N. Tomasic

Effect of High-Carbohydrate Diet on Plasma Metabolome in Mice with Mitochondrial Respiratory Chain Complex III Deficiency

V. Fellman, J. Kallijärvi, V. Velagapudi, 2016, International journal of molecular sciences.

The phenotype of polycythemia due to Croatian homozygous VHL (571C>G:H191D) mutation is different from that of Chuvash polycythemia (VHL 598C>T:R200W)

S. Nekhai, C. Huff, J. Prchal, 2013, Haematologica.

Fasting reveals largely intact systemic lipid mobilization mechanisms in respiratory chain complex III deficient mice.

V. Fellman, E. Eklund, M. Jauhiainen, 2019, Biochimica et biophysica acta. Molecular basis of disease.

Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model

V. Fellman, E. Eklund, J. Kallijärvi, 2017, Orphanet Journal of Rare Diseases.

Continuous remote monitoring of COPD patients—justification and explanation of the requirements and a survey of the available technologies

R. Trobec, T. Kelava, I. Tomasic, 2018, Medical & Biological Engineering & Computing.

Continuous remote monitoring of COPD patients—justification and explanation of the requirements and a survey of the available technologies

Roman Trobec, Ivan Tomasic, Tomislav Kelava, 2018, Medical & Biological Engineering & Computing.