CATALOGO DEI PRODOTTI DELLA RICERCA

SALVIATI, Alessandro
 Distribuzione geografica
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Continente #
NA - Nord America 4.150
EU - Europa 3.025
AS - Asia 2.023
SA - Sud America 266
AF - Africa 42
Continente sconosciuto - Info sul continente non disponibili 39
OC - Oceania 9
Totale 9.554
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Nazione #
US - Stati Uniti d'America 4.045
RU - Federazione Russa 967
SG - Singapore 837
GB - Regno Unito 722
CN - Cina 640
IT - Italia 343
BR - Brasile 212
SE - Svezia 212
FR - Francia 179
DE - Germania 160
VN - Vietnam 159
HK - Hong Kong 156
IE - Irlanda 144
FI - Finlandia 138
KR - Corea 66
UA - Ucraina 52
CA - Canada 51
BD - Bangladesh 32
AR - Argentina 25
JP - Giappone 25
IN - India 23
BE - Belgio 20
TR - Turchia 19
MX - Messico 17
PL - Polonia 17
NL - Olanda 16
NG - Nigeria 12
IQ - Iraq 10
AU - Australia 9
CH - Svizzera 9
ID - Indonesia 9
ES - Italia 8
AT - Austria 7
ZA - Sudafrica 7
CR - Costa Rica 6
CW - ???statistics.table.value.countryCode.CW??? 6
EC - Ecuador 6
IL - Israele 6
JM - Giamaica 6
CL - Cile 5
CO - Colombia 5
KZ - Kazakistan 5
NI - Nicaragua 5
SA - Arabia Saudita 5
EG - Egitto 4
GT - Guatemala 4
PH - Filippine 4
PY - Paraguay 4
SV - El Salvador 4
TN - Tunisia 4
VE - Venezuela 4
AL - Albania 3
CZ - Repubblica Ceca 3
DK - Danimarca 3
DZ - Algeria 3
EE - Estonia 3
JO - Giordania 3
LT - Lituania 3
MA - Marocco 3
MY - Malesia 3
NO - Norvegia 3
NP - Nepal 3
PK - Pakistan 3
PR - Porto Rico 3
UY - Uruguay 3
UZ - Uzbekistan 3
AZ - Azerbaigian 2
BB - Barbados 2
BG - Bulgaria 2
ET - Etiopia 2
GP - Guadalupe 2
GR - Grecia 2
LV - Lettonia 2
PA - Panama 2
PT - Portogallo 2
RO - Romania 2
TT - Trinidad e Tobago 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
IR - Iran 1
KH - Cambogia 1
LB - Libano 1
LY - Libia 1
MD - Moldavia 1
MG - Madagascar 1
MN - Mongolia 1
MU - Mauritius 1
PE - Perù 1
QA - Qatar 1
RS - Serbia 1
SO - Somalia 1
TH - Thailandia 1
TZ - Tanzania 1
Totale 9.521
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Città #
Southend 617
Ashburn 480
Singapore 466
Jacksonville 409
Chandler 404
Dallas 404
San Jose 354
Moscow 298
Woodbridge 254
Ann Arbor 171
Hong Kong 155
Dublin 144
Houston 141
Beijing 103
Verona 101
Council Bluffs 90
New York 73
The Dalles 72
Ho Chi Minh City 65
Wilmington 59
Lawrence 55
Princeton 55
Jinan 52
Hanoi 49
Los Angeles 49
Nanjing 45
Shenyang 44
Santa Clara 34
Tianjin 32
Hebei 30
São Paulo 29
Buffalo 28
Sindelfingen 28
Helsinki 27
Nanchang 27
Boardman 24
Haikou 22
Milan 22
Hangzhou 21
Munich 21
Tokyo 21
Brussels 20
Changsha 17
Columbus 17
Jiaxing 17
Annandale 16
Orem 16
Rome 16
San Francisco 16
Warsaw 16
Zhengzhou 16
Ningbo 15
Redondo Beach 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
Seattle 11
Denver 10
Detroit 10
Guangzhou 10
Montreal 10
Seoul 10
Brooklyn 9
Chicago 9
Fuzhou 9
Naples 9
Taizhou 9
Chennai 8
Mestre 8
Philadelphia 8
Stockholm 8
Belo Horizonte 7
London 7
Paris 7
Toronto 7
Atlanta 6
Auburn Hills 6
Da Nang 6
Palermo 6
Willemstad 6
Ankara 5
Baghdad 5
Barnet 5
Boston 5
Buenos Aires 5
Haiphong 5
Johannesburg 5
Kent 5
Kingston 5
Lanzhou 5
Madrid 5
Managua 5
Totale 6.162
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Nome #
A 48-bp insertion between exon 13 and 14 of the HEXB gene causes infantile-onset Sandhoff disease 293
La biopsia del nervo periferico. Indicazioni, metodiche e principali quadri patologici [Peripheral nerve biopsy. Indications, methods and principal pathological pictures] 288
A common beta hexosaminidase gene mutation in adult Sandhoff disease patients. 281
AZT-induced mitochondrial myopathy 250
FAbry STabilization indEX (FASTEX): an innovative tool for the assessment of clinical stabilization in Fabry disease 242
Prevalence of multiple sclerosis in Verona, Italy: an epidemiologic and genetic study 237
Effects of long-term conduction block on membrane properties of reinnervated and normally innervated rat skeletal muscle 224
A novel mutation which represents the fifth non-pathogenic polymorphism in the coding sequence of the arylsulfatase A gene 223
Anti-N-methyl-d-aspartate receptor encephalitis causing a prolonged depressive disorder evolving to inflammatory brain disease. 219
Potenziali evocati acustici troncoencefalici e rilievi anatomo-patologici in un caso di sindrome di Wallenberg 217
