Alicia Martinez-Pineiro
Overview
Explore the profile of Alicia Martinez-Pineiro including associated specialties, affiliations and a list of published articles.
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22
Citations
225
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Recent Articles
1.
Nunez-Manchon J, Capo J, Martinez-Pineiro A, Juanola E, Pesovic J, Mosqueira-Martin L, et al.
iScience
. 2024 Dec;
27(12):111499.
PMID: 39735432
[This corrects the article DOI: 10.1016/j.isci.2024.109930.].
2.
Nunez-Manchon J, Capo J, Martinez-Pineiro A, Juanola E, Pesovic J, Mosqueira-Martin L, et al.
iScience
. 2024 Jun;
27(6):109930.
PMID: 38832025
Historically, cellular models have been used as a tool to study myotonic dystrophy type 1 (DM1) and the validation of therapies in said pathology. However, there is a need for...
3.
Llados G, Massanella M, Coll-Fernandez R, Rodriguez R, Hernandez E, Lucente G, et al.
Clin Microbiol Infect
. 2023 Nov;
30(4):515-521.
PMID: 37984511
Objectives: The post-COVID-19 condition (PCC) is a disabling syndrome affecting at least 5%-10% of subjects who survive COVID-19. SARS-CoV-2 mediated vagus nerve dysfunction could explain some PCC symptoms, such as...
4.
Koehorst E, Odria R, Capo J, Nunez-Manchon J, Arbex A, Almendrote M, et al.
Biomedicines
. 2022 Jun;
10(6).
PMID: 35740394
Myotonic dystrophy type 1 (DM1) is a progressive, non-treatable, multi-systemic disorder. To investigate the contribution of epigenetics to the complexity of DM1, we compared DNA methylation profiles of four annotated...
5.
New spinocerebellar ataxia subtype caused by mutation triggering mitochondrial dysregulation (SCA49)
Corral-Juan M, Casquero P, Giraldo-Restrepo N, Laurie S, Martinez-Pineiro A, Mateo-Montero R, et al.
Brain Commun
. 2022 Mar;
4(2):fcac030.
PMID: 35310830
Spinocerebellar ataxias consist of a highly heterogeneous group of inherited movement disorders clinically characterized by progressive cerebellar ataxia variably associated with additional distinctive clinical signs. The genetic heterogeneity is evidenced...
6.
Koehorst E, Nunez-Manchon J, Ballester-Lopez A, Almendrote M, Lucente G, Arbex A, et al.
J Clin Med
. 2021 Dec;
10(23).
PMID: 34884222
Myotonic Dystrophy type 1 (DM1) is a muscular dystrophy with a multi-systemic nature. It was one of the first diseases in which repeat associated non-ATG (RAN) translation was described in...
7.
Lucente G, Corral J, Rodriguez-Esparragoza L, Castaner S, Ortiz H, Piqueras A, et al.
Front Neurol
. 2021 Nov;
12:755432.
PMID: 34790163
Previously published retrospective series show a high prevalence of fecal incontinence (FI) in stroke patients. We aimed to analyze in a prospective series the current incidence of FI in acute...
8.
Martin-Aguilar L, Lleixa C, Pascual-Goni E, Caballero-Avila M, Martinez-Martinez L, Diaz-Manera J, et al.
Neurol Neuroimmunol Neuroinflamm
. 2021 Nov;
9(1).
PMID: 34728497
Background And Objectives: To study the clinical and laboratory features of antineurofascin-155 (NF155)-positive autoimmune nodopathy (AN). Methods: Patients with anti-NF155 antibodies detected on routine immunologic testing were included. Clinical characteristics,...
9.
Higueras Sune C, Carrasco Lopez C, Malagon Lopez P, Senosiain O, Escribano M, Vila Poyatos J, et al.
J Plast Reconstr Aesthet Surg
. 2021 May;
74(11):3040-3047.
PMID: 34020902
Background: Long-term facial nerve palsy has a highly negative impact on patients' quality of life. In 2016, Alam reported one case of facial reanimation with the sternohyoid muscle after publishing...
10.
Alvarez-Velasco R, Gutierrez-Gutierrez G, Trujillo J, Martinez E, Segovia S, Arribas-Velasco M, et al.
Eur J Neurol
. 2021 Mar;
28(6):2083-2091.
PMID: 33721382
Background And Purpose: Prognosis of myasthenia gravis (MG) in patients with thymoma is not well established. Moreover, it is not clear whether thymoma recurrence or unresectable lesions entail a worse...