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Gorría-Redondo, Nerea
35
results:
Search for persons
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Format
Online (35)
Mediatypes
Articles (Online) (13)
OpenAccess-fulltext (22)
Languages
english (32)
spanish (1)
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1
Diverse faces of GNAO1: mild forms in epilepsy and autism:
Ludlam, William Grant
;
Soliani, Luca
;
Domínguez-Carral, Jana
...
Journal of Neurology. , 2024
Link:
https://doi.org/10.1007/..
?
2
Genetic Heterogeneity Underlying Phenotypes with Early-Onse..:
Martínez-Rubio, Dolores
;
Hinarejos, Isabel
;
Argente-Escrig, Herminia
...
International Journal of Molecular Sciences. 24 (2023) 22 - p. 16400 , 2023
Link:
https://doi.org/10.3390/..
?
3
Protein misfolding and clearance in the pathogenesis of a n..:
Martínez-Rubio, Dolores
;
Rodríguez-Prieto, Ángela
;
Sancho, Paula
...
Human Molecular Genetics. 31 (2022) 22 - p. 3897-3913 , 2022
Link:
https://doi.org/10.1093/..
?
4
Mutations, Genes, and Phenotypes Related to Movement Disord..:
Martínez-Rubio, Dolores
;
Hinarejos, Isabel
;
Sancho, Paula
...
International Journal of Molecular Sciences. 23 (2022) 19 - p. 11847 , 2022
Link:
https://doi.org/10.3390/..
?
5
Biallelic variants in SLC35B2 cause a novel chondrodysplasi..:
Guasto, Alessandra
;
Dubail, Johanne
;
Aguilera-Albesa, Sergio
...
Brain. 145 (2022) 10 - p. 3711-3722 , 2022
Link:
https://doi.org/10.1093/..
?
6
Expanding the β-III Spectrin-Associated Phenotypes toward N..:
Sancho, Paula
;
Andrés-Bordería, Amparo
;
Gorría-Redondo, Nerea
...
International Journal of Molecular Sciences. 22 (2021) 5 - p. 2505 , 2021
Link:
https://doi.org/10.3390/..
?
7
Case Report: Benign Infantile Seizures Temporally Associate..:
García-Howard, Marcos
;
Herranz-Aguirre, Mercedes
;
Moreno-Galarraga, Laura
...
Frontiers in Pediatrics. 8 (2020) - p. , 2020
Link:
https://doi.org/10.3389/..
?
8
Novel Variant in PLAG1 in a Familial Case with Silver–Russe..:
Vado, Yerai
;
Pereda, Arrate
;
Llano-Rivas, Isabel
...
Genes. 11 (2020) 12 - p. 1461 , 2020
Link:
https://doi.org/10.3390/..
?
9
Genetic Heterogeneity Underlying Phenotypes with Early-Onse..:
Martínez-Rubio, Dolores
;
Hinarejos, Isabel
;
Argente-Escrig, Herminia
...
doi:10.3390/ijms242216400. , 2023
Link:
http://hdl.handle.net/10..
?
10
Protein misfolding and clearance in the pathogenesis of a n..:
Martínez-Rubio, Dolores
;
Rodriguez-Prieto, Ángela
;
Sancho, Paula
...
Human Molecular Genetics;31(22). , 2022
Link:
https://hdl.handle.net/1..
?
11
Mutations, Genes, and Phenotypes Related to Movement Disord..:
Martínez-Rubio, Dolores
;
Hinarejos, Isabel
;
Sancho, Paula
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9570320/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
12
Protein misfolding and clearance in the pathogenesis of a n..:
Martínez-Rubio, Dolores
;
Rodríguez-Prieto, Ángela
;
Sancho, Paula
...
#PLACEHOLDER_PARENT_METADATA_VALUE#. , 2022
Link:
http://hdl.handle.net/10..
?
13
Mutations, Genes, and Phenotypes Related to Movement Disord..:
Martínez-Rubio, Dolores
;
Hinarejos Martínez, Isabel
;
Sancho, Paula
...
International Journal of Molecular Sciences;23(19). , 2022
Link:
https://hdl.handle.net/1..
?
14
Mutations, Genes, and Phenotypes Related to Movement Disord..:
Martínez-Rubio, Dolores
;
Hinarejos, Isabel
;
Sancho, Paula
...
#PLACEHOLDER_PARENT_METADATA_VALUE#. , 2022
Link:
http://hdl.handle.net/10..
?
15
Mutations, Genes, and Phenotypes Related to Movement Disord..:
Martínez-Rubio, Dolores
;
Hinarejos, Isabel
;
Sancho, Paula
...
http://hdl.handle.net/10668/21202. , 2022
Link:
http://hdl.handle.net/10..
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