Concepedia

Author

Cristina Guilera

Centre for Biomedical Network Research on Rare DiseasesORCID

Also Known As

C Guilera, Cristina Guilera

12

Publications

429

Citations

9

H-Index

24

Concepts

All Affiliations

Centre for Biomedical Network Research on Rare DiseasesInstitució Catalana de Recerca i Estudis AvançatsInstitut d'Investigació Biomédica de BellvitgeInstituto de Salud Carlos IIIBellvitge University Hospital
CG

About

Cristina Guilera is an author at Centre for Biomedical Network Research on Rare Diseases specializing in medicine, pharmacology, and physiology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

3

3

172

2

Neurology

2

2

141

3

Biochemistry

1

1

97

4

Immunology

1

1

31

5

Neuroscience

1

1

44

Cristina Guilera

×

9

Publications

408

Citations

9

H-Index

YearCitations

Valproic acid induces antioxidant effects in X-linked adrenoleukodystrophy

Stéphane Fourcade, Montserrat Ruíz, Cristina Guilera,

Human Molecular Genetics

2010

97

Oxidative Damage Compromises Energy Metabolism in the Axonal Degeneration Mouse Model of X-Adrenoleukodystrophy

Jorge Galino, Montserrat Ruíz, Stéphane Fourcade,

Antioxidants and Redox Signaling

2011

82

Autophagy induction halts axonal degeneration in a mouse model of X-adrenoleukodystrophy

Nathalie Launay, Carmen Aguado, Stéphane Fourcade,

Acta Neuropathologica

2014

49

Oxidative stress regulates the ubiquitin–proteasome system and immunoproteasome functioning in a mouse model of X-adrenoleukodystrophy

Nathalie Launay, Montserrat Ruíz, Stéphane Fourcade,

Brain

2013

45

Altered glycolipid and glycerophospholipid signaling drive inflammatory cascades in adrenomyeloneuropathy

Montserrat Ruíz, Mariona Jové, Agatha Schlüter,

Human Molecular Genetics

2015

44

Activation of sirtuin 1 as therapy for the peroxisomal disease adrenoleukodystrophy

Laia Morató, Montserrat Ruíz, Jordi Boada,

Cell Death and Differentiation

2015

31

Oxidative stress and mitochondrial dynamics malfunction are linked in <scp>P</scp>elizaeus‐<scp>M</scp>erzbacher disease

Montserrat Ruíz, Mélina Bégou, Nathalie Launay,

Brain Pathology

2017

25

Diagnosis of Genetic White Matter Disorders by Singleton Whole-Exome and Genome Sequencing Using Interactome-Driven Prioritization

Agatha Schlüter, Agustí Rodríguez‐Palmero, Edgard Verdura,

Neurology

2022

22

RINT1 deficiency disrupts lipid metabolism and underlies a complex hereditary spastic paraplegia

Nathalie Launay, Montserrat Ruíz, Laura Planas‐Serra,

Journal of Clinical Investigation

2023

13

Page 1