CATALOGO DEI PRODOTTI DELLA RICERCA

SIMONATI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 4.942
EU - Europa 4.034
AS - Asia 1.028
Continente sconosciuto - Info sul continente non disponibili 7
SA - Sud America 7
OC - Oceania 4
AF - Africa 1
Totale 10.023
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Nazione #
US - Stati Uniti d'America 4.930
GB - Regno Unito 1.250
CN - Cina 923
IT - Italia 783
FR - Francia 440
SE - Svezia 398
IE - Irlanda 333
FI - Finlandia 323
DE - Germania 269
UA - Ucraina 115
BE - Belgio 38
VN - Vietnam 35
NL - Olanda 31
KR - Corea 25
RU - Federazione Russa 19
TR - Turchia 12
AT - Austria 9
CA - Canada 8
EU - Europa 6
IR - Iran 5
JP - Giappone 5
BR - Brasile 4
CH - Svizzera 4
AU - Australia 3
BD - Bangladesh 3
BG - Bulgaria 3
DK - Danimarca 3
IL - Israele 3
IN - India 3
LV - Lettonia 3
PK - Pakistan 3
SG - Singapore 3
CL - Cile 2
ES - Italia 2
LK - Sri Lanka 2
MX - Messico 2
PH - Filippine 2
RO - Romania 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AR - Argentina 1
BY - Bielorussia 1
CR - Costa Rica 1
CZ - Repubblica Ceca 1
DZ - Algeria 1
GR - Grecia 1
HK - Hong Kong 1
HR - Croazia 1
ID - Indonesia 1
IS - Islanda 1
LT - Lituania 1
MD - Moldavia 1
MO - Macao, regione amministrativa speciale della Cina 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PA - Panama 1
PL - Polonia 1
UZ - Uzbekistan 1
Totale 10.023
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Città #
Southend 1.134
Jacksonville 1.078
Chandler 755
Woodbridge 617
Ann Arbor 430
Dublin 333
Houston 274
Ashburn 158
Lawrence 158
Princeton 158
Wilmington 154
Verona 153
Beijing 142
Nanjing 108
Jinan 103
Sindelfingen 88
Redmond 78
Shenyang 77
Milan 62
New York 57
Hebei 52
Helsinki 47
Nanchang 46
Ningbo 42
Changsha 38
Jiaxing 35
Boardman 33
Tianjin 33
Hangzhou 30
Zhengzhou 29
Brussels 27
Seoul 25
Haikou 24
Dong Ket 23
Taiyuan 19
Bologna 18
Norwalk 18
Seattle 18
Taizhou 18
Redwood City 17
Guangzhou 16
Detroit 15
Los Angeles 14
Lancaster 13
Lanzhou 12
Philadelphia 12
Auburn Hills 11
Fuzhou 11
Waanrode 11
Falls Church 10
Rome 10
Vienna 9
Riva 8
San Diego 8
Washington 8
Frattamaggiore 7
Chicago 6
Dongguan 6
Kemerovo 6
Lappeenranta 6
Augusta 5
Dearborn 5
Edinburgh 5
Phoenix 5
San Francisco 5
Venice 5
Cadelbosco 4
Cento 4
Clearwater 4
Como 4
Dallas 4
Fairfield 4
Mehlingen 4
Naples 4
Napoli 4
Palermo 4
Roverbella 4
Torino 4
Toronto 4
Trento 4
Catania 3
Florence 3
Genova 3
Karachi 3
L'aquila 3
Las Vegas 3
Pescia 3
Sacramento 3
Salerno 3
Terni 3
Tolentino 3
Abbadia Lariana 2
Alcamo 2
Amsterdam 2
Aquila 2
Aragona 2
Ardabil 2
Atlanta 2
Austin 2
Bari 2
Totale 7.045
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Nome #
Encefalopatie eredo-degenerative in età evolutiva 369
Polineuropatia da collanti. Contributo Istologico ed ultrastrutturale 222
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 208
Protocollo assistenziale di minima della Neurofibromatosi tipo 1 (NF1) 120
Cerebral cortex three-dimensional profiling in human fetuses by magnetic resonance imaging 107
Clinical features of Kleine-Levin syndrome with localized encephalitis 97
Congenital hypomyelination neuropathy with a novel mutation of PMP22 97
PMP22 related congenital hypomyelination neuropathy 96
Effects of pulsed electromagnetic fields on nerve regeneration: an experimental study in the rat 93
Chapter 22 - Ataxia in mitochondrial disorders. 92
Transcriptomic profiling discloses molecular and cellular events related to neuronal differentiation in SH-SY5Y neuroblastoma cells 92
The role of muscle biopsy in investigating isolated muscle pain 91
Dejerine-Sottas neuropathy with multiple nerve roots enlargement and hypomyelination associated with a missense mutation of the transmembrane domain of MPZ/P0 89
An experimental study on the neurotoxicity of n-hexane metabolites: hexanol-1 and hexanol-2 88
Diagnostic methods and emerging treatments for adult neuronal ceroid lipofuscinoses (Kufs disease) 88
