Nadia DAmbrosi
Overview
Explore the profile of Nadia DAmbrosi including associated specialties, affiliations and a list of published articles.
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Articles
50
Citations
1399
Followers
0
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Recent Articles
1.
Apolloni S, DAmbrosi N
Neural Regen Res
. 2024 Nov;
20(11):3229-3230.
PMID: 39589500
No abstract available.
2.
Felice F, De Falco P, Milani M, Castelli S, Ragnini-Wilson A, Lazzarino G, et al.
Cell Commun Signal
. 2024 Nov;
22(1):564.
PMID: 39587614
Background: Microglia play a crucial role in brain development and repair by facilitating processes such as synaptic pruning and debris clearance. They can be activated in response to various stimuli,...
3.
Della Valle I, Milani M, Rossi S, Turchi R, Tortolici F, Nesci V, et al.
Genes Dis
. 2024 Aug;
11(6):101178.
PMID: 39100202
No abstract available.
4.
Sciarretta F, Zaccaria F, Ninni A, Ceci V, Turchi R, Apolloni S, et al.
Life Sci Alliance
. 2024 Apr;
7(7).
PMID: 38631900
Immunometabolism investigates the intricate relationship between the immune system and cellular metabolism. This study delves into the consequences of mitochondrial frataxin (FXN) depletion, the primary cause of Friedreich's ataxia (FRDA),...
5.
Milani M, Della Valle I, Rossi S, Fabbrizio P, Margotta C, Nardo G, et al.
Neurotherapeutics
. 2024 Mar;
21(3):e00346.
PMID: 38493058
Amyotrophic lateral sclerosis (ALS) is a complex neurodegenerative disease influenced by genetic, epigenetic, and environmental factors, resulting in dysfunction in cellular and molecular pathways. The limited efficacy of current treatments...
6.
Rossi S, Di Salvio M, Bali M, De Simone A, Apolloni S, DAmbrosi N, et al.
Cells
. 2023 Aug;
12(15).
PMID: 37566088
Compelling evidence indicates that defects in nucleocytoplasmic transport contribute to the pathogenesis of amyotrophic lateral sclerosis (ALS). In particular, hexanucleotide (G4C2) repeat expansions in , the most common cause of...
7.
Apolloni S, DAmbrosi N
Neural Regen Res
. 2023 Jul;
18(12):2705-2706.
PMID: 37449632
No abstract available.
8.
Apolloni S, DAmbrosi N
Int J Mol Sci
. 2023 Jun;
24(11).
PMID: 37298369
Our understanding of the pathophysiology of the nervous system has advanced significantly in the last few years, but there are still many unanswered questions [...].
9.
Ciccarone F, Castelli S, Lazzarino G, Scaricamazza S, Mangione R, Bernardini S, et al.
Genes Dis
. 2023 May;
10(2):321-324.
PMID: 37223542
No abstract available.
10.
Apolloni S, Milani M, DAmbrosi N
Int J Mol Sci
. 2022 Jun;
23(11).
PMID: 35682973
Friedreich's ataxia (FRDA) is a rare genetic disorder caused by mutations in the gene frataxin, encoding for a mitochondrial protein involved in iron handling and in the biogenesis of iron-sulphur...