CATALOGO DEI PRODOTTI DELLA RICERCA

SIMONATI, Alessandro
 Distribuzione geografica
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Continente #
EU - Europa 6.661
NA - Nord America 6.622
AS - Asia 4.223
SA - Sud America 675
AF - Africa 43
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 8
Totale 18.242
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Nazione #
US - Stati Uniti d'America 6.539
RU - Federazione Russa 2.295
SG - Singapore 1.927
GB - Regno Unito 1.290
CN - Cina 1.278
IT - Italia 853
BR - Brasile 570
FR - Francia 455
SE - Svezia 408
HK - Hong Kong 378
FI - Finlandia 358
DE - Germania 343
IE - Irlanda 336
VN - Vietnam 257
KR - Corea 141
UA - Ucraina 125
CA - Canada 41
BE - Belgio 38
NL - Olanda 37
AR - Argentina 34
IN - India 31
ID - Indonesia 30
AT - Austria 29
BD - Bangladesh 28
TR - Turchia 24
JP - Giappone 22
IQ - Iraq 21
MX - Messico 21
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
LT - Lituania 8
LV - Lettonia 8
VE - Venezuela 8
CH - Svizzera 7
KE - Kenya 7
LB - Libano 7
SA - Arabia Saudita 7
UY - Uruguay 7
UZ - Uzbekistan 7
EU - Europa 6
RO - Romania 6
AE - Emirati Arabi Uniti 5
AU - Australia 5
CR - Costa Rica 5
IR - Iran 5
MA - Marocco 5
NP - Nepal 5
AZ - Azerbaigian 4
JO - Giordania 4
MD - Moldavia 4
TG - Togo 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
TN - Tunisia 3
AL - Albania 2
DZ - Algeria 2
EG - Egitto 2
GR - Grecia 2
HR - Croazia 2
KZ - Kazakistan 2
LK - Sri Lanka 2
NZ - Nuova Zelanda 2
SN - Senegal 2
SY - Repubblica araba siriana 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
GE - Georgia 1
GT - Guatemala 1
HN - Honduras 1
HT - Haiti 1
IS - Islanda 1
KG - Kirghizistan 1
KI - Kiribati 1
Totale 18.231
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Città #
Southend 1.134
Jacksonville 1.078
Singapore 914
Chandler 755
Moscow 655
Woodbridge 617
Dallas 525
Ann Arbor 430
Ashburn 381
Hong Kong 378
Dublin 336
Houston 277
Beijing 197
Verona 160
Lawrence 158
Princeton 158
Wilmington 154
Los Angeles 127
The Dalles 114
Nanjing 110
Jinan 104
New York 92
Sindelfingen 88
Ho Chi Minh City 84
Shenyang 79
Redmond 78
Buffalo 66
Milan 65
Helsinki 63
Hebei 52
Hanoi 50
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
Haikou 24
Rio de Janeiro 24
Dong Ket 23
Guangzhou 23
Seattle 21
Bologna 20
Taiyuan 19
Taizhou 19
Vienna 19
Warsaw 19
Jakarta 18
Norwalk 18
Tokyo 18
Nuremberg 17
Redwood City 17
Rome 17
Council Bluffs 15
Detroit 15
Kent 15
Belo Horizonte 14
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
Da Nang 8
Porto Alegre 8
Riva 8
Curitiba 7
Dhaka 7
Totale 10.799
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Nome #
Encefalopatie eredo-degenerative in età evolutiva 420
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 255
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-2 202
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 196
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing loss 177
Congenital hypomyelination neuropathy with a novel mutation of PMP22 175
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
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 171
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 167
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 167
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 162
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 160
Dysmyelinating neuropathies of infancy: defined and undefined forms 160
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 158
AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders. 158
Blood lymphocytes in neuronal ceroid lipofuscinosis 157
Diagnostic methods and emerging treatments for adult neuronal ceroid lipofuscinoses (Kufs disease) 156
A novel nonsense mutation (Q509X) in three Italian Late infantile neuronal ceroid-lipofuscinosis children 154
An unusual case of meningeal gliomatosis 153
Protocollo assistenziale di minima della Neurofibromatosi tipo 1 (NF1) 153
Clinical features of Kleine-Levin syndrome with localized encephalitis 152
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 152
A novel missense mutation in the L1CAM gene in a boy with L1-disease. 152
Congenital toxoplasmosis: histological and ultrastructural study 149
Transcriptomic profiling discloses molecular and cellular events related to neuronal differentiation in SH-SY5Y neuroblastoma cells 149
C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation. 148
Quantitative analysis of PPT1 interactome in human neuroblastoma cells 145
The networks of genes encoding palmitoylated proteins in axonal and synaptic compartments are affected in PPT1 overexpressing neuronal-like cells 144
The role of muscle biopsy in investigating isolated muscle pain 144
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 143
Functional transcriptome analysis in ARSACS KO cell model reveals a role of sacsin in autophagy 140
Age and sex prevalence estimate of Joubert syndrome in Italy 140
