Abdominal aortic aneurysm as an IgG4‐related disease

por Prucha, M., Sedivy, P., Stadler, P., Zdrahal, P., Prokopova, P., Voska, L., Sedlackova, L.
Publicado 2019

Biallelic variants in the SORD gene are one of the most common causes of hereditary neuropathy among Czech patients

por Laššuthová, P., Mazanec, R., Staněk, D., Sedláčková, L., Plevová, B., Haberlová, J., Seeman, P.
Publicado 2021