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Advances in Experimental Medicine and Biology|March 13, 2010
The role of mitochondrial network dynamics in the pathogenesis of Charcot-Marie-Tooth diseaseFrancesc Palau, Anna Estela, David Pla-Martín, et al.
International Journal of Molecular Sciences|January 24, 2019
Calcium Deregulation and Mitochondrial Bioenergetics in GDAP1-Related CMT DiseasePaloma González-Sánchez, Jorgina Satrústegui, Francesc Palau, et al.
Anales De Pediatria|June 7, 2021
Participant-funded clinical trials on rare diseasesRafael Dal-Ré, Francesc Palau, Encarna Guillén-Navarro, et al.
Anales De Pediatria|June 6, 2020
[Participant-funded clinical trials on rare diseases]Rafael Dal-Ré, Francesc Palau, Encarna Guillén-Navarro, et al.
Advances in Experimental Medicine and Biology|March 13, 2010
Friedreich ataxia: an update on animal models, frataxin function and therapiesPilar González-Cabo, José Vicente Llorens, Francesc Palau, et al.
Plos One|May 15, 2018
ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolismEstrella Rubio-Solsona, Salvador Martí, Juan J Vílchez, et al.
Plos One|June 7, 2018
Correction: ANKK1 is found in myogenic precursors and muscle fibers subtypes with glycolytic metabolismEstrella Rubio-Solsona, Salvador Martí, Juan J Vílchez, et al.
The Journal of Biological Chemistry|September 6, 2011
Charcot-Marie-Tooth-related gene GDAP1 complements cell cycle delay at G2/M phase in Saccharomyces cerevisiae fis1 gene-defective cellsAnna Estela, David Pla-Martín, Maribel Sánchez-Piris, et al.
Human Molecular Genetics|March 18, 2005
GDAP1, the protein causing Charcot-Marie-Tooth disease type 4A, is expressed in neurons and is associated with mitochondriaLaia Pedrola, Antonio Espert, Xingyao Wu, et al.
Frontiers in Cellular Neuroscience|May 27, 2014
Mitochondrial dysfunction induced by frataxin deficiency is associated with cellular senescence and abnormal calcium metabolismArantxa Bolinches-Amorós, Belén Mollá, David Pla-Martín, et al.
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