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

Year Number of Results
2009 1
2011 2
2012 1
2013 1
2016 1
2017 1
2018 1
2019 1
2021 1
2022 1
2023 4
2024 0

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14 results

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Page 1
[Neurological consequences of prematurity].
Cerisola A, Baltar F. Cerisola A, et al. Medicina (B Aires). 2023 Sep;83 Suppl 4:18-24. Medicina (B Aires). 2023. PMID: 37714118 Free article. Review. Spanish.
[Febrile seizures: questions and answers].
Cerisola A, Chaibún E, Rosas M, Cibils L. Cerisola A, et al. Medicina (B Aires). 2018;78 Suppl 2:18-24. Medicina (B Aires). 2018. PMID: 30199360 Free article. Review. Spanish.
Computational and mitochondrial functional studies of novel compound heterozygous variants in SPATA5 gene support a causal link with epileptogenic encephalopathy.
Raggio V, Graña M, Winiarski E, Mansilla S, Simoes C, Rodríguez S, Brandes M, Tapié A, Rodríguez L, Cibils L, Alonso M, Martínez J, Fernández-Calero T, Domínguez F, Mezquida MR, Castro L, Cerisola A, Naya H, Cassina A, Quijano C, Spangenberg L. Raggio V, et al. Among authors: cerisola a. Hum Genomics. 2023 Feb 27;17(1):14. doi: 10.1186/s40246-023-00463-x. Hum Genomics. 2023. PMID: 36849973 Free PMC article.
Exploring the Spectrum of RHOBTB2 Variants Associated with Developmental Encephalopathy 64: A Case Series and Literature Review.
de Pedro Baena S, Sariego Jamardo A, Castro P, López González FJ, Sánchez Carpintero R, Cerisola A, Troncoso M, Witting S, Barrios A, Fons C, López Pisón J, Ortigoza-Escobar JD. de Pedro Baena S, et al. Among authors: cerisola a. Mov Disord Clin Pract. 2023 Sep 25;10(11):1671-1679. doi: 10.1002/mdc3.13880. eCollection 2023 Nov. Mov Disord Clin Pract. 2023. PMID: 37982109 Review.
[Venous and cerebral sinus thrombosis in newborns and children].
Mora R, Ibarra L, Olivera V, Rosas M, Cibils L, Baltar F, Ruiz V, Turcatti E, Costa G, Mansilla S, Cerisola A, González G. Mora R, et al. Among authors: cerisola a. Medicina (B Aires). 2023 Sep;83 Suppl 4:95-101. Medicina (B Aires). 2023. PMID: 37714130 Free article. Spanish.
[Mechanisms of brain injury of the premature baby].
Cerisola A, Baltar F, Ferrán C, Turcatti E. Cerisola A, et al. Medicina (B Aires). 2019;79 Suppl 3:10-14. Medicina (B Aires). 2019. PMID: 31603836 Free article. Spanish.
Genetic, Phenotypic, and Interferon Biomarker Status in ADAR1-Related Neurological Disease.
Rice GI, Kitabayashi N, Barth M, Briggs TA, Burton ACE, Carpanelli ML, Cerisola AM, Colson C, Dale RC, Danti FR, Darin N, De Azua B, De Giorgis V, De Goede CGL, Desguerre I, De Laet C, Eslahi A, Fahey MC, Fallon P, Fay A, Fazzi E, Gorman MP, Gowrinathan NR, Hully M, Kurian MA, Leboucq N, Lin JS, Lines MA, Mar SS, Maroofian R, Martí-Sanchez L, McCullagh G, Mojarrad M, Narayanan V, Orcesi S, Ortigoza-Escobar JD, Pérez-Dueñas B, Petit F, Ramsey KM, Rasmussen M, Rivier F, Rodríguez-Pombo P, Roubertie A, Stödberg TI, Toosi MB, Toutain A, Uettwiller F, Ulrick N, Vanderver A, Waldman A, Livingston JH, Crow YJ. Rice GI, et al. Among authors: cerisola am. Neuropediatrics. 2017 Jun;48(3):166-184. doi: 10.1055/s-0037-1601449. Epub 2017 Apr 10. Neuropediatrics. 2017. PMID: 28561207 Free PMC article.
Blood cell respiration rates and mtDNA copy number: A promising tool for the diagnosis of mitochondrial disease.
Alonso M, Zabala C, Mansilla S, De Brun L, Martínez J, Garau M, Rivas G, Acosta C, Lens D, Cerisola A, Graña M, Naya H, Puentes R, Spangenberg L, Raggio V, Lemes A, Castro L, Quijano C. Alonso M, et al. Among authors: cerisola a. Mitochondrion. 2021 Nov;61:31-43. doi: 10.1016/j.mito.2021.09.004. Epub 2021 Sep 16. Mitochondrion. 2021. PMID: 34536563
3697G>A in MT-ND1 is a causative mutation in mitochondrial disease.
Spangenberg L, Graña M, Greif G, Suarez-Rivero JM, Krysztal K, Tapié A, Boidi M, Fraga V, Lemes A, Gueçaimburú R, Cerisola A, Sánchez-Alcázar JA, Robello C, Raggio V, Naya H. Spangenberg L, et al. Among authors: cerisola a. Mitochondrion. 2016 May;28:54-9. doi: 10.1016/j.mito.2016.03.006. Epub 2016 Mar 24. Mitochondrion. 2016. PMID: 27017994
14 results