CATALOGO DEI PRODOTTI DELLA RICERCA

SIMONATI, Alessandro
 Distribuzione geografica
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Continente #
EU - Europa 6.663
NA - Nord America 6.654
AS - Asia 4.341
SA - Sud America 681
AF - Africa 45
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 8
Totale 18.402
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Nazione #
US - Stati Uniti d'America 6.570
RU - Federazione Russa 2.295
SG - Singapore 2.001
GB - Regno Unito 1.290
CN - Cina 1.287
IT - Italia 853
BR - Brasile 575
FR - Francia 455
SE - Svezia 408
HK - Hong Kong 378
FI - Finlandia 358
DE - Germania 343
IE - Irlanda 336
VN - Vietnam 282
KR - Corea 141
UA - Ucraina 126
CA - Canada 41
BE - Belgio 38
NL - Olanda 38
AR - Argentina 35
IN - India 32
ID - Indonesia 30
AT - Austria 29
BD - Bangladesh 28
TR - Turchia 25
JP - Giappone 23
IQ - Iraq 22
MX - Messico 22
PL - Polonia 20
EC - Ecuador 19
ES - Italia 15
ZA - Sudafrica 14
CO - Colombia 13
CL - Cile 11
PK - Pakistan 10
IL - Israele 9
PY - Paraguay 9
LB - Libano 8
LT - Lituania 8
LV - Lettonia 8
VE - Venezuela 8
CH - Svizzera 7
KE - Kenya 7
SA - Arabia Saudita 7
UY - Uruguay 7
UZ - Uzbekistan 7
AE - Emirati Arabi Uniti 6
AZ - Azerbaigian 6
EU - Europa 6
RO - Romania 6
AU - Australia 5
CR - Costa Rica 5
IR - Iran 5
MA - Marocco 5
NP - Nepal 5
JO - Giordania 4
MD - Moldavia 4
TG - Togo 4
TN - Tunisia 4
BG - Bulgaria 3
BY - Bielorussia 3
CZ - Repubblica Ceca 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
JM - Giamaica 3
MT - Malta 3
OM - Oman 3
PA - Panama 3
PE - Perù 3
PH - Filippine 3
SY - Repubblica araba siriana 3
AL - Albania 2
DZ - Algeria 2
EG - Egitto 2
GR - Grecia 2
HR - Croazia 2
KG - Kirghizistan 2
KZ - Kazakistan 2
LK - Sri Lanka 2
NZ - Nuova Zelanda 2
SN - Senegal 2
TH - Thailandia 2
TT - Trinidad e Tobago 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AM - Armenia 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BH - Bahrain 1
BJ - Benin 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CG - Congo 1
CI - Costa d'Avorio 1
EE - Estonia 1
ET - Etiopia 1
GE - Georgia 1
GT - Guatemala 1
HN - Honduras 1
HT - Haiti 1
IS - Islanda 1
Totale 18.390
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Città #
Southend 1.134
Jacksonville 1.078
Singapore 988
Chandler 755
Moscow 655
Woodbridge 617
Dallas 525
Ann Arbor 430
Ashburn 384
Hong Kong 378
Dublin 336
Houston 277
Beijing 197
Verona 160
Lawrence 158
Princeton 158
Wilmington 154
The Dalles 138
Los Angeles 127
Nanjing 110
Jinan 104
New York 92
Ho Chi Minh City 90
Sindelfingen 88
Shenyang 79
Redmond 78
Buffalo 66
Milan 65
Helsinki 63
Hanoi 54
Hebei 52
Columbus 46
Nanchang 46
São Paulo 44
Ningbo 43
Tianjin 43
Changsha 42
Redondo Beach 38
Jiaxing 35
Boardman 33
Hangzhou 33
Zhengzhou 33
Seoul 32
Santa Clara 31
Munich 30
Brussels 27
Brooklyn 26
Denver 25
Guangzhou 25
Haikou 24
Rio de Janeiro 24
Dong Ket 23
Seattle 21
Bologna 20
Taiyuan 19
Taizhou 19
Tokyo 19
Vienna 19
Warsaw 19
Jakarta 18
Norwalk 18
Nuremberg 17
Redwood City 17
Rome 17
Belo Horizonte 15
Council Bluffs 15
Da Nang 15
Detroit 15
Kent 15
Chicago 14
Philadelphia 14
Phoenix 14
Lancaster 13
Orem 13
San Francisco 13
Toronto 13
Turku 13
Brasília 12
Lanzhou 12
Lappeenranta 12
London 12
Naples 12
Atlanta 11
Auburn Hills 11
Fuzhou 11
Waanrode 11
Falls Church 10
Chennai 9
Guarulhos 9
Haiphong 9
Montreal 9
San Diego 9
Stockholm 9
Washington 9
Biên Hòa 8
Boston 8
Porto Alegre 8
Riva 8
Curitiba 7
Dhaka 7
Totale 10.921
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Nome #
Encefalopatie eredo-degenerative in età evolutiva 421
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 257
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 248
Cerebral cortex three-dimensional profiling in human fetuses by magnetic resonance imaging 217
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 205
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 198
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing loss 179
Congenital hypomyelination neuropathy with a novel mutation of PMP22 175
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 173
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 172
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 169
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 168
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 165
Diagnostic methods and emerging treatments for adult neuronal ceroid lipofuscinoses (Kufs disease) 161
Dysmyelinating neuropathies of infancy: defined and undefined forms 161
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 160
AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders. 160
Blood lymphocytes in neuronal ceroid lipofuscinosis 159
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 159
An unusual case of meningeal gliomatosis 156
A novel nonsense mutation (Q509X) in three Italian Late infantile neuronal ceroid-lipofuscinosis children 156
A novel missense mutation in the L1CAM gene in a boy with L1-disease. 155
Clinical features of Kleine-Levin syndrome with localized encephalitis 153
Protocollo assistenziale di minima della Neurofibromatosi tipo 1 (NF1) 153
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 153
Congenital toxoplasmosis: histological and ultrastructural study 151
Transcriptomic profiling discloses molecular and cellular events related to neuronal differentiation in SH-SY5Y neuroblastoma cells 151
C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation. 150
Quantitative analysis of PPT1 interactome in human neuroblastoma cells 148
The role of muscle biopsy in investigating isolated muscle pain 146
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 146
