CATANIA, ALESSIA
 Distribuzione geografica
Continente #
NA - Nord America 205
EU - Europa 179
AS - Asia 110
SA - Sud America 16
AF - Africa 3
OC - Oceania 3
Totale 516
Nazione #
US - Stati Uniti d'America 198
IT - Italia 38
SG - Singapore 34
SE - Svezia 33
IE - Irlanda 25
DE - Germania 24
CN - Cina 18
RU - Federazione Russa 16
IR - Iran 13
HK - Hong Kong 12
GB - Regno Unito 10
FR - Francia 9
BR - Brasile 7
PK - Pakistan 7
CA - Canada 6
CL - Cile 6
BE - Belgio 5
IN - India 5
SA - Arabia Saudita 5
AT - Austria 4
ES - Italia 4
JP - Giappone 4
AU - Australia 3
CO - Colombia 3
ID - Indonesia 3
NL - Olanda 3
TR - Turchia 3
CZ - Repubblica Ceca 2
EG - Egitto 2
FI - Finlandia 2
PT - Portogallo 2
UA - Ucraina 2
AE - Emirati Arabi Uniti 1
AZ - Azerbaigian 1
BD - Bangladesh 1
KR - Corea 1
MU - Mauritius 1
MX - Messico 1
MY - Malesia 1
PH - Filippine 1
Totale 516
Città #
Singapore 29
Dublin 25
Chandler 22
Fairfield 21
Frankfurt am Main 17
Ann Arbor 16
Seattle 12
Milan 11
Cambridge 9
Hong Kong 9
New York 9
Woodbridge 9
Houston 8
Princeton 8
Ashburn 7
Altamura 6
Nunoa 6
Sao Goncalo 6
Brussels 5
Medina 5
Shanghai 5
Wilmington 5
Birmingham 4
Cagliari 4
Madrid 4
Santa Clara 4
Andover 3
Bogotá 3
Dearborn 3
Jacksonville 3
Jakarta 3
Lawrence 3
Melbourne 3
Ottawa 3
Amsterdam 2
Bani Suwayf 2
Edinburgh 2
Ferrara 2
Helsinki 2
Karachi 2
Kunming 2
Lahore 2
Los Angeles 2
Mumbai 2
Nanjing 2
San Diego 2
Saray 2
Thrissur 2
Toronto 2
Vialonga 2
Ankara 1
Atlanta 1
Baku 1
Beijing 1
Brighton 1
Brno 1
Cadelbosco 1
Canoas 1
Cardiff 1
Carugate 1
Changsha 1
Chicago 1
Cranford 1
Dhaka 1
Dottingen 1
Falkenstein 1
Falls Church 1
Florence 1
Fremont 1
Funabashi 1
Hebei 1
Hefei 1
Jinan 1
Kuala Lumpur 1
Lexington 1
Manila 1
Mexico City 1
Montesilvano 1
Montreal 1
Nagold 1
New Bedfont 1
Norwalk 1
Nottingham 1
Nuremberg 1
Shenyang 1
Strasbourg 1
Tehran 1
Verona 1
Totale 360
Nome #
Characterization of disease genes and mechanisms causing neurodegenerative phenotypes 190
Compound heterozygous missense and deep intronic variants in NDUFAF6 unraveled by exome sequencing and mRNA analysis 128
Neuro-telehealth for fragile patients in a tertiary referral neurological institute during the COVID-19 pandemic in Milan, Lombardy 101
R106C TFG variant causes infantile neuroaxonal dystrophy “plus” syndrome 86
Homozygous mutations in C1QBP as cause of progressive external ophthalmoplegia (PEO) and mitochondrial myopathy with multiple mtDNA deletions 9
Sex distribution and classification of GBA1 variants in an Italian cohort of Parkinson's disease patients analyzed over the last seventeen years 7
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy 6
Evaluation of Mitochondrial Dysfunction and Idebenone Responsiveness in Fibroblasts from Leber’s Hereditary Optic Neuropathy (LHON) Subjects 6
A novel MT-ATP6 variant associated with complicated ataxia in two unrelated Italian patients: case report and functional studies 6
Bi-allelic LETM1 variants perturb mitochondrial ion homeostasis leading to a clinical spectrum with predominant nervous system involvement 6
Biallelic Variants in ENDOG Associated with Mitochondrial Myopathy and Multiple mtDNA Deletions 5
Leber's Hereditary Optic Neuropathy: A Report on Novel mtDNA Pathogenic Variants 5
Role of pitrm1 in mitochondrial dysfunction and neurodegeneration 4
Multifocal vitelliform lesions associated with mitochondrial retinopathy 4
The m.3890G>A/MT-ND1 mtDNA rare pathogenic variant: Expanding clinical and MRI phenotypes 4
Totale 567
Categoria #
all - tutte 2.356
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.356


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202028 0 0 0 0 0 0 12 5 4 2 3 2
2020/202122 2 2 3 2 4 2 1 2 1 2 1 0
2021/202257 1 3 16 12 2 2 1 3 5 1 6 5
2022/2023106 10 39 6 6 2 15 1 14 9 0 4 0
2023/2024112 3 2 11 9 12 20 18 15 4 3 3 12
2024/2025179 8 25 23 9 18 14 82 0 0 0 0 0
Totale 567