Le anomalie della migrazione neuronale. 88
An unusual case of meningeal gliomatosis 87
Dysmyelinating neuropathies of infancy: defined and undefined forms 87
Botulinum toxin treatment of muscle cramps: a clinical and neurophysiological study 87
MELAS: clinical phenotypes and morphological brain abnormalities 86
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 86
A CLN2 gene nonsense mutation is associated with severe caudate atrophy and dystonia in LINCL 85
Unexpected subacute leucoencephalopathy following intrathecal methotrexate and cytarabine administration in a patient homozygous for MTHFR 677C→T polymorphism. 85
Multicystic encephalomalacia associated with symmetrical necrotizing brain stem lesions in an infant: a case report 84
Congenital hypomyelination neuropathy with Ser72Leu substitution in PMP22 83
Déjerine-Sottas syndrome with a silent nucleotide change of myelin protein zero gene. 82
Chapter 14 | Dysmyelinating neuropathies of infancy: defined and undefined forms 82
Chronic inflammatory demyelinating polyneuropathy 81
Quantitative analysis of PPT1 interactome in human neuroblastoma cells 81
Proteomic profiling in the brain of CLN1 disease model reveals affected functional modules 81
Progressive myoclonus epilepsy in congenital generalized lipodystrophy type 2: report of 3 cases and literature review 79
Congenital toxoplasmosis: histological and ultrastructural study 78
Changes in terminal sprout formation in rat sternocostalis muscle during chronic intoxication with 2,5 hexanedione 77
AHI1 gene mutations cause specific forms of Joubert syndrome-related disorders. 77
Phenotype and natural history of variant late infantile ceroid-lipofuscinosis 5 77
Novel CLN1 mutation in two Italian sibs with late-infantile ceroid lipofuscinosis 77
Ponto-cerebellar hypoplasia with dystonia: Clinico-pathological findings in a sporadic case 76
Hexacarbon axonopathy: the morphological expression of altered cytoskeletal translocation. 76
Stiff-man syndrome associated with nocturnal myoclonus and epilepsy 75
The networks of genes encoding palmitoylated proteins in axonal and synaptic compartments are affected in PPT1 overexpressing neuronal-like cells 75
Neuropatie immunitarie ed infiammatorie. 74
Neuropathological features of nerve regeneration in 2.5-HD intoxicated rats. 73
Neurotoxic effects of 2,5-hexanedione in rats: early morphological and functional changes in nerve fibres and neuromuscular junctions 72
High-field-magnetic resonance imaging of the developing human brain from the 10th to the 16th week of gestational age 71
Selected aspects of peripheral nerve pathology. 71
Neuronal ceroid lipofuscinosis: the increasing spectrum of an old disease. 71
Blood lymphocytes in neuronal ceroid lipofuscinosis 70
Functional transcriptome analysis in ARSACS KO cell model reveals a role of sacsin in autophagy 70
Cerebro-ocular dysplasia and muscular dystrophy: report of two cases 69
Molecular epidemiology of childhood neuronal ceroid-lipofuscinosis in Italy. 69
Cell proliferation and death: morphological evidence during corticogenesis in the developing human brain 69
Neurotoxic action of 2,5-hexanedione on the autonomic nervous system: ultrastructural and functional alterations in the rat sympathetic superior cervical ganglion 68
Gliomatosis cerebri diffusa. A case report 67
Sarcoidosis and inclusion body myositis. 67
The effects of 2,5-hexanedione on axonal regeneration after nerve crush in the rat 66
A novel nonsense mutation (Q509X) in three Italian Late infantile neuronal ceroid-lipofuscinosis children 66
La tomografia computerizzata nella diagnostica delle paralisi cerebrali infantili 66
Central-peripheral sensory axonopathy in a juvenile case of Alpers-Huttenlocher disease 66
Peripheral nerve allograft for nerve repair 65
Choroid plexus papilloma of the cerebello-pontine angle 65
Neuronal ceroid lipofuscinoses : many players, and more to come 65
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 65
