
[Myopathy with lipid accumulation and type-II glutaric aciduria] 229
A 49-year-old man with neuropsychiatric symptoms followed by progressive cognitive decline. 229
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 229
Lesione bilaterale della corteccia cingolata anteriore: studio polisonnografico ad autonomico di un caso. 228
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 227
[Hypertrophic neuropathies beginning in infancy: a study of 3 cases (author's transl)] 225
A case of multifocal CIS with unusual MRI features suggestive of Balo's concentric sclerosis 224
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 223
Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton. 223
Un caso di sclerosi multipla con esordio "tumor-like" e decorso benigno 223
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence study. 221
[Electromyographic study of 2 cases of nystagmus-myoclonus of the velum palatinum] 219
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 218
Potenziali evocati acustici troncoencefalici e rilievi anatomo-patologici in un caso di sindrome di Wallenberg 217
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 217
Cytoskeletal changes in cultured human fibroblasts following exposure to 2,5-hexanedione 214
[Alzheimer's disease. Histopathological and ultrastructural study of 6 cases (author's transl)] 214
Binding of monoclonal anti-myelin-associated glycoprotein antibodies to human foetal peripheral neurons in culture 212
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 209
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 207
Dysmyelinating neuropathies of infancy: defined and undefined forms 205
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 203
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 203
T-cell cytotoxicity of human Schwann cells: TNFalpha promotes fasL-mediated apoptosis and IFN gamma perforin-mediated lysis 203
Three-dimensional Structure of the Transthyretin (TTR) Phe64Leu Variant 202
[Oculo-facio-cervical dystonia syndrome revealed by plurisystematized degeneration of the central nervous system with pallidoreticular pigmentary condition] 201
Congenital hypomyelination neuropathy with a novel mutation of PMP22 200
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 200
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 200
Clinical features of Kleine-Levin syndrome with localized encephalitis 199
BAEP and autopsy findings in Wallenberg syndrome 199
Adhesion molecules expression on the vascular endothelium of peripheral nerve in HIV-associated Distal Sensory Polyneuropathy 196
[Seitelberger's infantile neuroaxonal dystrophy: anatomoclinical study of a sibling group] 195
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 195
Lower-limb lengthening in short stature. An electrophysiological and clinical assessment of peripheral nerve function 194
Botulinum toxin for the treatment of genital pain syndromes 193
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 193
[Hereditary sensory neuropathies with acrodystrophic lesions. Nosographic considerations] 192
pH-dependent prion protein conformation in classical Creutzfeldt-Jakob disease 192
Gene dosage sensitivity of a novel mutation in the intracellular domain of P0 associated with Charcot-Marie-Tooth disease type 1B 191
Glial cell and macrophage reactions in rat spinal ganglion after peripheral nerve lesions: an immuno-cytochemical and morphometric study 190
Cerebral amyloidoses: molecular pathways and therapeutic challenges 190
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 190
Satellite cells and interstitial macrophages activation in rat dorsal root ganglia following peripheral nerve lesions 188
[On a peculiar form of Creutzfeldt-Jakob disease, with anatomo-clinical dissociation] 187
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 187
Congenital toxoplasmosis: histological and ultrastructural study 187
A novel missense mutation in the L1CAM gene in a boy with L1-disease. 187
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 186
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 186
Eclamptic encephalopathy: imaging and pathogenetic considerations 185
Amyotrophy in Shy-Drager syndrome. 185
An unusual case of meningeal gliomatosis 185
Hepatitis C virus infection of peripheral nerves in type II cryoglobulinaemia 185
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 185
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 185
Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes. 185
Blood lymphocytes in neuronal ceroid lipofuscinosis 184
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 184
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 184
[Diffuse sclerosis. Anatomo-clinical study of a subacute case with a striated demyelination] 182
[Histopathologic and ultrastructural study of various amputation neuromas] 180
Inherited neuroaxonal dystrophy in C6 deficient rabbits 180
[Spino-olivo-cerebello-nigral degeneration. Study of a case begining in infancy] 180
Gonosomal mosaicism of a novel heterozygous mutation of P0 causes Charcot-Marie-Tooth neuropathy type 1B with apparent autosomal recessive inheritance 180
Brain metastases from post-radiation malignant peripheral nerve sheath tumour 180
Friedreich's ataxia. A light- and electron microscopic study of peripheral nerve biopsies 179
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 179
Hexacarbon axonopathy: the morphological expression of altered cytoskeletal translocation. 179
[4 cases of Jakob-Creutzfeldt's disease] 177
Impaired heteronymous somatosensory motor cortical inhibition in dystonia 177
T-cell anti-apoptotic mechanisms in inflammatory myopathies 177
PMP22 related congenital hypomyelination neuropathy 176
T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathy 176
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 174
Atypical Alzheimer's disease: a case report. 174
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 173
Prosopagnosia. Report of four cases 172
Human skeletal muscle as a target organ of trichloroethylene toxicity. 172
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 172
Splicing mutation causes infantile Sandhoff disease 171
Epilessia ed imaging 171
The role of muscle biopsy in investigating isolated muscle pain 171
Cytoskeletal changes induced by 2,5-hexanedione on developing human neurons in vitro 170
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 170
Charcot-Marie-Tooth disease with giant axons:a clinicopathological and genetic study 170
Totale 20.267
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Categoria #
all - tutte 138.889
article - articoli 121.714
book - libri 0
conference - conferenze 9.976
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 7.199
Totale 277.778
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.131 0 0 0 0 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
2025/202613.695 1.078 817 1.136 2.047 3.428 982 1.291 609 1.197 707 200 203
2026/20273.191 146 364 626 1.981 74 0 0 0 0 0 0 0
Totale 42.348