Agosta GE - Search Results

1

Treatment of refractory epilepsy with the modified Atkins diet.

Vaccarezza MM, Toma MV, Ramos Guevara JD, Diez CG, Agosta GE. Vaccarezza MM, et al. Among authors: agosta ge. Arch Argent Pediatr. 2014 Aug;112(4):348-51. doi: 10.5546/aap.2014.eng.348. Arch Argent Pediatr. 2014. PMID: 24955906 Free article. English, Spanish.

2

Epilepsia partialis continua associated with levamisole.

Aberastury MN, Silva WH, Vaccarezza MM, Maxit C, Agosta G. Aberastury MN, et al. Pediatr Neurol. 2011 May;44(5):385-8. doi: 10.1016/j.pediatrneurol.2010.11.020. Pediatr Neurol. 2011. PMID: 21481750

3

Long-term follow-up of the ketogenic diet for refractory epilepsy: multicenter Argentinean experience in 216 pediatric patients.

Caraballo R, Vaccarezza M, Cersósimo R, Rios V, Soraru A, Arroyo H, Agosta G, Escobal N, Demartini M, Maxit C, Cresta A, Marchione D, Carniello M, Paníco L. Caraballo R, et al. Seizure. 2011 Oct;20(8):640-5. doi: 10.1016/j.seizure.2011.06.009. Epub 2011 Jul 16. Seizure. 2011. PMID: 21763159 Free article.

4

[Super-refractory status epilepticus: treatment with ketogenic diet in pediatrics].

Vaccarezza M, Silva W, Maxit C, Agosta G. Vaccarezza M, et al. Rev Neurol. 2012 Jul 1;55(1):20-5. Rev Neurol. 2012. PMID: 22718405 Free article. Spanish.

5

[Long chain 3-hydroxyacyl-coA dehydrogenase deficiency, association with HELLP and magnetic resonance spectroscopy findings].

Deltetto N, Maxit C, Marchione D, Szlago M, Schenone A, Besada CH, Vaccarezza M, Agosta G. Deltetto N, et al. Arch Argent Pediatr. 2012 Aug;110(4):e63-6. doi: 10.5546/aap.2012.e63. Arch Argent Pediatr. 2012. PMID: 22859334 Free article. Spanish.

6

Epilepsy surgery in children and adolescents: Report on 43 cases.

Aberastury M, Comas B, García M, Besocke A, Ciraolo C, Agosta G, Silva W. Aberastury M, et al. Arch Argent Pediatr. 2016 Oct 1;114(5):458-63. doi: 10.5546/aap.2016.eng.458. Epub 2016 Oct 1. Arch Argent Pediatr. 2016. PMID: 27606645 Free article. English, Spanish.

7

Identification of a somatic mutation in the RHEB gene through high depth and ultra-high depth next generation sequencing in a patient with Hemimegalencephaly and drug resistant Epilepsy.

Salinas V, Vega P, Piccirilli MV, Chicco C, Ciraolo C, Christiansen S, Consalvo D, Perez-Maturo J, Medina N, González-Morón D, Novaro V, Perrone C, García MDC, Agosta G, Silva W, Kauffman M. Salinas V, et al. Eur J Med Genet. 2019 Nov;62(11):103571. doi: 10.1016/j.ejmg.2018.11.005. Epub 2018 Nov 8. Eur J Med Genet. 2019. PMID: 30414531

8

[Prevalence and incidence of disability based on the Unique Certificate of Disability at a teaching hospital in the Metropolitan Area of Buenos Aires].

Puga C, Pagotto V, Giunta D, Vicens J, Leist M, Vaucheret Paz E, Hornstein L, Garfi L, Agosta G. Puga C, et al. Arch Argent Pediatr. 2019 Jun 1;117(3):183-187. doi: 10.5546/aap.2019.eng.183. Arch Argent Pediatr. 2019. PMID: 31063306 Free article. Spanish.

9

DEPDC5 mutation and familial focal epilepsy with variable foci: genotype and phenotype of a family.

Aberastury M, Fernández R, Córdoba M, Comas B, Peralta M, Agosta G, Kauffman M, Silva W. Aberastury M, et al. Epileptic Disord. 2019 Feb 1;21(1):42-47. doi: 10.1684/epd.2019.1025. Epileptic Disord. 2019. PMID: 30767899

10

[Transient reading disorders associated with interictal epileptiform paroxysmal discharges in invasive videocorticography].

Vaucheret E, Peralta J, Garcia-Basalo M, Agosta G, Silva W. Vaucheret E, et al. Rev Neurol. 2019 Jun 16;68(12):517-523. doi: 10.33588/rn.6812.2018391. Rev Neurol. 2019. PMID: 31173332 Free article. Spanish.

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