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Page 1
Hereditary thrombotic thrombocytopenic purpura and the hereditary TTP registry.
Mansouri Taleghani M, von Krogh AS, Fujimura Y, George JN, Hrachovinová I, Knöbl PN, Quist-Paulsen P, Schneppenheim R, Lämmle B, Kremer Hovinga JA. Mansouri Taleghani M, et al. Among authors: hrachovinova i. Hamostaseologie. 2013 May 29;33(2):138-43. doi: 10.5482/HAMO-13-04-0026. Hamostaseologie. 2013. PMID: 23715103 Review.
The International Hereditary Thrombotic Thrombocytopenic Purpura Registry: key findings at enrollment until 2017.
van Dorland HA, Taleghani MM, Sakai K, Friedman KD, George JN, Hrachovinova I, Knöbl PN, von Krogh AS, Schneppenheim R, Aebi-Huber I, Bütikofer L, Largiadèr CR, Cermakova Z, Kokame K, Miyata T, Yagi H, Terrell DR, Vesely SK, Matsumoto M, Lämmle B, Fujimura Y, Kremer Hovinga JA; Hereditary TTP Registry. van Dorland HA, et al. Among authors: hrachovinova i. Haematologica. 2019 Oct;104(10):2107-2115. doi: 10.3324/haematol.2019.216796. Epub 2019 Feb 21. Haematologica. 2019. PMID: 30792199 Free PMC article. Clinical Trial.
Annual incidence and severity of acute episodes in hereditary thrombotic thrombocytopenic purpura.
Tarasco E, Bütikofer L, Friedman KD, George JN, Hrachovinova I, Knöbl PN, Matsumoto M, von Krogh AS, Aebi-Huber I, Cermakova Z, Górska-Kosicka M, Jalowiec KA, Largiadèr CR, Prohászka Z, Sinkovits G, Windyga J, Lämmle B, Kremer Hovinga JA. Tarasco E, et al. Among authors: hrachovinova i. Blood. 2021 Jun 24;137(25):3563-3575. doi: 10.1182/blood.2020009801. Blood. 2021. PMID: 33649760 Free article.
A common origin of the 4143insA ADAMTS13 mutation.
Schneppenheim R, Kremer Hovinga JA, Becker T, Budde U, Karpman D, Brockhaus W, Hrachovinová I, Korczowski B, Oyen F, Rittich S, von Rosen J, Tjønnfjord GE, Pimanda JE, Wienker TF, Lämmle B. Schneppenheim R, et al. Among authors: hrachovinova i. Thromb Haemost. 2006 Jul;96(1):3-6. doi: 10.1160/TH05-12-0817. Thromb Haemost. 2006. PMID: 16807643
[Hereditary form of thrombotic thrombocytopenic purpura].
Hrachovinová I, Rittich S, Salaj P, Suttnar J, Dyr JE, Suláková T, Pták J, Dulícek P, Seeman T. Hrachovinová I, et al. Cas Lek Cesk. 2006;145(5):390-2. Cas Lek Cesk. 2006. PMID: 16755777 Czech.
[Molecular study of type 2 von Willebrand disease].
Habart D, Smejkal P, Matýsková M, Turek P, Hrachovinová I, Vorlová Z. Habart D, et al. Among authors: hrachovinova i. Cas Lek Cesk. 2003;142(6):373-6. Cas Lek Cesk. 2003. PMID: 12924038 Czech.
High-resolution melting analysis for detection of MYH9 mutations.
Provaznikova D, Kumstyrova T, Kotlin R, Salaj P, Matoska V, Hrachovinova I, Rittich S. Provaznikova D, et al. Among authors: hrachovinova i. Platelets. 2008 Sep;19(6):471-5. doi: 10.1080/09537100802140013. Platelets. 2008. PMID: 18925516
48 results