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Page 1
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. Among authors: campins romeu m. Neurol Genet. 2022 Nov 14;8(6):e200038. doi: 10.1212/NXG.0000000000200038. eCollection 2022 Dec. Neurol Genet. 2022. PMID: 36530930 Free PMC article.
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. Among authors: campins romeu m. 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
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. Among authors: campins romeu m. 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.
[Adverse effects and complications of continuous intestinal infusion of levodopa-carbidopa in a cohort of patients with Parkinson's disease in a tertiary hospital].
Campins-Romeu M, Sastre-Bataller I, Pons-Beltrán V, Baviera-Muñoz R, Losada-López M, Morata-Martínez C, Pérez-García J, Martínez-Torres I. Campins-Romeu M, et al. Rev Neurol. 2022 Mar 1;74(5):143-148. doi: 10.33588/rn.7405.2021482. Rev Neurol. 2022. PMID: 35211947 Free article. Spanish.
Refractory status epilepticus due to vitamin B6 deficit in a Parkinson's disease patient in treatment with levodopa/carbidopa intestinal gel.
Baviera-Muñoz R, Buigues-Lafuente A, Campins-Romeu M, Garcés-Sánchez M, Martinez-Torres I. Baviera-Muñoz R, et al. Among authors: campins romeu m. Neurologia (Engl Ed). 2022 Sep;37(7):608-609. doi: 10.1016/j.nrleng.2021.10.002. Epub 2022 May 6. Neurologia (Engl Ed). 2022. PMID: 35527110 Free article. No abstract available.
Gait Function after High-Intensity Focused Ultrasound Thalamotomy for Essential Tremor: Searching for Technique Optimization.
Sastre-Bataller I, Campins-Romeu M, Marcos-Carrión A, Gutiérrez-Martín A, Conde-Sardón R, Losada-López M, Santabárbara-Gómez JM, León-Guijarro JL, Belloch V, Lozano AM, Martínez-Torres I. Sastre-Bataller I, et al. Among authors: campins romeu m. Stereotact Funct Neurosurg. 2023;101(1):12-21. doi: 10.1159/000527374. Epub 2023 Jan 25. Stereotact Funct Neurosurg. 2023. PMID: 36696885
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. Among authors: campins romeu m. 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.
11 results