1. A concentration-QTc analysis of vericiguat. (14th October 2021) Authors: Meyer, M; Ruehs, H; Solms, A; Frei, M; Becker, C; Trujillo, M; Garmann, D Journal: European heart journal Issue: Volume 42(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Acute encephalopathy with parvovirus B19 infection in sickle cell disease. Issue 6 (1st December 2002) Authors: Bakhshi, S; Sarnaik, S A; Becker, C; Shurney, W W; Nigro, M; Savaşan, S Journal: Archives of disease in childhood Issue: Volume 87:Issue 6(2002) Page Start: 541 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Estimating prevalence and characteristics of statin intolerance among high and very high cardiovascular risk patients in Germany between 2017–2020. (3rd October 2022) Authors: Parhofer, K G; Anastassopoulou, A; Calver, H; Becker, C; Singh Rathore, A Journal: European heart journal Issue: Volume 43(2022)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Estimating prevalence and characteristics of statin intolerance among high and very high cardiovascular risk patients in Germany between 2017–2020. Issue 4 (22nd December 2022) Authors: Parhofer, K G; Anastassopoulou, A; Calver, H; Becker, C; Singh Rathore, A Journal: European heart journal Issue: Volume 3:Issue 4(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. F14 8OHdG is not a biomarker for Huntington's disease; lessons for future biomarker studies. (29th August 2012) Authors: Borowsky, B; Warner, J; Matson, W; Johnson, H; Durr, A; Roos, R; Tabrizi, SJ; Leavitt, B; Becker, C; Tobin, A; Schulman, H Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 83(2012)Supplement 1 Page Start: A25 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Hypomorphic mutations in meckelin (MKS3/TMEM67) cause nephronophthisis with liver fibrosis (NPHP11). Issue 10 (8th June 2009) Authors: Otto, E A; Tory, K; Attanasio, M; Zhou, W; Chaki, M; Paruchuri, Y; Wise, E L; Wolf, M T F; Utsch, B; Becker, C; Nürnberg, G; Nürnberg, P; Nayir, A; Saunier, S; Antignac, C; Hildebrandt, F Journal: Journal of medical genetics Issue: Volume 46:Issue 10(2009) Page Start: 663 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. In vivo imaging of colitis and colon cancer development in mice using high resolution chromoendoscopy. Issue 7 (10th June 2005) Authors: Becker, C; Fantini, M C; Wirtz, S; Nikolaev, A; Kiesslich, R; Lehr, H A; Galle, P R; Neurath, M F Journal: Gut Issue: Volume 54:Issue 7(2005) Page Start: 950 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Leveraging translational approaches for accelerated clinical development of vericiguat. (14th October 2021) Authors: Meyer, M; Schneckener, S; Loosen, R; Coboeken, K; Willmann, S; Burghaus, R; Lippert, J; Mueck, W; Becker, C Journal: European heart journal Issue: Volume 42(2021)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Missense mutations of ACTA1 cause dominant congenital myopathy with cores. Issue 11 (1st November 2004) Authors: Kaindl, A M; Rüschendorf, F; Krause, S; Goebel, H-H; Koehler, K; Becker, C; Pongratz, D; Müller-Höcker, J; Nürnberg, P; Stoltenburg-Didinger, G; Lochmüller, H; Huebner, A Journal: Journal of medical genetics Issue: Volume 41:Issue 11(2004) Page Start: 842 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Molecular karyotyping using an SNP array for genomewide genotyping. Issue 12 (9th December 2004) Authors: Rauch, A; Rüschendorf, F; Huang, J; Trautmann, U; Becker, C; Thiel, C; Jones, K W; Reis, A; Nürnberg, P Journal: Journal of medical genetics Issue: Volume 41:Issue 12(2004) Page Start: 916 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