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Page 1
The worldwide distribution of the VHL 598C>T mutation indicates a single founding event.
Liu E, Percy MJ, Amos CI, Guan Y, Shete S, Stockton DW, McMullin MF, Polyakova LA, Ang SO, Pastore YD, Jedlickova K, Lappin TR, Gordeuk V, Prchal JT. Liu E, et al. Among authors: jedlickova k. Blood. 2004 Mar 1;103(5):1937-40. doi: 10.1182/blood-2003-07-2550. Epub 2003 Nov 6. Blood. 2004. PMID: 14604959 Free article.
Mutations in the VHL gene in sporadic apparently congenital polycythemia.
Pastore YD, Jelinek J, Ang S, Guan Y, Liu E, Jedlickova K, Krishnamurti L, Prchal JT. Pastore YD, et al. Among authors: jedlickova k. Blood. 2003 Feb 15;101(4):1591-5. doi: 10.1182/blood-2002-06-1843. Epub 2002 Oct 10. Blood. 2003. PMID: 12393546 Free article.
Congenital disorder of oxygen sensing: association of the homozygous Chuvash polycythemia VHL mutation with thrombosis and vascular abnormalities but not tumors.
Gordeuk VR, Sergueeva AI, Miasnikova GY, Okhotin D, Voloshin Y, Choyke PL, Butman JA, Jedlickova K, Prchal JT, Polyakova LA. Gordeuk VR, et al. Among authors: jedlickova k. Blood. 2004 May 15;103(10):3924-32. doi: 10.1182/blood-2003-07-2535. Epub 2004 Jan 15. Blood. 2004. PMID: 14726398 Free article.
Inflammation and fibrosis characterize different stages of myocardial remodeling in patients after stereotactic body radiotherapy of ventricular myocardium for recurrent ventricular tachycardia.
Kučera T, Jedličková K, Šramko M, Peichl P, Cvek J, Knybel L, Hurník P, Neuwirth R, Jiravský O, Voska L, Kautzner J. Kučera T, et al. Among authors: jedlickova k. Cardiovasc Pathol. 2023 Jan-Feb;62:107488. doi: 10.1016/j.carpath.2022.107488. Epub 2022 Oct 4. Cardiovasc Pathol. 2023. PMID: 36206914 Free PMC article.
20 results