1. A critical appraisal of one‐stage and chromogenic assays of factor VIII activity. (1st February 2016) Authors: Peyvandi, F.; Oldenburg, J.; Friedman, K. D. Journal: Journal of thrombosis and haemostasis Issue: Volume 14:Number 2(2016:Feb.) Page Start: 248 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A new cell culture‐based assay quantifies vitamin K 2, 3‐epoxide reductase complex subunit 1 function and reveals warfarin resistance phenotypes not shown by the dithiothreitol‐driven VKOR assay. Issue 5 (15th May 2013) Authors: Fregin, A.; Czogalla, K. J.; Gansler, J.; Rost, S.; Taverna, M.; Watzka, M.; Bevans, C. G.; MüLler, C. R.; Oldenburg, J. Journal: Journal of thrombosis and haemostasis Issue: Volume 11:Issue 5(2013) Page Start: 872 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Analysis of F8 mRNA in haemophilia A patients with silent mutations or presumptive splice site mutations. (23rd October 2012) Authors: Zimmermann, M. A.; Gehrig, A.; Oldenburg, J.; Müller, C. R.; Rost, S. Journal: Haemophilia Issue: Volume 19:Number 2(2013:Mar.) Page Start: 310 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Chromogenic analysis of FIX activity in haemophilia B patients treated with nonacog beta pegol. Issue 6 (18th September 2017) Authors: Young, G.; Ezban, M.; Clausen, W. H. O.; Negrier, C.; Oldenburg, J.; Shima, M. Journal: Haemophilia Issue: Volume 23:Issue 6(2017) Page Start: e528 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Clinical overview of Fanhdi/Alphanate (plasma‐derived, VWF‐containing FVIII concentrate) in immune tolerance induction in haemophilia A patients with inhibitors. (27th November 2015) Authors: Jiménez‐Yuste, V.; Oldenburg, J.; Rangarajan, S.; Kurth, M. H; Bozzo, J.; Santagostino, E. Journal: Haemophilia Issue: Volume 22:Number 1(2016:Jan.) Page Start: e71 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII‐A2. Issue 3 (May 2017) Authors: Ivaškevičius, V.; Biswas, A.; Garly, M.‐L.; Oldenburg, J. Journal: Haemophilia Issue: Volume 23:Issue 3(2017) Page Start: e194 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Congenital combined deficiency of coagulation factors VII and X – different genetic mechanisms. (13th January 2015) Authors: Pavlova, A.; Preisler, B.; Driesen, J.; de Moerloose, P.; Zieger, B.; Hütker, S.; Dengler, K.; Harbrecht, U.; Oldenburg, J. Journal: Haemophilia Issue: Volume 21:Number 3(2015:May) Page Start: 386 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Controlled, cross‐sectional MRI evaluation of joint status in severe haemophilia A patients treated with prophylaxis vs. on demand. (2nd December 2014) Authors: Oldenburg, J.; Zimmermann, R.; Katsarou, O.; Theodossiades, G.; Zanon, E.; Niemann, B.; Kellermann, E.; Lundin, B.; the Cross‐sectional MRI study investigators Journal: Haemophilia Issue: Volume 21:Number 2(2015:Mar.) Page Start: 171 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Controlled, cross‐sectional MRI evaluation of joint status in severe haemophilia A patients treated with prophylaxis vs. on demand. (2nd December 2014) Authors: Oldenburg, J.; Zimmermann, R.; Katsarou, O.; Theodossiades, G.; Zanon, E.; Niemann, B.; Kellermann, E.; Lundin, B. Journal: Haemophilia Issue: Volume 21:Number 2(2015:Mar.) Page Start: 171 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Deep intronic 'mutations' cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNA. (12th September 2013) Authors: Pezeshkpoor, B.; Zimmer, N.; Marquardt, N.; Nanda, I.; Haaf, T.; Budde, U.; Oldenburg, J.; El‐Maarri, O. Journal: Journal of thrombosis and haemostasis Issue: Volume 11:Number 9(2013:Sep.) Page Start: 1679 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