CATALOGO DEI PRODOTTI DELLA RICERCA

SIMONATI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 9.871
EU - Europa 7.115
AS - Asia 5.125
SA - Sud America 800
Continente sconosciuto - Info sul continente non disponibili 166
AF - Africa 101
OC - Oceania 11
Totale 23.189
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Nazione #
US - Stati Uniti d'America 9.596
RU - Federazione Russa 2.309
SG - Singapore 2.278
CN - Cina 1.378
GB - Regno Unito 1.320
IT - Italia 1.171
BR - Brasile 644
FR - Francia 468
VN - Vietnam 438
SE - Svezia 409
HK - Hong Kong 405
FI - Finlandia 368
DE - Germania 359
IE - Irlanda 338
KR - Corea 191
UA - Ucraina 134
CA - Canada 130
BD - Bangladesh 96
IN - India 57
NL - Olanda 46
AR - Argentina 43
BE - Belgio 39
ID - Indonesia 37
TR - Turchia 31
AT - Austria 30
MX - Messico 30
EC - Ecuador 28
JP - Giappone 28
IL - Israele 26
IQ - Iraq 25
NG - Nigeria 25
PL - Polonia 25
ES - Italia 23
ZA - Sudafrica 23
CR - Costa Rica 22
CO - Colombia 20
VE - Venezuela 20
PK - Pakistan 19
CL - Cile 17
UZ - Uzbekistan 14
GT - Guatemala 13
NI - Nicaragua 13
PR - Porto Rico 13
HN - Honduras 12
LT - Lituania 11
PY - Paraguay 11
SA - Arabia Saudita 11
CW - ???statistics.table.value.countryCode.CW??? 10
JM - Giamaica 10
SV - El Salvador 10
LB - Libano 9
LV - Lettonia 9
MA - Marocco 9
TT - Trinidad e Tobago 9
UY - Uruguay 9
CH - Svizzera 8
KE - Kenya 8
MY - Malesia 8
AE - Emirati Arabi Uniti 7
AZ - Azerbaigian 7
JO - Giordania 7
NP - Nepal 7
PH - Filippine 7
AL - Albania 6
EU - Europa 6
OM - Oman 6
RO - Romania 6
SC - Seychelles 6
TN - Tunisia 6
AU - Australia 5
BO - Bolivia 5
EG - Egitto 5
IR - Iran 5
KZ - Kazakistan 5
BG - Bulgaria 4
BY - Bielorussia 4
MD - Moldavia 4
PA - Panama 4
SN - Senegal 4
TG - Togo 4
TH - Thailandia 4
CZ - Repubblica Ceca 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
EE - Estonia 3
GE - Georgia 3
GR - Grecia 3
HR - Croazia 3
MT - Malta 3
NZ - Nuova Zelanda 3
PE - Perù 3
SY - Repubblica araba siriana 3
DZ - Algeria 2
ET - Etiopia 2
HT - Haiti 2
KG - Kirghizistan 2
LC - Santa Lucia 2
LK - Sri Lanka 2
PS - Palestinian Territory 2
A2 - ???statistics.table.value.countryCode.A2??? 1
Totale 23.015
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Città #
Singapore 1.227
Ashburn 1.216
Southend 1.134
Jacksonville 1.083
San Jose 909
Chandler 755
Moscow 655
Woodbridge 617
Dallas 544
Ann Arbor 430
Hong Kong 400
Verona 348
Dublin 337
Houston 287
Council Bluffs 279
The Dalles 246
Beijing 217
Lawrence 158
Princeton 158
Wilmington 154
Los Angeles 146
Ho Chi Minh City 141
New York 114
Nanjing 110
Jinan 104
Hanoi 90
Sindelfingen 88
Milan 82
Buffalo 80
Shenyang 79
Redmond 78
Santa Clara 77
Helsinki 73
São Paulo 72
Hebei 52
Columbus 47
Nanchang 46
Tianjin 44
Ningbo 43
Changsha 42
Redondo Beach 38
Orem 37
Boardman 36
Jiaxing 35
Brooklyn 33
Hangzhou 33
Zhengzhou 33
Annandale 32
Seoul 32
Munich 31
Rome 31
Las Vegas 29
Brussels 28
Denver 28
Guangzhou 26
Rio de Janeiro 26
Abuja 25
Chicago 25
Toronto 25
Da Nang 24
Haikou 24
Montreal 24
Tokyo 24
Bologna 23
Dong Ket 23
Seattle 23
Warsaw 23
London 21
Philadelphia 21
Detroit 20
Jakarta 20
Naples 19
Norwalk 19
Phoenix 19
San Francisco 19
Taiyuan 19
Taizhou 19
Vienna 19
Atlanta 18
Belo Horizonte 18
Frankfurt am Main 18
San José 18
Nuremberg 17
Redwood City 17
Chennai 16
Brasília 15
Haiphong 15
Kent 15
Lancaster 15
Turku 13
Johannesburg 12
Lanzhou 12
Lappeenranta 12
Managua 12
North Bergen 12
Auburn Hills 11
Dhaka 11
Fuzhou 11
San Diego 11
Waanrode 11
Totale 14.058
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Nome #
Encefalopatie eredo-degenerative in età evolutiva 453
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 288
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 279
Cerebral cortex three-dimensional profiling in human fetuses by magnetic resonance imaging 276
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 243
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 237
