CATALOGO DEI PRODOTTI DELLA RICERCA

SIMONATI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 9.241
EU - Europa 7.045
AS - Asia 5.105
SA - Sud America 785
Continente sconosciuto - Info sul continente non disponibili 156
AF - Africa 94
OC - Oceania 11
Totale 22.437
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Nazione #
US - Stati Uniti d'America 9.107
RU - Federazione Russa 2.298
SG - Singapore 2.276
CN - Cina 1.377
GB - Regno Unito 1.317
IT - Italia 1.125
BR - Brasile 632
FR - Francia 465
VN - Vietnam 438
SE - Svezia 409
HK - Hong Kong 405
FI - Finlandia 368
DE - Germania 356
IE - Irlanda 338
KR - Corea 191
UA - Ucraina 133
BD - Bangladesh 96
CA - Canada 76
IN - India 57
NL - Olanda 46
AR - Argentina 41
BE - Belgio 39
ID - Indonesia 37
TR - Turchia 31
AT - Austria 30
JP - Giappone 28
EC - Ecuador 27
MX - Messico 26
IQ - Iraq 25
NG - Nigeria 25
PL - Polonia 25
ZA - Sudafrica 22
ES - Italia 21
CO - Colombia 20
VE - Venezuela 20
PK - Pakistan 18
CL - Cile 17
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
UY - Uruguay 9
CH - Svizzera 8
KE - Kenya 8
MY - Malesia 8
AE - Emirati Arabi Uniti 7
AZ - Azerbaigian 7
CR - Costa Rica 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
EG - Egitto 5
IR - Iran 5
JM - Giamaica 5
KZ - Kazakistan 5
BG - Bulgaria 4
BY - Bielorussia 4
MD - Moldavia 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
GT - Guatemala 3
HR - Croazia 3
MT - Malta 3
NZ - Nuova Zelanda 3
PA - Panama 3
PE - Perù 3
SY - Repubblica araba siriana 3
TT - Trinidad e Tobago 3
DZ - Algeria 2
ET - Etiopia 2
KG - Kirghizistan 2
LC - Santa Lucia 2
LK - Sri Lanka 2
PR - Porto Rico 2
PS - Palestinian Territory 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
Totale 22.267
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Città #
Singapore 1.226
Southend 1.134
Jacksonville 1.082
Ashburn 947
San Jose 907
Chandler 755
Moscow 655
Woodbridge 617
Dallas 542
Ann Arbor 430
Hong Kong 400
Verona 348
Dublin 337
Houston 286
Council Bluffs 279
The Dalles 246
Beijing 217
Lawrence 158
Princeton 158
Wilmington 154
Los Angeles 143
Ho Chi Minh City 141
Nanjing 110
New York 109
Jinan 104
Hanoi 90
Sindelfingen 88
Buffalo 79
Milan 79
Shenyang 79
Redmond 78
Helsinki 73
Santa Clara 71
São Paulo 63
Hebei 52
Columbus 47
Nanchang 46
Tianjin 44
Ningbo 43
Changsha 42
Redondo Beach 38
Boardman 36
Jiaxing 35
Orem 35
Brooklyn 33
Hangzhou 33
Zhengzhou 33
Annandale 32
Seoul 32
Munich 31
Brussels 28
Denver 27
Las Vegas 27
Guangzhou 26
Rio de Janeiro 26
Rome 26
Abuja 25
Chicago 24
Da Nang 24
Haikou 24
Tokyo 24
Dong Ket 23
Warsaw 23
Bologna 22
Seattle 22
Jakarta 20
Philadelphia 20
Toronto 20
Detroit 19
London 19
Norwalk 19
Taiyuan 19
Taizhou 19
Vienna 19
Frankfurt am Main 18
Phoenix 18
Belo Horizonte 17
Nuremberg 17
Redwood City 17
Chennai 16
Naples 16
San Francisco 16
Atlanta 15
Brasília 15
Haiphong 15
Kent 15
Lancaster 15
Montreal 15
Turku 13
Johannesburg 12
Lanzhou 12
Lappeenranta 12
Auburn Hills 11
Dhaka 11
Fuzhou 11
San Diego 11
Waanrode 11
Falls Church 10
Tashkent 10
Washington 10
Totale 13.701
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Nome #
Encefalopatie eredo-degenerative in età evolutiva 438
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 278
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 274
Cerebral cortex three-dimensional profiling in human fetuses by magnetic resonance imaging 267
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 239
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 232
AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders. 205
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 205
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing loss 201
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 199
Congenital hypomyelination neuropathy with a novel mutation of PMP22 196
Clinical features of Kleine-Levin syndrome with localized encephalitis 195
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 195
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 195
Dysmyelinating neuropathies of infancy: defined and undefined forms 193
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 191
A novel nonsense mutation (Q509X) in three Italian Late infantile neuronal ceroid-lipofuscinosis children 187
Diagnostic methods and emerging treatments for adult neuronal ceroid lipofuscinoses (Kufs disease) 186
Congenital toxoplasmosis: histological and ultrastructural study 185
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. 184
Blood lymphocytes in neuronal ceroid lipofuscinosis 183
Age and sex prevalence estimate of Joubert syndrome in Italy 183
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 183
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 183
An unusual case of meningeal gliomatosis 181
The networks of genes encoding palmitoylated proteins in axonal and synaptic compartments are affected in PPT1 overexpressing neuronal-like cells 181
Transcriptomic profiling discloses molecular and cellular events related to neuronal differentiation in SH-SY5Y neuroblastoma cells 181
A novel missense mutation in the L1CAM gene in a boy with L1-disease. 180
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 178
C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation. 178
Functional transcriptome analysis in ARSACS KO cell model reveals a role of sacsin in autophagy 178
Protocollo assistenziale di minima della Neurofibromatosi tipo 1 (NF1) 177
PMP22 related congenital hypomyelination neuropathy 175
Quantitative analysis of PPT1 interactome in human neuroblastoma cells 170
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 169
