Lars Allan Larsen

Lars Allan Larsen

Professor

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    Publication year:
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    1 - 8 out of 8Page size: 10
    1. 2005
    2. Published

      Delineation of an interstitial 9q22 deletion in basal cell nevus syndrome

      Boonen, S. E., Stahl, D., Kreiborg, S., Rosenberg, T., Kalscheuer, V., Larsen, Lars Allan, Tommerup, Niels & Brøndum-Nielsen, K., 2005, In: American Journal of Medical Genetics. Part A. Vol. 132, p. 324-328

      Research output: Contribution to journal › Journal article › Research › peer-review

    3. Published

      High Throughput Single-Strand Conformation Polymorphism Analysis on a Microfabricated Capillary Array Electrophoresis Dervice

      Tian, H., Emrich, C. A., Scherer, J., Mathies, R. A., Andersen, P. S., Larsen, Lars Allan & Christiansen, M., 2005, In: Electrophoresis. Vol. 26, p. 1834-1842

      Research output: Contribution to journal › Journal article › Research › peer-review

    4. Published

      Mutations in the HERG ion channel: A novel link between long QT syndrome and sudden death syndrome

      Christiansen, M., Tønder, N., Larsen, Lars Allan, Andersen, P. S., Simonsen, H. B., Øyen, N., Kanters, J. K., Jacobsen, J. R., Fosdal, I., Wettrell, G. & Kjeldsen, K., 2005, In: American Journal of Cardiology. Vol. 95, p. 433-434

      Research output: Contribution to journal › Journal article › Research › peer-review

    5. Published

      Mutations in the genes KCND2 and KCND3 encoding the ion-channels Kv 4.2. and Kv 4.3, conducting the cardiac fast transient outward current ( ITo,f), are not a frequent cause of Long QT syndrome

      Frank-Hansen, R., Larsen, Lars Allan, Andersen, P. S., Jespersgård, C. & Christiansen, M., 2005, In: Clinica Chimica Acta. Vol. 351, p. 95-100

      Research output: Contribution to journal › Journal article › Research › peer-review

    6. Published

      One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region

      Hougs, L., Havndrup, O., Bundgård, Henning, Køber, Lars Valeur, Vuust, J., Larsen, Lars Allan, Christiansen, M. & Andersen, P. S., 2005, In: European Journal of Human Genetics. 13, 2, p. 161-5 4 p.

      Research output: Contribution to journal › Journal article › Research › peer-review

    7. Published

      One-third of Danish hyperytrophic cardiomyopathy patients with MYH7 mutations have mutations in rod region

      Hougs, L., Havndrup, O., Bundgaard, H., Køber, L., Vuust, J., Larsen, Lars Allan, Christiansen, M. & Andersen, P. S., 2005, In: European Journal of Human Genetics. Vol. 13, p. 161-165

      Research output: Contribution to journal › Journal article › Research › peer-review

    8. Published

      Potassium Must Be Considered in Congenital Long QT Syndrome

      Christiansen, M., Kjeldsen, K., Wettrell, G., Larsen, Lars Allan, Lundkvist, L., Andersen, P. S., Tran, C. T., Kanters, J. K. & Vuust, J., 2005, In: Cardiology. Vol. 5, p. 54-58

      Research output: Contribution to journal › Journal article › Research › peer-review

    9. Published

      The eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1. Mb of chromosome 21 and osteoporosis in Down syndrome

      Tümer, Asuman Zeynep, Henriksen, A. M., Bache, Iben, Larsen, Lars Allan, Brixen, K., Illum, N., Rasmussen, K. & Tommerup, Niels, 2005, In: American Journal of Medical Genetics. Part C: Seminars in Medical Genetics. Vol. 135A, p. 339-341

      Research output: Contribution to journal › Journal article › Research › peer-review

    ID: 2949