Vol. 64 No. 4 (2018): Rare diseases special issue

View Vol. 64 No. 4 (2018): Rare diseases special issue

Edited by Teresa Zoładek i Joanna Kruszewska

Published: 2018-12-29

Editorials

Articles

  • Molecular mechanisms of genistein action in the light of therapies for genetic and immunological diseases

    Grzegorz Węgrzyn, Karolina Pierzynowska, Magdalena Podlacha, Joanna Brokowska, Lidia Gaffke, Jagoda Mantej, Zuzanna Cyske, Estera Rintz, Marta Osiadły, Michał Bartkowski, Michał Puchalski, Michał Grabski, Michał Pierzynowski, Dominika Pankanin, Ewa Piotrowska, Stefan Tukaj
    262 - 276
    DOI: https://doi.org/10.18388/pb.2018_140

  • Proteins from Vps13 family: from molecular function to pathogenesis of neurodegenerative disorders

    Joanna Kamińska, Damian Kolakowski
    275 - 287
    DOI: https://doi.org/10.18388/pb.2018_141

  • Therapeutic perspective in hereditary polyneuropathies

    Andrzej Kochański, Dagmara Kabzińska, Weronika Rzepnikowska, Katarzyna Binięda, Artur Kiepura
    288 - 299
    DOI: https://doi.org/10.18388/pb.2018_142

  • Mitochondrial diseases 2018, progress in research and treatment

    Ewa Bartnik, Katarzyna Tońska, Joanna Rusecka
    300 - 303
    DOI: https://doi.org/10.18388/pb.2018_143

  • Molecular bases of diseases caused by mutations in genes encoding subunits of ATP synthase

    Emilia Baranowska, Joanna Rytka, Róża Kucharczyk
    304 - 317
    DOI: https://doi.org/10.18388/pb.2018_144

  • Gene therapy of haemophilia â has the cure come within reach?

    Radosław Kaczmarek
    318 - 322
    DOI: https://doi.org/10.18388/pb.2018_145

  • Preeclampsia â a disease of pregnant women

    Anna Filipek, Ewelina Jurewicz
    232 - 229
    DOI: https://doi.org/10.18388/pb.2018_146

  • Rare diseases with epigenetic background

    Wiesława Leśniak
    330 - 337
    DOI: https://doi.org/10.18388/pb.2018_147

  • Ciliopaties â diseases caused by abnormal cilia functioning

    Ewa Joachimiak, Dorota Włoga, Anna Filipek, Hanna Fabczak
    338 - 350
    DOI: https://doi.org/10.18388/pb.2018_148

  • Genodermatoses â pathogenesis and molecular diagnostics

    Katarzyna Wertheim- Tysarowska
    351 - 358
    DOI: https://doi.org/10.18388/pb.2018_149

  • Peroxisomal disorders

    Tresa J. Stradomska
    359 - 367
    DOI: https://doi.org/10.18388/pb.2018_150

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