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 218
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 209
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing loss 208
AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders. 208
Dysmyelinating neuropathies of infancy: defined and undefined forms 205
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 204
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
Congenital hypomyelination neuropathy with a novel mutation of PMP22 201
Clinical features of Kleine-Levin syndrome with localized encephalitis 199
Age and sex prevalence estimate of Joubert syndrome in Italy 195
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 193
A novel nonsense mutation (Q509X) in three Italian Late infantile neuronal ceroid-lipofuscinosis children 191
Diagnostic methods and emerging treatments for adult neuronal ceroid lipofuscinoses (Kufs disease) 191
Protocollo assistenziale di minima della Neurofibromatosi tipo 1 (NF1) 189
Congenital toxoplasmosis: histological and ultrastructural study 188
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. 188
Transcriptomic profiling discloses molecular and cellular events related to neuronal differentiation in SH-SY5Y neuroblastoma cells 188
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 188
A novel missense mutation in the L1CAM gene in a boy with L1-disease. 187
An unusual case of meningeal gliomatosis 186
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 186
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 185
Unexpected subacute leucoencephalopathy following intrathecal methotrexate and cytarabine administration in a patient homozygous for MTHFR 677C→T polymorphism. 185
Blood lymphocytes in neuronal ceroid lipofuscinosis 184
The networks of genes encoding palmitoylated proteins in axonal and synaptic compartments are affected in PPT1 overexpressing neuronal-like cells 184
C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation. 182
Functional transcriptome analysis in ARSACS KO cell model reveals a role of sacsin in autophagy 181
Hexacarbon axonopathy: the morphological expression of altered cytoskeletal translocation. 179
PMP22 related congenital hypomyelination neuropathy 176
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 173
Quantitative analysis of PPT1 interactome in human neuroblastoma cells 173
The role of muscle biopsy in investigating isolated muscle pain 171
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 170
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 169
Chapter 22 - Ataxia in mitochondrial disorders. 168
Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD 165
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 164
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 162
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria 160
Neuropatie immunitarie ed infiammatorie. 158
Anatomia normale del lobo temporale:approccio morfologico mediante studio per immagini 156
Sarcoidosis and inclusion body myositis. 153
Neurotoxic effects of 2,5-hexanedione in rats: Early morphological and functional changes in nerve fibres and neuromuscular junctions 153
Le anomalie della migrazione neuronale. 151
Neuropathology of mitochondrial diseases 151
Involvement of the mitochondrial compartment in human NCL fibroblasts. 150
Early white matter involvement in an infant carrying a novel mutation in ACOX1 149
Neuronal ceroid lipofuscinosis: the increasing spectrum of an old disease. 148
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 147
NCL diseases - clinical perspectives. 147
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. 146
MELAS: clinical phenotypes and morphological brain abnormalities 145
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy. 144
Ponto-cerebellar hypoplasia with dystonia: Clinico-pathological findings in a sporadic case 143
