CATALOGO DEI PRODOTTI DELLA RICERCA

SALVIATI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 3.519
EU - Europa 2.963
AS - Asia 1.985
SA - Sud America 253
AF - Africa 42
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 1
Totale 8.772
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Nazione #
US - Stati Uniti d'America 3.476
RU - Federazione Russa 964
SG - Singapore 836
GB - Regno Unito 719
CN - Cina 637
IT - Italia 297
SE - Svezia 211
BR - Brasile 203
FR - Francia 178
DE - Germania 159
VN - Vietnam 158
HK - Hong Kong 154
IE - Irlanda 144
FI - Finlandia 138
KR - Corea 65
UA - Ucraina 51
AR - Argentina 24
JP - Giappone 24
IN - India 23
BE - Belgio 20
TR - Turchia 18
PL - Polonia 17
CA - Canada 16
MX - Messico 16
NL - Olanda 15
BD - Bangladesh 13
NG - Nigeria 12
IQ - Iraq 10
AU - Australia 9
CH - Svizzera 9
AT - Austria 7
ES - Italia 7
ID - Indonesia 7
ZA - Sudafrica 7
CL - Cile 5
EC - Ecuador 5
KZ - Kazakistan 5
EG - Egitto 4
JM - Giamaica 4
PY - Paraguay 4
SA - Arabia Saudita 4
TN - Tunisia 4
VE - Venezuela 4
AL - Albania 3
CO - Colombia 3
CZ - Repubblica Ceca 3
DZ - Algeria 3
IL - Israele 3
JO - Giordania 3
LT - Lituania 3
MA - Marocco 3
MY - Malesia 3
NO - Norvegia 3
NP - Nepal 3
PK - Pakistan 3
UY - Uruguay 3
UZ - Uzbekistan 3
AZ - Azerbaigian 2
BB - Barbados 2
DK - Danimarca 2
EE - Estonia 2
ET - Etiopia 2
GR - Grecia 2
LV - Lettonia 2
NI - Nicaragua 2
PH - Filippine 2
RO - Romania 2
AE - Emirati Arabi Uniti 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
BJ - Benin 1
BN - Brunei Darussalam 1
BO - Bolivia 1
DO - Repubblica Dominicana 1
EU - Europa 1
GE - Georgia 1
IR - Iran 1
KH - Cambogia 1
LB - Libano 1
LY - Libia 1
MD - Moldavia 1
MG - Madagascar 1
MN - Mongolia 1
MU - Mauritius 1
PA - Panama 1
PE - Perù 1
PT - Portogallo 1
RS - Serbia 1
SO - Somalia 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
TZ - Tanzania 1
UG - Uganda 1
Totale 8.772
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Città #
Southend 617
Singapore 466
Jacksonville 408
Chandler 404
Dallas 396
Ashburn 332
Moscow 298
San Jose 277
Woodbridge 254
Ann Arbor 171
Hong Kong 153
Dublin 144
Houston 139
Beijing 103
Verona 101
The Dalles 72
Ho Chi Minh City 65
New York 65
Wilmington 57
Lawrence 55
Princeton 55
Jinan 52
Hanoi 49
Nanjing 45
Los Angeles 44
Shenyang 44
Tianjin 32
Hebei 30
Sindelfingen 28
Helsinki 27
Nanchang 27
Buffalo 25
Boardman 24
Haikou 22
São Paulo 22
Hangzhou 21
Munich 21
Brussels 20
Tokyo 20
Changsha 17
Columbus 17
Jiaxing 17
Santa Clara 17
Milan 16
Orem 16
Zhengzhou 16
Ningbo 15
Redondo Beach 15
San Francisco 15
Warsaw 15
Taiyuan 14
Dearborn 13
Frankfurt am Main 13
Rio de Janeiro 13
Turku 13
Lancaster 12
Redmond 12
Abuja 11
Düsseldorf 11
Norwalk 11
Redwood City 11
Council Bluffs 10
Guangzhou 10
Montreal 10
Rome 10
Seattle 10
Brooklyn 9
Chicago 9
Denver 9
Detroit 9
Fuzhou 9
Seoul 9
Taizhou 9
Chennai 8
Mestre 8
Stockholm 8
Belo Horizonte 7
London 7
Paris 7
Philadelphia 7
Auburn Hills 6
Da Nang 6
Naples 6
Ankara 5
Baghdad 5
Barnet 5
Boston 5
Buenos Aires 5
Johannesburg 5
Kent 5
Lanzhou 5
Porto Alegre 5
Atlanta 4
Cairo 4
Clearwater 4
Haiphong 4
Kingston 4
Leeds 4
Madrid 4
Mexico City 4
Totale 5.755
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Nome #
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 284
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 268
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 261
FAbry STabilization indEX (FASTEX): an innovative tool for the assessment of clinical stabilization in Fabry disease 233
AZT-induced mitochondrial myopathy 224
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 214
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 212
Effects of long-term conduction block on membrane properties of reinnervated and normally innervated rat skeletal muscle 212
Anti-N-methyl-d-aspartate receptor encephalitis causing a prolonged depressive disorder evolving to inflammatory brain disease. 202
