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Page 1
Study of paediatric patients with the clinical and biochemical phenotype of glucose transporter type 1 deficiency syndrome.
Jiménez Legido M, Cortés Ledesma C, Bernardino Cuesta B, López Marín L, Cantarín Extremera V, Pérez-Cerdá C, Pérez González B, López Martín E, González Gutiérrez-Solana L. Jiménez Legido M, et al. Among authors: cantarin extremera v. Neurologia (Engl Ed). 2022 Mar;37(2):91-100. doi: 10.1016/j.nrl.2018.10.006. Epub 2019 Apr 29. Neurologia (Engl Ed). 2022. PMID: 31047728 Free article. English, Spanish.
[Panayiotopoulos syndrome: academic difficulties and behavioural disorders].
Pérez-Villena A, López-Marín L, Cantarín-Extremera V, Leon-Gonzalez M, Fournier-Del Castillo C, Ruiz-Falcó ML. Pérez-Villena A, et al. Among authors: cantarin extremera v. Rev Neurol. 2011 Jun 16;52(12):705-12. Rev Neurol. 2011. PMID: 21594855 Free article. Spanish.
Procalcitonin, a high acute phase reactant in antiepileptic hypersentivity syndrome in pediatric age.
Cantarín-Extremera V, Castaño-De La Mota C, Alvarez-Coca J, Rojas MR, Gutierrez-Solana LG, García Peñas JJ, Martínez-Pérez J, Duat-Rodríguez A, López-Marín L, Losada-Del Pozo R. Cantarín-Extremera V, et al. Eur J Paediatr Neurol. 2012 Mar;16(2):200-2. doi: 10.1016/j.ejpn.2011.06.007. Epub 2011 Jul 28. Eur J Paediatr Neurol. 2012. PMID: 21798772
[Characteristics and evolution of patients with Alice in Wonderland syndrome].
Losada-Del Pozo R, Cantarín-Extremera V, García-Peñas JJ, Duat-Rodríguez A, López-Marín L, Gutiérrez-Solana LG, Ruiz-Falcó ML. Losada-Del Pozo R, et al. Among authors: cantarin extremera v. Rev Neurol. 2011 Dec 1;53(11):641-8. Rev Neurol. 2011. PMID: 22086425 Free article. Spanish.
[Von Hippel-Lindau disease in a patient with l-2-hydroxyglutaric aciduria].
Duat Rodríguez A, Ruiz-Falcó Rojas ML, González Gutiérrez-Solana L, Cantarín Extremera V, Pedrón Giner C. Duat Rodríguez A, et al. Among authors: cantarin extremera v. An Pediatr (Barc). 2012 Jul;77(1):63-4. doi: 10.1016/j.anpedi.2012.02.006. Epub 2012 Apr 4. An Pediatr (Barc). 2012. PMID: 22481001 Free article. Spanish. No abstract available.
Immune-mediated mechanisms in the pathogenesis of Hopkins syndrome.
Cantarín-Extremera V, González-Gutiérrez-Solana L, Ramírez-Orellana M, López-Marín L, Duat-Rodríguez A, Ruíz-Falcó-Rojas ML. Cantarín-Extremera V, et al. Pediatr Neurol. 2012 Nov;47(5):373-4. doi: 10.1016/j.pediatrneurol.2012.08.006. Pediatr Neurol. 2012. PMID: 23044022
[Clinical phenotype of a patient with FOXP1 deletion].
Blanco Sánchez T, Duat Rodríguez A, Cantarín Extremera V, Lapunzina P, Palomares Bralo M, Nevado Blanco J. Blanco Sánchez T, et al. Among authors: cantarin extremera v. An Pediatr (Barc). 2015 Apr;82(4):280-1. doi: 10.1016/j.anpedi.2014.06.007. Epub 2014 Jul 16. An Pediatr (Barc). 2015. PMID: 25037997 Free article. Spanish. No abstract available.
53 results