CATALOGO DEI PRODOTTI DELLA RICERCA

SIMONATI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 5.089
EU - Europa 4.447
AS - Asia 1.775
SA - Sud America 14
Continente sconosciuto - Info sul continente non disponibili 7
AF - Africa 6
OC - Oceania 5
Totale 11.343
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Nazione #
US - Stati Uniti d'America 5.075
GB - Regno Unito 1.250
CN - Cina 1.031
IT - Italia 819
SG - Singapore 618
FR - Francia 440
SE - Svezia 398
RU - Federazione Russa 373
IE - Irlanda 333
FI - Finlandia 329
DE - Germania 273
UA - Ucraina 115
BE - Belgio 38
VN - Vietnam 35
NL - Olanda 31
KR - Corea 25
ID - Indonesia 14
TR - Turchia 12
AT - Austria 9
BR - Brasile 9
CA - Canada 9
CH - Svizzera 7
LV - Lettonia 7
EU - Europa 6
IL - Israele 6
JP - Giappone 6
IR - Iran 5
AU - Australia 4
TG - Togo 4
BD - Bangladesh 3
BG - Bulgaria 3
DK - Danimarca 3
ES - Italia 3
IN - India 3
PK - Pakistan 3
RO - Romania 3
SA - Arabia Saudita 3
AE - Emirati Arabi Uniti 2
CL - Cile 2
GR - Grecia 2
LK - Sri Lanka 2
LT - Lituania 2
MX - Messico 2
PA - Panama 2
PH - Filippine 2
PL - Polonia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AR - Argentina 1
BN - Brunei Darussalam 1
BY - Bielorussia 1
CO - Colombia 1
CR - Costa Rica 1
CZ - Repubblica Ceca 1
DZ - Algeria 1
EC - Ecuador 1
EE - Estonia 1
EG - Egitto 1
HK - Hong Kong 1
HR - Croazia 1
IS - Islanda 1
MD - Moldavia 1
MO - Macao, regione amministrativa speciale della Cina 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
TH - Thailandia 1
UZ - Uzbekistan 1
Totale 11.343
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Città #
Southend 1.134
Jacksonville 1.078
Chandler 755
Woodbridge 617
Singapore 512
Ann Arbor 430
Dublin 333
Houston 274
Ashburn 183
Verona 160
Lawrence 158
Princeton 158
Beijing 155
Wilmington 154
Nanjing 108
Jinan 103
Sindelfingen 88
Redmond 78
Shenyang 77
Milan 62
New York 57
Hebei 52
Helsinki 51
Nanchang 46
Ningbo 42
Changsha 38
Jiaxing 35
Boardman 33
Tianjin 33
Hangzhou 31
Zhengzhou 30
Brussels 27
Seoul 25
Haikou 24
Dong Ket 23
Santa Clara 20
Bologna 19
Guangzhou 19
Taiyuan 19
Norwalk 18
Seattle 18
Taizhou 18
Los Angeles 17
Redwood City 17
Detroit 15
Kent 15
Moscow 15
Dallas 14
Jakarta 13
Lancaster 13
Lanzhou 12
Philadelphia 12
Auburn Hills 11
Fuzhou 11
Rome 11
Waanrode 11
Falls Church 10
Naples 10
Vienna 9
Lappeenranta 8
Riva 8
San Diego 8
Washington 8
Frattamaggiore 7
Augusta 6
Chicago 6
Dongguan 6
Kemerovo 6
San Francisco 6
Dearborn 5
Edinburgh 5
Messina 5
Palermo 5
Phoenix 5
Toronto 5
Venice 5
Bari 4
Cadelbosco 4
Cento 4
Clearwater 4
Como 4
Fairfield 4
Las Vegas 4
Lomé 4
Mehlingen 4
Munich 4
Napoli 4
Riga 4
Roverbella 4
Torino 4
Trento 4
Bern 3
Catania 3
Florence 3
Genova 3
Karachi 3
L'aquila 3
Pescia 3
Riyadh 3
Sacramento 3
Totale 7.702
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Nome #
Encefalopatie eredo-degenerative in età evolutiva 380
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 230
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 225
Protocollo assistenziale di minima della Neurofibromatosi tipo 1 (NF1) 126
Cerebral cortex three-dimensional profiling in human fetuses by magnetic resonance imaging 125
Congenital hypomyelination neuropathy with a novel mutation of PMP22 107
Clinical features of Kleine-Levin syndrome with localized encephalitis 106
PMP22 related congenital hypomyelination neuropathy 105
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 103
Chapter 22 - Ataxia in mitochondrial disorders. 102
Transcriptomic profiling discloses molecular and cellular events related to neuronal differentiation in SH-SY5Y neuroblastoma cells 100
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 99
The role of muscle biopsy in investigating isolated muscle pain 99
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 98
An unusual case of meningeal gliomatosis 97
Dysmyelinating neuropathies of infancy: defined and undefined forms 97
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 96
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 96
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 96
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 95
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 95
Diagnostic methods and emerging treatments for adult neuronal ceroid lipofuscinoses (Kufs disease) 94
Le anomalie della migrazione neuronale. 94
MELAS: clinical phenotypes and morphological brain abnormalities 93
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 92
Congenital toxoplasmosis: histological and ultrastructural study 91
Unexpected subacute leucoencephalopathy following intrathecal methotrexate and cytarabine administration in a patient homozygous for MTHFR 677C→T polymorphism. 91
Multicystic encephalomalacia associated with symmetrical necrotizing brain stem lesions in an infant: a case report 90
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 90
Quantitative analysis of PPT1 interactome in human neuroblastoma cells 90
Chronic inflammatory demyelinating polyneuropathy 88
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 88
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5 88
Changes in terminal sprout formation in rat sternocostalis muscle during chronic intoxication with 2,5 hexanedione 86
Hexacarbon axonopathy: the morphological expression of altered cytoskeletal translocation. 86
AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders. 86
