CATALOGO DEI PRODOTTI DELLA RICERCA

SIMONATI, Alessandro
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 7.981
EU - Europa 6.974
AS - Asia 4.996
SA - Sud America 750
AF - Africa 93
OC - Oceania 11
Continente sconosciuto - Info sul continente non disponibili 8
Totale 20.813
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 7.886
RU - Federazione Russa 2.298
SG - Singapore 2.256
CN - Cina 1.350
GB - Regno Unito 1.310
IT - Italia 1.075
BR - Brasile 612
FR - Francia 464
VN - Vietnam 435
SE - Svezia 408
HK - Hong Kong 402
FI - Finlandia 368
DE - Germania 356
IE - Irlanda 337
KR - Corea 191
UA - Ucraina 133
IN - India 55
CA - Canada 46
BD - Bangladesh 45
NL - Olanda 43
AR - Argentina 41
BE - Belgio 39
ID - Indonesia 35
TR - Turchia 31
AT - Austria 30
JP - Giappone 28
IQ - Iraq 25
MX - Messico 25
NG - Nigeria 25
PL - Polonia 24
EC - Ecuador 23
ZA - Sudafrica 22
ES - Italia 18
PK - Pakistan 18
VE - Venezuela 17
CL - Cile 16
CO - Colombia 15
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
CR - Costa Rica 5
IR - Iran 5
BO - Bolivia 4
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
GE - Georgia 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
EE - Estonia 2
ET - Etiopia 2
GR - Grecia 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 20.793
Salva come PNG Salva come JPEG
Città #
Singapore 1.224
Southend 1.134
Jacksonville 1.079
Chandler 755
Ashburn 743
San Jose 719
Moscow 655
Woodbridge 617
Dallas 530
Ann Arbor 430
Hong Kong 397
Verona 348
Dublin 337
Houston 277
The Dalles 243
Beijing 202
Lawrence 158
Princeton 158
Wilmington 154
Ho Chi Minh City 140
Los Angeles 131
Nanjing 110
Jinan 104
New York 97
Hanoi 89
Sindelfingen 88
Shenyang 79
Redmond 78
Milan 74
Helsinki 73
Buffalo 70
São Paulo 54
Hebei 52
Columbus 46
Nanchang 46
Tianjin 44
Ningbo 43
Santa Clara 43
Changsha 42
Redondo Beach 38
Boardman 36
Jiaxing 35
Orem 34
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
Seattle 21
Bologna 20
Council Bluffs 20
Jakarta 20
Rome 19
Taiyuan 19
Taizhou 19
Vienna 19
Frankfurt am Main 18
Norwalk 18
Belo Horizonte 17
Nuremberg 17
Redwood City 17
Chennai 16
London 16
Chicago 15
Detroit 15
Haiphong 15
Kent 15
Philadelphia 15
Phoenix 14
Toronto 14
Brasília 13
Lancaster 13
San Francisco 13
Turku 13
Atlanta 12
Johannesburg 12
Lanzhou 12
Lappeenranta 12
Naples 12
Auburn Hills 11
Fuzhou 11
Waanrode 11
Dhaka 10
Falls Church 10
Montreal 10
San Diego 10
Tashkent 10
Boston 9
Curitiba 9
Guarulhos 9
Totale 12.811
Salva come PNG Salva come JPEG
Nome #
Encefalopatie eredo-degenerative in età evolutiva 433
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 256
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 230
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 223
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 194
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing loss 193
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 192
AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders. 191
Congenital hypomyelination neuropathy with a novel mutation of PMP22 188
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 184
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 184
Dysmyelinating neuropathies of infancy: defined and undefined forms 181
Diagnostic methods and emerging treatments for adult neuronal ceroid lipofuscinoses (Kufs disease) 180
A novel nonsense mutation (Q509X) in three Italian Late infantile neuronal ceroid-lipofuscinosis children 178
Blood lymphocytes in neuronal ceroid lipofuscinosis 177
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 176
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 176
Clinical features of Kleine-Levin syndrome with localized encephalitis 175
Age and sex prevalence estimate of Joubert syndrome in Italy 175
An unusual case of meningeal gliomatosis 174
Congenital toxoplasmosis: histological and ultrastructural study 173
C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation. 173
Transcriptomic profiling discloses molecular and cellular events related to neuronal differentiation in SH-SY5Y neuroblastoma cells 173
A novel missense mutation in the L1CAM gene in a boy with L1-disease. 171
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 170
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 169
Functional transcriptome analysis in ARSACS KO cell model reveals a role of sacsin in autophagy 168
The networks of genes encoding palmitoylated proteins in axonal and synaptic compartments are affected in PPT1 overexpressing neuronal-like cells 167
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 163
Quantitative analysis of PPT1 interactome in human neuroblastoma cells 160
The role of muscle biopsy in investigating isolated muscle pain 160
PMP22 related congenital hypomyelination neuropathy 159
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 159
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 157
