CATALOGO DEI PRODOTTI DELLA RICERCA

RIZZUTO, Nicolo'
 Distribuzione geografica
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Continente #
NA - Nord America 16.048
EU - Europa 13.368
AS - Asia 8.832
SA - Sud America 1.054
Continente sconosciuto - Info sul continente non disponibili 170
AF - Africa 167
OC - Oceania 28
Totale 39.667
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Nazione #
US - Stati Uniti d'America 15.845
RU - Federazione Russa 4.146
SG - Singapore 3.857
GB - Regno Unito 3.648
CN - Cina 2.798
IT - Italia 1.094
SE - Svezia 1.031
FR - Francia 910
BR - Brasile 864
FI - Finlandia 693
HK - Hong Kong 692
DE - Germania 665
VN - Vietnam 615
IE - Irlanda 563
KR - Corea 307
UA - Ucraina 284
CA - Canada 101
IN - India 93
BD - Bangladesh 88
TR - Turchia 76
AR - Argentina 70
NL - Olanda 64
MX - Messico 55
JP - Giappone 49
BE - Belgio 46
NG - Nigeria 45
ES - Italia 42
PL - Polonia 39
ZA - Sudafrica 38
IQ - Iraq 34
ID - Indonesia 30
CL - Cile 26
AU - Australia 24
CO - Colombia 24
EC - Ecuador 22
LT - Lituania 20
AT - Austria 19
PK - Pakistan 19
IL - Israele 17
SA - Arabia Saudita 16
IR - Iran 15
KE - Kenya 14
VE - Venezuela 14
AZ - Azerbaigian 13
CH - Svizzera 12
EG - Egitto 12
NP - Nepal 12
PH - Filippine 12
UZ - Uzbekistan 12
EU - Europa 11
MA - Marocco 11
AL - Albania 10
JO - Giordania 10
LB - Libano 10
RO - Romania 10
TN - Tunisia 10
BO - Bolivia 9
DZ - Algeria 9
BG - Bulgaria 8
CR - Costa Rica 8
DO - Repubblica Dominicana 8
GR - Grecia 8
HU - Ungheria 8
MY - Malesia 8
PE - Perù 8
PY - Paraguay 8
UY - Uruguay 8
KG - Kirghizistan 7
LV - Lettonia 7
OM - Oman 7
CZ - Repubblica Ceca 6
KZ - Kazakistan 6
SN - Senegal 6
AE - Emirati Arabi Uniti 5
CI - Costa d'Avorio 5
HR - Croazia 5
NO - Norvegia 5
DK - Danimarca 4
EE - Estonia 4
JM - Giamaica 4
PA - Panama 4
PT - Portogallo 4
TH - Thailandia 4
AM - Armenia 3
ET - Etiopia 3
HN - Honduras 3
LK - Sri Lanka 3
NI - Nicaragua 3
TT - Trinidad e Tobago 3
A2 - ???statistics.table.value.countryCode.A2??? 2
BB - Barbados 2
BW - Botswana 2
BY - Bielorussia 2
GE - Georgia 2
GT - Guatemala 2
MN - Mongolia 2
MU - Mauritius 2
NZ - Nuova Zelanda 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
Totale 39.470
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Città #
Southend 3.143
Jacksonville 2.355
Singapore 2.110
Chandler 1.466
Ashburn 1.424
San Jose 1.378
Moscow 1.237
Woodbridge 1.164
Dallas 1.132
Ann Arbor 742
Hong Kong 686
Houston 638
Dublin 562
Verona 426
Council Bluffs 393
The Dalles 357
Beijing 327
New York 301
Los Angeles 291
Wilmington 276
Lawrence 263
Princeton 263
Nanjing 252
Jinan 233
Ho Chi Minh City 221
Shenyang 189
Buffalo 184
Sindelfingen 157
Hanoi 141
Hebei 139
Tianjin 124
Helsinki 114
Milan 108
Boardman 104
Santa Clara 104
Munich 99
Nanchang 91
Changsha 85
Ningbo 85
Zhengzhou 80
Hangzhou 77
São Paulo 76
Columbus 74
Haikou 72
Philadelphia 72
Taizhou 71
Guangzhou 69
Jiaxing 64
Orem 60
Redondo Beach 59
Lancaster 58
Taiyuan 53
San Francisco 52
Chicago 50
Seattle 49
Turku 49
Abuja 42
Rio de Janeiro 42
Brussels 41
Auburn Hills 40
London 40
Tokyo 40
Fuzhou 37
Brooklyn 36
Seoul 36
Denver 35
Warsaw 35
Frankfurt am Main 34
Chennai 33
Da Nang 33
Lanzhou 33
Falls Church 31
Norwalk 31
Rome 31
Istanbul 30
Montreal 30
Detroit 29
Fairfield 29
Dearborn 26
Toronto 26
Atlanta 25
Washington 24
Stockholm 23
Belo Horizonte 21
Boston 21
Phoenix 21
Curitiba 20
Haiphong 20
Johannesburg 20
Kent 20
Redwood City 19
Cambridge 17
Clearwater 17
Amsterdam 16
Biên Hòa 16
Manchester 16
Paris 16
Brasília 15
Mumbai 15
Redmond 14
Totale 25.645
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Nome #
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 286
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 273
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 270
Complement-mediated demyelination in patients with IgM monoclonal gammopathy and polyneuropathy 264
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 264
AZT-induced mitochondrial myopathy 239
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 239
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 238
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 235
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 232
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 228
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 227
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 221
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 220
A 49-year-old man with neuropsychiatric symptoms followed by progressive cognitive decline. 220
Un caso di sclerosi multipla con esordio "tumor-like" e decorso benigno 220
[Myopathy with lipid accumulation and type-II glutaric aciduria] 219
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 218
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 216
Acute reversible paralysis in critically ill patients 216
[Hypertrophic neuropathies beginning in infancy: a study of 3 cases (author's transl)] 213
[Electromyographic study of 2 cases of nystagmus-myoclonus of the velum palatinum] 211
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence study. 210
A case of multifocal CIS with unusual MRI features suggestive of Balo's concentric sclerosis 209
Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton. 208
Lesione bilaterale della corteccia cingolata anteriore: studio polisonnografico ad autonomico di un caso. 207
[Alzheimer's disease. Histopathological and ultrastructural study of 6 cases (author's transl)] 206
Cytoskeletal changes in cultured human fibroblasts following exposure to 2,5-hexanedione 205
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 205
Binding of monoclonal anti-myelin-associated glycoprotein antibodies to human foetal peripheral neurons in culture 204
