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Automatic identification of atypical clinical fMRI results.
Neuroradiology. 2020 Dec;62(12):1677-1688. doi: 10.1007/s00234-020-02510-z. Epub 2020 Aug 18.
Neuroradiology. 2020.
PMID: 32812070
Free PMC article.
Correction to: Automatic identification of atypical clinical fMRI results.
Jansma JM, Rutten GJ, Ramsey LE, Snijders TJ, Bizzi A, Rosengarth K, Dodoo-Schittko F, Hattingen E, de la Peña MJ, von Campe G, Jehna M, Ramsey NF.
Jansma JM, et al. Among authors: de la pena mj.
Neuroradiology. 2020 Dec;62(12):1723. doi: 10.1007/s00234-020-02565-y.
Neuroradiology. 2020.
PMID: 32986199
Free PMC article.
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A Practical Approach to Imaging of the Supplementary Motor Area and Its Subcortical Connections.
de la Peña MJ, Gil-Robles S, de Vega VM, Aracil C, Acevedo A, Rodríguez MR.
de la Peña MJ, et al.
Curr Neurol Neurosci Rep. 2020 Sep 15;20(11):50. doi: 10.1007/s11910-020-01070-2.
Curr Neurol Neurosci Rep. 2020.
PMID: 32930895
Review.
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Spontaneous skull base meningoencephaloceles and cerebrospinal fluid fistulas.
Alonso RC, de la Peña MJ, Caicoya AG, Rodriguez MR, Moreno EA, de Vega Fernandez VM.
Alonso RC, et al. Among authors: de la pena mj.
Radiographics. 2013 Mar-Apr;33(2):553-70. doi: 10.1148/rg.332125028.
Radiographics. 2013.
PMID: 23479713
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Early perfusion changes in multiple sclerosis patients as assessed by MRI using arterial spin labeling.
de la Peña MJ, Peña IC, García PG, Gavilán ML, Malpica N, Rubio M, González RA, de Vega VM.
de la Peña MJ, et al.
Acta Radiol Open. 2019 Dec 30;8(12):2058460119894214. doi: 10.1177/2058460119894214. eCollection 2019 Dec.
Acta Radiol Open. 2019.
PMID: 32002192
Free PMC article.
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Cortical thickness differences in the prefrontal cortex in children and adolescents with ADHD in relation to dopamine transporter (DAT1) genotype.
Fernández-Jaén A, López-Martín S, Albert J, Fernández-Mayoralas DM, Fernández-Perrone AL, de La Peña MJ, Calleja-Pérez B, Rodríguez MR, López-Arribas S, Muñoz-Jareño N.
Fernández-Jaén A, et al. Among authors: de la pena mj.
Psychiatry Res. 2015 Sep 30;233(3):409-17. doi: 10.1016/j.pscychresns.2015.07.005. Epub 2015 Jul 8.
Psychiatry Res. 2015.
PMID: 26206710
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Bi-Allelic c.1746G>T; p.Leu582= Variants in TUBGCP4 in a Boy with Autism: Clinical Data and Literature Review.
Martín Fernández-Mayoralas D, Albert J, López-Martín S, de la Peña MJ, Fernández-Perrone AL, Jiménez de Domingo A, Calleja-Pérez B, Martínez-García M, Álvarez S, Fernández-Jaén A.
Martín Fernández-Mayoralas D, et al. Among authors: de la pena mj.
Mol Syndromol. 2022 Feb;13(2):165-170. doi: 10.1159/000519365. Epub 2021 Dec 2.
Mol Syndromol. 2022.
PMID: 35418825
Free PMC article.
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Biallelic SYNE2 Missense Mutations Leading to Nesprin-2 Giant Hypo-Expression Are Associated with Intellectual Disability and Autism.
Young N, Asif M, Jackson M, Fernández-Mayoralas DM, de la Peña MJ, Calleja-Pérez B, Álvarez S, Hunter-Featherstone E, Noegel AA, Höhne W, Nürnberg P, Obara B, Hussain MS, Karakesisoglou I, Fernández-Jaén A.
Young N, et al. Among authors: de la pena mj.
Genes (Basel). 2021 Aug 24;12(9):1294. doi: 10.3390/genes12091294.
Genes (Basel). 2021.
PMID: 34573277
Free PMC article.
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