CATALOGO DEI PRODOTTI DELLA RICERCA

SALVIATI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 2.953
EU - Europa 2.690
AS - Asia 1.611
SA - Sud America 232
AF - Africa 20
OC - Oceania 8
Continente sconosciuto - Info sul continente non disponibili 1
Totale 7.515
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Nazione #
US - Stati Uniti d'America 2.921
RU - Federazione Russa 801
GB - Regno Unito 704
SG - Singapore 650
CN - Cina 608
IT - Italia 230
SE - Svezia 211
BR - Brasile 189
FR - Francia 172
DE - Germania 153
HK - Hong Kong 145
IE - Irlanda 144
FI - Finlandia 137
VN - Vietnam 69
UA - Ucraina 51
KR - Corea 47
AR - Argentina 21
BE - Belgio 20
JP - Giappone 17
PL - Polonia 15
IN - India 14
TR - Turchia 14
MX - Messico 13
NL - Olanda 12
BD - Bangladesh 10
CA - Canada 10
CH - Svizzera 9
AU - Australia 8
ID - Indonesia 7
AT - Austria 6
CL - Cile 5
ES - Italia 5
KZ - Kazakistan 5
ZA - Sudafrica 5
EC - Ecuador 4
IQ - Iraq 4
PY - Paraguay 4
CZ - Repubblica Ceca 3
EG - Egitto 3
IL - Israele 3
JM - Giamaica 3
LT - Lituania 3
NO - Norvegia 3
TN - Tunisia 3
UY - Uruguay 3
UZ - Uzbekistan 3
VE - Venezuela 3
AZ - Azerbaigian 2
BB - Barbados 2
DZ - Algeria 2
EE - Estonia 2
LV - Lettonia 2
NP - Nepal 2
PK - Pakistan 2
RO - Romania 2
SA - Arabia Saudita 2
AL - Albania 1
BG - Bulgaria 1
BH - Bahrain 1
BJ - Benin 1
BN - Brunei Darussalam 1
BO - Bolivia 1
CO - Colombia 1
DK - Danimarca 1
DO - Repubblica Dominicana 1
EU - Europa 1
GE - Georgia 1
GR - Grecia 1
IR - Iran 1
LB - Libano 1
LY - Libia 1
MA - Marocco 1
MD - Moldavia 1
MG - Madagascar 1
MN - Mongolia 1
MU - Mauritius 1
NG - Nigeria 1
NI - Nicaragua 1
PA - Panama 1
PE - Perù 1
SO - Somalia 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
Totale 7.515
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Città #
Southend 617
Jacksonville 408
Chandler 404
Dallas 395
Singapore 288
Woodbridge 254
Moscow 252
Ashburn 188
Ann Arbor 171
Hong Kong 145
Dublin 144
Houston 137
Beijing 103
New York 59
Wilmington 57
Lawrence 55
Princeton 55
Jinan 52
Verona 46
Nanjing 45
Shenyang 44
Los Angeles 41
Tianjin 32
Hebei 30
Sindelfingen 28
Nanchang 27
Helsinki 26
Ho Chi Minh City 25
Boardman 24
Buffalo 23
Haikou 22
Hanoi 22
Hangzhou 21
Munich 21
São Paulo 21
Brussels 20
Changsha 17
Columbus 17
Jiaxing 17
Milan 16
Zhengzhou 16
Ningbo 15
Redondo Beach 15
San Francisco 14
Taiyuan 14
Tokyo 14
Dearborn 13
Rio de Janeiro 13
Turku 13
Warsaw 13
Lancaster 12
Redmond 12
Santa Clara 12
Düsseldorf 11
Norwalk 11
Redwood City 11
Guangzhou 10
Seattle 10
The Dalles 10
Detroit 9
Fuzhou 9
Seoul 9
Taizhou 9
Brooklyn 8
Chicago 8
Council Bluffs 8
Mestre 8
Stockholm 8
Belo Horizonte 7
Denver 7
Frankfurt am Main 7
Philadelphia 7
Rome 7
Auburn Hills 6
London 6
Naples 6
Buenos Aires 5
Kent 5
Lanzhou 5
Montreal 5
Orem 5
Porto Alegre 5
Ankara 4
Boston 4
Clearwater 4
Haiphong 4
Johannesburg 4
Leeds 4
Washington 4
Bern 3
Bologna 3
Brasília 3
Cairo 3
Chennai 3
Dhaka 3
Kingston 3
Mehlingen 3
Melbourne 3
Mexico City 3
Montevideo 3
Totale 4.828
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Nome #
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 249
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 244
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 241
FAbry STabilization indEX (FASTEX): an innovative tool for the assessment of clinical stabilization in Fabry disease 207
AZT-induced mitochondrial myopathy 195
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 189
Effects of long-term conduction block on membrane properties of reinnervated and normally innervated rat skeletal muscle 182
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 180
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 176
Anti-N-methyl-d-aspartate receptor encephalitis causing a prolonged depressive disorder evolving to inflammatory brain disease. 176
