Allan Meldgaard Lund

Allan Meldgaard Lund

Clinical Professor

Member of:

  • Paediatrics


Publication year:
All
31 - 40 out of 52Page size: 10
  1. 2015
  2. Published

    Mild lesch–nyhan disease in a boy with a null mutation in HPRT1: An exception to the known genotype–phenotype correlation

    Bayat, Allan, Christensen, M., Wibrand, F., Duno, M. & Lund, Allan Meldgaard, 2015, JIMD Reports. Springer, p. 135-137 3 p. (JIMD Reports, Vol. 18).

    Research output: Chapter in Book/Report/Conference proceeding › Book chapter › Research › peer-review

  3. Published

    Diagnostik og behandling af fenylketonuri

    Bayat, Allan, Møller, L. B. & Lund, Allan Meldgaard, 16 Feb 2015, In: Ugeskrift for Laeger. 177, 8

    Research output: Contribution to journal › Review › Research › peer-review

  4. 2016
  5. Published

    >Svar: Vi beskriver ikkekomplekse tilstande

    Leganger, J., Lund, Allan Meldgaard, Farholt, S., Søborg, M. L. K., Burcharth, Jakob & Rosenberg, Jacob, 2016, In: Ugeskrift for Laeger. 178, 12, p. 1191 1 p.

    Research output: Contribution to journal › Comment/debate › Research › peer-review

  6. 2017
  7. Published

    The D313Y variant in the GLA gene–no evidence of a pathogenic role in Fabry disease

    Hasholt, Lis Frydenreich, Ballegaard, Martin, Bundgård, Henning, Christiansen, M., Law, Ian, Lund, Allan Meldgaard, Nørremølle, Anne, Krogh Rasmussen, A., Ravn, K., Tümer, Asuman Zeynep, Wibrand, F. & Feldt-Rasmussen, Ulla, 2017, In: Scandinavian Journal of Clinical and Laboratory Investigation. 77, 8, p. 617-621 5 p.

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

  8. 2020
  9. Published

    Behandling af monogene sygdomme ved viral transduktion af hæmatopoietiske stamceller

    Ifversen, M. S., Masmas, T. N., Kornblit, B., Rieneck, K., Kaastrup, E. K., Lund, Allan Meldgaard, Fischer-Nielsen, A. & Glenthøj, Andreas Birkedal, 2020, In: Ugeskrift for Laeger. 182, 46, 5 p., V06200458.

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

  10. Published

    Increased risk of sudden death in untreated primary carnitine deficiency

    Rasmussen, J., Dunø, M., Lund, Allan Meldgaard, Steuerwald, U., Hansen, Steen Holger, Joensen, H. D., Køber, Lars Valeur & Nielsen, Olav Wendelboe, 2020, In: Journal of Inherited Metabolic Disease. 43, 2, p. 290-296 7 p.

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

  11. 2021
  12. Published

    Excellent response to asfotase alfa treatment in an adolescent patient with hypophosphatasia

    Strandbech, O. S., Lund, Allan Meldgaard & Østergaard, Elsebet, 2021, In: JIMD Reports. 59, 1, p. 10-15

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

  13. Published

    Genetic disease is a common cause of bilateral childhood cataract in Denmark

    Kessel, Line, Bach-Holm, Daniella, Al-Bakri, M., Roos, L., Lund, Allan Meldgaard & Grønskov, K., 2021, In: Ophthalmic Genetics. 42, 6, p. 650-658

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

  14. Published

    Use of molecular genetic analyses in danish routine newborn screening

    Lund, Allan Meldgaard, Wibrand, F., Skogstrand, K., Bækvad-Hansen, M., Gregersen, N., Andresen, B. S., Hougaard, D. M., Dunø, M. & Olsen, R. K. J., 2021, In: International Journal of Neonatal Screening. 7, 3, 50.

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

  15. 2022
  16. Published

    Influence of early identification and therapy on long-term outcomes in early-onset MTHFR deficiency

    E-HOD Consortium, E. C., 2022, In: Journal of Inherited Metabolic Disease. 45, 4, p. 848-861

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

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