Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry von Pecina, Petr, Houšťková, Hana, Mráček, Tomáš, Pecinová, Alena, Nůsková, Hana, Tesařová, Markéta, Hansíková, Hana, Janota, Jan, Zeman, Jiří, Houštěk, Josef

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Anti-IL6 Autoantibodies in an Infant With CRP-Less Septic Shock von Bloomfield, Marketa, Parackova, Zuzana, Cabelova, Tamara, Pospisilova, Iva, Kabicek, Pavel, Houstkova, Hana, Sediva, Anna

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Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome von Pecina, Petr, Čapková, Markéta, Chowdhury, Subir K.R., Drahota, Zdeněk, Dubot, Audrey, Vojtíšková, Alena, Hansíková, Hana, Houšt'ková, Hana, Zeman, Jiří, Godinot, Catherine, Houštěk, Josef

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Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family von Kaplanová, Vilma, Zeman, Jiřı́, Hansı́ková, Hana, Černá, Leona, Houšt'ková, Hana, Mišovicová, Naděžda, Houštěk, Josef

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A Novel Deficiency of Mitochondrial ATPase of Nuclear Origin von Houštek, Josef, Klement, Petr, Floryk, Daniel, Antonická, Hana, Hermanská, Jana, Kalous, Martin, Hansíková, Hana, Houšt'ková, Hana, Chowdhury, Subir K. R., Rosipal, Štefan, Kmoch, Stanislav, Stratilová, Leona, Zeman, Jirí

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Retrospective, multicentric study of 180 children with cytochrome c oxidase deficiency von BÖHM, Marek, PRONICKA, Ewa, HOUSTKOVA, Hana, HOUSTEK, Josef, ZEMAN, Jiri, KARCZMAREWICZ, Elzbieta, PRONICKI, Maciej, PIEKUTOWSKA-ABRAMCZUK, Dorota, SYKUT-CEGIELSKA, Jolanta, MIERZEWSKA, Hanna, HANSIKOVA, Hana, VESELA, Katerina, TESAROVA, Marketa

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Defective kinetics of cytochrome c oxidase and alteration of mitochondrial membrane potential in fibroblasts and cytoplasmic hybrid cells with the mutation for myoclonus epilepsy w... von Antonická, H, Floryk, D, Klement, P, Stratilová, L, Hermanská, J, Houstková, H, Kalous, M, Drahota, Z, Zeman, J, Houstek, J

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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 von Houštek, Josef, Klement, Petr, Hermanska, Jana, Houšťková, Hana, Hansíková, Hana, Van den Bogert, Coby, Zeman, Jiri

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Complex approach to prenatal diagnosis of cytochromec oxidase deficiencies von Houštěk, Josef, Klement, Petr, Heřmanská, Jana, Antonická, Hana, Houšťková, Hana, Stratilová, Leona, Wanders, Ronald J. A., Zeman, Jiří

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Complex approach to prenatal diagnosis of cytochrome c oxidase deficiencies von Houštěk, Josef, Klement, Petr, Heřmanská, Jana, Antonická, Hana, Houšťková, Hana, Stratilová, Leona, Wanders, Ronald J. A., Zeman, Jiří

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A Novel Mutation in SURF1 Causes Skipping of Exon 8 in a Patient with Cytochrome c Oxidase-Deficient Leigh Syndrome and Hypertrichosis von Williams, Siôn L, Taanman, Jan-Willem, Hansı́ková, Hana, Houšt'ková, Hana, Chowdhury, Subir, Zeman, Jiřı́, Houštěk, Josef

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