PMP22 related congenital hypomyelination neuropathy 139
Chapter 22 - Ataxia in mitochondrial disorders. 139
Unexpected subacute leucoencephalopathy following intrathecal methotrexate and cytarabine administration in a patient homozygous for MTHFR 677C→T polymorphism. 139
Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD 138
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 137
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 135
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 132
Sarcoidosis and inclusion body myositis. 132
Hexacarbon axonopathy: the morphological expression of altered cytoskeletal translocation. 130
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 128
Le anomalie della migrazione neuronale. 127
Involvement of the mitochondrial compartment in human NCL fibroblasts. 125
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria 125
MELAS: clinical phenotypes and morphological brain abnormalities 122
Neuropatie immunitarie ed infiammatorie. 122
Anatomia normale del lobo temporale:approccio morfologico mediante studio per immagini 120
Neuropathology of mitochondrial diseases 120
Multicystic encephalomalacia associated with symmetrical necrotizing brain stem lesions in an infant: a case report 119
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. 118
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy. 117
Ponto-cerebellar hypoplasia with dystonia: Clinico-pathological findings in a sporadic case 116
Chronic inflammatory demyelinating polyneuropathy 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
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 113
Selected aspects of peripheral nerve pathology. 113
Cerebro-ocular dysplasia and muscular dystrophy: report of two cases 112
Early white matter involvement in an infant carrying a novel mutation in ACOX1 112
Stiff-man syndrome associated with nocturnal myoclonus and epilepsy 111
Neurotoxic effects of 2,5-hexanedione in rats: Early morphological and functional changes in nerve fibres and neuromuscular junctions 111
High-field-magnetic resonance imaging of the developing human brain from the 10th to the 16th week of gestational age 110
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 110
Neuronal ceroid lipofuscinosis: the increasing spectrum of an old disease. 109
Clinical, ultrastructural, and molecular studies in a patient with Kufs disease 109
Neuropatie immunitarie. 107
NCL diseases - clinical perspectives. 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
Novel CLN1 mutation in two Italian sibs with late-infantile ceroid lipofuscinosis 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
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 102
Le neuropatie genetiche. Inquadramento fisiopatologico e clinico 102
La tomografia computerizzata nella diagnostica delle paralisi cerebrali infantili 102
Mechanisms of corticogenesis: cell proliferation and death in the developing human central nervous system 102
CLN8 is an endoplasmic reticulum cargo receptor that regulates lysosome biogenesis 102
Peripheral neuropathies associated with coeliac disease 101
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 101
Gliomatosis cerebri diffusa. A case report 100
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: another genetic hit in the Mediterranean 100
Human pathology in NCL. 100
Neurotoxic action of 2,5-hexanedione on the autonomic nervous system: ultrastructural and functional alterations in the rat sympathetic superior cervical ganglion 99
Peripheral nerve allograft for nerve repair 99
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 99
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. 99
Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs disease. 99
La patologia delle neuropatie periferiche. 98
Le neuropatie genetiche 97
Disease characteristics and progression in patients with late-infantile neuronal ceroid lipofuscinosis type 2 (CLN2) disease: an observational cohort study 97
A novel IRF2BPL truncating variant is associated with endolysosomal storage 97
Lysosomal proteomics links disturbances in lipid homeostasis and sphingolipid metabolism to CLN5 disease 97
Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome. 96
Pontine tegmental cap dysplasia: developmental and cognitive outcome in three adolescent patients. 96
Electrophysiological profile remodeling via selective suppression of voltage-gated currents by CLN1/PPT1 overexpression in human neuronal-like cells 96
Totale 13.274
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Categoria #
all - tutte 64.782
article - articoli 55.782
book - libri 0
conference - conferenze 1.322
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 7.678
Totale 129.564
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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
2025/20265.117 607 505 560 1.184 1.920 341 0 0 0 0 0 0
Totale 18.390