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Volume: Vol. 49, No 3, july - september 2005



    Primarijus docent dr. Miljenko Mrakovčić (26. 3. 1920. – 4. 2. 2005.)


    Diagnosis and treatment of Gaucher disease
    M. Mrsić


    Laboratory diagnosis of lysosomal storage diseases: new potentials
    K. Fumić


    Assessment of bone turnover by bone markers: clinical application and significance
    V. Kušec


    The role of densitometry in the diagnosis of osteogenesis imperfecta
    D. Dodig, Ž. Jurašinović, S. Divošević


    Treatment of mucopolysaccharidoses
    D. Petković, I. Barić


    Current management of musculo-skeletal complications in children with mucopolysaccharidosis andosteogenesis imperfecta
    D. Antičević, M. Bergovec, T. Đapić


    Renal complications of Anderson-Fabry disease
    P. Kes, N. Bašić-Jukić, B. Brunetta, I. Jurić, I. Blajić, N. Dumančić, M. Blažev


    Genetic and phenotypic heterogenity of mucopolysaccharidoses
    I. Barišić


    Genetics of serum lipoprotein disorders
    Ž. Reiner


    Neurological indications and complications of storage diseases
    M. Čačić Hribljan


    First results of enzyme replacement therapy in two patients with mucopolysaccharidosis ih
    V. Petković, I. Barišić, N. Huzjak, G. Petković, K. Fumić

About us

The editor is Children's Hospital Zagreb. It is published four times per year by Children's University Hospital Zagreb, Klaićeva 16, HR-10000 Zagreb, Croatia.
Practicing pediatricians, pediatric subspecialists, neonatologists, family physicians, and other health care professionals that have children in their care.
Journal is open-access.

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