A Closer Look at Frederic Chopin's Cause of Death.
Witt M, Szklener A, Kaweckki J, Rużyłło W, Negrusz-Kawecka M, Jeleń M, Langfort R, Marchiwca W, Dobosz T;
Am J Medicine, 2018, 131 (2): 211-212, Epub 2017 Oct 11, IF-5.55, MNiSW-40.
Publications
Publikacje pracowników w ePub
Human sperm morphology analysis using a Digital holographic microscope.
Fabian E, Kamieniczna M, Kurpisz M, Stachowska E;
W: Innovations in Biomedical Engineering, (series editor J.Kacprzyk), vol. 623, Advances in Inteligent Systems and Computing”, edited by: M.Gzik, Z. Paszenda, E. Tkacz, E. Pietka, ISBN 978-3-319-70062-5, 2018, str.: 61-68.
Methylenetetrahydrofolate reductase 677T-1298C haplotype is a risk factor for acute lymphoblastic leukemia in children.
Kałużna EM, Strauss E, Świątek-Kościelna B, Zając O, Gowin E, Nowak J, Rembowska J, Januszkiewicz-Lewandowska D;
Medicine (Baltimore), 2017, 96: 51 (e9290), 5 pages, dx.doi.org/10.1097/MD.0000000000009290.
Vitamin D status in recurrent aphtous stomatitis.
Krawiecka E, Ślebioda Z, Szponar E, Kowalska A, Dorocka-Bobkowska B;
Advances in Dermatology and Allergology, 2017, 6: 612-617.
Perspective in optimization of stem cell therapies for heart regeneration.
Gapska P, Kurpisz M;
Postepy Hig Med Dosw, 2017 (7.12), 71: 975-987.
Familial adenomatous polyposis: age of onset and association with mutations oft the APC gene in patients from West Ukraine.
Lozynska MR, Lozynskyy YS, Plawski A, Pinyazhko RO, Prokopchuk NM, Fedota OM;
Biopolymers and Cell, 2017, 33 (2): 102-115.
Cryptorchidism and varicocele: another look at the reasons for launching autoaggression.
Havrylyuk AM, Chopyak VV, Nakonechnyi IA, Fraczek M, Kurpisz M
Paediatric Surgery, 2017; 3(56):75-83.
Distribution of polymorphisms rs12979860, rs8099917 and rs12980275 IL28B in patients with chronic hepatitis C.
Wysocka-Leszczyńska J, Kałużna E, Świątek-Kościelna B, Gowin E, Nowak J, Bereszyńska I, Mozer-Lisewska I, Wysocki J, Januszkiewicz-Lewandowska D;
Adv Clin Exp Med (Wrocław), 2017, 26 (8): 1257-1261.
Translocation t(8;14)(q24;q11) with concurrent PTEN alterations and deletions of STIL/TAL1 and CDKN2A/B in a pediatric case of acute T-lymphoblastic leukemia: A genetic profile associated with adverse prognosis.
Skalska-Sadowska J, Dawidowska M, Szarzyńska-Zawadzka B, Jarmuż-Szymczak M, Czerwińska-Rybak J, Machowska L, Derwich K;
Pediatr Blood Cancer. 2017 Apr;64(4). doi: 10.1002/pbc.26266. Epub 2016 Oct 19.
Cost-effective screening of DNMT3A coding sequence identifies somatic mutation in pediatric T-cell acute lymphoblastic leukemia.
Szarzyńska-Zawadzka B, Kosmalska M, Sędek Ł, Sonsala A, Twardoch M, Kowalczyk JR, Szczepański T, Witt M, Dawidowska M
Eur J Haematol., 2017, 99 (6): 514-519.