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 197
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 197
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 196
[Oculo-facio-cervical dystonia syndrome revealed by plurisystematized degeneration of the central nervous system with pallidoreticular pigmentary condition] 194
T-cell cytotoxicity of human Schwann cells: TNFalpha promotes fasL-mediated apoptosis and IFN gamma perforin-mediated lysis 194
Congenital hypomyelination neuropathy with a novel mutation of PMP22 191
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 191
[Seitelberger's infantile neuroaxonal dystrophy: anatomoclinical study of a sibling group] 190
Potenziali evocati acustici troncoencefalici e rilievi anatomo-patologici in un caso di sindrome di Wallenberg 190
Lower-limb lengthening in short stature. An electrophysiological and clinical assessment of peripheral nerve function 189
BAEP and autopsy findings in Wallenberg syndrome 188
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 188
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 188
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 187
[Hereditary sensory neuropathies with acrodystrophic lesions. Nosographic considerations] 186
Clinical features of Kleine-Levin syndrome with localized encephalitis 185
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 185
Dysmyelinating neuropathies of infancy: defined and undefined forms 184
Botulinum toxin for the treatment of genital pain syndromes 183
Gene dosage sensitivity of a novel mutation in the intracellular domain of P0 associated with Charcot-Marie-Tooth disease type 1B 183
Glial cell and macrophage reactions in rat spinal ganglion after peripheral nerve lesions: an immuno-cytochemical and morphometric study 182
[On a peculiar form of Creutzfeldt-Jakob disease, with anatomo-clinical dissociation] 181
Cerebral amyloidoses: molecular pathways and therapeutic challenges 181
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 181
Blood lymphocytes in neuronal ceroid lipofuscinosis 179
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 178
An unusual case of meningeal gliomatosis 177
Congenital toxoplasmosis: histological and ultrastructural study 177
Amyotrophy in Shy-Drager syndrome. 176
[Diffuse sclerosis. Anatomo-clinical study of a subacute case with a striated demyelination] 176
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 176
Three-dimensional Structure of the Transthyretin (TTR) Phe64Leu Variant 176
[Spino-olivo-cerebello-nigral degeneration. Study of a case begining in infancy] 175
Eclamptic encephalopathy: imaging and pathogenetic considerations 175
A novel missense mutation in the L1CAM gene in a boy with L1-disease. 175
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 175
[Histopathologic and ultrastructural study of various amputation neuromas] 174
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 174
Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes. 174
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 173
Brain metastases from post-radiation malignant peripheral nerve sheath tumour 173
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 173
pH-dependent prion protein conformation in classical Creutzfeldt-Jakob disease 173
[4 cases of Jakob-Creutzfeldt's disease] 172
Hepatitis C virus infection of peripheral nerves in type II cryoglobulinaemia 172
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 171
Inherited neuroaxonal dystrophy in C6 deficient rabbits 169
T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathy 169
Friedreich's ataxia. A light- and electron microscopic study of peripheral nerve biopsies 168
Gonosomal mosaicism of a novel heterozygous mutation of P0 causes Charcot-Marie-Tooth neuropathy type 1B with apparent autosomal recessive inheritance 168
Satellite cells and interstitial macrophages activation in rat dorsal root ganglia following peripheral nerve lesions 167
Adhesion molecules expression on the vascular endothelium of peripheral nerve in HIV-associated Distal Sensory Polyneuropathy 167
T-cell anti-apoptotic mechanisms in inflammatory myopathies 167
Prosopagnosia. Report of four cases 166
Impaired heteronymous somatosensory motor cortical inhibition in dystonia 166
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 166
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 166
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 165
Atypical Alzheimer's disease: a case report. 165
Splicing mutation causes infantile Sandhoff disease 164
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 164
Effetti della luce laser He-Ne sulla rigenerazione assonale del nervo safeno di ratto sottoposto a neurotmesi e neurorrafia. 163
[Cerebral calcinosis in postoperative hypoparathyroidism. Presentation of an anatomo-clinical case] 162
[Flaccid paralysis of the foot in rolandic parasagittal tumors] 162
PMP22 related congenital hypomyelination neuropathy 162
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 162
Epilepsy in glioblastoma multiforme: correlation with glutamine synthetase levels. 162
The role of muscle biopsy in investigating isolated muscle pain 162
Human skeletal muscle as a target organ of trichloroethylene toxicity. 161
[Juvenile thrombosis of the basilar artery] 160
Totale 19.131
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Categoria #
all - tutte 130.930
article - articoli 114.950
book - libri 0
conference - conferenze 9.298
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 6.682
Totale 261.860
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.233 0 850 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
2025/202613.695 1.078 817 1.136 2.047 3.428 982 1.291 609 1.197 707 200 203
2026/2027510 146 364 0 0 0 0 0 0 0 0 0 0
Totale 39.667