CATALOGO DEI PRODOTTI DELLA RICERCA

RIZZUTO, Nicolo'
 Distribuzione geografica
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Continente #
NA - Nord America 9.905
EU - Europa 8.883
AS - Asia 3.397
SA - Sud America 33
OC - Oceania 21
Continente sconosciuto - Info sul continente non disponibili 13
AF - Africa 6
Totale 22.258
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Nazione #
US - Stati Uniti d'America 9.881
GB - Regno Unito 3.523
CN - Cina 2.162
SG - Singapore 1.080
SE - Svezia 1.008
FR - Francia 867
IT - Italia 701
RU - Federazione Russa 653
FI - Finlandia 628
IE - Irlanda 557
DE - Germania 507
UA - Ucraina 262
BE - Belgio 45
NL - Olanda 43
KR - Corea 34
TR - Turchia 29
AU - Australia 20
IN - India 17
BR - Brasile 16
IR - Iran 15
ES - Italia 13
IL - Israele 13
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 22.258
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Città #
Southend 3.143
Jacksonville 2.352
Chandler 1.466
Woodbridge 1.163
Singapore 919
Ann Arbor 742
Houston 618
Dublin 557
Ashburn 482
Wilmington 276
Lawrence 263
Princeton 263
Nanjing 250
Jinan 232
Beijing 200
New York 195
Shenyang 186
Sindelfingen 157
Verona 152
Hebei 139
Tianjin 116
Boardman 104
Helsinki 98
Nanchang 90
Milan 85
Ningbo 84
Changsha 78
Zhengzhou 75
Hangzhou 74
Haikou 72
Taizhou 69
Philadelphia 67
Jiaxing 64
Lancaster 58
Guangzhou 57
Taiyuan 53
Auburn Hills 40
Brussels 40
Seattle 39
Santa Clara 38
Fuzhou 37
Los Angeles 36
Lanzhou 32
Falls Church 31
Norwalk 30
Fairfield 29
Moscow 29
Chicago 27
Detroit 27
San Francisco 27
Dearborn 26
Dallas 25
Seoul 25
Washington 20
Kent 19
Redwood City 19
Cambridge 17
Clearwater 16
Munich 16
Rome 15
Redmond 14
Riva 13
Edinburgh 12
Kemerovo 11
San Mateo 11
Bologna 10
Leawood 9
Curitiba 8
Andover 7
Bolzano 7
London 7
Melbourne 7
Palermo 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
Totale 15.922
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Nome #
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 230
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 225
Un caso di sclerosi multipla con esordio "tumor-like" e decorso benigno 176
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 154
Complement-mediated demyelination in patients with IgM monoclonal gammopathy and polyneuropathy 148
Potenziali evocati acustici troncoencefalici e rilievi anatomo-patologici in un caso di sindrome di Wallenberg 147
Malattia di Charco-Marie-Tooth. Guida alla diagnosi molecolare. 147
Lesione bilaterale della corteccia cingolata anteriore: studio polisonnografico ad autonomico di un caso. 142
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 140
Lower-limb lengthening in short stature. An electrophysiological and clinical assessment of peripheral nerve function 122
Acute reversible paralysis in critically ill patients 120
Cytoskeletal changes in cultured human fibroblasts following exposure to 2,5-hexanedione 119
Binding of monoclonal anti-myelin-associated glycoprotein antibodies to human foetal peripheral neurons in culture 119
An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy 117
Three-dimensional Structure of the Transthyretin (TTR) Phe64Leu Variant 115
AZT-induced mitochondrial myopathy 115
Splicing mutation causes infantile Sandhoff disease 114
A case of multifocal CIS with unusual MRI features suggestive of Balo's concentric sclerosis 114
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 113
Antisulfatide polyneuropathy: antibody-mediated complement attack on peripheral myelin 113
Charcot-Marie-Tooth disease type 2E, a disorder of the cytoskeleton. 113
X-linked dominant Charcot-Marie Tooth neuropathy: analysis of a pedigree with a novel mutation of connexin32 112
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 111
Cutis verticis gyrata, mental retardation and Lennox-Gastaut syndrome: a case report 110
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease. 110
Phosphorylated 14-3-3zeta protein in the CSF of neuroleptic-treated patients 108
Cytoskeletal pathology in ataxia-telangiectasia. 107
Prosopagnosia. Report of four cases 107
Congenital hypomyelination neuropathy with a novel mutation of PMP22 107
T-cell-mediated epineurial vasculitis and humoral-mediated microangiopathy in cryoglobulinemic neuropathy 107
Gene dosage sensitivity of a novel mutation in the intracellular domain of P0 associated with Charcot-Marie-Tooth disease type 1B 107
Giant axon and neurofilament accumulation in Charcot-Marie-Tooth disease type 2E 107
Clinical features of Kleine-Levin syndrome with localized encephalitis 106
A 49-year-old man with neuropsychiatric symptoms followed by progressive cognitive decline. 106
Anatomical and clinical study of a case of subacute encephalomyelitis with hyperekplexia syndrome. 106
Gonosomal mosaicism of a novel heterozygous mutation of P0 causes Charcot-Marie-Tooth neuropathy type 1B with apparent autosomal recessive inheritance 105
PMP22 related congenital hypomyelination neuropathy 105
Human skeletal muscle as a target organ of trichloroethylene toxicity. 105
Detection of pathologic prion protein in the olfactory epithelium in sporadic Creutzfeldt-Jakob disease 105
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 104
[Myopathy with lipid accumulation and type-II glutaric aciduria] 103
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 103