Multicystic encephalomalacia associated with symmetrical necrotizing brain stem lesions in an infant: a case report 143
Selected aspects of peripheral nerve pathology. 143
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5 143
Availability, accessibility and delivery to patients of the 28 orphan medicines approved by the European Medicine Agency for hereditary metabolic diseases in the MetabERN network 143
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 142
Proteomic profiling in the brain of CLN1 disease model reveals affected functional modules 142
Changes in terminal sprout formation in rat sternocostalis muscle during chronic intoxication with 2,5 hexanedione 141
Disease characteristics and progression in patients with late-infantile neuronal ceroid lipofuscinosis type 2 (CLN2) disease: an observational cohort study 140
Stiff-man syndrome associated with nocturnal myoclonus and epilepsy 138
Cerebro-ocular dysplasia and muscular dystrophy: report of two cases 137
Le neuropatie genetiche. Inquadramento fisiopatologico e clinico 136
Peripheral nerve allograft for nerve repair 136
Chronic inflammatory demyelinating polyneuropathy 134
Mechanisms of corticogenesis: cell proliferation and death in the developing human central nervous system 134
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 134
Choroid plexus papilloma of the cerebello-pontine angle 134
CLN8 is an endoplasmic reticulum cargo receptor that regulates lysosome biogenesis 134
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. 133
Gliomatosis cerebri diffusa. A case report 132
High-field-magnetic resonance imaging of the developing human brain from the 10th to the 16th week of gestational age 132
Clinical, ultrastructural, and molecular studies in a patient with Kufs disease 132
Proteomic analysis of the palmitoyl protein thioesterase 1 interactome in SH-SY5Y human neuroblastoma cells. 131
Novel CLN1 mutation in two Italian sibs with late-infantile ceroid lipofuscinosis 131
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 130
Survey on treatments for primary headaches in 13 specialized juvenile Headache Centers: The first multicenter Italian study 130
The effects of 2,5-hexanedione on axonal regeneration after nerve crush in the rat 129
Neuronal ceroid lipofuscinoses : many players, and more to come 129
Lysosomal proteomics links disturbances in lipid homeostasis and sphingolipid metabolism to CLN5 disease 129
La valutazione neuropatologica nella malattia di Alzheimer (AD): correlazioni con il quadro clinico ed analisi delle problematiche 128
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 128
Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome. 128
Human pathology in NCL. 128
A novel IRF2BPL truncating variant is associated with endolysosomal storage 128
Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs disease. 127
Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6. 126
Electrophysiological profile remodeling via selective suppression of voltage-gated currents by CLN1/PPT1 overexpression in human neuronal-like cells 126
Spinal cord lesions 125
Neuropatie immunitarie. 125
Peripheral neuropathies associated with coeliac disease 124
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 124
Totale 16.582
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Categoria #
all - tutte 82.403
article - articoli 70.994
book - libri 0
conference - conferenze 1.672
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 9.737
Totale 164.806
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022624 0 0 0 0 32 41 15 103 48 41 99 245
2022/20232.314 194 179 267 385 222 521 20 153 259 16 66 32
2023/2024970 58 98 79 150 133 109 35 45 9 42 135 77
2024/20252.900 185 203 89 496 169 55 147 134 480 200 192 550
2025/20268.067 607 505 560 1.184 1.920 558 734 456 782 410 162 189
2026/20271.849 114 233 372 1.027 103 0 0 0 0 0 0 0
Totale 23.189