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Cuteness and the Power of Emotion.
Paz EV, Leis M, Garcia Basalo MJ, Giacchino M, Agosta G. Paz EV, et al. Among authors: agosta g. Neurol India. 2023 Jul-Aug;71(4):737-741. doi: 10.4103/0028-3886.383846. Neurol India. 2023. PMID: 37635507 Free article.
Epilepsia partialis continua associated with levamisole.
Aberastury MN, Silva WH, Vaccarezza MM, Maxit C, Agosta G. Aberastury MN, et al. Among authors: agosta g. Pediatr Neurol. 2011 May;44(5):385-8. doi: 10.1016/j.pediatrneurol.2010.11.020. Pediatr Neurol. 2011. PMID: 21481750
Inferring parental gonadal mosaicism in LMNA-associated muscular dystrophy by ultra-deep next generation sequencing: A sensitive approach providing valuable information for genetic counseling.
Perez Maturo J, Vega P, Medina N, Salinas V, Pauni M, Agosta G, Muntadas Rausei J, Kauffman M. Perez Maturo J, et al. Among authors: agosta g. Am J Med Genet A. 2019 Jun;179(6):1074-1076. doi: 10.1002/ajmg.a.61135. Epub 2019 Mar 26. Am J Med Genet A. 2019. PMID: 30912254 No abstract available.
Novel Protein Biomarkers of Monoamine Metabolism Defects Correlate with Disease Severity.
Tristán-Noguero A, Borràs E, Molero-Luis M, Wassenberg T, Peters T, Verbeek MM, Willemsen M, Opladen T, Jeltsch K, Pons R, Thony B, Horvath G, Yapici Z, Friedman J, Hyland K, Agosta GE, López-Laso E, Artuch R, Sabidó E, García-Cazorla À. Tristán-Noguero A, et al. Among authors: agosta ge. Mov Disord. 2021 Mar;36(3):690-703. doi: 10.1002/mds.28362. Epub 2020 Nov 5. Mov Disord. 2021. PMID: 33152132
Clinical next generation sequencing in developmental and epileptic encephalopathies: Diagnostic relevance of data re-analysis and variants re-interpretation.
Salinas V, Martínez N, Maturo JP, Rodriguez-Quiroga SA, Zavala L, Medina N, Amartino H, Sfaello I, Agosta G, Serafín EM, Morón DG, Kauffman MA, Vega P. Salinas V, et al. Among authors: agosta g. Eur J Med Genet. 2021 Dec;64(12):104363. doi: 10.1016/j.ejmg.2021.104363. Epub 2021 Oct 18. Eur J Med Genet. 2021. PMID: 34673242
45 results