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Published in Frontiers in immunology (08.11.2019)
Published in Frontiers in immunology (08.11.2019)
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Noninvasive diagnostics of mitochondrial disorders in isolated lymphocytes with high resolution respirometry
Pecina, Petr, Houšťková, Hana, Mráček, Tomáš, Pecinová, Alena, Nůsková, Hana, Tesařová, Markéta, Hansíková, Hana, Janota, Jan, Zeman, Jiří, Houštěk, Josef
Published in BBA clinical (01.12.2014)
Published in BBA clinical (01.12.2014)
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Functional alteration of cytochrome c oxidase by SURF1 mutations in Leigh syndrome
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
Published in Biochimica et biophysica acta (01.09.2003)
Published in Biochimica et biophysica acta (01.09.2003)
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Segregation pattern and biochemical effect of the G3460A mtDNA mutation in 27 members of LHON family
Kaplanová, Vilma, Zeman, Jiřı́, Hansı́ková, Hana, Černá, Leona, Houšt'ková, Hana, Mišovicová, Naděžda, Houštěk, Josef
Published in Journal of the neurological sciences (30.08.2004)
Published in Journal of the neurological sciences (30.08.2004)
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A Novel Deficiency of Mitochondrial ATPase of Nuclear Origin
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
Published in Human molecular genetics (01.10.1999)
Published in Human molecular genetics (01.10.1999)
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Retrospective, multicentric study of 180 children with cytochrome c oxidase deficiency
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
Published in Pediatric research (2006)
Published in Pediatric research (2006)
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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
Williams, Siôn L, Taanman, Jan-Willem, Hansı́ková, Hana, Houšt'ková, Hana, Chowdhury, Subir, Zeman, Jiřı́, Houštěk, Josef
Published in Molecular genetics and metabolism (01.08.2001)
Published in Molecular genetics and metabolism (01.08.2001)
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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 with ragged-red fibres ('MERRF') at position 8344 nt
Antonická, H, Floryk, D, Klement, P, Stratilová, L, Hermanská, J, Houstková, H, Kalous, M, Drahota, Z, Zeman, J, Houstek, J
Published in Biochemical journal (15.09.1999)
Published in Biochemical journal (15.09.1999)
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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
Houštek, Josef, Klement, Petr, Hermanska, Jana, Houšťková, Hana, Hansíková, Hana, Van den Bogert, Coby, Zeman, Jiri
Published in Biochimica et biophysica acta (09.06.1995)
Published in Biochimica et biophysica acta (09.06.1995)
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Complex approach to prenatal diagnosis of cytochromec oxidase deficiencies
Houštěk, Josef, Klement, Petr, Heřmanská, Jana, Antonická, Hana, Houšťková, Hana, Stratilová, Leona, Wanders, Ronald J. A., Zeman, Jiří
Published in Prenatal diagnosis (01.06.1999)
Published in Prenatal diagnosis (01.06.1999)
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Complex approach to prenatal diagnosis of cytochrome c oxidase deficiencies
Houštěk, Josef, Klement, Petr, Heřmanská, Jana, Antonická, Hana, Houšťková, Hana, Stratilová, Leona, Wanders, Ronald J. A., Zeman, Jiří
Published in Prenatal diagnosis (01.06.1999)
Published in Prenatal diagnosis (01.06.1999)
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Resin hemoperfusion in hepatic porphyrias
Horák, J, Martásek, P, Kordac, V, Mertl, L, Jirsa, M, Tlustáková, M, Houstková, H
Published in Artificial organs (01.05.1985)
Published in Artificial organs (01.05.1985)
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