- Klinická, biochemická a molekulární studie sedmi polských pacientů s deficitem adenylosukcinátlyázy2008 | 1. lékařská fakulta
- Clinical, biochemical and molecular findings in seven Polish patients with adenylosuccinate lyase deficiency2008 | Publikace bez příslušnosti k fakultě
- Identification and Functional Analysis of Two Novel Mutations in the CBS Gene in Polish Patients with Homocystinuria2004 | 1. lékařská fakulta
- Léčba čtyř polských pacientů s deficitem adenylosukcinátlyázy pomocí D-Ribózy: Bez pozitivního efektu.2008 | 1. lékařská fakulta
- Identification and functional analysis of two novel mutations in CBS gene in Polish patients with homocystinuria2004 | 1. lékařská fakulta
- Identification and functional analysis of two novel mutations in CBS gene in Polish patients with homocysteinuria2004 | Fakulta tělesné výchovy a sportu
- Identification and functional analysis of two novel mutations in CBS gene in Polish patients with homocystinuria2004 | Fakulta tělesné výchovy a sportu
- Identification and functional analysis of two novel mutations in the CBS gene in Polish patients with homocystinuria2004 | Fakulta tělesné výchovy a sportu
- D-Ribose therapy in four Polish patients with adenylosuccinate lyase deficiency: Absence of positive effect.2008 | Publikace bez příslušnosti k fakultě
- Chronic visceral acid sphingomyelinase deficiency (Niemann-Pick disease type B) in 16 Polish patients: long-term follow-up2019 | 1. lékařská fakulta
- Attenuated Adenylosuccinate Lyase Deficiency: A Report of One Case and a Review of the Literature2014 | 1. lékařská fakulta
- The frequency of mitochondrial polymerase gamma related disorders in a large Polish population cohort2019 | 1. lékařská fakulta
- L239F founder mutation in GDAP1 is associated with a mild Charcot-Marie-Tooth type 4C4 (CMT4C4) phenotype2010 | 2. lékařská fakulta