Jordi Corral

Spinocerebellar ataxias in Spanish patients: genetic analysis of familial and sporadic cases

Miguel Angel Pujana, Jordi Corral, Mónica Gratacòs et al. · Human Genetics · 1999 · 131 citations

Genetic Analysis, Mendelian Disorder, Genetic Disorder +9

A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome.

Antoni Barrientos, V. Volpini, Jordi Casademont et al. · Journal of Clinical Investigation · 1996 · 109 citations · Full text

Genetics, Molecular Biology, Pathology +20

Cerebellar ataxia with coenzyme Q10 deficiency: Diagnosis and follow-up after coenzyme Q10 supplementation

Rafael Artuch, Gloria Brea‐Calvo, Paz Briones et al. · Journal of the Neurological Sciences · 2006 · 99 citations

Coenzyme Q10 Supplementation, Neurology, Cerebellar Ataxia +3

Presymptomatic analysis of spinocerebellar ataxia type 1 (SCA1) via the expansion of the <i>SCA1</i> CAG-repeat in a large pedigree displaying anticipation and parental male bias

T. Matilla, V. Volpinl, D. E. Genis et al. · Human Molecular Genetics · 1993 · 84 citations

Roles of Efflux Pumps from Different Superfamilies in the Surface-Associated Motility and Virulence of <i>Acinetobacter baumannii</i> ATCC 17978

María Pérez−Varela, Jordi Corral, Jesús Aranda et al. · Antimicrobial Agents and Chemotherapy · 2019 · 77 citations · Full text