N. Starčević-Čižmarević

The impact of hemochromatosis mutations and transferrin genotype on gonadotropin serum levels in infertile men.

S. Ristić, I. Vlastelic, S. Nadalin, 2009, Fertility and sterility.

The effects of microbiota abundance on symptom severity in Parkinson’s disease: A systematic review

B. Peterlin, G. Hauser, A. Kovanda, 2022, Frontiers in Aging Neuroscience.

Angiotensin‐converting enzyme I/D gene polymorphism and risk of multiple sclerosis

B. Peterlin, S. Ristić, L. Lovrečić, 2006, Acta neurologica Scandinavica.

Tumor Necrosis Factor-α-308 Gene Polymorphism in Croatian and Slovenian Multiple Sclerosis Patients

B. Peterlin, S. Ristić, L. Lovrečić, 2007, European Neurology.

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.

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

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

Mutations in the hemochromatosis gene (HFE) and multiple sclerosis

B. Peterlin, S. Ristić, L. Lovrečić, 2005, Neuroscience Letters.

PAI and TPA gene polymorphisms in multiple sclerosis

B. Peterlin, S. Ristić, L. Lovrečić, 2008, Multiple sclerosis.

Tumor necrosis factor-alpha-308 gene polymorphism in Croatian and Slovenian multiple sclerosis patients.

B. Peterlin, S. Ristić, L. Lovrečić, 2007, European Neurology.

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.