CATALOGO DEI PRODOTTI DELLA RICERCA

SALVIATI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 3.711
EU - Europa 2.988
AS - Asia 2.011
SA - Sud America 257
AF - Africa 42
Continente sconosciuto - Info sul continente non disponibili 33
OC - Oceania 9
Totale 9.051
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Nazione #
US - Stati Uniti d'America 3.657
RU - Federazione Russa 964
SG - Singapore 837
GB - Regno Unito 719
CN - Cina 640
IT - Italia 316
SE - Svezia 212
BR - Brasile 206
FR - Francia 179
DE - Germania 159
VN - Vietnam 158
HK - Hong Kong 156
IE - Irlanda 144
FI - Finlandia 138
KR - Corea 66
UA - Ucraina 51
BD - Bangladesh 32
AR - Argentina 25
JP - Giappone 24
IN - India 23
CA - Canada 22
BE - Belgio 20
TR - Turchia 18
PL - Polonia 17
MX - Messico 16
NL - Olanda 16
NG - Nigeria 12
IQ - Iraq 10
AU - Australia 9
CH - Svizzera 9
ES - Italia 8
AT - Austria 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
NI - Nicaragua 3
NO - Norvegia 3
NP - Nepal 3
PK - Pakistan 3
UY - Uruguay 3
UZ - Uzbekistan 3
AZ - Azerbaigian 2
BB - Barbados 2
BG - Bulgaria 2
CR - Costa Rica 2
DK - Danimarca 2
EE - Estonia 2
ET - Etiopia 2
GR - Grecia 2
LV - Lettonia 2
PH - Filippine 2
PT - Portogallo 2
RO - Romania 2
AE - Emirati Arabi Uniti 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BJ - Benin 1
BN - Brunei Darussalam 1
BO - Bolivia 1
DO - Repubblica Dominicana 1
EU - Europa 1
GE - Georgia 1
GP - Guadalupe 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
RS - Serbia 1
SO - Somalia 1
SV - El Salvador 1
TH - Thailandia 1
TT - Trinidad e Tobago 1
TZ - Tanzania 1
UG - Uganda 1
Totale 9.019
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Città #
Southend 617
Singapore 466
Jacksonville 408
Chandler 404
Dallas 398
Ashburn 342
San Jose 302
Moscow 298
Woodbridge 254
Ann Arbor 171
Hong Kong 155
Dublin 144
Houston 140
Beijing 103
Verona 101
Council Bluffs 90
The Dalles 72
New York 69
Ho Chi Minh City 65
Wilmington 58
Lawrence 55
Princeton 55
Jinan 52
Hanoi 49
Los Angeles 45
Nanjing 45
Shenyang 44
Tianjin 32
Hebei 30
Buffalo 28
Sindelfingen 28
Helsinki 27
Nanchang 27
Santa Clara 27
Boardman 24
São Paulo 23
Haikou 22
Hangzhou 21
Munich 21
Brussels 20
Milan 20
Tokyo 20
Changsha 17
Columbus 17
Jiaxing 17
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
Rome 12
Abuja 11
Düsseldorf 11
Norwalk 11
Redwood City 11
Guangzhou 10
Montreal 10
Seattle 10
Seoul 10
Brooklyn 9
Chicago 9
Denver 9
Detroit 9
Fuzhou 9
Taizhou 9
Chennai 8
Mestre 8
Philadelphia 8
Stockholm 8
Belo Horizonte 7
London 7
Paris 7
Auburn Hills 6
Da Nang 6
Naples 6
Ankara 5
Atlanta 5
Baghdad 5
Barnet 5
Boston 5
Buenos Aires 5
Johannesburg 5
Kent 5
Lanzhou 5
Palermo 5
Phoenix 5
Porto Alegre 5
Cairo 4
Clearwater 4
Haiphong 4
Kingston 4
Leeds 4
Totale 5.906
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Nome #
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 286
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 273
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 264
AZT-induced mitochondrial myopathy 239
FAbry STabilization indEX (FASTEX): an innovative tool for the assessment of clinical stabilization in Fabry disease 237
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 218
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 216
Effects of long-term conduction block on membrane properties of reinnervated and normally innervated rat skeletal muscle 215
Anti-N-methyl-d-aspartate receptor encephalitis causing a prolonged depressive disorder evolving to inflammatory brain disease. 208
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 199
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 197
Aortic and Mitral Valve Involvement in Maroteaux-Lamy Syndrome VI: Surgical Implications in the Enzyme Replacement Therapy Era 191
Potenziali evocati acustici troncoencefalici e rilievi anatomo-patologici in un caso di sindrome di Wallenberg 190
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 190
A case of Fabry disease with central nervous system (CNS) demyelinating lesions: a double trouble? 190
BAEP and autopsy findings in Wallenberg syndrome 188
Atypical presentation of thalamic post-stroke pain. 188
[Hereditary sensory neuropathies with acrodystrophic lesions. Nosographic considerations] 186
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 181
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 181
Amyotrophy in Shy-Drager syndrome. 176
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 174
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 171
Inherited neuroaxonal dystrophy in C6 deficient rabbits 169
Forma e attività intermedia della malattia di Farber (Deficit di Ceramidasi acida) in gemelli omozigoti 166
Splicing mutation causes infantile Sandhoff disease 164
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? 163
Unusual renal presentation of Fabry disease in a female patient. 163
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 161
Characterization of FMR1 Repeat Expansion and Intragenic Variants by Indirect Sequence Capture 156
Familial cavernous hemangioma with atypical neuroimaging 151
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 147
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 146
Mitochondrial DNA haplogroups may influence Fabry Disease phenotypei. 143
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 142
Neuropatie immunitarie ed infiammatorie. 142
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 139
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)) 137
Teaching NeuroImages: Brain MRI and DaT-SPECT imaging in adult GM1 gangliosidosis 136
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 133
Pre-diagnosing and managing patients with GM1 gangliosidosis and related disorders by the evaluation of GM1 ganglioside content 133
Transduced fibroblasts and metachromatic leukodystrophy lymphocytes transfer arylsulfatase A to myelinating glia and deficient cells in vitro. 132
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 132
Delphi consensus on the current clinical and therapeutic knowledge on Anderson-Fabry disease. 130
Mutations associated with very late-onset metachromatic leukodystrophy. 128
Late onset MLD with normal nerve conduction associated with two novel missense mutations in the ASA gene 126
Oxidative stress biomarkers in Fabry disease: is there a room for them? 121
Vascular dementia in a population-based autopsy study 114
Neuropathology of cognitively normal elderly 112
Sensory involvement in X-linked spino-bulbar muscolar atrophy (Kennedy's syndrome): an electrophysiological study 112
Nervous system and Fabry disease, from symptoms to diagnosis: damage evaluation and follow-up in adult patients, enzyme replacement, and support therapy. 104
No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis. 103
Neuroaxonal dystrophy with dystonia and pallidal involvement 100
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 97
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients. 91
Totale 9.051
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Categoria #
all - tutte 29.536
article - articoli 29.082
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 454
Totale 59.072
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022536 0 195 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
2025/20263.363 237 228 377 506 800 247 290 146 238 174 47 73
2026/2027115 41 74 0 0 0 0 0 0 0 0 0 0
Totale 9.051