CATALOGO DEI PRODOTTI DELLA RICERCA

SIMONATI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 8.257
EU - Europa 7.003
AS - Asia 5.060
SA - Sud America 756
AF - Africa 93
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 8
Totale 21.188
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Nazione #
US - Stati Uniti d'America 8.153
RU - Federazione Russa 2.298
SG - Singapore 2.268
CN - Cina 1.357
GB - Regno Unito 1.311
IT - Italia 1.096
BR - Brasile 616
FR - Francia 464
VN - Vietnam 435
SE - Svezia 408
HK - Hong Kong 403
FI - Finlandia 368
DE - Germania 356
IE - Irlanda 338
KR - Corea 191
UA - Ucraina 133
BD - Bangladesh 89
IN - India 55
CA - Canada 54
NL - Olanda 45
AR - Argentina 41
BE - Belgio 39
ID - Indonesia 35
TR - Turchia 31
AT - Austria 30
JP - Giappone 28
MX - Messico 26
IQ - Iraq 25
NG - Nigeria 25
PL - Polonia 24
EC - Ecuador 23
ZA - Sudafrica 22
ES - Italia 19
PK - Pakistan 18
VE - Venezuela 17
CL - Cile 16
CO - Colombia 16
UZ - Uzbekistan 14
PY - Paraguay 11
SA - Arabia Saudita 11
IL - Israele 10
LT - Lituania 10
LB - Libano 9
LV - Lettonia 9
MA - Marocco 9
CH - Svizzera 8
KE - Kenya 8
MY - Malesia 8
UY - Uruguay 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
TN - Tunisia 6
AU - Australia 5
BO - Bolivia 5
CR - Costa Rica 5
IR - Iran 5
BY - Bielorussia 4
EG - Egitto 4
JM - Giamaica 4
KZ - Kazakistan 4
MD - Moldavia 4
SN - Senegal 4
TG - Togo 4
TH - Thailandia 4
BG - Bulgaria 3
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
PA - Panama 3
PE - Perù 3
SY - Repubblica araba siriana 3
DZ - Algeria 2
ET - Etiopia 2
KG - Kirghizistan 2
LK - Sri Lanka 2
PR - Porto Rico 2
PS - Palestinian Territory 2
TT - Trinidad e Tobago 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BH - Bahrain 1
BJ - Benin 1
BN - Brunei Darussalam 1
CG - Congo 1
Totale 21.167
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Città #
Singapore 1.225
Southend 1.134
Jacksonville 1.081
Ashburn 762
San Jose 760
Chandler 755
Moscow 655
Woodbridge 617
Dallas 534
Ann Arbor 430
Hong Kong 398
Verona 348
Dublin 337
Houston 278
The Dalles 244
Beijing 205
Lawrence 158
Princeton 158
Wilmington 154
Ho Chi Minh City 140
Los Angeles 140
Council Bluffs 134
Nanjing 110
New York 107
Jinan 104
Hanoi 89
Sindelfingen 88
Shenyang 79
Redmond 78
Buffalo 75
Milan 74
Helsinki 73
São Paulo 55
Hebei 52
Santa Clara 48
Columbus 46
Nanchang 46
Tianjin 44
Ningbo 43
Changsha 42
Redondo Beach 38
Boardman 36
Jiaxing 35
Orem 35
Hangzhou 33
Zhengzhou 33
Seoul 32
Munich 31
Brussels 28
Brooklyn 27
Denver 26
Guangzhou 26
Abuja 25
Rio de Janeiro 25
Da Nang 24
Haikou 24
Tokyo 24
Dong Ket 23
Warsaw 23
Rome 22
Seattle 21
Bologna 20
Jakarta 20
Taiyuan 19
Taizhou 19
Vienna 19
Chicago 18
Frankfurt am Main 18
Norwalk 18
Belo Horizonte 17
London 17
Nuremberg 17
Redwood City 17
Chennai 16
Philadelphia 16
Toronto 16
Detroit 15
Haiphong 15
Kent 15
Phoenix 14
San Francisco 14
Atlanta 13
Brasília 13
Lancaster 13
Naples 13
Turku 13
Johannesburg 12
Lanzhou 12
Lappeenranta 12
Montreal 12
Auburn Hills 11
Fuzhou 11
Waanrode 11
Dhaka 10
Falls Church 10
San Diego 10
Tashkent 10
Boston 9
Curitiba 9
Guarulhos 9
Totale 13.044
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Nome #
Encefalopatie eredo-degenerative in età evolutiva 434
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 268
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 261
Cerebral cortex three-dimensional profiling in human fetuses by magnetic resonance imaging 257
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 232
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 223
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing loss 196
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 195
AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders. 194
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 193
Congenital hypomyelination neuropathy with a novel mutation of PMP22 189
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
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
Dysmyelinating neuropathies of infancy: defined and undefined forms 183
Diagnostic methods and emerging treatments for adult neuronal ceroid lipofuscinoses (Kufs disease) 182
A novel nonsense mutation (Q509X) in three Italian Late infantile neuronal ceroid-lipofuscinosis children 180
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 180
Blood lymphocytes in neuronal ceroid lipofuscinosis 177
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 177
An unusual case of meningeal gliomatosis 176
Transcriptomic profiling discloses molecular and cellular events related to neuronal differentiation in SH-SY5Y neuroblastoma cells 176
Age and sex prevalence estimate of Joubert syndrome in Italy 175
Congenital toxoplasmosis: histological and ultrastructural study 174
C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation. 174
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. 174
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 174
The networks of genes encoding palmitoylated proteins in axonal and synaptic compartments are affected in PPT1 overexpressing neuronal-like cells 173
A novel missense mutation in the L1CAM gene in a boy with L1-disease. 172
Functional transcriptome analysis in ARSACS KO cell model reveals a role of sacsin in autophagy 170
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 169
Protocollo assistenziale di minima della Neurofibromatosi tipo 1 (NF1) 166
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 164
Quantitative analysis of PPT1 interactome in human neuroblastoma cells 164
