Jochmans K - Search Results

1

Diagnostic accuracy of the Triage D-dimer test for exclusion of venous thromboembolism in outpatients.

Ghys T, Achtergael W, Verschraegen I, Leus B, Jochmans K. Ghys T, et al. Among authors: jochmans k. Thromb Res. 2008;121(6):735-41. doi: 10.1016/j.thromres.2007.07.012. Epub 2007 Sep 20. Thromb Res. 2008. PMID: 17888501

2

Diagnostic potential of CD34+ cell antigen expression in myelodysplastic syndromes.

De Smet D, Trullemans F, Jochmans K, Renmans W, Smet L, Heylen O, Bael AM, Schots R, Leus B, De Waele M. De Smet D, et al. Among authors: jochmans k. Am J Clin Pathol. 2012 Nov;138(5):732-43. doi: 10.1309/AJCPAGVO27RPTOTV. Am J Clin Pathol. 2012. PMID: 23086775

3

Antithrombin heparin binding site deficiency: A challenging diagnosis of a not so benign thrombophilia.

Orlando C, Heylen O, Lissens W, Jochmans K. Orlando C, et al. Among authors: jochmans k. Thromb Res. 2015 Jun;135(6):1179-85. doi: 10.1016/j.thromres.2015.03.013. Epub 2015 Mar 14. Thromb Res. 2015. PMID: 25837307

4

Plasma D-dimer concentrations in different clinical conditions.

Ver Elst K, Jochmans K, De Pauw A, De Waele M. Ver Elst K, et al. Among authors: jochmans k. Acta Clin Belg. 2002 Nov-Dec;57(6):325-30. doi: 10.1179/acb.2002.060. Acta Clin Belg. 2002. PMID: 12723250

5

Heterozygous FGA p.Asp473Ter (fibrinogen Nieuwegein) presenting as antepartum cerebral thrombosis.

Tajdar M, Orlando C, Casini A, Herpol M, De Bisschop B, Govaert P, Neerman-Arbez M, Jochmans K. Tajdar M, et al. Among authors: jochmans k. Thromb Res. 2018 Mar;163:185-189. doi: 10.1016/j.thromres.2017.10.020. Epub 2017 Oct 28. Thromb Res. 2018. PMID: 29122299

6

Thrombotic storm under DOAC treatment in a patient with homozygous antithrombin Budapest III mutation.

Condoluci A, Alberio L, Gomez FJ, Studt JD, Orlando C, Jochmans K, Gerber B. Condoluci A, et al. Among authors: jochmans k. Thromb Res. 2021 May;201:161-163. doi: 10.1016/j.thromres.2021.04.002. Epub 2021 Apr 9. Thromb Res. 2021. PMID: 33866212 No abstract available.

7

Nonsense mutation Arg197stop in a Dutch family with type 1 hereditary antithrombin (AT) deficiency causing thrombophilia.

Michiels JJ, van der Luit L, van Vliet HH, Jochmans K, Lissens W. Michiels JJ, et al. Among authors: jochmans k. Thromb Res. 1995 May 1;78(3):251-4. doi: 10.1016/0049-3848(95)90875-g. Thromb Res. 1995. PMID: 7631305 No abstract available.

8

Routine haematology parameters in COVID-19 patients and clinical outcome: A Belgian single-centre study.

Demeester S, Demuyser T, Fauconnier C, Heestermans R, Orlando C, Depreter B, Jochmans K. Demeester S, et al. Among authors: jochmans k. Int J Lab Hematol. 2020 Dec;42(6):e252-e255. doi: 10.1111/ijlh.13313. Epub 2020 Sep 11. Int J Lab Hematol. 2020. PMID: 32915507 No abstract available.

9

The molecular basis of antithrombin deficiency in Belgian and Dutch families.

Jochmans K, Lissens W, Seneca S, Capel P, Chatelain B, Meeus P, Osselaer JC, Peerlinck K, Seghers J, Slacmeulder M, Stibbe J, van de Loo J, Vermylen J, Liebaers I, De Waele M. Jochmans K, et al. Thromb Haemost. 1998 Sep;80(3):376-81. Thromb Haemost. 1998. PMID: 9759613

10

Antithrombin p.Thr147Ala: The First Founder Mutation in People of African Origin Responsible for Inherited Antithrombin Deficiency.

Orlando C, de la Morena-Barrio B, Pareyn I, Vanhoorelbeke K, Martínez-Martínez I, Vicente V, Corral J, Jochmans K, de la Morena-Barrio ME. Orlando C, et al. Among authors: jochmans k. Thromb Haemost. 2021 Feb;121(2):182-191. doi: 10.1055/s-0040-1716531. Epub 2020 Sep 13. Thromb Haemost. 2021. PMID: 32920809

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