Search Results - Bielecka, Liliana

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  1. 1
    The natural history of SCO2 deficiency in 36 Polish children confirmed the genotype-phenotype correlation

    The natural history of SCO2 deficiency in 36 Polish children confirmed the genotype-phenotype correlation by Pronicka, Ewa, Piekutowska-Abramczuk, Dorota, Szymańska-Dębińska, Tamara, Bielecka, Liliana, Kowalski, Paweł, Luczak, Sylwia, Karkucińska-Więckowska, Agnieszka, Migdał, Marek, Kubalska, Jolanta, Zimowski, Janusz, Jamroz, Ewa, Wierzba, Jolanta, Sykut-Cegielska, Jolanta, Pronicki, Maciej, Zaremba, Jacek, Krajewska-Walasek, Małgorzata

    Published in Mitochondrion
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  2. 2
    High prevalence of SURF1 c.845_846delCT mutation in Polish Leigh patients

    High prevalence of SURF1 c.845_846delCT mutation in Polish Leigh patients by Piekutowska-Abramczuk, Dorota, Popowska, Ewa, Pronicki, Maciej, Karczmarewicz, Elzbieta, Tylek-Lemanska, Dorota, Sykut-Cegielska, Jolanta, Szymanska-Dembinska, Tamara, Bielecka, Liliana, Krajewska-Walasek, Malgorzata, Pronicka, Ewa

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    Molecular studies of Polish patients with respiratory chain complex I deficiency

    Molecular studies of Polish patients with respiratory chain complex I deficiency by Kowalski, Paweł, Piekutowska-Abramczuk, Dorota, Popowska, Ewa, Karczmarewicz, Elżbieta, Bielecka, Liliana, Kryśkiewicz, Edyta, Jamroz, Ewa, Pilch, Jacek, Ciara, Elżbieta, Jurkiewicz, Dorota, Borucka-Mankiewicz, Maria, Tańska, Anna, Łuczak, Sylwia, Pelc, Magdalena, Trubicka, Joanna, Krajewska-Walasek, Małgorzata, Elpeleg, Orly, Smeitink, Jan, Pronicka, Ewa

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