I agree that this site is using cookies. You can find further informations here.
X
Catania, Alessia
81  results:
Search for persons X
?
1

Genetic variants affecting NQO1 protein levels impact the e..:

Aleo, Serena Jasmine ; Del Dotto, Valentina ; Romagnoli, Martina...
Cell Reports Medicine.  5 (2024)  2 - p. 101383 , 2024
Link: https://doi.org/10.1016/..
 
?
2

New insights into idebenone therapy in relation to NQO1:

La Morgia, Chiara ; Aleo, Serena Jasmine ; Del Dotto, Valentina...
Acta Ophthalmologica.  102 (2024)  S279 - p. , 2024
Link: https://doi.org/10.1111/..
 
?
3

A novel MT-ATP6 variant associated with complicated ataxia ..:

Sala, Daniele ; Marchet, Silvia ; Nanetti, Lorenzo...
Orphanet Journal of Rare Diseases.  19 (2024)  1 - p. , 2024
Link: https://doi.org/10.1186/..
 
?
4

Sex distribution and classification of GBA1 variants in an ..:

Panteghini, Celeste ; Reale, Chiara ; Colangelo, Isabel...
Parkinsonism & Related Disorders.  117 (2023)  - p. 105919 , 2023
Link: https://doi.org/10.1016/..
 
?
5

Evaluation of Mitochondrial Dysfunction and Idebenone Respo..:

Baglivo, Mirko ; Nasca, Alessia ; Lamantea, Eleonora...
International Journal of Molecular Sciences.  24 (2023)  16 - p. 12580 , 2023
Link: https://doi.org/10.3390/..
 
?
6

Biallelic Variants in ENDOG Associated with Mitochondrial M..:

Nasca, Alessia ; Legati, Andrea ; Meneri, Megi...
Cells.  11 (2022)  6 - p. 974 , 2022
Link: https://doi.org/10.3390/..
 
?
7

Bi-allelic LETM1 variants perturb mitochondrial ion homeost..:

Kaiyrzhanov, Rauan ; Mohammed, Sami E.M. ; Maroofian, Reza...
The American Journal of Human Genetics.  109 (2022)  9 - p. 1692-1712 , 2022
Link: https://doi.org/10.1016/..
 
?
8

Role of PITRM1 in Mitochondrial Dysfunction and Neurodegene..:

Brunetti, Dario ; Catania, Alessia ; Viscomi, Carlo...
Biomedicines.  9 (2021)  7 - p. 833 , 2021
Link: https://doi.org/10.3390/..
 
?
9

The m.3890G>A/MT-ND1 mtDNA rare pathogenic variant: Expandi..:

Vacchiano, Veria ; Caporali, Leonardo ; La Morgia, Chiara...
Mitochondrion.  60 (2021)  - p. 142-149 , 2021
Link: https://doi.org/10.1016/..
 
?
10

Leber's Hereditary Optic Neuropathy: A Report on Novel mtDN..:

Peverelli, Lorenzo ; Catania, Alessia ; Marchet, Silvia...
Frontiers in Neurology.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
?
11

DNMT1-complex disorder caused by a novel mutation associate..:

Catania, Alessia ; Peverelli, Lorenzo ; Tabano, Silvia..
Neurological Sciences.  40 (2019)  9 - p. 1963-1966 , 2019
Link: https://doi.org/10.1007/..
 
?
12

Arabidopsis thaliana alternative dehydrogenases: a potentia..:

Catania, Alessia ; Iuso, Arcangela ; Bouchereau, Juliette...
Orphanet Journal of Rare Diseases.  14 (2019)  1 - p. , 2019
Link: https://doi.org/10.1186/..
 
?
13

Homozygous variant in OTX2 and possible genetic modifiers i..:

Catania, Alessia ; Legati, Andrea ; Peverelli, Lorenzo...
American Journal of Medical Genetics Part A.  179 (2019)  5 - p. 827-831 , 2019
Link: https://doi.org/10.1002/..
 
?
14

Compound heterozygous missense and deep intronic variants i..:

Catania, Alessia ; Ardissone, Anna ; Verrigni, Daniela...
Journal of Human Genetics.  63 (2018)  5 - p. 563-568 , 2018
Link: https://doi.org/10.1038/..
 
?
15

Roles of neutrophil gelatinase-associated lipocalin (NGAL) ..:

Candido, Saverio ; Maestro, Roberta ; Polesel, Jerry...
Oncotarget.  5 (2014)  6 - p. 1576-1594 , 2014
Link: https://doi.org/10.18632..
 
1-15