CATALOGO DEI PRODOTTI DELLA RICERCA

RIZZUTO, Nicolo'
 Distribuzione geografica
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Continente #
NA - Nord America 15.607
EU - Europa 13.344
AS - Asia 8.792
SA - Sud America 1.043
AF - Africa 166
OC - Oceania 28
Continente sconosciuto - Info sul continente non disponibili 14
Totale 38.994
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Nazione #
US - Stati Uniti d'America 15.425
RU - Federazione Russa 4.146
SG - Singapore 3.838
GB - Regno Unito 3.648
CN - Cina 2.787
IT - Italia 1.081
SE - Svezia 1.030
FR - Francia 909
BR - Brasile 857
FI - Finlandia 693
HK - Hong Kong 689
DE - Germania 665
VN - Vietnam 615
IE - Irlanda 563
KR - Corea 307
UA - Ucraina 283
CA - Canada 93
IN - India 93
BD - Bangladesh 83
TR - Turchia 76
AR - Argentina 69
NL - Olanda 64
MX - Messico 52
JP - Giappone 49
BE - Belgio 46
NG - Nigeria 45
PL - Polonia 39
ES - Italia 38
ZA - Sudafrica 38
IQ - Iraq 34
ID - Indonesia 30
CL - Cile 26
AU - Australia 24
CO - Colombia 22
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
UZ - Uzbekistan 12
EU - Europa 11
MA - Marocco 11
JO - Giordania 10
LB - Libano 10
PH - Filippine 10
RO - Romania 10
TN - Tunisia 10
AL - Albania 9
BO - Bolivia 9
DZ - Algeria 9
DO - Repubblica Dominicana 8
GR - Grecia 8
HU - Ungheria 8
MY - Malesia 8
PE - Perù 8
PY - Paraguay 8
BG - Bulgaria 7
CR - Costa Rica 7
KG - Kirghizistan 7
LV - Lettonia 7
OM - Oman 7
UY - Uruguay 7
CZ - Repubblica Ceca 6
KZ - Kazakistan 6
SN - Senegal 6
AE - Emirati Arabi Uniti 5
CI - Costa d'Avorio 5
NO - Norvegia 5
DK - Danimarca 4
EE - Estonia 4
HR - Croazia 4
PA - Panama 4
TH - Thailandia 4
AM - Armenia 3
ET - Etiopia 3
LK - Sri Lanka 3
NI - Nicaragua 3
PT - Portogallo 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
HN - Honduras 2
JM - Giamaica 2
MN - Mongolia 2
MU - Mauritius 2
NZ - Nuova Zelanda 2
RS - Serbia 2
SK - Slovacchia (Repubblica Slovacca) 2
TW - Taiwan 2
Totale 38.960
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Città #
Southend 3.143
Jacksonville 2.353
Singapore 2.106
Chandler 1.466
Ashburn 1.411
San Jose 1.372
Moscow 1.237
Woodbridge 1.163
Dallas 1.131
Ann Arbor 742
Hong Kong 683
Houston 636
Dublin 562
Verona 426
The Dalles 357
Beijing 323
New York 299
Los Angeles 290
Wilmington 276
Lawrence 263
Princeton 263
Nanjing 252
Jinan 233
Ho Chi Minh City 221
Shenyang 189
Buffalo 183
Sindelfingen 157
Hanoi 141
Hebei 139
Council Bluffs 137
Tianjin 124
Helsinki 114
Milan 106
Boardman 104
Munich 99
Nanchang 91
Santa Clara 86
Changsha 85
Ningbo 85
Zhengzhou 80
Hangzhou 77
São Paulo 76
Columbus 74
Haikou 72
Philadelphia 71
Taizhou 71
Guangzhou 69
Jiaxing 64
Orem 60
Redondo Beach 59
Lancaster 58
Taiyuan 53
San Francisco 51
Seattle 49
Turku 49
Chicago 48
Abuja 42
Rio de Janeiro 42
Brussels 41
Auburn Hills 40
London 40
Tokyo 40
Fuzhou 37
Seoul 36
Warsaw 35
Denver 34
Frankfurt am Main 34
Brooklyn 33
Chennai 33
Da Nang 33
Lanzhou 33
Falls Church 31
Istanbul 30
Montreal 30
Norwalk 30
Fairfield 29
Detroit 28
Rome 27
Dearborn 26
Toronto 24
Stockholm 23
Washington 23
Atlanta 22
Belo Horizonte 21
Boston 20
Curitiba 20
Haiphong 20
Johannesburg 20
Kent 19
Redwood City 19
Cambridge 17
Clearwater 17
Amsterdam 16
Biên Hòa 16
Manchester 16
Paris 16
Phoenix 16
Brasília 15
Mumbai 15
Redmond 14
Totale 25.302
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Nome #
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 284
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 269
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 268
Complement-mediated demyelination in patients with IgM monoclonal gammopathy and polyneuropathy 263
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 261
AZT-induced mitochondrial myopathy 238
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 236
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 236
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 232
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 230
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 225
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 223
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 220
A 49-year-old man with neuropsychiatric symptoms followed by progressive cognitive decline. 219
Un caso di sclerosi multipla con esordio "tumor-like" e decorso benigno 219
[Myopathy with lipid accumulation and type-II glutaric aciduria] 218
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 218
Acute reversible paralysis in critically ill patients 215
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 214
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 213
[Hypertrophic neuropathies beginning in infancy: a study of 3 cases (author's transl)] 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. 209
[Electromyographic study of 2 cases of nystagmus-myoclonus of the velum palatinum] 207
Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton. 206
Cytoskeletal changes in cultured human fibroblasts following exposure to 2,5-hexanedione 204
Lesione bilaterale della corteccia cingolata anteriore: studio polisonnografico ad autonomico di un caso. 204
A case of multifocal CIS with unusual MRI features suggestive of Balo's concentric sclerosis 203
Binding of monoclonal anti-myelin-associated glycoprotein antibodies to human foetal peripheral neurons in culture 202
[Alzheimer's disease. Histopathological and ultrastructural study of 6 cases (author's transl)] 202
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 200
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 196
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 195
[Oculo-facio-cervical dystonia syndrome revealed by plurisystematized degeneration of the central nervous system with pallidoreticular pigmentary condition] 193
