Peroxisomal D-bifunctional protein deficiency: First case reports from Slovakia
Konkoľová, J., Petrovič, R., Chandoga, J., Repiský, M., Zelinková, H., Kršiaková, J., Kolníková, M., Kantarská, D., Šutovský, S., Böhmer, D.
Published in Gene (15.08.2015)
Published in Gene (15.08.2015)
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Influence of different spectra of NOTCH3 variants on the clinical phenotype of CADASIL – experience from Slovakia
Juhosová, M., Chandoga, J., Cisárik, F., Dallemule, S., Ďurina, P., Jarásková, D., Jungová, P., Kantarská, D., Kvasnicová, M., Mistrík, M., Pastoráková, A., Petrovič, R., Valachová, A., Zelinková, H., Barošová, J., Böhmer, D., Štofko, J.
Published in Neurogenetics (01.01.2023)
Published in Neurogenetics (01.01.2023)
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Two siblings with bilateral congenital knee dislocations: case report
Kubinec, V, Polakovičová, L, Kantarská, D
Published in Acta chirurgiae orthopaedicae et traumatologiae Čechoslovaca (01.04.2015)
Published in Acta chirurgiae orthopaedicae et traumatologiae Čechoslovaca (01.04.2015)
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