CATALOGO DEI PRODOTTI DELLA RICERCA

SALVIATI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 2.482
EU - Europa 1.989
AS - Asia 1.349
SA - Sud America 178
AF - Africa 12
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 1
Totale 6.019
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Nazione #
US - Stati Uniti d'America 2.463
GB - Regno Unito 698
SG - Singapore 567
CN - Cina 528
IT - Italia 225
SE - Svezia 205
FR - Francia 171
BR - Brasile 153
DE - Germania 152
IE - Irlanda 144
HK - Hong Kong 140
FI - Finlandia 137
RU - Federazione Russa 135
UA - Ucraina 50
KR - Corea 38
BE - Belgio 20
VN - Vietnam 17
NL - Olanda 12
TR - Turchia 11
IN - India 10
AR - Argentina 9
AU - Australia 8
CH - Svizzera 8
AT - Austria 6
JP - Giappone 6
MX - Messico 6
BD - Bangladesh 5
CA - Canada 5
CL - Cile 4
PL - Polonia 4
ZA - Sudafrica 4
CZ - Repubblica Ceca 3
ES - Italia 3
ID - Indonesia 3
IL - Israele 3
IQ - Iraq 3
JM - Giamaica 3
NO - Norvegia 3
UZ - Uzbekistan 3
VE - Venezuela 3
EC - Ecuador 2
EE - Estonia 2
EG - Egitto 2
KZ - Kazakistan 2
LT - Lituania 2
LV - Lettonia 2
NP - Nepal 2
PK - Pakistan 2
PY - Paraguay 2
RO - Romania 2
SA - Arabia Saudita 2
TN - Tunisia 2
UY - Uruguay 2
AL - Albania 1
AZ - Azerbaigian 1
BB - Barbados 1
BG - Bulgaria 1
BH - Bahrain 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CO - Colombia 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EU - Europa 1
GE - Georgia 1
GR - Grecia 1
IR - Iran 1
MA - Marocco 1
MD - Moldavia 1
MN - Mongolia 1
MU - Mauritius 1
NI - Nicaragua 1
PA - Panama 1
PE - Perù 1
SO - Somalia 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
Totale 6.019
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Città #
Southend 617
Jacksonville 408
Chandler 404
Singapore 285
Woodbridge 254
Ann Arbor 171
Dallas 153
Dublin 144
Hong Kong 140
Houston 133
Ashburn 124
Beijing 80
Wilmington 57
Lawrence 55
Princeton 55
Jinan 52
Nanjing 45
Verona 45
New York 44
Shenyang 43
Hebei 30
Tianjin 29
Sindelfingen 28
Nanchang 27
Helsinki 26
Boardman 24
Haikou 22
Munich 21
Brussels 20
Hangzhou 20
Columbus 17
Jiaxing 17
Changsha 16
Milan 16
Ningbo 15
Zhengzhou 15
San Francisco 14
Taiyuan 14
Dearborn 13
Turku 13
Lancaster 12
Redmond 12
Rio de Janeiro 12
São Paulo 12
Düsseldorf 11
Norwalk 11
Redwood City 11
Guangzhou 10
The Dalles 10
Detroit 9
Fuzhou 9
Seattle 9
Seoul 9
Council Bluffs 8
Los Angeles 8
Mestre 8
Santa Clara 8
Taizhou 8
Chicago 7
Frankfurt am Main 7
Ho Chi Minh City 7
Philadelphia 7
Auburn Hills 6
Naples 6
Rome 6
Hanoi 5
Kent 5
Lanzhou 5
Moscow 5
Belo Horizonte 4
Brooklyn 4
Clearwater 4
Leeds 4
London 4
Porto Alegre 4
Washington 4
Bern 3
Bologna 3
Brasília 3
Johannesburg 3
Kingston 3
Mehlingen 3
Melbourne 3
Oslo 3
Palermo 3
Tashkent 3
Tokyo 3
Venezia 3
Warsaw 3
West Bromwich 3
Baghdad 2
Barbacena 2
Bexley 2
Boston 2
Brno 2
Buenos Aires 2
Cairo 2
Charleston 2
Concordia Sagittaria 2
Conselice 2
Totale 4.039
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Nome #
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 238
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 189
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 174
FAbry STabilization indEX (FASTEX): an innovative tool for the assessment of clinical stabilization in Fabry disease 163
Potenziali evocati acustici troncoencefalici e rilievi anatomo-patologici in un caso di sindrome di Wallenberg 158
AZT-induced mitochondrial myopathy 154
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 145
Anti-N-methyl-d-aspartate receptor encephalitis causing a prolonged depressive disorder evolving to inflammatory brain disease. 140
Effects of long-term conduction block on membrane properties of reinnervated and normally innervated rat skeletal muscle 139
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 135
Atypical presentation of thalamic post-stroke pain. 130
Splicing mutation causes infantile Sandhoff disease 127
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 126