Hexacarbon axonopathy: the morphological expression of altered cytoskeletal translocation. 169
Unexpected subacute leucoencephalopathy following intrathecal methotrexate and cytarabine administration in a patient homozygous for MTHFR 677C→T polymorphism. 169
The role of muscle biopsy in investigating isolated muscle pain 166
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 165
Chapter 22 - Ataxia in mitochondrial disorders. 165
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 164
Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD 161
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 158
ATP1A2- and ATP1A3-associated early profound epileptic encephalopathy and polymicrogyria 158
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional study 157
Sarcoidosis and inclusion body myositis. 152
Involvement of the mitochondrial compartment in human NCL fibroblasts. 148
Neuropatie immunitarie ed infiammatorie. 148
Neurotoxic effects of 2,5-hexanedione in rats: Early morphological and functional changes in nerve fibres and neuromuscular junctions 148
Neuropathology of mitochondrial diseases 147
Neuronal ceroid lipofuscinosis: the increasing spectrum of an old disease. 145
Early white matter involvement in an infant carrying a novel mutation in ACOX1 145
Anatomia normale del lobo temporale:approccio morfologico mediante studio per immagini 144
Le anomalie della migrazione neuronale. 143
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5 142
Ponto-cerebellar hypoplasia with dystonia: Clinico-pathological findings in a sporadic case 141
Multicystic encephalomalacia associated with symmetrical necrotizing brain stem lesions in an infant: a case report 141
MELAS: clinical phenotypes and morphological brain abnormalities 141
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. 141
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy. 141
Proteomic profiling in the brain of CLN1 disease model reveals affected functional modules 140
Changes in terminal sprout formation in rat sternocostalis muscle during chronic intoxication with 2,5 hexanedione 139
NCL diseases - clinical perspectives. 139
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 138
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 137
Cerebro-ocular dysplasia and muscular dystrophy: report of two cases 135
Stiff-man syndrome associated with nocturnal myoclonus and epilepsy 135
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 135
Selected aspects of peripheral nerve pathology. 135
Chronic inflammatory demyelinating polyneuropathy 132
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 131
Disease characteristics and progression in patients with late-infantile neuronal ceroid lipofuscinosis type 2 (CLN2) disease: an observational cohort study 131
CLN8 is an endoplasmic reticulum cargo receptor that regulates lysosome biogenesis 131
High-field-magnetic resonance imaging of the developing human brain from the 10th to the 16th week of gestational age 130
Choroid plexus papilloma of the cerebello-pontine angle 130
Clinical, ultrastructural, and molecular studies in a patient with Kufs disease 129
Proteomic analysis of the palmitoyl protein thioesterase 1 interactome in SH-SY5Y human neuroblastoma cells. 129
Mutations in the cilia gene ARL13B lead to the classical form of Joubert syndrome. 128
Survey on treatments for primary headaches in 13 specialized juvenile Headache Centers: The first multicenter Italian study 127
Novel CLN1 mutation in two Italian sibs with late-infantile ceroid lipofuscinosis 127
The effects of 2,5-hexanedione on axonal regeneration after nerve crush in the rat 126
Neuronal ceroid lipofuscinoses : many players, and more to come 126
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 125
Human pathology in NCL. 125
Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs disease. 125
Lysosomal proteomics links disturbances in lipid homeostasis and sphingolipid metabolism to CLN5 disease 125
Gliomatosis cerebri diffusa. A case report 124
Mechanisms of corticogenesis: cell proliferation and death in the developing human central nervous system 124
Le neuropatie genetiche. Inquadramento fisiopatologico e clinico 123
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 123
Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome. 123
A novel IRF2BPL truncating variant is associated with endolysosomal storage 123
Peripheral neuropathies associated with coeliac disease 122
Pontine tegmental cap dysplasia: developmental and cognitive outcome in three adolescent patients. 122
Neuropatie immunitarie. 122
Neurotoxic action of 2,5-hexanedione on the autonomic nervous system: ultrastructural and functional alterations in the rat sympathetic superior cervical ganglion 121
Peripheral nerve allograft for nerve repair 121
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 121
Congenital myopathies: clinical phenotypes and new diagnostic tools 121
Electrophysiological profile remodeling via selective suppression of voltage-gated currents by CLN1/PPT1 overexpression in human neuronal-like cells 121
Totale 16.045
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Categoria #
all - tutte 79.969
article - articoli 68.996
book - libri 0
conference - conferenze 1.611
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 9.362
Totale 159.938
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022707 0 0 0 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
2025/20268.067 607 505 560 1.184 1.920 558 734 456 782 410 162 189
2026/20271.097 114 233 372 378 0 0 0 0 0 0 0 0
Totale 22.437