Early white matter involvement in an infant carrying a novel mutation in ACOX1 64
Le neuropatie genetiche. Inquadramento fisiopatologico e clinico 63
C19orf12 and FA2H mutations are rare in Italian patients with neurodegeneration with brain iron accumulation. 63
Migrating focal seizures and myoclonic status in ARV1-related encephalopathy 63
Physicochemical characters of a ribonucleoprotein fragment extracted from rat brain, and their modification due to either enviromental or chemical influence 62
Le neuropatie genetiche 62
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 62
Involvement of the mitochondrial compartment in human NCL fibroblasts. 62
Coeliac disease associated with peripheral neuropathy in a child: A case report 62
Peripheral neuropathies associated with coeliac disease 61
PLA2G6, encoding a phospholipase A(2), is mutated in neurodegenerative disorders with high brain iron 61
Spinal cord lesions 61
La valutazione neuropatologica nella malattia di Alzheimer (AD): correlazioni con il quadro clinico ed analisi delle problematiche 60
Protein glutathionylation in human central nervous system: potential role in redox regulation of neuronal defense against free radicals 60
Features of cell death in brain and liver, the target tissues of progressive neuronal degeneration of childhood with liver disease (Alpers-Huttenlocher disease) 60
Neuropatie immunitarie. 60
Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions. 60
Focally folded myelin in Charcot-Marie-Tooth neuropathy type 1B with Ser49Leu in the myelin protein zero 59
Myelin uncompaction in Charcot-Marie-Tooth neuropathy type 1A with a point mutation of peripheral myelin protein-22 59
Neuropathology of mitochondrial diseases 59
Neuropatia sperimentale da acrilamide. Studio istologico ed ultrastrutturale. [Experimental neuropathy due to acrilamide. Histological and ultrastructural studies (author's transl)] 58
Early infantile neuronal ceroid lipofuscinosis (CLN10 disease) associated with a novel mutation in CTSD 58
Disease characteristics and progression in patients with late-infantile neuronal ceroid lipofuscinosis type 2 (CLN2) disease: an observational cohort study 58
Mechanisms of corticogenesis: cell proliferation and death in the developing human central nervous system 57
Neuronal ceroid lipofuscinoses: pathological features of bioptic specimens from 28 patients 57
Novel mutation of the P0 extracellular domain causes a Dejerine-Sottas syndrome 57
Lumbar epidural Ewing sarcoma. Light and electron microscopic investigation 57
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders. 57
DNA fragmentation in normal development of the human central nervous system: A morphological study during corticogenesis 56
Pontine tegmental cap dysplasia: developmental and cognitive outcome in three adolescent patients. 56
NCL diseases - clinical perspectives. 56
Pseudo-dominant inheritance of a novel CTSF mutation associated with type B Kufs disease. 56
Neuroaxonal dystrophy with dystonia and pallidal involvement 55
Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1 54
Human pathology in NCL. 54
Microgyria associated with Sturge-Weber angiomatosis 53
Neuronal-specific roles of the survival motor neuron protein: evidence from survival motor neuron expression patterns in the developing human central nervous system. 53
Novel mutations in CLN8 in Italian variant late infantile neuronal ceroid lipofuscinosis: another genetic hit in the Mediterranean 53
Totale 7.714
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Categoria #
all - tutte 31.813
article - articoli 27.026
book - libri 0
conference - conferenze 678
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 4.109
Totale 63.626
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201944 0 0 0 0 0 0 0 0 0 0 22 22
2019/20201.383 195 10 13 146 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
2023/2024768 58 98 79 150 133 109 35 45 9 42 10 0
Totale 10.171