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Six molecular patterns leading to hemophilia A phenotype in 18 females from Poland.
Thromb Res. 2020 Sep;193:9-14. doi: 10.1016/j.thromres.2020.05.041. Epub 2020 May 28.
Thromb Res. 2020.
PMID: 32497951
Free article.
Puzzling outcome of the nationwide genetic survey of severe/moderate female haemophilia B in Poland.
Janczar S, Babol-Pokora K, Jatczak-Pawlik I, Windyga J, Odnoczko E, Madetko-Talowska A, Sadowska B, Zdziarska J, Iwaniec T, Pietrys D, Balwierz W, Gazda HT, Ploski R, Mlynarski W.
Janczar S, et al. Among authors: odnoczko e.
Haemophilia. 2019 Nov;25(6):e373-e376. doi: 10.1111/hae.13854. Epub 2019 Oct 2.
Haemophilia. 2019.
PMID: 31577376
No abstract available.
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Severe bleeding due to hypersensitivity to vitamin K antagonist caused by the c.109G>A (p.Ala37Thr) mutation in the F9 gene in a patient with mechanical heart valve prosthesis.
Odnoczko E, Falkowska J, Baran B, Buczma A, Stefanska-Windyga E, Windyga J.
Odnoczko E, et al.
Thromb Res. 2019 Feb;174:59-61. doi: 10.1016/j.thromres.2018.12.005. Epub 2018 Dec 12.
Thromb Res. 2019.
PMID: 30576981
No abstract available.
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Successful perioperative prophylaxis with susoctocog alfa in a patient with acquired haemophilia A: A case study.
Buczma A, Baran B, Korwin M, Odnoczko E, Windyga J.
Buczma A, et al. Among authors: odnoczko e.
Haemophilia. 2022 Mar;28(2):e39-e41. doi: 10.1111/hae.14468. Epub 2021 Dec 8.
Haemophilia. 2022.
PMID: 34878208
No abstract available.
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Treatment guidelines for acquired hemophilia A.
Windyga J, Baran B, Odnoczko E, Buczma A, Drews K, Laudanski P, Pietrzak B, Sieroszewski P.
Windyga J, et al. Among authors: odnoczko e.
Ginekol Pol. 2019;90(6):353-364. doi: 10.5603/GP.2019.0063.
Ginekol Pol. 2019.
PMID: 31276188
Free article.
Review.
No abstract available.
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Activated prothrombin complex concentrate in combination with tranexamic acid: a single centre experience for the treatment of mucosal bleeding and dental extraction in haemophilia patients with inhibitors.
Windyga J, Stefanska-Windyga E, Odnoczko E, Baran B, Czubak G.
Windyga J, et al. Among authors: odnoczko e.
Haemophilia. 2016 Sep;22(5):e465-8. doi: 10.1111/hae.13035. Epub 2016 Jul 25.
Haemophilia. 2016.
PMID: 27457184
No abstract available.
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Neurodevelopmental disorder in a patient with HMBS and SCN3A variants-A possibly blended phenotype further delineating autosomal recessive HMBS related disease.
M K, M R, J B, A BI, K IP, R W, E O, A ZK, R S, R P.
M K, et al. Among authors: e o.
Am J Med Genet A. 2024 Apr 3:e63617. doi: 10.1002/ajmg.a.63617. Online ahead of print.
Am J Med Genet A. 2024.
PMID: 38568055
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