Petr Jarolim

Distinct Subgroups in Hypertrophic Cardiomyopathy in the NHLBI Registry

M. Desai, M. Jerosch-Herold, M. Maron, 2019 .

Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency.

J. Prchal, P. Jarolim, L. Snyder, 1996, Blood.

Mutations of conserved arginines in the membrane domain of erythroid band 3 lead to a decrease in membrane-associated band 3 and to the phenotype of hereditary spherocytosis.

H. Wichterle, C. Brugnara, P. Jarolim, 1995, Blood.

Combination of two mutant alpha spectrin alleles underlies a severe spherocytic hemolytic anemia.

H. Wichterle, P. Jarolim, J. Palek, 1996, The Journal of clinical investigation.

Effect of hemoglobin oxidation products on the stability of red cell membrane skeletons and the associations of skeletal proteins: correlation with a release of hemin.

P. Jarolim, Shih-Chun Liu, S. Liu, 1990, Blood.

Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency.

P. Njølstad, J. Rogus, J. Palek, 1997, Blood.