The networks of genes encoding palmitoylated proteins in axonal and synaptic compartments are affected in PPT1 overexpressing neuronal-like cells 145
Age and sex prevalence estimate of Joubert syndrome in Italy 143
Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD 141
Chapter 22 - Ataxia in mitochondrial disorders. 140
Functional transcriptome analysis in ARSACS KO cell model reveals a role of sacsin in autophagy 140
PMP22 related congenital hypomyelination neuropathy 139
Unexpected subacute leucoencephalopathy following intrathecal methotrexate and cytarabine administration in a patient homozygous for MTHFR 677C→T polymorphism. 139
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 139
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 136
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 135
Sarcoidosis and inclusion body myositis. 132
Hexacarbon axonopathy: the morphological expression of altered cytoskeletal translocation. 131
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 130
Le anomalie della migrazione neuronale. 129
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria 127
Involvement of the mitochondrial compartment in human NCL fibroblasts. 126
Anatomia normale del lobo temporale:approccio morfologico mediante studio per immagini 123
MELAS: clinical phenotypes and morphological brain abnormalities 123
Neuropatie immunitarie ed infiammatorie. 123
Multicystic encephalomalacia associated with symmetrical necrotizing brain stem lesions in an infant: a case report 120
Neuropathology of mitochondrial diseases 120
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. 119
Chronic inflammatory demyelinating polyneuropathy 117
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy. 117
Ponto-cerebellar hypoplasia with dystonia: Clinico-pathological findings in a sporadic case 116
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5 116
Changes in terminal sprout formation in rat sternocostalis muscle during chronic intoxication with 2,5 hexanedione 115
Proteomic profiling in the brain of CLN1 disease model reveals affected functional modules 115
Selected aspects of peripheral nerve pathology. 114
Stiff-man syndrome associated with nocturnal myoclonus and epilepsy 113
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 113
Early white matter involvement in an infant carrying a novel mutation in ACOX1 113
Cerebro-ocular dysplasia and muscular dystrophy: report of two cases 112
Neurotoxic effects of 2,5-hexanedione in rats: Early morphological and functional changes in nerve fibres and neuromuscular junctions 112
High-field-magnetic resonance imaging of the developing human brain from the 10th to the 16th week of gestational age 111
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 111
Neuronal ceroid lipofuscinosis: the increasing spectrum of an old disease. 111
Clinical, ultrastructural, and molecular studies in a patient with Kufs disease 110
Neuropatie immunitarie. 109
NCL diseases - clinical perspectives. 108
Novel CLN1 mutation in two Italian sibs with late-infantile ceroid lipofuscinosis 107
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 106
Neuronal ceroid lipofuscinoses : many players, and more to come 106
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 105
La tomografia computerizzata nella diagnostica delle paralisi cerebrali infantili 104
Choroid plexus papilloma of the cerebello-pontine angle 104
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 104
The effects of 2,5-hexanedione on axonal regeneration after nerve crush in the rat 103
Mechanisms of corticogenesis: cell proliferation and death in the developing human central nervous system 103
Le neuropatie genetiche. Inquadramento fisiopatologico e clinico 102
Peripheral neuropathies associated with coeliac disease 102
CLN8 is an endoplasmic reticulum cargo receptor that regulates lysosome biogenesis 102
Gliomatosis cerebri diffusa. A case report 101
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 101
Human pathology in NCL. 101
A novel IRF2BPL truncating variant is associated with endolysosomal storage 101
Neurotoxic action of 2,5-hexanedione on the autonomic nervous system: ultrastructural and functional alterations in the rat sympathetic superior cervical ganglion 100
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: another genetic hit in the Mediterranean 100
Peripheral nerve allograft for nerve repair 99
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 99
La patologia delle neuropatie periferiche. 99
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. 99
Electrophysiological profile remodeling via selective suppression of voltage-gated currents by CLN1/PPT1 overexpression in human neuronal-like cells 99
Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs disease. 99
Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome. 98
Lysosomal proteomics links disturbances in lipid homeostasis and sphingolipid metabolism to CLN5 disease 98
Le neuropatie genetiche 97
TSEN54 mutation in a child with pontocerebellar hypoplasia type 1. 97
Pontine tegmental cap dysplasia: developmental and cognitive outcome in three adolescent patients. 97
Totale 13.391
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Categoria #
all - tutte 65.110
article - articoli 56.063
book - libri 0
conference - conferenze 1.328
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 7.719
Totale 130.220
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021708 0 0 0 0 0 141 35 124 135 26 174 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
2025/20265.277 607 505 560 1.184 1.920 501 0 0 0 0 0 0
Totale 18.550