Centro Andaluz de Biología del Desarrollo (CABD)
Centro de investigación
Hospital Vall d'Hebron
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Hospital Vall d'Hebron (7)
2024
-
Chromosomal breaks: another differential gap between early-onset and late-onset colorectal cancers
British Journal of Surgery, Vol. 111, Núm. 3
2021
2019
-
Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy
Nature Communications, Vol. 10, Núm. 1
2016
-
Dominant-negative mutation p.Arg324Thr in KCNA1 impairs Kv1.1 channel function in episodic ataxia
Movement Disorders, Vol. 31, Núm. 11, pp. 1743-1748
2012
-
Guidelines for the use and interpretation of assays for monitoring autophagy
Autophagy, Vol. 8, Núm. 4, pp. 445-544
2009
-
Coenzyme Q10 deficiency associated with a mitochondrial DNA depletion syndrome: A case report
Clinical Biochemistry, Vol. 42, Núm. 7-8, pp. 742-745
2006
-
Cerebellar ataxia with coenzyme Q10 deficiency: Diagnosis and follow-up after coenzyme Q10 supplementation
Journal of the Neurological Sciences, Vol. 246, Núm. 1-2, pp. 153-158