Simón R - Search Results

1

Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients.

Fernández-Marmiesse A, Roca I, Díaz-Flores F, Cantarín V, Pérez-Poyato MS, Fontalba A, Laranjeira F, Quintans S, Moldovan O, Felgueroso B, Rodríguez-Pedreira M, Simón R, Camacho A, Quijada P, Ibanez-Mico S, Domingno MR, Benito C, Calvo R, Pérez-Cejas A, Carrasco ML, Ramos F, Couce ML, Ruiz-Falcó ML, Gutierrez-Solana L, Martínez-Atienza M. Fernández-Marmiesse A, et al. Among authors: simon r. Front Neurosci. 2019 Nov 8;13:1135. doi: 10.3389/fnins.2019.01135. eCollection 2019. Front Neurosci. 2019. PMID: 31780880 Free PMC article.

2

Cognitive and behavioral profile in females with epilepsy with PDCH19 mutation: two novel mutations and review of the literature.

Camacho A, Simón R, Sanz R, Viñuela A, Martínez-Salio A, Mateos F. Camacho A, et al. Among authors: simon r. Epilepsy Behav. 2012 May;24(1):134-7. doi: 10.1016/j.yebeh.2012.02.023. Epub 2012 Apr 14. Epilepsy Behav. 2012. PMID: 22504056 Review.

3

Levetiracetam-induced reversible autistic regression.

Camacho A, Espín JC, Nuñez N, Simón R. Camacho A, et al. Among authors: simon r. Pediatr Neurol. 2012 Jul;47(1):65-7. doi: 10.1016/j.pediatrneurol.2012.04.002. Pediatr Neurol. 2012. PMID: 22704022

4

Myorhythmia-Like Dyskinesia Affecting the Face and Ear Associated With Anti-N-Methyl-d-Aspartate Receptor Encephalitis.

Camacho A, Núñez N, Armangué T, Simón R. Camacho A, et al. Among authors: simon r. Mov Disord Clin Pract. 2015 Dec 24;3(4):425-426. doi: 10.1002/mdc3.12300. eCollection 2016 Jul-Aug. Mov Disord Clin Pract. 2015. PMID: 30713936 Free PMC article. No abstract available.

5

Clinical and histologic changes in the follow-up of a congenital myopathy.

Camacho A, Villarejo A, Simón R, Mateos F, Cabello A. Camacho A, et al. Among authors: simon r. Pediatr Neurol. 2005 Aug;33(2):139-41. doi: 10.1016/j.pediatrneurol.2005.02.012. Pediatr Neurol. 2005. PMID: 16087062

6

LAMA2-related congenital muscular dystrophy complicated by West syndrome.

Camacho A, Núñez N, Dekomien G, Hernández-Laín A, de Aragón AM, Simón R. Camacho A, et al. Among authors: simon r. Eur J Paediatr Neurol. 2015 Mar;19(2):243-7. doi: 10.1016/j.ejpn.2014.11.005. Epub 2014 Dec 2. Eur J Paediatr Neurol. 2015. PMID: 25500573

7

[No title available]

[No authors listed] [No authors listed] PMID: 35871522

8

Mechanical Thrombectomy for Acute Stroke in a 2-Month-Old Patient and Review of the Literature in Infancy.

Rodríguez-López A, Gimeno I, Vila S, Seoane A, Ballenilla F, Ramos A, Hilario A, Núñez N, Camacho A, Simón R. Rodríguez-López A, et al. Among authors: simon r. Neuropediatrics. 2022 Oct;53(5):376-380. doi: 10.1055/a-1844-8780. Epub 2022 May 5. Neuropediatrics. 2022. PMID: 35512844 Review.

9

Spontaneous carotid and vertebral artery dissection in children.

Camacho A, Villarejo A, de Aragón AM, Simón R, Mateos F. Camacho A, et al. Among authors: simon r. Pediatr Neurol. 2001 Sep;25(3):250-3. doi: 10.1016/s0887-8994(01)00294-6. Pediatr Neurol. 2001. PMID: 11587883

10

Vertebral artery fibromuscular dysplasia: an unusual cause of stroke in a 3-year-old child.

Camacho A, Villarejo A, Moreno T, Simón R, Muñoz A, Mateos F. Camacho A, et al. Among authors: simon r. Dev Med Child Neurol. 2003 Oct;45(10):709-11. doi: 10.1017/s0012162203001312. Dev Med Child Neurol. 2003. PMID: 14515944 Free article.

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