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Handbook of Experimental Pharmacology|January 6, 2007
Conditional mouse models for Friedreich ataxia, a neurodegenerative disorder associating cardiomyopathyH PuccioHuman Molecular Genetics|April 18, 2000
Recent advances in the molecular pathogenesis of Friedreich ataxiaH Puccio, M KoenigRevue Neurologique|May 6, 2014
Pathophysiogical and therapeutic progress in Friedreich ataxiaH Puccio, M Anheim, C TranchantHuman Molecular Genetics|October 9, 2001
Disabled early recruitment of antioxidant defenses in Friedreich's ataxiaK Chantrel-Groussard, V Geromel, H Puccio, et al.Human Molecular Genetics|April 18, 2000
Inactivation of the Friedreich ataxia mouse gene leads to early embryonic lethality without iron accumulationM Cossée, H Puccio, A Gansmuller, et al.Nature Genetics|February 15, 2001
Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron depositsH Puccio, D Simon, M Cossée, et al.Neurogenetics|November 21, 2001
Rescue of the Friedreich's ataxia knockout mouse by human YAC transgenesisM A Pook, S Al-Mahdawi, C J Carroll, et al.Pageof 1