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Year | Number of Results |
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2021 | 3 |
2022 | 2 |
2023 | 1 |
2024 | 0 |
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Page 1
Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias.
Int J Mol Sci. 2022 Oct 6;23(19):11847. doi: 10.3390/ijms231911847.
Int J Mol Sci. 2022.
PMID: 36233161
Free PMC article.
Diagnostic Efficacy of Genetic Studies in a Series of Hereditary Cerebellar Ataxias in Eastern Spain.
Baviera-Muñoz R, Carretero-Vilarroig L, Vázquez-Costa JF, Morata-Martínez C, Campins-Romeu M, Muelas N, Sastre-Bataller I, Martínez-Torres I, Pérez-García J, Sivera R, Sevilla T, Vilchez JJ, Jaijo T, Espinós C, Millán JM, Bataller L, Aller E.
Baviera-Muñoz R, et al.
Neurol Genet. 2022 Nov 14;8(6):e200038. doi: 10.1212/NXG.0000000000200038. eCollection 2022 Dec.
Neurol Genet. 2022.
PMID: 36530930
Free PMC article.
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Clinical and genetic characteristics of 21 Spanish patients with biallelic pathogenic SPG7 mutations.
Baviera-Muñoz R, Campins-Romeu M, Carretero-Vilarroig L, Sastre-Bataller I, Martínez-Torres I, Vázquez-Costa JF, Muelas N, Sevilla T, Vílchez JJ, Aller E, Jaijo T, Bataller L, Espinós C.
Baviera-Muñoz R, et al.
J Neurol Sci. 2021 Oct 15;429:118062. doi: 10.1016/j.jns.2021.118062. Epub 2021 Aug 30.
J Neurol Sci. 2021.
PMID: 34500365
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Spinocerebellar Ataxia 36 is a Frequent Cause of Hereditary Ataxia in Eastern Spain.
Baviera-Muñoz R, Carretero-Vilarroig L, Muelas N, Sivera R, Sopena-Novales P, Martínez-Sanchis B, Sastre-Bataller I, Campins-Romeu M, Martínez-Torres I, García-Verdugo JM, Millán JM, Jaijo T, Aller E, Bataller L.
Baviera-Muñoz R, et al.
Mov Disord Clin Pract. 2023 May 5;10(6):992-997. doi: 10.1002/mdc3.13740. eCollection 2023 Jun.
Mov Disord Clin Pract. 2023.
PMID: 37332636
Free PMC article.
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Hereditary Spastic Paraplegia 7 Presenting as Multifocal Dystonia with Prominent Cranio-Cervical Involvement.
Campins-Romeu M, Baviera-Muñoz R, Sastre-Bataller I, Bataller L, Jaijo T, Martínez-Torres I.
Campins-Romeu M, et al. Among authors: baviera munoz r.
Mov Disord Clin Pract. 2021 Jun 22;8(6):966-968. doi: 10.1002/mdc3.13257. eCollection 2021 Aug.
Mov Disord Clin Pract. 2021.
PMID: 34405107
Free PMC article.
No abstract available.
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A 3.9-Mb Deletion on 2p11.2 Comprising the REEP1 Gene Causes Early-Onset Atypical Parkinsonism.
Baviera-Muñoz R, Martínez-Rubio D, Sastre-Bataller I, Campins-Romeu M, Losada-López M, Pérez-García J, Novella-Maestre E, Martínez-Torres I, Espinós C.
Baviera-Muñoz R, et al.
Neurol Genet. 2021 Nov 19;7(6):e642. doi: 10.1212/NXG.0000000000000642. eCollection 2021 Dec.
Neurol Genet. 2021.
PMID: 34825060
Free PMC article.
No abstract available.
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