The networks of genes encoding palmitoylated proteins in axonal and synaptic compartments are affected in PPT1 overexpressing neuronal-like cells 86
Ponto-cerebellar hypoplasia with dystonia: Clinico-pathological findings in a sporadic case 85
Proteomic profiling in the brain of CLN1 disease model reveals affected functional modules 85
Cerebro-ocular dysplasia and muscular dystrophy: report of two cases 83
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 83
Neuropatie immunitarie ed infiammatorie. 82
Novel CLN1 mutation in two Italian sibs with late-infantile ceroid lipofuscinosis 82
Blood lymphocytes in neuronal ceroid lipofuscinosis 81
Stiff-man syndrome associated with nocturnal myoclonus and epilepsy 81
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy. 81
High-field-magnetic resonance imaging of the developing human brain from the 10th to the 16th week of gestational age 80
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 79
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 79
Functional transcriptome analysis in ARSACS KO cell model reveals a role of sacsin in autophagy 79
Neurotoxic effects of 2,5-hexanedione in rats: Early morphological and functional changes in nerve fibres and neuromuscular junctions 79
Selected aspects of peripheral nerve pathology. 78
Neuronal ceroid lipofuscinosis: the increasing spectrum of an old disease. 77
The effects of 2,5-hexanedione on axonal regeneration after nerve crush in the rat 76
Gliomatosis cerebri diffusa. A case report 75
A novel nonsense mutation (Q509X) in three Italian Late infantile neuronal ceroid-lipofuscinosis children 75
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 74
Sarcoidosis and inclusion body myositis. 74
NCL diseases - clinical perspectives. 74
Neurotoxic action of 2,5-hexanedione on the autonomic nervous system: ultrastructural and functional alterations in the rat sympathetic superior cervical ganglion 73
Peripheral nerve allograft for nerve repair 73
Involvement of the mitochondrial compartment in human NCL fibroblasts. 73
C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation. 73
La tomografia computerizzata nella diagnostica delle paralisi cerebrali infantili 72
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 72
Early white matter involvement in an infant carrying a novel mutation in ACOX1 72
Le neuropatie genetiche. Inquadramento fisiopatologico e clinico 71
Choroid plexus papilloma of the cerebello-pontine angle 71
La valutazione neuropatologica nella malattia di Alzheimer (AD): correlazioni con il quadro clinico ed analisi delle problematiche 70
Peripheral neuropathies associated with coeliac disease 70
Neuronal ceroid lipofuscinoses : many players, and more to come 70
DNA fragmentation in normal development of the human central nervous system: A morphological study during corticogenesis 69
Coeliac disease associated with peripheral neuropathy in a child: A case report 69
Physicochemical characters of a ribonucleoprotein fragment extracted from rat brain, and their modification due to either enviromental or chemical influence 68
Le neuropatie genetiche 68
Spinal cord lesions 68
Mechanisms of corticogenesis: cell proliferation and death in the developing human central nervous system 67
PLA2G6, encoding a phospholipase A(2), is mutated in neurodegenerative disorders with high brain iron 67
Protein glutathionylation in human central nervous system: potential role in redox regulation of neuronal defense against free radicals 67
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 67
Neuropatie immunitarie. 67
Neuropathology of mitochondrial diseases 67
Human pathology in NCL. 66
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. 66
Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD 66
Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs disease. 66
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 65
Neuronal ceroid lipofuscinoses: pathological features of bioptic specimens from 28 patients 64
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 64
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 64
Lumbar epidural Ewing sarcoma. Light and electron microscopic investigation 64
Disease characteristics and progression in patients with late-infantile neuronal ceroid lipofuscinosis type 2 (CLN2) disease: an observational cohort study 64
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. 63
Neuropatia sperimentale da acrilamide. Studio istologico ed ultrastrutturale. [Experimental neuropathy due to acrilamide. Histological and ultrastructural studies (author's transl)] 62
Anatomia normale del lobo temporale:approccio morfologico mediante studio per immagini 62
A novel missense mutation in the L1CAM gene in a boy with L1-disease. 62
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 62
La patologia delle neuropatie periferiche. 62
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: another genetic hit in the Mediterranean 61
TSEN54 mutation in a child with pontocerebellar hypoplasia type 1. 61
Totale 8.600
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Categoria #
all - tutte 40.530
article - articoli 34.540
book - libri 0
conference - conferenze 831
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 5.159
Totale 81.060
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.019 0 0 0 0 88 187 132 134 70 167 57 184
2020/20211.306 80 226 56 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
2024/20251.118 185 203 89 496 145 0 0 0 0 0 0 0
Totale 11.491