Vladimir Sarnavka

<i>S</i> -adenosylhomocysteine hydrolase deficiency in a human: A genetic disorder of methionine metabolism

Ivo Barić, Ksenija Fumić, B. Glenn et al. · Proceedings of the National Academy of Sciences · 2004 · 220 citations · Full text

<i>S</i>‐Adenosylhomocysteine hydrolase deficiency: A second patient, the younger brother of the index patient, and outcomes during therapy

Ivo Barić, M. Ćuk, Ksenija Fumić et al. · Journal of Inherited Metabolic Disease · 2005 · 75 citations · Full text

Genotype-predicted tetrahydrobiopterin (BH4)-responsiveness and molecular genetics in Croatian patients with phenylalanine hydroxylase (PAH) deficiency

Iva Karačić, David Meili, Vladimir Sarnavka et al. · Molecular Genetics and Metabolism · 2009 · 70 citations

Croatian Patients, Mendelian Disorder, Biochemistry +10

Newborn screening in southeastern Europe

Urh Grošelj, Mojca Žerjav Tanšek, Andraž Šmon et al. · Molecular Genetics and Metabolism · 2014 · 56 citations

Newborn Screening, Neonatology, International Health +7

Phenylketonuria screening and management in southeastern Europe – survey results from 11 countries

Mojca Žerjav Tanšek, Urh Grošelj, Natalija Angelkova et al. · Orphanet Journal of Rare Diseases · 2015 · 47 citations · Full text