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 124
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 118
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 118
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 116
BAEP and autopsy findings in Wallenberg syndrome 115
Forma e attività intermedia della malattia di Farber (Deficit di Ceramidasi acida) in gemelli omozigoti 114
Amyotrophy in Shy-Drager syndrome. 113
Familial cavernous hemangioma with atypical neuroimaging 113
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 112
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 111
A case of Fabry disease with central nervous system (CNS) demyelinating lesions: a double trouble? 110
Inherited neuroaxonal dystrophy in C6 deficient rabbits 109
[Hereditary sensory neuropathies with acrodystrophic lesions. Nosographic considerations] 108
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? 108
Molecular genetic characterization of two metachromatic leukodystrophy patients who carry the T799G mutation acid show different phenotypes; description of a novel null-type mutation (Human Genetics (1998) 102 (459-463)) 106
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 105
Unusual renal presentation of Fabry disease in a female patient. 102
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 102
Neuropatie immunitarie ed infiammatorie. 102
Aortic and Mitral Valve Involvement in Maroteaux-Lamy Syndrome VI: Surgical Implications in the Enzyme Replacement Therapy Era 102
Transduced fibroblasts and metachromatic leukodystrophy lymphocytes transfer arylsulfatase A to myelinating glia and deficient cells in vitro. 101
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 98
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 96
Mutations associated with very late-onset metachromatic leukodystrophy. 95
Late onset MLD with normal nerve conduction associated with two novel missense mutations in the ASA gene 94
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 93
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 91
Vascular dementia in a population-based autopsy study 89
Pre-diagnosing and managing patients with GM1 gangliosidosis and related disorders by the evaluation of GM1 ganglioside content 88
Teaching NeuroImages: Brain MRI and DaT-SPECT imaging in adult GM1 gangliosidosis 86
Neuropathology of cognitively normal elderly 84
Sensory involvement in X-linked spino-bulbar muscolar atrophy (Kennedy's syndrome): an electrophysiological study 84
Neuroaxonal dystrophy with dystonia and pallidal involvement 81
Delphi consensus on the current clinical and therapeutic knowledge on Anderson-Fabry disease. 81
Mitochondrial DNA haplogroups may influence Fabry Disease phenotypei. 80
Characterization of FMR1 Repeat Expansion and Intragenic Variants by Indirect Sequence Capture 78
Oxidative stress biomarkers in Fabry disease: is there a room for them? 76
No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis. 74
Nervous system and Fabry disease, from symptoms to diagnosis: damage evaluation and follow-up in adult patients, enzyme replacement, and support therapy. 71
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients. 62
Whole-exome sequencing of the mummified remains of Cangrande della Scala (1291{ extendash}1329 {CE}) indicates the first known case of late-onset Pompe disease 62
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 61
Totale 6.051
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Categoria #
all - tutte 20.876
article - articoli 20.543
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 333
Totale 41.752
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021368 0 0 31 44 49 56 14 42 41 11 59 21
2021/2022570 34 195 7 63 1 19 7 48 28 17 42 109
2022/20231.026 71 110 101 184 96 240 10 70 105 5 23 11
2023/2024410 14 41 29 59 72 60 19 23 4 16 42 31
2024/20251.077 78 73 30 163 81 34 50 41 171 42 80 234
2025/2026478 237 228 13 0 0 0 0 0 0 0 0 0
Totale 6.051