The KCNE genes in hypertrophic cardiomyopathy: a candidate gene study

por Hedley, Paula L, Haundrup, Ole, Andersen, Paal S, Aidt, Frederik H, Jensen, Morten, Moolman-Smook, Johanna C, Bundgaard, Henning, Christiansen, Michael
Publicado 2011

Private Mitochondrial DNA Variants in Danish Patients with Hypertrophic Cardiomyopathy

por Hagen, Christian M., Aidt, Frederik H., Havndrup, Ole, Hedley, Paula L., Jensen, Morten K., Kanters, Jørgen K., Pham, Tam T., Bundgaard, Henning, Christiansen, Michael
Publicado 2015

Mitochondrial Haplogroups Modify the Risk of Developing Hypertrophic Cardiomyopathy in a Danish Population

por Hagen, Christian M., Aidt, Frederik H., Hedley, Paula L., Jensen, Morten K., Havndrup, Ole, Kanters, Jørgen K., Moolman-Smook, Johanna C., Larsen, Severin O., Bundgaard, Henning, Christiansen, Michael
Publicado 2013

MT-CYB mutations in hypertrophic cardiomyopathy

por Hagen, Christian M, Aidt, Frederik H, Havndrup, Ole, Hedley, Paula L, Jespersgaard, Cathrine, Jensen, Morten, Kanters, Jørgen K, Moolman-Smook, Johanna C, Møller, Daniel V, Bundgaard, Henning, Christiansen, Michael
Publicado 2013

MT-CYB mutations in hypertrophic cardiomyopathy

por Hagen, Christian M, Aidt, Frederik H, Havndrup, Ole, Hedley, Paula L, Jespersgaard, Cathrine, Jensen, Morten, Kanters, Jørgen K, Moolman-Smook, Johanna C, Møller, Daniel V, Bundgaard, Henning, Christiansen, Michael
Publicado 2013

Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2

por Christiansen, Michael, Hedley, Paula L, Theilade, Juliane, Stoevring, Birgitte, Leren, Trond P, Eschen, Ole, Sørensen, Karina M, Tybjærg-Hansen, Anne, Ousager, Lilian B, Pedersen, Lisbeth N, Frikke-Schmidt, Ruth, Aidt, Frederik H, Hansen, Michael G, Hansen, Jim, Bloch Thomsen, Poul E, Toft, Egon, Henriksen, Finn L, Bundgaard, Henning, Jensen, Henrik K, Kanters, Jørgen K
Publicado 2014