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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