Potenziali evocati acustici troncoencefalici e rilievi anatomo-patologici in un caso di sindrome di Wallenberg 168
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 167
Atypical presentation of thalamic post-stroke pain. 162
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 159
A case of Fabry disease with central nervous system (CNS) demyelinating lesions: a double trouble? 156
BAEP and autopsy findings in Wallenberg syndrome 152
Aortic and Mitral Valve Involvement in Maroteaux-Lamy Syndrome VI: Surgical Implications in the Enzyme Replacement Therapy Era 152
Amyotrophy in Shy-Drager syndrome. 151
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 150
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 149
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 146
[Hereditary sensory neuropathies with acrodystrophic lesions. Nosographic considerations] 145
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 144
Splicing mutation causes infantile Sandhoff disease 142
Unusual renal presentation of Fabry disease in a female patient. 141
Forma e attività intermedia della malattia di Farber (Deficit di Ceramidasi acida) in gemelli omozigoti 136
Inherited neuroaxonal dystrophy in C6 deficient rabbits 133
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? 133
Familial cavernous hemangioma with atypical neuroimaging 129
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 128
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)) 123
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 123
Characterization of FMR1 Repeat Expansion and Intragenic Variants by Indirect Sequence Capture 123
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 118
Mitochondrial DNA haplogroups may influence Fabry Disease phenotypei. 117
Neuropatie immunitarie ed infiammatorie. 116
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 112
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 110
Mutations associated with very late-onset metachromatic leukodystrophy. 109
Transduced fibroblasts and metachromatic leukodystrophy lymphocytes transfer arylsulfatase A to myelinating glia and deficient cells in vitro. 109
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 108
Delphi consensus on the current clinical and therapeutic knowledge on Anderson-Fabry disease. 105
Pre-diagnosing and managing patients with GM1 gangliosidosis and related disorders by the evaluation of GM1 ganglioside content 104
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 104
Teaching NeuroImages: Brain MRI and DaT-SPECT imaging in adult GM1 gangliosidosis 103
Late onset MLD with normal nerve conduction associated with two novel missense mutations in the ASA gene 101
Vascular dementia in a population-based autopsy study 97
Sensory involvement in X-linked spino-bulbar muscolar atrophy (Kennedy's syndrome): an electrophysiological study 95
Oxidative stress biomarkers in Fabry disease: is there a room for them? 95
Neuropathology of cognitively normal elderly 92
Neuroaxonal dystrophy with dystonia and pallidal involvement 90
No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis. 84
Nervous system and Fabry disease, from symptoms to diagnosis: damage evaluation and follow-up in adult patients, enzyme replacement, and support therapy. 81
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients. 74
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 72
Totale 7.547
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Categoria #
all - tutte 24.410
article - articoli 24.033
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 377
Totale 48.820
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021293 0 0 0 0 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
2025/20261.974 237 228 377 506 626 0 0 0 0 0 0 0
Totale 7.547