Search Results - Berankova, Kamila

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  1. 1
    Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I

    Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I by Danhelovska, Tereza, Kolarova, Hana, Zeman, Jiri, Hansikova, Hana, Vaneckova, Manuela, Lambert, Lukas, Kucerova-Vidrova, Vendula, Berankova, Kamila, Honzik, Tomas, Tesarova, Marketa

    Published in BMC pediatrics
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  2. 2
    Muckle-Wells Syndrome Across Four Generations in One Czech Family: Natural Course of the Disease

    Muckle-Wells Syndrome Across Four Generations in One Czech Family: Natural Course of the Disease by Fingerhutová, Šárka, Fráňová, Jana, Hlaváčková, Eva, Jančová, Eva, Procházková, Leona, Beránková, Kamila, Tesařová, Markéta, Honsová, Eva, Doležalová, Pavla

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  3. 3
    GP224 Multisystem mitochondrial diseases in children with maternally inherited complex I deficiency

    GP224 Multisystem mitochondrial diseases in children with maternally inherited complex I deficiency by Danhelovska, Tereza, Kolarova, Hana, Langer, Jan, Berankova, Kamila, Hansikova, Hana, Tesarova, Marketa, Honzik, Tomas, Zeman, Jiri

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  4. 4
    Sideroblastic anemia associated with multisystem mitochondrial disorders

    Sideroblastic anemia associated with multisystem mitochondrial disorders by Tesarova, Marketa, Vondrackova, Alzbeta, Stufkova, Hana, Veprekova, Lenka, Stranecky, Viktor, Berankova, Kamila, Hansikova, Hana, Magner, Martin, Galoova, Natalia, Honzik, Tomas, Vodickova, Elena, Stary, Jan, Zeman, Jiri

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    Muckle-Wells Syndrome Across Four Generations in One Czech Family: Natural Course of the Disease

    Muckle-Wells Syndrome Across Four Generations in One Czech Family: Natural Course of the Disease by Fingerhutová, Šárka, Fráňová, Jana, Hlaváčková, Eva, Jančová, Eva, Procházková, Leona, Beránková, Kamila, Tesařová, Markéta, Honsová, Eva, Doležalová, Pavla

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