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Page 1
Efficacy and Safety of Ketogenic Diet Treatment in Pediatric Patients with Mitochondrial Disease.
Wesół-Kucharska D, Greczan M, Kaczor M, Ehmke Vel Emczyńska-Seliga E, Hajdacka M, Czekuć-Kryśkiewicz E, Piekutowska-Abramczuk D, Halat-Wolska P, Ciara E, Jaworski M, Jezela-Stanek A, Rokicki D. Wesół-Kucharska D, et al. Among authors: greczan m. Nutrients. 2024 Mar 13;16(6):812. doi: 10.3390/nu16060812. Nutrients. 2024. PMID: 38542723 Free PMC article.
Neutrophil functions in patients with neutropenia due to glycogen storage disease type 1b treated with empagliflozin.
Kaczor M, Malicki S, Folkert J, Dobosz E, Bryzek D, Chruścicka-Smaga B, Greczan M, Wesół-Kucharska D, Piatosa B Prof, Samborowska E, Madzio J, Książyk J, Vel Emczyńska EE, Hajdacka M, Potempa J, Młynarski W, Rokicki D, Veillard F. Kaczor M, et al. Among authors: greczan m. Blood Adv. 2024 Mar 26:bloodadvances.2023012403. doi: 10.1182/bloodadvances.2023012403. Online ahead of print. Blood Adv. 2024. PMID: 38531056
The fibroblast growth factor 21 concentration in children with mitochondrial disease does not depend on the disease stage, but rather on the disease genotype.
Wesół-Kucharska D, Rokicki D, Greczan M, Kaczor M, Czekuć-Kryśkiewicz E, Piekutowska-Abramczuk D, Halat-Wolska P, Ciara E, Jaworski M, Jezela-Stanek A. Wesół-Kucharska D, et al. Among authors: greczan m. Pediatr Endocrinol Diabetes Metab. 2022;28(2):141-151. doi: 10.5114/pedm.2022.116116. Pediatr Endocrinol Diabetes Metab. 2022. PMID: 35620925 Free PMC article.
Clinical characteristics and long-term outcomes of patients with glycogen storage disease type 1b: a retrospective multi-center experience in Poland.
Kaczor M, Wesół-Kucharska D, Greczan M, Kierus K, Kałużny Ł, Duś-Żuchowska M, Ehmke Vel Emczyńska-Seliga E, Ciara E, Książyk J, Rokicki D. Kaczor M, et al. Among authors: greczan m. Pediatr Endocrinol Diabetes Metab. 2022;28(3):207-212. doi: 10.5114/pedm.2022.116115. Pediatr Endocrinol Diabetes Metab. 2022. PMID: 35620924 Free PMC article.
Early treatment of biotin-thiamine-responsive basal ganglia disease improves the prognosis.
Wesół-Kucharska D, Greczan M, Kaczor M, Pajdowska M, Piekutowska-Abramczuk D, Ciara E, Halat-Wolska P, Kowalski P, Jurkiewicz E, Rokicki D. Wesół-Kucharska D, et al. Among authors: greczan m. Mol Genet Metab Rep. 2021 Sep 29;29:100801. doi: 10.1016/j.ymgmr.2021.100801. eCollection 2021 Dec. Mol Genet Metab Rep. 2021. PMID: 34631424 Free PMC article.
NBAS deficiency due to biallelic c.2809C > G variant presenting with recurrent acute liver failure with severe hyperammonemia, acquired microcephaly and progressive brain atrophy.
Lipiński P, Greczan M, Piekutowska-Abramczuk D, Jurkiewicz E, Bakuła A, Socha P, Jankowska I, Rokicki D, Tylki-Szymańska A. Lipiński P, et al. Among authors: greczan m. Metab Brain Dis. 2021 Oct;36(7):2169-2172. doi: 10.1007/s11011-021-00827-z. Epub 2021 Aug 24. Metab Brain Dis. 2021. PMID: 34427841 Free PMC article.