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

Year Number of Results
2004 1
2005 1
2006 1
2007 1
2008 3
2009 3
2010 3
2011 1
2012 2
2013 6
2014 4
2015 5
2016 3
2017 1
2018 2
2019 4
2020 1
2021 7
2022 7
2023 5
2024 3

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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: albert j. 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: albert j. Medicina (B Aires). 2024 Mar;84 Suppl 1:26-30. Medicina (B Aires). 2024. PMID: 38350621 Free article. Review. Spanish.
Selective Inhibitory Control in Middle Childhood.
Rincón-Pérez I, Sánchez-Carmona AJ, Arroyo-Lozano S, García-Rubio C, Hinojosa JA, Fernández-Jaén A, López-Martín S, Albert J. Rincón-Pérez I, et al. Among authors: albert j. Int J Environ Res Public Health. 2021 Jun 10;18(12):6300. doi: 10.3390/ijerph18126300. Int J Environ Res Public Health. 2021. PMID: 34200757 Free PMC article.
[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: albert j. Medicina (B Aires). 2019;79(Suppl 1):57-61. Medicina (B Aires). 2019. PMID: 30776281 Free article. 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: albert j. 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
Mutations in the COL18A1 gen associated with knobloch syndrome and structural brain anomalies: a novel case report and literature review of neuroimaging findings.
Irene Díez García-Prieto I, Lopez-Martín S, Albert J, Jiménez de la Peña M, Fernández-Mayoralas DM, Calleja-Pérez B, Gómez Fernández MT, Álvarez S, Pihlajaniemi T, Izzi V, Fernández-Jaén A. Irene Díez García-Prieto I, et al. Among authors: albert j. Neurocase. 2022 Feb;28(1):11-18. doi: 10.1080/13554794.2021.1928228. Epub 2022 Mar 6. Neurocase. 2022. PMID: 35253627 Review.
50 results