H Houst'ková

Retrospective, Multicentric Study of 180 Children with Cytochrome c Oxidase Deficiency

Marek Böhm, Ewa Pronicka, Elżbieta Karczmarewicz et al. · Pediatric Research · 2005 · 109 citations · Full text

Life Sciences, Child Health, Pediatrics +3

Altered properties of mitochondrial ATP-synthase in patients with a T → G mutation in the ATPase 6 (subunit a) gene at position 8993 of mtDNA

J Houštěk, Petr Klement, Jana Heřmanská et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 1995 · 105 citations

Life Sciences, Genetics, Molecular Genetics +16

Genetic defects of cytochrome c oxidase assembly

Petr Pecina, H Houst'ková, J Zeman et al. · Physiological Research · 2004 · 99 citations · Full text

Life Sciences, Genetics, Molecular Biology +15

Deficiency of mitochondrial ATP synthase of nuclear genetic origin

Wolfgang Sperl, Pavel Ješina, J Zeman et al. · Neuromuscular Disorders · 2006 · 73 citations

Life Sciences, Genetics, Molecular Genetics +12

Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome

Petr Pecina, Markéta Čapková, Subir Roy Chowdhury et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 2003 · 53 citations

Life Sciences, Genetics, Molecular Genetics +8