Neuropsychological and neuroimaging correlates in corticobasal degeneration 103
Remitting infratentorial leukoencephalopathy in a patient with HIV infection. 103
Peripheral nerve vasculitis: a clinico-pathological study 103
Cytoskeletal changes induced by 2,5-hexanedione on developing human neurons in vitro 101
Cerebral amyloidoses: molecular pathways and therapeutic challenges 101
T-cell anti-apoptotic mechanisms in inflammatory myopathies 101
Friedreich's ataxia. A light- and electron microscopic study of peripheral nerve biopsies 100
Endothelial adhesion molecule expression is unaltered in the peripheral nerve from patients with AIDS and distal sensory polyneuropathy 100
Segmental conduction abnormalities and myelin thickenings in Val102/fs null mutation of MPZ gene 100
Axillary injection of botulinum. A toxin in a patient with muscle craps associated with severe axillary hyperhydrosis 100
T-cell cytotoxicity of human Schwann cells: TNFalpha promotes fasL-mediated apoptosis and IFN gamma perforin-mediated lysis 100
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence study. 100
[Hypertrophic neuropathies beginning in infancy: a study of 3 cases (author's transl)] 99
[Alzheimer's disease. Histopathological and ultrastructural study of 6 cases (author's transl)] 99
Demyelinating polyradiculoneuritis following Coxiella burnetti infection (Q fever) 99
Glial cell and macrophage reactions in rat spinal ganglion after peripheral nerve lesions: an immuno-cytochemical and morphometric study 99
Satellite cells and interstitial macrophages activation in rat dorsal root ganglia following peripheral nerve lesions 99
Botulinum toxin for the treatment of genital pain syndromes 99
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 99
Endothelial dysfunction in mitochondrial diseases: biological and biochemical evidence of increased oxidative stress and peroxinitrite generation 99
The role of muscle biopsy in investigating isolated muscle pain 99
Programmed cell death occurs in muscle fibers with mitochondrial dysfunction 98
pH-dependent prion protein conformation in classical Creutzfeldt-Jakob disease 98
An unusual case of meningeal gliomatosis 97
Dysmyelinating neuropathies of infancy: defined and undefined forms 97
BAEP and autopsy findings in Wallenberg syndrome 96
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 96
Epilessia ed imaging 96
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 96
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 96
Antioxidant agents have a different expression pattern in muscle fibers of patients with mitochondrial diseases 96
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 95
Human peripheral nerve macrophages in normal and pathological conditions 94
[Oculo-facio-cervical dystonia syndrome revealed by plurisystematized degeneration of the central nervous system with pallidoreticular pigmentary condition] 94
Transcription factors c-Jun/activator protein-1 and nuclear factor-kappa B in oxidative stress response in mithocondrial diseases 94
Inherited neuroaxonal dystrophy in C6 deficient rabbits 93
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)) 93
[Thrombosis of the extracranial carotid caused by traumatic lesions of the soft palate in childhood] 93
[On a peculiar form of Creutzfeldt-Jakob disease, with anatomo-clinical dissociation] 93
[Seitelberger's infantile neuroaxonal dystrophy: anatomoclinical study of a sibling group] 93
Hepatitis C virus infection of peripheral nerves in type II cryoglobulinaemia 93
MELAS: clinical phenotypes and morphological brain abnormalities 93
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 93
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy 93
A novel mutation of aprataxin associated with ataxia ocular apraxia type 1: Phenotypical and genotypical characterization 93
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 92
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy 92
Further evidence that mutations in FGD4/frabin cause Charcot-Marie-Tooth disease type 4H. 92
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 92
[Histopathologic and ultrastructural study of various amputation neuromas] 91
SERCA1 and calsequestrin storage myopathy: a new surplus protein myopathy. 91
Brain metastases from post-radiation malignant peripheral nerve sheath tumour 91
Congenital toxoplasmosis: histological and ultrastructural study 91
HIV-associated PML presenting as epilepsia partialis continua 91
Effetti della luce laser He-Ne sulla rigenerazione assonale del nervo safeno di ratto sottoposto a neurotmesi e neurorrafia. 91
Motor neuron disease with pyramidal tract dysfunction involves the cortical generators of the early somatosensory evoked potential to tibial nerve stimulation 91
Complement neoantigen and vitronectin are components of plaques in amyloid AL neuropathy 90
Amyotrophy in Shy-Drager syndrome. 90
Totale 10.705
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Categoria #
all - tutte 70.853
article - articoli 62.036
book - libri 0
conference - conferenze 5.140
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 3.677
Totale 141.706
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.333 0 0 0 0 316 406 353 292 109 309 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
2024/20251.804 335 375 99 795 200 0 0 0 0 0 0 0
Totale 22.414