The role of muscle biopsy in investigating isolated muscle pain 161
PMP22 related congenital hypomyelination neuropathy 160
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 160
Unexpected subacute leucoencephalopathy following intrathecal methotrexate and cytarabine administration in a patient homozygous for MTHFR 677C→T polymorphism. 160
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 160
Chapter 22 - Ataxia in mitochondrial disorders. 157
Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD 156
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 153
Hexacarbon axonopathy: the morphological expression of altered cytoskeletal translocation. 152
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 151
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria 151
Sarcoidosis and inclusion body myositis. 147
Involvement of the mitochondrial compartment in human NCL fibroblasts. 144
Neurotoxic effects of 2,5-hexanedione in rats: Early morphological and functional changes in nerve fibres and neuromuscular junctions 142
Neuropatie immunitarie ed infiammatorie. 140
Anatomia normale del lobo temporale:approccio morfologico mediante studio per immagini 139
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. 137
MELAS: clinical phenotypes and morphological brain abnormalities 136
Le anomalie della migrazione neuronale. 136
Neuronal ceroid lipofuscinosis: the increasing spectrum of an old disease. 136
Early white matter involvement in an infant carrying a novel mutation in ACOX1 136
Neuropathology of mitochondrial diseases 136
Ponto-cerebellar hypoplasia with dystonia: Clinico-pathological findings in a sporadic case 135
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy. 135
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5 134
Proteomic profiling in the brain of CLN1 disease model reveals affected functional modules 134
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 134
Changes in terminal sprout formation in rat sternocostalis muscle during chronic intoxication with 2,5 hexanedione 132
Multicystic encephalomalacia associated with symmetrical necrotizing brain stem lesions in an infant: a case report 131
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 131
Cerebro-ocular dysplasia and muscular dystrophy: report of two cases 129
NCL diseases - clinical perspectives. 129
Selected aspects of peripheral nerve pathology. 128
Stiff-man syndrome associated with nocturnal myoclonus and epilepsy 127
Clinical, ultrastructural, and molecular studies in a patient with Kufs disease 126
Chronic inflammatory demyelinating polyneuropathy 125
Neuronal ceroid lipofuscinoses : many players, and more to come 124
CLN8 is an endoplasmic reticulum cargo receptor that regulates lysosome biogenesis 124
High-field-magnetic resonance imaging of the developing human brain from the 10th to the 16th week of gestational age 123
Lysosomal proteomics links disturbances in lipid homeostasis and sphingolipid metabolism to CLN5 disease 123
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 122
Proteomic analysis of the palmitoyl protein thioesterase 1 interactome in SH-SY5Y human neuroblastoma cells. 122
Novel CLN1 mutation in two Italian sibs with late-infantile ceroid lipofuscinosis 122
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. 121
The effects of 2,5-hexanedione on axonal regeneration after nerve crush in the rat 120
Choroid plexus papilloma of the cerebello-pontine angle 120
Neuropatie immunitarie. 120
Disease characteristics and progression in patients with late-infantile neuronal ceroid lipofuscinosis type 2 (CLN2) disease: an observational cohort study 120
Peripheral neuropathies associated with coeliac disease 119
Le neuropatie genetiche. Inquadramento fisiopatologico e clinico 118
A novel IRF2BPL truncating variant is associated with endolysosomal storage 118
Electrophysiological profile remodeling via selective suppression of voltage-gated currents by CLN1/PPT1 overexpression in human neuronal-like cells 118
Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs disease. 118
Gliomatosis cerebri diffusa. A case report 117
Human pathology in NCL. 117
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 116
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 116
Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6. 116
Survey on treatments for primary headaches in 13 specialized juvenile Headache Centers: The first multicenter Italian study 116
Congenital myopathies: clinical phenotypes and new diagnostic tools 116
Neurotoxic action of 2,5-hexanedione on the autonomic nervous system: ultrastructural and functional alterations in the rat sympathetic superior cervical ganglion 115
Mechanisms of corticogenesis: cell proliferation and death in the developing human central nervous system 115
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 115
Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome. 115
Coeliac disease associated with peripheral neuropathy in a child: A case report 115
PLA2G6, encoding a phospholipase A(2), is mutated in neurodegenerative disorders with high brain iron 114
Totale 15.309
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Categoria #
all - tutte 73.956
article - articoli 63.777
book - libri 0
conference - conferenze 1.501
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 8.678
Totale 147.912
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202173 0 0 0 0 0 0 0 0 0 0 0 73
2021/20221.116 87 313 9 83 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
2025/20268.063 607 505 560 1.184 1.920 558 734 456 782 410 162 185
Totale 21.336