Corticobasal Syndrome in a Family with Early‐Onset Alzheimer's Disease Linked to a Presenilin‐1 Gene Mutation

por Navarro, Eloisa, De Andrés, Clara, Guerrero, Carmen, Giménez‐Roldán, Santiago
Publicado en Mov Disord Clin Pract (2015)

Comorbidity of Narcolepsy Type 1 With Autoimmune Diseases and Other Immunopathological Disorders: A Case-Control Study

por Martinez-Orozco, Francisco Javier, Vicario, Jose Luis, De Andres, Clara, Fernandez-Arquero, Miguel, Peraita-Adrados, Rosa
Publicado en J Clin Med Res (2016)

Activation of Blood CD3(+)CD56(+)CD8(+) T Cells during Pregnancy and Multiple Sclerosis

por de Andrés, Clara, Fernández-Paredes, Lidia, Tejera-Alhambra, Marta, Alonso, Bárbara, Ramos-Medina, Rocío, Sánchez-Ramón, Silvia
Publicado en Front Immunol (2017)

Perforin Expression by CD4+ Regulatory T Cells Increases at Multiple Sclerosis Relapse: Sex Differences

por Tejera-Alhambra, Marta, Alonso, Bárbara, Teijeiro, Roseta, Ramos-Medina, Rocío, Aristimuño, Carol, Valor, Larissa, de Andrés, Clara, Sánchez-Ramón, Silvia
Publicado 2012

Long-Term Decrease in VLA-4 Expression and Functional Impairment of Dendritic Cells during Natalizumab Therapy in Patients with Multiple Sclerosis

por de Andrés, Clara, Teijeiro, Roseta, Alonso, Bárbara, Sánchez-Madrid, Francisco, Martínez, M. Luisa, de Villoria, Juan Guzmán, Fernández-Cruz, Eduardo, Sánchez-Ramón, Silvia
Publicado 2012

Profiling of Canonical and Non-Traditional Cytokine Levels in Interferon-β-Treated Relapsing–Remitting-Multiple Sclerosis Patients

por D’Angelo, Chiara, Reale, Marcella, Costantini, Erica, Di Nicola, Marta, Porfilio, Italo, de Andrés, Clara, Fernández-Paredes, Lidia, Sánchez-Ramón, Silvia, Pasquali, Livia
Publicado en Front Immunol (2018)

A Missense Mutation in Myelin Oligodendrocyte Glycoprotein as a Cause of Familial Narcolepsy with Cataplexy

por Hor, Hyun, Bartesaghi, Luca, Kutalik, Zoltán, Vicário, José L., de Andrés, Clara, Pfister, Corinne, Lammers, Gert J., Guex, Nicolas, Chrast, Roman, Tafti, Mehdi, Peraita-Adrados, Rosa
Publicado 2011

A Missense Mutation in Myelin Oligodendrocyte Glycoprotein as a Cause of Familial Narcolepsy with Cataplexy

por Hor, Hyun, Bartesaghi, Luca, Kutalik, Zoltán, Vicário, José L., de Andrés, Clara, Pfister, Corinne, Lammers, Gert J., Guex, Nicolas, Chrast, Roman, Tafti, Mehdi, Peraita-Adrados, Rosa
Publicado 2012

Plasma Biomarkers Discriminate Clinical Forms of Multiple Sclerosis

por Tejera-Alhambra, Marta, Casrouge, Armanda, de Andrés, Clara, Seyfferth, Ansgar, Ramos-Medina, Rocío, Alonso, Bárbara, Vega, Janet, Fernández-Paredes, Lidia, Albert, Matthew L., Sánchez-Ramón, Silvia
Publicado en PLoS One (2015)

Neuromyelitis optica spectrum disorders: Comparison according to the phenotype and serostatus

por Sepúlveda, Maria, Armangué, Thaís, Sola-Valls, Nuria, Arrambide, Georgina, Meca-Lallana, José E., Oreja-Guevara, Celia, Mendibe, Mar, Alvarez de Arcaya, Amaya, Aladro, Yolanda, Casanova, Bonaventura, Olascoaga, Javier, Jiménez-Huete, Adolfo, Fernández-Fournier, Mireya, Ramió-Torrentà, Lluis, Cobo-Calvo, Alvaro, Viñals, Montserrat, de Andrés, Clara, Meca-Lallana, Virginia, Cervelló, Angeles, Calles, Carmen, Rubio, Manuel Barón, Ramo-Tello, Cristina, Caminero, Ana, Munteis, Elvira, Antigüedad, Alfredo R., Blanco, Yolanda, Villoslada, Pablo, Montalban, Xavier, Graus, Francesc, Saiz, Albert
Publicado en Neurol Neuroimmunol Neuroinflamm (2016)