Arrate Pereda

ResearcherID Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 9

Top Venues

Genes

European journal of endocrinology

Journal of neurology

European journal of neurology

BioAraba National Health Institute, OSI Araba University Hospital

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

Affiliation History

BioAraba National Health Institute, OSI Araba University Hospital Feb 01 2017

Spain

INVESTIGADORA POSTDOCTORAL :: Molecular (Epi)Genetics Laboratory

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)
Diana-Alexandra Ertl, Guiomar Perez de Nanclares, Harald Jüppner, Patrick Hanna, Angela Pagnano, Arrate Pereda, Anya Rothenbuhler, Giulia Del Sindaco, Pilar Ruiz-Cuevas, Christelle Audrain, Arancha Escribano, Jugurtha Berkenou, Andreas Gleiss, Mantovani Giovanna, Agnès Linglart
Recombinant Growth Hormone Improves Growth and Adult Height in Patients with Maternal Inactivating Gnas Mutations. European journal of endocrinology (2023)
Hasier Eraña, Beatriz San Millán, Carlos M Díaz-Domínguez, Jorge M Charco, Rosa Rodríguez, Irene Viéitez, Arrate Pereda, Rosa Yañez, María V Geijo, Carmen Navarro, Guiomar Perez de Nanclares, Susana Teijeira, Joaquín Castilla
Description of the first Spanish case of Gerstmann-Sträussler-Scheinker disease with A117V variant: clinical, histopathological and biochemical characterization. Journal of neurology 269 (8) (2022)
Izaro Kortazar-Zubizarreta, Hasier Eraña, Arrate Pereda, Jorge M Charco, Africa Manero-Azua, Rebeca Ruiz-Onandi, Urko Aguirre Larracoechea, Gonzalo Gonzalez-Chinchon, null null, Guiomar Perez de Nanclares, Joaquín Castilla
Analysis of a large case series of fatal familial insomnia to determine tests with the highest diagnostic value. Journal of neuropathology and experimental neurology (2022)
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, 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)

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Publication Activity (10 Years)

Top Topics

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Arrate Pereda