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2. Coexistence of mutations in keratin 10 (KRT10) and the mitochondrial genome in a patient with ichthyosis with confetti and Leber's hereditary optic neuropathy. Issue 11 (25th September 2017)

3. Coexistence of mutations in keratin 10 (KRT10) and the mitochondrial genome in a patient with ichthyosis with confetti and Leber's hereditary optic neuropathy. Issue 11 (25th September 2017)

4. Coexistence of pemphigus foliaceus and acquired hemophilia A: A case report. Issue 6 (9th April 2015)

6. Dominant ELOVL1 mutation causes neurological disorder with ichthyotic keratoderma, spasticity, hypomyelination and dysmorphic features. Issue 6 (1st March 2018)

7. Dynamics of Acute Local Inflammatory Response after Autologous Transplantation of Muscle-Derived Cells into the Skeletal Muscle. (27th August 2014)