Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

19 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study.
Armangue T, Olivé-Cirera G, Martínez-Hernandez E, Sepulveda M, Ruiz-Garcia R, Muñoz-Batista M, Ariño H, González-Álvarez V, Felipe-Rucián A, Jesús Martínez-González M, Cantarín-Extremera V, Concepción Miranda-Herrero M, Monge-Galindo L, Tomás-Vila M, Miravet E, Málaga I, Arrambide G, Auger C, Tintoré M, Montalban X, Vanderver A, Graus F, Saiz A, Dalmau J; Spanish Pediatric anti-MOG Study Group. Armangue T, et al. Lancet Neurol. 2020 Mar;19(3):234-246. doi: 10.1016/S1474-4422(19)30488-0. Epub 2020 Feb 10. Lancet Neurol. 2020. PMID: 32057303
"Leukodystrophy-Like" Phenotype in Anti-MOG Antibody-Associated Disorders.
Ortiz de Zarate Z, Felipe-Rucián A, Sánchez-Montáñez Á, Armangué T, Gómez-Andrés D. Ortiz de Zarate Z, et al. Neuropediatrics. 2022 Apr;53(2):147-148. doi: 10.1055/a-1740-9649. Epub 2022 Mar 8. Neuropediatrics. 2022. PMID: 35030636 No abstract available.
Characteristic retinal atrophy pattern allows differentiation between pediatric MOGAD and MS after a single optic neuritis episode.
Pakeerathan T, Havla J, Schwake C, Salmen A, Bigi S, Abegg M, Brügger D, Ferrazzini T, Runge AK, Breu M, Kornek B, Bsteh G, Felipe-Rucián A, Ringelstein M, Aktas O, Karenfort M, Wendel E, Kleiter I, Hellwig K, Kümpfel T, Thiels C, Lücke T, Gold R, Rostasy K, Ayzenberg I. Pakeerathan T, et al. Among authors: felipe rucian a. J Neurol. 2022 Dec;269(12):6366-6376. doi: 10.1007/s00415-022-11256-y. Epub 2022 Jul 23. J Neurol. 2022. PMID: 35869995 Free PMC article.
EPITRANS. Quality assessment of the epilepsy transition process.
Ortiz de Zarate Z, Fonseca E, Abraira L, Santamarina E, Campos-Fernández D, Quintana M, Sánchez J, Goméz-Andrés D, Sala J, Raspall M, Felipe-Rucián A, Del Toro M, Macaya A, Toledo M. Ortiz de Zarate Z, et al. Among authors: felipe rucian a. Eur J Paediatr Neurol. 2024 Jan;48:121-128. doi: 10.1016/j.ejpn.2024.01.004. Epub 2024 Jan 12. Eur J Paediatr Neurol. 2024. PMID: 38241904
Impact of COVID19 pandemic on patients with rare diseases in Spain, with a special focus on inherited metabolic diseases.
Rovira-Remisa MM, Moreira M, Ventura PS, Gonzalez-Alvarez P, Mestres N, Graterol Torres F, Joaquín C, Seuma AR, Del Mar Martínez-Colls M, Roche A, Ibáñez-Micó S, López-Laso E, Méndez-Hernández MJ, Murillo M, Monlleó-Neila L, Maqueda-Castellote E, Del Toro Riera M, Felipe-Rucián A, Giralt-López M, Cortès-Saladelafont E. Rovira-Remisa MM, et al. Among authors: felipe rucian a. Mol Genet Metab Rep. 2023 Jun;35:100962. doi: 10.1016/j.ymgmr.2023.100962. Epub 2023 Mar 6. Mol Genet Metab Rep. 2023. PMID: 36909454 Free PMC article.
19 results