Antonell A - Search Results

1

Galectin-3 is upregulated in frontotemporal dementia patients with subtype specificity.

Borrego-Écija S, Pérez-Millan A, Antonell A, Fort-Aznar L, Kaya-Tilki E, León-Halcón A, Lladó A, Molina-Porcel L, Balasa M, Juncà-Parella J, Vitorica J, Venero JL, Deierborg T, Boza-Serrano A, Sánchez-Valle R. Borrego-Écija S, et al. Among authors: antonell a. Alzheimers Dement. 2024 Mar;20(3):1515-1526. doi: 10.1002/alz.13536. Epub 2023 Nov 29. Alzheimers Dement. 2024. PMID: 38018380 Free PMC article.

2

[Williams syndrome: its clinical aspects and molecular bases].

Antonell A, Del Campo M, Flores R, Campuzano V, Perez-Jurado LA. Antonell A, et al. Rev Neurol. 2006 Jan 7;42 Suppl 1:S69-75. Rev Neurol. 2006. PMID: 16506136 Free article. Review. Spanish.

3

Cellular crosstalk between TNF-α, NADPH oxidase, PKCβ2, and C2GNT in human leukocytes.

Tarr JM, Ding N, Kaul K, Antonell A, Pérez-Jurado LA, Chibber R. Tarr JM, et al. Among authors: antonell a. Cell Signal. 2012 Apr;24(4):873-8. doi: 10.1016/j.cellsig.2011.12.003. Epub 2011 Dec 13. Cell Signal. 2012. PMID: 22182514

4

Evolutionary mechanisms shaping the genomic structure of the Williams-Beuren syndrome chromosomal region at human 7q11.23.

Antonell A, de Luis O, Domingo-Roura X, Pérez-Jurado LA. Antonell A, et al. Genome Res. 2005 Sep;15(9):1179-88. doi: 10.1101/gr.3944605. Genome Res. 2005. PMID: 16140988 Free PMC article.

5

Partial 7q11.23 deletions further implicate GTF2I and GTF2IRD1 as the main genes responsible for the Williams-Beuren syndrome neurocognitive profile.

Antonell A, Del Campo M, Magano LF, Kaufmann L, de la Iglesia JM, Gallastegui F, Flores R, Schweigmann U, Fauth C, Kotzot D, Pérez-Jurado LA. Antonell A, et al. J Med Genet. 2010 May;47(5):312-20. doi: 10.1136/jmg.2009.071712. Epub 2009 Nov 5. J Med Genet. 2010. PMID: 19897463

6

Transcriptome profile in Williams-Beuren syndrome lymphoblast cells reveals gene pathways implicated in glucose intolerance and visuospatial construction deficits.

Antonell A, Vilardell M, Pérez Jurado LA. Antonell A, et al. Hum Genet. 2010 Jul;128(1):27-37. doi: 10.1007/s00439-010-0817-4. Epub 2010 Apr 17. Hum Genet. 2010. PMID: 20401492

7

MAPT gene duplications are not a cause of frontotemporal lobar degeneration.

Lladó A, Rodríguez-Santiago B, Antonell A, Sánchez-Valle R, Molinuevo JL, Reñé R, Pérez-Jurado LA. Lladó A, et al. Among authors: antonell a. Neurosci Lett. 2007 Aug 31;424(1):61-5. doi: 10.1016/j.neulet.2007.07.008. Epub 2007 Aug 1. Neurosci Lett. 2007. PMID: 17707586

8

Clinical features and APOE genotype of pathologically proven early-onset Alzheimer disease.

Balasa M, Gelpi E, Antonell A, Rey MJ, Sánchez-Valle R, Molinuevo JL, Lladó A; Neurological Tissue Bank/University of Barcelona/Hospital Clínic NTB/UB/HC Collaborative Group. Balasa M, et al. Among authors: antonell a. Neurology. 2011 May 17;76(20):1720-5. doi: 10.1212/WNL.0b013e31821a44dd. Neurology. 2011. PMID: 21576687

9

Neuroimaging and biochemical markers in the three variants of primary progressive aphasia.

Gil-Navarro S, Lladó A, Rami L, Castellví M, Bosch B, Bargalló N, Lomeña F, Reñé R, Montagut N, Antonell A, Molinuevo JL, Sánchez-Valle R. Gil-Navarro S, et al. Among authors: antonell a. Dement Geriatr Cogn Disord. 2013;35(1-2):106-17. doi: 10.1159/000346289. Epub 2013 Feb 6. Dement Geriatr Cogn Disord. 2013. PMID: 23392204

10

Decreased striatal dopamine transporter uptake in the non-fluent/agrammatic variant of primary progressive aphasia.

Gil-Navarro S, Lomeña F, Cot A, Lladó A, Montagut N, Castellví M, Bosch B, Rami L, Antonell A, Balasa M, Pavia J, Iranzo A, Molinuevo JL, Sánchez-Valle R. Gil-Navarro S, et al. Among authors: antonell a. Eur J Neurol. 2013 Nov;20(11):1459-e126. doi: 10.1111/ene.12196. Epub 2013 May 17. Eur J Neurol. 2013. PMID: 23679075

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