Concepedia

Vilma Kaplanová

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Statistics

Publications

10

Citations

658

H-Index

10

Active since

2004

Affiliations

Czech Academy of Sciences(Current)

Czech Academy of Sciences, Institute of Physiology

Charles University

Paracelsus Medical University

Vilma Kaplanová is an author at Czech Academy of Sciences specializing in life sciences, mitochondrial genetics, and mitochondrial disorders.

ORCID

Publications per year

2004–2019

10

Publications

10

TMEM70 mutations cause isolated ATP synthase deficiency and neonatal mitochondrial encephalocardiomyopathy

Alena Čížková, Viktor Stránecký, Johannes A. Mayr et al. · Nature Genetics · 2008 · 200 citations

, , +16

Mitochondrial ATP synthase deficiency due to a mutation in the ATP5E gene for the F1   subunit

Johannes A. Mayr, Vendula Havlíčková, Franz Zimmermann et al. · Human Molecular Genetics · 2010 · 138 citations

, , +17

Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6

Hana Hartmannová, Lenka Piherová, Kateřina Tauchmannová et al. · Human Molecular Genetics · 2016 · 80 citations · Full text

, , +17

Diminished synthesis of subunit a (ATP6) and altered function of ATP synthase and cytochrome <i>c</i> oxidase due to the mtDNA 2 bp microdeletion of TA at positions 9205 and 9206

Pavel Ješina, Markéta Tesařová, Daniela Fornůsková et al. · Biochemical Journal · 2004 · 62 citations · Full text

, , +17

Mitochondrial Membrane Potential and ATP Production in Primary Disorders of ATP Synthase

Alena Vojtı́šková, Pavel Ješina, Martin Kalous et al. · Toxicology Mechanisms and Methods · 2004 · 43 citations

, , +17

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