Vol. 64 No. 4 (2020)

Published: 2020-12-30

Original Scientific Paper

  • Neuronal ceroid lipofuscinosis – the most common neurodegenerative disorder in childhood

    Ružica Kravljanac
    213-220
    DOI: https://doi.org/10.13112/PC.2020.33

Case Report

  • Diagnostic, clinical and therapeutic challenges in patients with Duchenne muscular dystrophy – patient series reports

    Radenka Kuzmanić Šamija, Marta Plejić
    282-288
    DOI: https://doi.org/10.13112/PC.2020.41

  • Neurological manifestations and complications of autoimmune gastrointestinal diseases in children

    Radenka Kuzmanić Šamija, Kristina Lovrić
    290-294
    DOI: https://doi.org/10.13112/PC.2020.42

Review

  • Early diagnosis of neuronal ceroid lipofuscinosis type 2 – a myth or reality?

    Igor Prpić
    223-228
    DOI: https://doi.org/10.13112/PC.2020.34

  • Spinal muscular atrophy: do we know enough about initial symptoms and importance of early diagnosis?

    Ivan Lehman
    230-234
    DOI: https://doi.org/10.13112/PC.2020.35

  • Treatment of patients with spinal muscular atrophy in Croatia - positive results from the national registry and new challenges

    Nina Barišić, Vana Vukić, Ivan Lehman, Milivoj Novak, Tomislav Đapić, Jadranka Sertić, Katarina Bošnjak Nađ, Ivana Kern, Boris Najdanović, Lana Omerza, Duje Braovac, Dorotea Bartoniček, Daniel Turudić, Josipa Tomas
    236-251
    DOI: https://doi.org/10.13112/PC.2020.36

  • Pompe disease – a progressive multisystemic disorder: diagnostic and treatment challenges

    Danijela Petković Ramadža
    253-259
    DOI: https://doi.org/10.13112/PC.2020.37

  • Neurological manifestations of mucopolysaccharidoses

    Mijana Kero
    261-266
    DOI: https://doi.org/10.13112/PC.2020.38

  • The role of laboratory diagnostics in diagnostic workup of children with suspected rare neurometabolic diseases

    Ksenija Fumić
    269-275
    DOI: https://doi.org/10.13112/PC.2020.39

  • Challenges and possibilities of selective laboratory diagnostics of neuronal ceroid lipofuscinosis types 1 and 2 in Croatia

    Ksenija Fumić, Iva Bilandžija Kuš
    277-281
    DOI: https://doi.org/10.13112/PC.2020.40