M. Maradin

Capillary blood sampling: national recommendations on behalf of the Croatian Society of Medical Biochemistry and Laboratory Medicine

J. L. Krleza, Adrijana Dorotić, Ana Grzunov, 2015, Biochemia medica.

S-Adenosylhomocysteine hydrolase deficiency: A second patient, the younger brother of the index patient, and outcomes during therapy

I. Pogribny, S. Zeisel, M. Radoš, 2005, Journal of Inherited Metabolic Disease.

Mucopolysaccharidosis type 1 : First experiences with enzyme replacement therapy (ERT) in Croatia

D. Antičević, I. Barić, K. Fumic, 2004 .

Novel OCTN2 mutations: no genotype-phenotype correlations: early carnitine therapy prevents cardiomyopathy.

L. de Meirleir, P. Divry, G. Besley, 2002, American journal of medical genetics.

[Vitamin B12 deficiency in children--underestimated danger in the light of new knowledge].

M. Baumgartner, S. Puseljic, I. Barić, 2011, Lijecnicki vjesnik.

Fumaric aciduria: Mild phenotype in a 8-year-old girl with novel mutations

M. Tesařová, J. Zeman, I. Barić, 2006, Journal of Inherited Metabolic Disease.

Hrvatsko društvo za medicinsku biokemiju i laboratorijsku medicinu: Nacionalne preporuke za kapilarno uzorkovanje krvi

J. L. Krleza, Adrijana Dorotić, Ana Grzunov, 2016 .