Boutakoglou E - Search Results

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Successful repurposing of empagliflozin to treat neutropenia in a severe congenital neutropenia patient with G6PC3 mutations.

Tsaknakis G, Boutakoglou E, Mavroudi I, Mantzoros CS, Cunha MV, Papadaki HA. Tsaknakis G, et al. Among authors: boutakoglou e. Metabolism. 2025 Jan;162:156077. doi: 10.1016/j.metabol.2024.156077. Epub 2024 Nov 16. Metabolism. 2025. PMID: 39557394 No abstract available.

Expanding the genetic landscape of congenital neutropenia: CXCR2 mutations in three families revealed through whole exome sequencing.

Klimiankou M, Tesakov I, Tsaknakis G, Boutakoglou E, Mavroudi I, Ritter M, Sturm M, Skokowa J, Papadaki HA. Klimiankou M, et al. Among authors: boutakoglou e. Haematologica. 2024 Dec 1;109(12):4140-4144. doi: 10.3324/haematol.2024.285569. Haematologica. 2024. PMID: 39086298 Free PMC article. No abstract available.

Identification of GFI1 mutations in adult patients with congenital neutropenia.

Boutakoglou E, Klimiankou M, Tsaknakis G, Drakos E, Skokowa J, Papadaki HA. Boutakoglou E, et al. Ann Hematol. 2022 Dec;101(12):2771-2773. doi: 10.1007/s00277-022-04977-7. Epub 2022 Sep 16. Ann Hematol. 2022. PMID: 36112213 No abstract available.

Erythroderma as a paraneoplastic manifestation of small cell lung cancer.

Zervakis SG, Spernovasilis N, Boutakoglou E, Panagiotakis S, Thomopoulou K, Samonis G. Zervakis SG, et al. Among authors: boutakoglou e. Curr Probl Cancer. 2020 Apr;44(2):100499. doi: 10.1016/j.currproblcancer.2019.100499. Epub 2019 Aug 30. Curr Probl Cancer. 2020. PMID: 31493907

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