CATALOGO DEI PRODOTTI DELLA RICERCA

SIMONATI, Alessandro
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 6.144
EU - Europa 4.677
AS - Asia 3.490
SA - Sud America 540
AF - Africa 32
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 8
Totale 14.901
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 6.089
SG - Singapore 1.534
GB - Regno Unito 1.276
CN - Cina 1.155
IT - Italia 844
BR - Brasile 477
FR - Francia 452
SE - Svezia 400
RU - Federazione Russa 380
HK - Hong Kong 376
FI - Finlandia 356
DE - Germania 337
IE - Irlanda 336
VN - Vietnam 126
UA - Ucraina 123
KR - Corea 116
BE - Belgio 38
NL - Olanda 36
AT - Austria 27
CA - Canada 27
ID - Indonesia 25
BD - Bangladesh 21
TR - Turchia 21
IN - India 19
AR - Argentina 18
JP - Giappone 18
IQ - Iraq 15
MX - Messico 12
EC - Ecuador 10
PL - Polonia 10
CO - Colombia 9
ES - Italia 9
ZA - Sudafrica 9
CL - Cile 8
LV - Lettonia 8
PK - Pakistan 8
CH - Svizzera 7
SA - Arabia Saudita 7
EU - Europa 6
IL - Israele 6
RO - Romania 6
UZ - Uzbekistan 6
VE - Venezuela 6
AU - Australia 5
IR - Iran 5
MA - Marocco 5
UY - Uruguay 5
KE - Kenya 4
LT - Lituania 4
MD - Moldavia 4
NP - Nepal 4
PY - Paraguay 4
TG - Togo 4
AE - Emirati Arabi Uniti 3
AZ - Azerbaigian 3
BG - Bulgaria 3
BY - Bielorussia 3
CR - Costa Rica 3
CZ - Repubblica Ceca 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
LB - Libano 3
MT - Malta 3
OM - Oman 3
PE - Perù 3
PH - Filippine 3
TN - Tunisia 3
DZ - Algeria 2
EG - Egitto 2
GR - Grecia 2
HR - Croazia 2
JM - Giamaica 2
JO - Giordania 2
LK - Sri Lanka 2
NZ - Nuova Zelanda 2
PA - Panama 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
BN - Brunei Darussalam 1
CI - Costa d'Avorio 1
EE - Estonia 1
GE - Georgia 1
HN - Honduras 1
HT - Haiti 1
IS - Islanda 1
KG - Kirghizistan 1
KI - Kiribati 1
LU - Lussemburgo 1
MN - Mongolia 1
MO - Macao, regione amministrativa speciale della Cina 1
MZ - Mozambico 1
NO - Norvegia 1
PG - Papua Nuova Guinea 1
PR - Porto Rico 1
PS - Palestinian Territory 1
SN - Senegal 1
Totale 14.899
Salva come PNG Salva come JPEG
Città #
Southend 1.134
Jacksonville 1.078
Chandler 755
Singapore 732
Woodbridge 617
Dallas 521
Ann Arbor 430
Hong Kong 376
Dublin 336
Houston 274
Ashburn 210
Beijing 174
Verona 160
Lawrence 158
Princeton 158
Wilmington 154
Nanjing 109
Jinan 104
Sindelfingen 88
Los Angeles 86
Redmond 78
Shenyang 78
New York 66
Milan 64
Helsinki 63
The Dalles 62
Buffalo 59
Hebei 52
Columbus 46
Nanchang 46
Ningbo 43
Changsha 41
Tianjin 39
Jiaxing 35
São Paulo 35
Boardman 33
Hangzhou 33
Zhengzhou 33
Seoul 32
Ho Chi Minh City 31
Munich 30
Redondo Beach 30
Brussels 27
Santa Clara 26
Haikou 24
Dong Ket 23
Guangzhou 21
Bologna 20
Hanoi 19
Rio de Janeiro 19
Seattle 19
Taiyuan 19
Taizhou 19
Vienna 19
Norwalk 18
Brooklyn 17
Nuremberg 17
Redwood City 17
Jakarta 16
Council Bluffs 15
Detroit 15
Kent 15
Moscow 15
Rome 15
Tokyo 15
Belo Horizonte 14
Philadelphia 14
Lancaster 13
San Francisco 13
Lanzhou 12
Naples 12
Turku 12
Auburn Hills 11
Fuzhou 11
Lappeenranta 11
Toronto 11
Waanrode 11
Brasília 10
Falls Church 10
Chicago 9
Phoenix 9
San Diego 9
Warsaw 9
Washington 9
Riva 8
Atlanta 7
Boston 7
Frankfurt am Main 7
Frattamaggiore 7
Augusta 6
Campinas 6
Dhaka 6
Dongguan 6
Goiânia 6
Kemerovo 6
London 6
Manaus 6
Palermo 6
Riyadh 6
Tashkent 6
Totale 9.425
Salva come PNG Salva come JPEG
Nome #
Encefalopatie eredo-degenerative in età evolutiva 403
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 244
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 238
Cerebral cortex three-dimensional profiling in human fetuses by magnetic resonance imaging 173
Congenital hypomyelination neuropathy with a novel mutation of PMP22 140
Protocollo assistenziale di minima della Neurofibromatosi tipo 1 (NF1) 140
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 139
An inherited large-scale rearrangement in SACS associated with spastic ataxia and hearing loss 136
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 134
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 134
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 132
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 128
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 128
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 127
PMP22 related congenital hypomyelination neuropathy 125
Chapter 22 - Ataxia in mitochondrial disorders. 125
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 124
Dysmyelinating neuropathies of infancy: defined and undefined forms 124
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 124
The role of muscle biopsy in investigating isolated muscle pain 124
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 123
Unexpected subacute leucoencephalopathy following intrathecal methotrexate and cytarabine administration in a patient homozygous for MTHFR 677C→T polymorphism. 123
Clinical features of Kleine-Levin syndrome with localized encephalitis 122
An unusual case of meningeal gliomatosis 122
Quantitative analysis of PPT1 interactome in human neuroblastoma cells 122
AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders. 122
Transcriptomic profiling discloses molecular and cellular events related to neuronal differentiation in SH-SY5Y neuroblastoma cells 122
Blood lymphocytes in neuronal ceroid lipofuscinosis 121
The networks of genes encoding palmitoylated proteins in axonal and synaptic compartments are affected in PPT1 overexpressing neuronal-like cells 117
Congenital toxoplasmosis: histological and ultrastructural study 115
Diagnostic methods and emerging treatments for adult neuronal ceroid lipofuscinoses (Kufs disease) 114
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 114
