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European Young Pediatricians Association: Laying the Foundations for Collaboration, Integration, and Networking among Pediatricians of the Future.
Gray S, Raschetti R, Beşer ÖF, Elicin PU, Aversa S, Pamuk G, Ozdil M, Berlese P, Ferreira-Magalhães M, Magner M, Ignat A, Lupu VV, Zsigmond B, Ghazaryan H, Rosenbaum S, Bendavid M, Bacquet M, Varga N, James D, Bon A, Vecchio D. Gray S, et al. Among authors: magner m. J Pediatr. 2016 Apr;171:324-5.e1. doi: 10.1016/j.jpeds.2015.12.013. J Pediatr. 2016. PMID: 27017465 Free article. No abstract available.
SURF1 missense mutations promote a mild Leigh phenotype.
Piekutowska-Abramczuk D, Magner M, Popowska E, Pronicki M, Karczmarewicz E, Sykut-Cegielska J, Kmiec T, Jurkiewicz E, Szymanska-Debinska T, Bielecka L, Krajewska-Walasek M, Vesela K, Zeman J, Pronicka E. Piekutowska-Abramczuk D, et al. Among authors: magner m. Clin Genet. 2009 Aug;76(2):195-204. doi: 10.1111/j.1399-0004.2009.01195.x. Clin Genet. 2009. PMID: 19780766
[Tracheal stent implantation in an adult patient with Hunter syndrome].
Murgašová L, Votruba J, Otáhal M, Michálek P, Zeman J, Magner M. Murgašová L, et al. Among authors: magner m. Laryngorhinootologie. 2020 Mar;99(3):173-175. doi: 10.1055/a-1018-5878. Epub 2020 Jan 9. Laryngorhinootologie. 2020. PMID: 31918447 German. No abstract available.
Clinical manifestation of mitochondrial diseases.
Magner M, Kolářová H, Honzik T, Švandová I, Zeman J. Magner M, et al. Dev Period Med. 2015 Oct-Dec;19(4):441-9. Dev Period Med. 2015. PMID: 26982751 Review.
Transient Hyperphosphatasemia in a Child with Autism Spectrum Disorder.
Kutílek Š, Rondziková-Mlynarčíková E, Pečenková K, Pikner R, Šmída T, Sládková E, Honzík T, Kolářová H, Magner M. Kutílek Š, et al. Among authors: magner m. Acta Medica (Hradec Kralove). 2022;65(1):41-43. doi: 10.14712/18059694.2022.16. Acta Medica (Hradec Kralove). 2022. PMID: 35793509 Free article.
105 results