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2015 1
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Page 1
Evans syndrome caused by a deleterious mutation affecting the adaptor protein SASH3.
Novak W, Berner J, Svaton M, Jimenez-Heredia R, Segarra-Roca A, Frohne A, Guiliani S, Rouhani D, Eder SK, Rottal A, Trapin D, Scheuchenstuhl A, Pickl WF, Simonitsch-Klupp I, Kager L, Boztug K. Novak W, et al. Among authors: eder sk. Br J Haematol. 2023 Nov;203(4):678-683. doi: 10.1111/bjh.19061. Epub 2023 Aug 30. Br J Haematol. 2023. PMID: 37646304
Trans-Iliac Bypass Grafting for Vascular Groin Complications.
Enzmann FK, Nierlich P, Eder SK, Aspalter M, Dabernig W, Aschacher T, Linni K, Hölzenbein TJ. Enzmann FK, et al. Among authors: eder sk. Eur J Vasc Endovasc Surg. 2019 Dec;58(6):930-935. doi: 10.1016/j.ejvs.2018.11.003. Epub 2019 Aug 8. Eur J Vasc Endovasc Surg. 2019. PMID: 31402084 Free article.
Local MRI-based measures of thigh adipose tissue derived from fully automated deep convolutional neural network-based segmentation show a comparable responsiveness to bidirectional change in body weight as from quality controlled manual segmentation.
Kemnitz J, Steidle-Kloc E, Wirth W, Fuerst D, Wisser A, Eder SK, Eckstein F. Kemnitz J, et al. Among authors: eder sk. Ann Anat. 2022 Feb;240:151866. doi: 10.1016/j.aanat.2021.151866. Epub 2021 Nov 23. Ann Anat. 2022. PMID: 34823014 Free article.
A single-center cohort study of patients with hereditary spherocytosis in Central Europe reveals a high frequency of novel disease-causing genotypes.
Kager L, Jimenez-Heredia R, Zeitlhofer P, Novak W, Eder SK, Segarra-Roca A, Frohne A, Nebral K, Haimel M, Geyeregger R, Roetzer-Londgin K, Haas OA, Boztug K. Kager L, et al. Among authors: eder sk. Hemasphere. 2024 Jan 26;8(1):e31. doi: 10.1002/hem3.31. eCollection 2024 Jan. Hemasphere. 2024. PMID: 38434532 Free PMC article. No abstract available.
14 results