Yerai Vado

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 7

Top Topics

Dna Methylation

Preterm Infants

Top Venues

European journal of neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Yerai Vado, Africa Manero-Azua, Arrate Pereda, Guiomar Perez de Nanclares
Choosing the Best Tissue and Technique to Detect Mosaicism in Fibrous Dysplasia/McCune-Albright Syndrome (FD/MAS). Genes 15 (1) (2024)
Yerai Vado, Africa Manero-Azua, Arrate Pereda, Guiomar Perez de Nanclares
Choosing the Best Tissue and Technique to Detect Mosaicism in Fibrous Dysplasia/McCune-Albright Syndrome (FD/MAS). Genes 15 (1) (2024)
Yerai Vado, Africa Manero-Azua, Arrate Pereda, Guiomar Perez de Nanclares
Choosing the Best Tissue and Technique to Detect Mosaicism in Fibrous Dysplasia/McCune-Albright Syndrome (FD/MAS). Genes 15 (1) (2024)
Yerai Vado, Africa Manero-Azua, Arrate Pereda, Guiomar Perez de Nanclares
Choosing the Best Tissue and Technique to Detect Mosaicism in Fibrous Dysplasia/McCune-Albright Syndrome (FD/MAS). Genes 15 (1) (2024)
Izaro Kortazar-Zubizarreta, Rebeca Ruiz-Onandi, Arrate Pereda, Yerai Vado, Gonzalo Gonzalez-Chinchon, Hasier Eraña, Guiomar Perez de Nanclares, Joaquín Castilla
Sporadic Creutzfeldt-Jakob disease with extremely long 14-year survival period. European journal of neurology 28 (9) (2021)
Yerai Vado, Gustavo Puras, Melania Rosique, Martín César, José Luis Pedraz, Shifa Jebari-Benslaiman, Marian M de Pancorbo, Jon Zarate, Guiomar Perez de Nanclares
Design and Validation of a Process Based on Cationic Niosomes for Gene Delivery into Novel Urine-Derived Mesenchymal Stem Cells. Pharmaceutics 13 (5) (2021)
Yerai Vado, Arrate Pereda, Isabel Llano-Rivas, Nerea Gorria-Redondo, Ignacio Díez López, Guiomar Perez de Nanclares
Novel Variant in PLAG1 in a Familial Case with Silver-Russell Syndrome Suspicion. Genes 11 (12) (2020)