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Year | Number of Results |
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2020 | 1 |
2021 | 1 |
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Page 1
Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy.
Int J Mol Sci. 2023 Nov 16;24(22):16400. doi: 10.3390/ijms242216400.
Int J Mol Sci. 2023.
PMID: 38003592
Free PMC article.
Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias.
Martínez-Rubio D, Hinarejos I, Sancho P, Gorría-Redondo N, Bernadó-Fonz R, Tello C, Marco-Marín C, Martí-Carrera I, Martínez-González MJ, García-Ribes A, Baviera-Muñoz R, Sastre-Bataller I, Martínez-Torres I, Duat-Rodríguez A, Janeiro P, Moreno E, Pías-Peleteiro L, Gordo MO, Ruiz-Gómez Á, Muñoz E, Martí MJ, Sánchez-Monteagudo A, Fuster C, Andrés-Bordería A, Pons RM, Jesús-Maestre S, Mir P, Lupo V, Pérez-Dueñas B, Darling A, Aguilera-Albesa S, Espinós C.
Martínez-Rubio D, et al. Among authors: hinarejos i.
Int J Mol Sci. 2022 Oct 6;23(19):11847. doi: 10.3390/ijms231911847.
Int J Mol Sci. 2022.
PMID: 36233161
Free PMC article.
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Mitochondrial Dysfunction, Oxidative Stress and Neuroinflammation in Neurodegeneration with Brain Iron Accumulation (NBIA).
Hinarejos I, Machuca-Arellano C, Sancho P, Espinós C.
Hinarejos I, et al.
Antioxidants (Basel). 2020 Oct 20;9(10):1020. doi: 10.3390/antiox9101020.
Antioxidants (Basel). 2020.
PMID: 33092153
Free PMC article.
Review.
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NR4A2 Mutations Can Cause Intellectual Disability and Language Impairment With Persistent Dystonia-Parkinsonism.
Jesús S, Hinarejos I, Carrillo F, Martínez-Rubio D, Macías-García D, Sánchez-Monteagudo A, Adarmes A, Lupo V, Pérez-Dueñas B, Mir P, Espinós C.
Jesús S, et al. Among authors: hinarejos i.
Neurol Genet. 2021 Jan 21;7(1):e543. doi: 10.1212/NXG.0000000000000543. eCollection 2021 Feb.
Neurol Genet. 2021.
PMID: 33585677
Free PMC article.
No abstract available.
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