N. Starčević-Čizmarević

Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis

G. Zamolo, B. Peterlin, A. Maver, 2017, Scientific Reports.

Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis

B. Peterlin, D. S̆timac, S. Ristić, 2011, Medical science monitor : international medical journal of experimental and clinical research.

The Role of Iron and Iron Overload in Chronic Liver Disease

D. S̆timac, S. Ristić, L. Orlić, 2016, Medical science monitor : international medical journal of experimental and clinical research.

No association of CCR5D32 gene mutation with multiple sclerosis in Croatian and Slovenian patients

B. Peterlin, S. Ristić, L. Lovrečić, 2005, Multiple sclerosis.