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

Year Number of Results
2007 1
2008 5
2009 6
2010 8
2011 6
2012 2
2013 2
2014 3
2015 1
2019 1
2020 4
2021 4
2022 2
2024 1

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39 results

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Page 1
[Epilepsy and inborn errors of metabolism].
Moya-López S, Ruiz-Colodrero A, Sainz-García J, Fariña-Jara V, García-Jiménez MC, Castejón-Ponce E, López-Pisón J, Pérez-Delgado R. Moya-López S, et al. Among authors: perez delgado r. Rev Neurol. 2024 Sep 29;79(5):129-135. doi: 10.33588/rn.7905.2024088. Rev Neurol. 2024. PMID: 39207127 Free PMC article. Spanish.
KCNQ2 gene mutations and neonatal epilepsy.
García Castellanos MT, López Pisón J, Pérez Delgado R. García Castellanos MT, et al. Among authors: perez delgado r. Med Clin (Barc). 2021 Dec 24;157(12):589-590. doi: 10.1016/j.medcli.2021.01.019. Epub 2021 May 4. Med Clin (Barc). 2021. PMID: 33962768 English, Spanish. No abstract available.
Aproximación etiológica a la hipoglucemia en urgencias: revisión de un protocolo.
Pérez Delgado R, Soria Marzo A, García Jiménez I, Campos Calleja C, García Mata JR, Lafuente Hidalgo M, García Oguiza A, López Pisón J, Luis Peña Segura J, Baldellou Vázquez A. Pérez Delgado R, et al. Rev Calid Asist. 2008 Jul;23(4):194-6. doi: 10.1016/S1134-282X(08)72133-X. Epub 2008 Oct 26. Rev Calid Asist. 2008. PMID: 23040192 Spanish. No abstract available.
[Progressive spastic paraparesis and static syringomyelia: Silver syndrome/SPG17].
Lafuente-Hidalgo M, Peña-Segura JL, Ranz-Angulo R, García-Oguiza A, Pérez-Delgado R, Izquierdo-Álvarez S, López-Pisón J. Lafuente-Hidalgo M, et al. Among authors: perez delgado r. Rev Neurol. 2015 Aug 16;61(4):188-91. Rev Neurol. 2015. PMID: 26204091 Free article. Review. Spanish. No abstract available.
[Satisfaction surveys on neurofibromatosis type 1 information sheets].
Sánchez Marco SB, López Pisón J, Peña Segura JL, López Lafuente A, Monge Galindo L, Pérez Delgado R. Sánchez Marco SB, et al. Among authors: perez delgado r. J Healthc Qual Res. 2021 Jul-Aug;36(4):240-241. doi: 10.1016/j.jhqr.2021.03.006. Epub 2021 May 8. J Healthc Qual Res. 2021. PMID: 33975814 Spanish. No abstract available.
[Infant with intracranial calcifications and retinopathy].
Hidalgo-Sanz J, Perez-Delgado R, Garcia-Jimenez I, Lopez-Pison J, Castillo-Castejon O, Poch ML, Izquierdo-Alvarez S. Hidalgo-Sanz J, et al. Among authors: perez delgado r. Rev Neurol. 2019 Oct 1;69(7):289-292. doi: 10.33588/rn.6907.2019166. Rev Neurol. 2019. PMID: 31559627 Free article. Spanish.
[Early infantile epileptic encephalopathy due to ITPA mutation].
Alcón-Grases M, Ferrer-Aliaga N, Salinas-Salvador B, Pérez-Delgado R, Castejón-Ponce E, García-Jiménez MC, Izquierdo-Álvarez S, López-Pisón J. Alcón-Grases M, et al. Among authors: perez delgado r. Rev Neurol. 2020 Sep 1;71(5):197-198. doi: 10.33588/rn.7105.2020239. Rev Neurol. 2020. PMID: 32729112 Free article. Spanish.
[Intestinal lymphangiectasia in a patient with Sanfilippo B syndrome].
Barbed Ferrández SM, García Romero R, Pérez Delgado R, Romagosa Sánchez-Monge I, Ros Arnal I, Torrecilla Idoipe N. Barbed Ferrández SM, et al. Among authors: perez delgado r. Arch Argent Pediatr. 2021 Apr;119(2):e138-e141. doi: 10.5546/aap.2021.e138. Arch Argent Pediatr. 2021. PMID: 33749204 Free article. Spanish.
A new overgrowth syndrome is due to mutations in RNF125.
Tenorio J, Mansilla A, Valencia M, Martínez-Glez V, Romanelli V, Arias P, Castrejón N, Poletta F, Guillén-Navarro E, Gordo G, Mansilla E, García-Santiago F, González-Casado I, Vallespín E, Palomares M, Mori MA, Santos-Simarro F, García-Miñaur S, Fernández L, Mena R, Benito-Sanz S, del Pozo Á, Silla JC, Ibañez K, López-Granados E, Martín-Trujillo A, Montaner D; SOGRI Consortium; Heath KE, Campos-Barros Á, Dopazo J, Nevado J, Monk D, Ruiz-Pérez VL, Lapunzina P. Tenorio J, et al. Hum Mutat. 2014 Dec;35(12):1436-41. doi: 10.1002/humu.22689. Hum Mutat. 2014. PMID: 25196541
39 results