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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2012 3
2013 6
2014 10
2015 2
2016 5
2017 3
2018 2
2019 2
2020 4
2021 6
2022 6
2023 2
2024 2

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40 results

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Page 1
[The impact of ADHD on reading].
Sánchez-Carmona AJ, Albert J, López-Martín S, Calleja-Pérez B, Fernández-Mayoralas DM, Jiménez De Domingo A, Fernández-Perrone AL, Fernández-Jaén A. Sánchez-Carmona AJ, et al. Among authors: fernandez perrone al. Medicina (B Aires). 2023 Mar;83 Suppl 2:22-26. Medicina (B Aires). 2023. PMID: 36820478 Free article. Review. Spanish.
[Genetics of ADHD in clinical practice].
López-Martín S, Albert J, Calleja-Pérez B, Fernández-Mayoralas DM, Fernández-Perrone AL, Jiménez De Domingo A, Fernández-Jaén A. López-Martín S, et al. Among authors: fernandez perrone al. Medicina (B Aires). 2024 Mar;84 Suppl 1:26-30. Medicina (B Aires). 2024. PMID: 38350621 Free article. Review. Spanish.
[Attention deficit/hyperactivity disorder. Study habits].
Calleja-Pérez B, Párraga JL, Albert J, López-Martín S, Jiménez de Domingo A, Fernández-Perrone AL, Fernández-Mayoralas DM, Tirado P, Suárez-Guinea R, López-Arribas S, Fernández-Jaén A. Calleja-Pérez B, et al. Among authors: fernandez perrone al. Medicina (B Aires). 2019;79(Suppl 1):57-61. Medicina (B Aires). 2019. PMID: 30776281 Free article. Spanish.
[Genetic studies and neurodevelopment. From effectiveness to genetic models].
Calleja-Pérez B, Fernández-Perrone AL, Fernández-Mayoralas DM, Jiménez de Domingo A, Tirado P, López-Arribas S, Suárez-Guinea R, Fernández-Jaén A. Calleja-Pérez B, et al. Among authors: fernandez perrone al. Medicina (B Aires). 2020;80 Suppl 2:26-30. Medicina (B Aires). 2020. PMID: 32150709 Free article. Review. Spanish.
ANO3 and early-onset dyskinetic encephalopathy.
Jiménez de Domingo A, Lopez-Martín S, Albert J, Jiménez de la Peña M, Tirado P, Fernández-Mayoralas DM, Fernández-Perrone AL, Calleja-Pérez B, Martínez-García M, Álvarez S, Fernández-Jaén A. Jiménez de Domingo A, et al. Among authors: fernandez perrone al. Eur J Med Genet. 2020 Dec;63(12):104085. doi: 10.1016/j.ejmg.2020.104085. Epub 2020 Oct 9. Eur J Med Genet. 2020. PMID: 33045406
DYNC1H1de novo mutation, spinal muscular atrophy and attention problems.
Fernández Perrone AL, Moreno Fernández P, Álvarez S, Fernández-Jaén A. Fernández Perrone AL, et al. Neurologia (Engl Ed). 2022 Jun;37(5):406-409. doi: 10.1016/j.nrl.2021.08.001. Epub 2021 Sep 10. Neurologia (Engl Ed). 2022. PMID: 34518024 Free article. English, Spanish. No abstract available.
DYNC1H1 de novo mutation, spinal muscular atrophy and attention problems.
Fernández Perrone AL, Moreno Fernández P, Álvarez S, Fernández-Jaén A. Fernández Perrone AL, et al. Neurologia (Engl Ed). 2022 Jun;37(5):406-409. doi: 10.1016/j.nrleng.2021.08.001. Epub 2022 May 21. Neurologia (Engl Ed). 2022. PMID: 35606327 Free article. No abstract available.
40 results