Unexpected subacute leucoencephalopathy following intrathecal methotrexate and cytarabine administration in a patient homozygous for MTHFR 677C→T polymorphism. 157
Chapter 22 - Ataxia in mitochondrial disorders. 155
Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD 154
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 151
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 150
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria 148
Hexacarbon axonopathy: the morphological expression of altered cytoskeletal translocation. 146
Sarcoidosis and inclusion body myositis. 145
Involvement of the mitochondrial compartment in human NCL fibroblasts. 142
Neurotoxic effects of 2,5-hexanedione in rats: Early morphological and functional changes in nerve fibres and neuromuscular junctions 139
Anatomia normale del lobo temporale:approccio morfologico mediante studio per immagini 138
MELAS: clinical phenotypes and morphological brain abnormalities 136
Le anomalie della migrazione neuronale. 136
Early white matter involvement in an infant carrying a novel mutation in ACOX1 136
Neuropathology of mitochondrial diseases 136
Neuropatie immunitarie ed infiammatorie. 135
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy. 135
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. 133
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5 132
Proteomic profiling in the brain of CLN1 disease model reveals affected functional modules 132
Ponto-cerebellar hypoplasia with dystonia: Clinico-pathological findings in a sporadic case 131
Changes in terminal sprout formation in rat sternocostalis muscle during chronic intoxication with 2,5 hexanedione 130
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 130
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 130
Cerebro-ocular dysplasia and muscular dystrophy: report of two cases 129
Multicystic encephalomalacia associated with symmetrical necrotizing brain stem lesions in an infant: a case report 129
NCL diseases - clinical perspectives. 127
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. 127
Chronic inflammatory demyelinating polyneuropathy 125
Stiff-man syndrome associated with nocturnal myoclonus and epilepsy 125
Selected aspects of peripheral nerve pathology. 125
Neuronal ceroid lipofuscinosis: the increasing spectrum of an old disease. 124
Clinical, ultrastructural, and molecular studies in a patient with Kufs disease 124
High-field-magnetic resonance imaging of the developing human brain from the 10th to the 16th week of gestational age 121
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 121
The effects of 2,5-hexanedione on axonal regeneration after nerve crush in the rat 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
CLN8 is an endoplasmic reticulum cargo receptor that regulates lysosome biogenesis 120
Lysosomal proteomics links disturbances in lipid homeostasis and sphingolipid metabolism to CLN5 disease 120
Choroid plexus papilloma of the cerebello-pontine angle 119
Novel CLN1 mutation in two Italian sibs with late-infantile ceroid lipofuscinosis 119
Le neuropatie genetiche. Inquadramento fisiopatologico e clinico 118
Peripheral neuropathies associated with coeliac disease 118
Neuronal ceroid lipofuscinoses : many players, and more to come 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
Proteomic analysis of the palmitoyl protein thioesterase 1 interactome in SH-SY5Y human neuroblastoma cells. 117
Human pathology in NCL. 116
Gliomatosis cerebri diffusa. A case report 115
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 115
Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs disease. 115
Mechanisms of corticogenesis: cell proliferation and death in the developing human central nervous system 114
Neurotoxic action of 2,5-hexanedione on the autonomic nervous system: ultrastructural and functional alterations in the rat sympathetic superior cervical ganglion 113
La tomografia computerizzata nella diagnostica delle paralisi cerebrali infantili 113
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 113
Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6. 113
Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome. 113
Congenital myopathies: clinical phenotypes and new diagnostic tools 113
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 112
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. 112
Coeliac disease associated with peripheral neuropathy in a child: A case report 112
Integrative organelle-based functional proteomics: in silico prediction of impaired functional annotations in SACS KO cell model 111
Totale 15.056
Salva come PNG Salva come JPEG
Categoria #
all - tutte 69.804
article - articoli 60.144
book - libri 0
conference - conferenze 1.428
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 8.232
Totale 139.608
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021273 0 0 0 0 0 0 0 0 0 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
2025/20267.688 607 505 560 1.184 1.920 558 734 456 782 382 0 0
Totale 20.961