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 194
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 193
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 188
Aortic and Mitral Valve Involvement in Maroteaux-Lamy Syndrome VI: Surgical Implications in the Enzyme Replacement Therapy Era 188
Atypical presentation of thalamic post-stroke pain. 185
Potenziali evocati acustici troncoencefalici e rilievi anatomo-patologici in un caso di sindrome di Wallenberg 184
BAEP and autopsy findings in Wallenberg syndrome 183
[Hereditary sensory neuropathies with acrodystrophic lesions. Nosographic considerations] 179
A case of Fabry disease with central nervous system (CNS) demyelinating lesions: a double trouble? 178
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 178
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 176
Amyotrophy in Shy-Drager syndrome. 171
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 171
Inherited neuroaxonal dystrophy in C6 deficient rabbits 166
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 165
Forma e attività intermedia della malattia di Farber (Deficit di Ceramidasi acida) in gemelli omozigoti 162
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? 160
Splicing mutation causes infantile Sandhoff disease 158
Unusual renal presentation of Fabry disease in a female patient. 157
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 157
Characterization of FMR1 Repeat Expansion and Intragenic Variants by Indirect Sequence Capture 154
Familial cavernous hemangioma with atypical neuroimaging 147
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 144
Mitochondrial DNA haplogroups may influence Fabry Disease phenotypei. 139
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 138
Neuropatie immunitarie ed infiammatorie. 135
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)) 134
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 134
Teaching NeuroImages: Brain MRI and DaT-SPECT imaging in adult GM1 gangliosidosis 131
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 130
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 130
Pre-diagnosing and managing patients with GM1 gangliosidosis and related disorders by the evaluation of GM1 ganglioside content 129
Transduced fibroblasts and metachromatic leukodystrophy lymphocytes transfer arylsulfatase A to myelinating glia and deficient cells in vitro. 128
Mutations associated with very late-onset metachromatic leukodystrophy. 127
Delphi consensus on the current clinical and therapeutic knowledge on Anderson-Fabry disease. 125
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 123
Late onset MLD with normal nerve conduction associated with two novel missense mutations in the ASA gene 122
Oxidative stress biomarkers in Fabry disease: is there a room for them? 114
Vascular dementia in a population-based autopsy study 112
Neuropathology of cognitively normal elderly 112
Sensory involvement in X-linked spino-bulbar muscolar atrophy (Kennedy's syndrome): an electrophysiological study 111
Nervous system and Fabry disease, from symptoms to diagnosis: damage evaluation and follow-up in adult patients, enzyme replacement, and support therapy. 101
No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis. 100
Neuroaxonal dystrophy with dystonia and pallidal involvement 99
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 94
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients. 88
Totale 8.804
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Categoria #
all - tutte 26.965
article - articoli 26.546
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 419
Totale 53.930
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202191 0 0 0 0 0 0 0 0 0 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
2025/20263.231 237 228 377 506 800 247 290 146 238 162 0 0
Totale 8.804