Le anomalie della migrazione neuronale. 113
C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation. 112
MELAS: clinical phenotypes and morphological brain abnormalities 111
Functional transcriptome analysis in ARSACS KO cell model reveals a role of sacsin in autophagy 110
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 109
Multicystic encephalomalacia associated with symmetrical necrotizing brain stem lesions in an infant: a case report 108
A novel nonsense mutation (Q509X) in three Italian Late infantile neuronal ceroid-lipofuscinosis children 106
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 106
Chronic inflammatory demyelinating polyneuropathy 105
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 105
Sarcoidosis and inclusion body myositis. 105
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5 105
Changes in terminal sprout formation in rat sternocostalis muscle during chronic intoxication with 2,5 hexanedione 104
Hexacarbon axonopathy: the morphological expression of altered cytoskeletal translocation. 104
Neuropatie immunitarie ed infiammatorie. 103
Proteomic profiling in the brain of CLN1 disease model reveals affected functional modules 103
Stiff-man syndrome associated with nocturnal myoclonus and epilepsy 101
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 101
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy. 100
Ponto-cerebellar hypoplasia with dystonia: Clinico-pathological findings in a sporadic case 99
Neurotoxic effects of 2,5-hexanedione in rats: Early morphological and functional changes in nerve fibres and neuromuscular junctions 99
High-field-magnetic resonance imaging of the developing human brain from the 10th to the 16th week of gestational age 98
Cerebro-ocular dysplasia and muscular dystrophy: report of two cases 97
A novel missense mutation in the L1CAM gene in a boy with L1-disease. 97
Novel CLN1 mutation in two Italian sibs with late-infantile ceroid lipofuscinosis 96
Anatomia normale del lobo temporale:approccio morfologico mediante studio per immagini 95
Age and sex prevalence estimate of Joubert syndrome in Italy 95
Involvement of the mitochondrial compartment in human NCL fibroblasts. 94
Selected aspects of peripheral nerve pathology. 94
NCL diseases - clinical perspectives. 94
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 93
Choroid plexus papilloma of the cerebello-pontine angle 92
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. 92
Neuronal ceroid lipofuscinosis: the increasing spectrum of an old disease. 92
Early white matter involvement in an infant carrying a novel mutation in ACOX1 92
Neuronal ceroid lipofuscinoses : many players, and more to come 91
The effects of 2,5-hexanedione on axonal regeneration after nerve crush in the rat 90
La tomografia computerizzata nella diagnostica delle paralisi cerebrali infantili 90
Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD 90
Le neuropatie genetiche. Inquadramento fisiopatologico e clinico 89
Neurotoxic action of 2,5-hexanedione on the autonomic nervous system: ultrastructural and functional alterations in the rat sympathetic superior cervical ganglion 88
Peripheral nerve allograft for nerve repair 88
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 88
Le neuropatie genetiche 87
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 87
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 87
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 87
Human pathology in NCL. 87
Neuropathology of mitochondrial diseases 87
Gliomatosis cerebri diffusa. A case report 86
Protein glutathionylation in human central nervous system: potential role in redox regulation of neuronal defense against free radicals 86
La valutazione neuropatologica nella malattia di Alzheimer (AD): correlazioni con il quadro clinico ed analisi delle problematiche 85
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 85
Neuropatie immunitarie. 85
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. 85
Physicochemical characters of a ribonucleoprotein fragment extracted from rat brain, and their modification due to either enviromental or chemical influence 84
Peripheral neuropathies associated with coeliac disease 84
PLA2G6, encoding a phospholipase A(2), is mutated in neurodegenerative disorders with high brain iron 84
DNA fragmentation in normal development of the human central nervous system: A morphological study during corticogenesis 83
Mechanisms of corticogenesis: cell proliferation and death in the developing human central nervous system 83
Disease characteristics and progression in patients with late-infantile neuronal ceroid lipofuscinosis type 2 (CLN2) disease: an observational cohort study 83
Spinal cord lesions 82
Neuroaxonal dystrophy with dystonia and pallidal involvement 82
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: another genetic hit in the Mediterranean 81
Revelation of a novel CLN5 mutation in early juvenile neuronal ceroid lipofuscinosis 81
Variant late infantile ceroid lipofuscinoses associated with novel mutations in CLN6. 81
Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome. 81
Lumbar epidural Ewing sarcoma. Light and electron microscopic investigation 80
Totale 10.926
Salva come PNG Salva come JPEG
Categoria #
all - tutte 57.720
article - articoli 49.613
book - libri 0
conference - conferenze 1.176
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 6.931
Totale 115.440
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021944 0 0 0 99 137 141 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
2025/20261.776 607 505 560 104 0 0 0 0 0 0 0 0
Totale 15.049