1. Bone morphogenetic protein 1 cleaves the linker region between ligand-binding repeats 4 and 5 of the LDL receptor and makes the LDL receptor non-functional. (10th October 2019) Authors: Strøm, Thea Bismo; Bjune, Katrine; Leren, Trond P Journal: Human molecular genetics Issue: Volume 29:Number 8(2020) Page Start: 1229 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Cardiovascular disease in patients with genotyped familial hypercholesterolemia in Norway during 1994–2009, a registry study. (29th August 2020) Authors: Mundal, Liv; Veierød, Marit B; Halvorsen, Thomas; Holven, Kirsten B; Ose, Leiv; Iversen, Per Ole; Tell, Grethe S; Leren, Trond P; Retterstøl, Kjetil Journal: European journal of preventive cardiology Issue: Volume 23:Number 18(2016) Page Start: 1962 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cardiovascular disease in patients with genotyped familial hypercholesterolemia in Norway during 1994–2009, a registry study. (December 2016) Authors: Mundal, Liv; Veierød, Marit B; Halvorsen, Thomas; Holven, Kirsten B; Ose, Leiv; Iversen, Per Ole; Tell, Grethe S; Leren, Trond P; Retterstøl, Kjetil Journal: European journal of preventive cardiology Issue: Volume 23:Number 18(2016) Page Start: 1962 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Cardiovascular disease mortality in patients with genetically verified familial hypercholesterolemia in Norway during 1992–2013. (29th August 2020) Authors: Mundal, Liv; Igland, Jannicke; Ose, Leiv; Holven, Kirsten B; Veierød, Marit B; Leren, Trond P; Retterstøl, Kjetil Journal: European journal of preventive cardiology Issue: Volume 24:Number 2(2017) Page Start: 137 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Cardiovascular disease mortality in patients with genetically verified familial hypercholesterolemia in Norway during 1992–2013. (January 2017) Authors: Mundal, Liv; Igland, Jannicke; Ose, Leiv; Holven, Kirsten B; Veierød, Marit B; Leren, Trond P; Retterstøl, Kjetil Journal: European journal of preventive cardiology Issue: Volume 24:Number 2(2017) Page Start: 137 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Characterization of the mechanisms by which missense mutations in the lysosomal acid lipase gene disrupt enzymatic activity. (27th May 2019) Authors: Vinje, Terje; Laerdahl, Jon K; Bjune, Katrine; Leren, Trond P; Strøm, Thea Bismo Journal: Human molecular genetics Issue: Volume 28:Number 18(2019) Page Start: 3043 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Comparison of clinical and molecular genetic criteria for diagnosing familial hypercholesterolemia. (June 2009) Authors: Leren, Trond P; Berge, Knut Erik Journal: Clinical lipidology Issue: Volume 4:Number 3(2009) Page Start: 303 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Impact of age on excess risk of coronary heart disease in patients with familial hypercholesterolaemia. Issue 19 (5th April 2018) Authors: Mundal, Liv J; Igland, Jannicke; Veierød, Marit B; Holven, Kirsten Bjørklund; Ose, Leiv; Selmer, Randi Marie; Wisloff, Torbjorn; Kristiansen, Ivar S; Tell, Grethe S; Leren, Trond P; Retterstøl, Kjetil Journal: Heart Issue: Volume 104:Issue 19(2018) Page Start: 1600 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Strategies to prevent cleavage of the linker region between ligand-binding repeats 4 and 5 of the LDL receptor. (23rd July 2019) Authors: Strøm, Thea Bismo; Bjune, Katrine; Costa, Luís Teixeira da; Leren, Trond P Journal: Human molecular genetics Issue: Volume 28:Number 22(2019) Page Start: 3734 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Unexpected myopathy associated with a mutation in MYBPC3 and misplacement of the cardiac myosin binding protein C. Issue 8 (26th October 2009) Authors: Tajsharghi, Homa; Leren, Trond P; Abdul-Hussein, Saba; Tulinius, Mar; Brunvand, Leif; Dahl, Hilde M; Oldfors, Anders Journal: Journal of medical genetics Issue: Volume 47:Issue 8(2010) Page Start: 575 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