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 193
T-cell cytotoxicity of human Schwann cells: TNFalpha promotes fasL-mediated apoptosis and IFN gamma perforin-mediated lysis 192
[Seitelberger's infantile neuroaxonal dystrophy: anatomoclinical study of a sibling group] 189
Congenital hypomyelination neuropathy with a novel mutation of PMP22 189
Lower-limb lengthening in short stature. An electrophysiological and clinical assessment of peripheral nerve function 188
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia 188
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 186
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 186
Potenziali evocati acustici troncoencefalici e rilievi anatomo-patologici in un caso di sindrome di Wallenberg 185
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 185
BAEP and autopsy findings in Wallenberg syndrome 184
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 184
Clinical features of Kleine-Levin syndrome with localized encephalitis 183
[Hereditary sensory neuropathies with acrodystrophic lesions. Nosographic considerations] 183
Dysmyelinating neuropathies of infancy: defined and undefined forms 183
Gene dosage sensitivity of a novel mutation in the intracellular domain of P0 associated with Charcot-Marie-Tooth disease type 1B 182
Botulinum toxin for the treatment of genital pain syndromes 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
[On a peculiar form of Creutzfeldt-Jakob disease, with anatomo-clinical dissociation] 180
Cerebral amyloidoses: molecular pathways and therapeutic challenges 180
Glial cell and macrophage reactions in rat spinal ganglion after peripheral nerve lesions: an immuno-cytochemical and morphometric study 179
Blood lymphocytes in neuronal ceroid lipofuscinosis 177
An unusual case of meningeal gliomatosis 176
[Spino-olivo-cerebello-nigral degeneration. Study of a case begining in infancy] 174
Eclamptic encephalopathy: imaging and pathogenetic considerations 174
[Diffuse sclerosis. Anatomo-clinical study of a subacute case with a striated demyelination] 174
Congenital toxoplasmosis: histological and ultrastructural study 174
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 174
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 174
[Histopathologic and ultrastructural study of various amputation neuromas] 173
Amyotrophy in Shy-Drager syndrome. 173
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 173
Three-dimensional Structure of the Transthyretin (TTR) Phe64Leu Variant 173
Identification of distinct N-terminal truncated forms of prion protein in different Creutzfeldt-Jakob disease subtypes. 173
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 172
A novel missense mutation in the L1CAM gene in a boy with L1-disease. 172
Hepatitis C virus infection of peripheral nerves in type II cryoglobulinaemia 170
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 170
Brain metastases from post-radiation malignant peripheral nerve sheath tumour 170
[4 cases of Jakob-Creutzfeldt's disease] 169
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 169
pH-dependent prion protein conformation in classical Creutzfeldt-Jakob disease 169
Inherited neuroaxonal dystrophy in C6 deficient rabbits 168
T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathy 168
Friedreich's ataxia. A light- and electron microscopic study of peripheral nerve biopsies 167
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 167
Gonosomal mosaicism of a novel heterozygous mutation of P0 causes Charcot-Marie-Tooth neuropathy type 1B with apparent autosomal recessive inheritance 166
Satellite cells and interstitial macrophages activation in rat dorsal root ganglia following peripheral nerve lesions 166
T-cell anti-apoptotic mechanisms in inflammatory myopathies 166
Impaired heteronymous somatosensory motor cortical inhibition in dystonia 165
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 165
Prosopagnosia. Report of four cases 164
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 164
Adhesion molecules expression on the vascular endothelium of peripheral nerve in HIV-associated Distal Sensory Polyneuropathy 163
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 163
A somatic and germline mosaic mutation in MPZ/P0 mimics recessive inheritance of CMT1B 163
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 161
Epilepsy in glioblastoma multiforme: correlation with glutamine synthetase levels. 161
Effetti della luce laser He-Ne sulla rigenerazione assonale del nervo safeno di ratto sottoposto a neurotmesi e neurorrafia. 161
The role of muscle biopsy in investigating isolated muscle pain 161
Splicing mutation causes infantile Sandhoff disease 160
PMP22 related congenital hypomyelination neuropathy 160
[Cerebral calcinosis in postoperative hypoparathyroidism. Presentation of an anatomo-clinical case] 159
[Flaccid paralysis of the foot in rolandic parasagittal tumors] 159
[Myoclonic form of Hallervorden-Spatz disease. Clinical aspect simulating a subacute spongiform encephalitis] 159
Atypical Alzheimer's disease: a case report. 159
Human peripheral nerve macrophages in normal and pathological conditions 158
Totale 18.910
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Categoria #
all - tutte 125.672
article - articoli 110.295
book - libri 0
conference - conferenze 8.938
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 6.439
Totale 251.344
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021105 0 0 0 0 0 0 0 0 0 0 0 105
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
2025/202613.688 1.078 817 1.136 2.047 3.428 982 1.291 609 1.197 707 200 196
Totale 39.150