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations 206
COX-2 promoter region polymorphisms in multiple sclerosis: lack of association of -765G>C with disease risk 203
CD45 and multiple sclerosis: the exon 4 C77G polymorphism (additional studies and meta-analysis) and new markers 201
A case of Fabry disease with central nervous system (CNS) demyelinating lesions: a double trouble? 201
Aortic and Mitral Valve Involvement in Maroteaux-Lamy Syndrome VI: Surgical Implications in the Enzyme Replacement Therapy Era 200
BAEP and autopsy findings in Wallenberg syndrome 198
Atypical presentation of thalamic post-stroke pain. 195
[Hereditary sensory neuropathies with acrodystrophic lesions. Nosographic considerations] 192
A novel 4-bp deletion creates a premature stop codon and dramatically decreases HEXB mRNA levels in a severe case of Sandhoff disease 187
Prevalence of multiple sclerosis in Verona, Italy: an epidemiological and genetic study. 187
Forma e attività intermedia della malattia di Farber (Deficit di Ceramidasi acida) in gemelli omozigoti 186
Myelin oligodendrocyte glycoprotein polymorphisms and multiple sclerosis. 185
Amyotrophy in Shy-Drager syndrome. 184
Two novel frameshift mutations in the adrenoleukodystrophy gene in Italian patients 184
Inherited neuroaxonal dystrophy in C6 deficient rabbits 179
Could mitochondrial haplogroups play a role in sporadic amyotrophic lateral sclerosis? 172
Splicing mutation causes infantile Sandhoff disease 171
Unusual renal presentation of Fabry disease in a female patient. 170
GM1 gangliosidosis and Morquio B disease: An update on genetic alterations and clinical findings. 168
Characterization of FMR1 Repeat Expansion and Intragenic Variants by Indirect Sequence Capture 167
Familial cavernous hemangioma with atypical neuroimaging 160
Neuropatie immunitarie ed infiammatorie. 157
Prevalence of dementia and apoliprotein E genotype distribution in the elderly of Buttapietra, Verona Province, Italy 156
Natural history of motor neuron disease in adult onset GM2-gangliosidosis: a case report with 25 years of follow-up 155
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 151
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)) 149
Two novel missense mutations causing adrenoleukodystrophy in Italian patients 148
Mitochondrial DNA haplogroups may influence Fabry Disease phenotypei. 148
Myelin Oligodendrocyte glycoprotein (MOG) polymorphisms and adrenoleukodystrophy 142
La guaina mielinica causa di neuropatia. Identificazione delle radicolonevriti demielinizzanti. 142
Teaching NeuroImages: Brain MRI and DaT-SPECT imaging in adult GM1 gangliosidosis 141
Transduced fibroblasts and metachromatic leukodystrophy lymphocytes transfer arylsulfatase A to myelinating glia and deficient cells in vitro. 140
Pre-diagnosing and managing patients with GM1 gangliosidosis and related disorders by the evaluation of GM1 ganglioside content 137
Oxidative stress biomarkers in Fabry disease: is there a room for them? 137
Late onset MLD with normal nerve conduction associated with two novel missense mutations in the ASA gene 136
Delphi consensus on the current clinical and therapeutic knowledge on Anderson-Fabry disease. 135
Mutations associated with very late-onset metachromatic leukodystrophy. 134
Vascular dementia in a population-based autopsy study 122
Neuropathology of cognitively normal elderly 118
Sensory involvement in X-linked spino-bulbar muscolar atrophy (Kennedy's syndrome): an electrophysiological study 118
Nervous system and Fabry disease, from symptoms to diagnosis: damage evaluation and follow-up in adult patients, enzyme replacement, and support therapy. 108
No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis. 108
Neuroaxonal dystrophy with dystonia and pallidal involvement 106
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis. 100
Genetic association and altered gene expression of mir-155 in multiple sclerosis patients. 96
Totale 9.554
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Categoria #
all - tutte 31.115
article - articoli 30.630
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 485
Totale 62.230
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022334 0 0 0 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
2026/2027618 41 75 133 369 0 0 0 0 0 0 0 0
Totale 9.554