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Prevalence of hyperthyroidism and hypothyroidism in liver transplant recipients and associated risk factors.
Suarez-Zdunek MA, Arentoft NS, Krohn PS, Lauridsen EHE, Afzal S, Høgh J, Thomsen MT, Knudsen AD, Nordestgaard BG, Hillingsø JG, Villadsen GE, Holland-Fischer P, Rasmussen A, Fialla AD, Feldt-Rasmussen U, Nielsen SD. Suarez-Zdunek MA, et al. Among authors: fialla ad. Sci Rep. 2024 Apr 3;14(1):7828. doi: 10.1038/s41598-024-58544-3. Sci Rep. 2024. PMID: 38570629 Free PMC article.
Fraction of exhaled nitric oxide is higher in liver transplant recipients than in controls from the general population: a cohort study.
Arentoft NS, Fialla AD, Krohn PS, Patursson MT, Thudium RF, Suarez-Zdunek MA, Høgh J, Lauridsen EHE, Hansen JB, Jensen JS, Perch M, Møller DL, Pommergaard HC, Aagaard NK, Davidsen JR, Lange P, Çolak Y, Afzal S, Nordestgaard BG, Rasmussen A, Nielsen SD. Arentoft NS, et al. Among authors: fialla ad. Front Immunol. 2024 Feb 1;15:1330923. doi: 10.3389/fimmu.2024.1330923. eCollection 2024. Front Immunol. 2024. PMID: 38361926 Free PMC article.
[Telomere biology disorders].
Byrjalsen A, Bygum A, Lautrup CK, Frederiksen AL, Fialla AD, Raaschou-Jensen K, Bendstrup E, Madsen TN, Klarskov M, Jelsig AM. Byrjalsen A, et al. Among authors: fialla ad. Ugeskr Laeger. 2022 Jul 11;184(28):V03220220. Ugeskr Laeger. 2022. PMID: 35959813 Free article. Review. Danish.
European Reference Network for Rare Vascular Diseases (VASCERN): When and how to use intravenous bevacizumab in Hereditary Haemorrhagic Telangiectasia (HHT)?
Dupuis-Girod S, Shovlin CL, Kjeldsen AD, Mager HJ, Sabba C, Droege F, Fargeton AE, Fialla AD, Gandolfi S, Hermann R, Lenato GM, Manfredi G, Post MC, Rennie C, Suppressa P, Sure U; ePag group; Buscarini E. Dupuis-Girod S, et al. Among authors: fialla ad. Eur J Med Genet. 2022 Oct;65(10):104575. doi: 10.1016/j.ejmg.2022.104575. Epub 2022 Aug 5. Eur J Med Genet. 2022. PMID: 35940549 Free article.
The European Rare Disease Network for HHT Frameworks for management of hereditary haemorrhagic telangiectasia in general and speciality care.
Shovlin CL, Buscarini E, Sabbà C, Mager HJ, Kjeldsen AD, Pagella F, Sure U, Ugolini S, Torring PM, Suppressa P, Rennie C, Post MC, Patel MC, Nielsen TH, Manfredi G, Lenato GM, Lefroy D, Kariholu U, Jones B, Fialla AD, Eker OF, Dupuis O, Droege F, Coote N, Boccardi E, Alsafi A, Alicante S, Dupuis-Girod S. Shovlin CL, et al. Among authors: fialla ad. Eur J Med Genet. 2022 Jan;65(1):104370. doi: 10.1016/j.ejmg.2021.104370. Epub 2021 Nov 1. Eur J Med Genet. 2022. PMID: 34737116 Free article.
28 results