Allan Meldgaard Lund

Allan Meldgaard Lund

Clinical Professor

Member of:

  • Paediatrics


Publication year:
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  1. Published

    The effect of casein glycomacropeptide versus free synthetic amino acids for early treatment of phenylketonuria in a mice model

    Ahring, K. K., Dagnaes-Hansen, F., Bruel, A., Christensen, M., Jensen, E., Jensen, T. G., Johannsen, M., Johansen, K. S., Lund, Allan Meldgaard, Madsen, J. G., Brondum-Nielsen, K., Pedersen, M., Sorensen, L. K., Kjolby, M. & Moller, L. B., 11 Jan 2022, In: PLoS ONE. 17, 1, 26 p., 0261150.

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

  2. Published

    Impact of citrulline substitution on clinical outcome after liver transplantation in carbamoyl phosphate synthetase 1 and ornithine transcarbamylase deficiency

    Aldrian, D., Waldner, B., Vogel, G. F., El-Gharbawy, A. H., McKiernan, P., Vockley, J., Landau, Y. E., Al Mutairi, F., Stepien, K. M., Kwok, A. M. K., Yıldız, Y., Honzik, T., Kelifova, S., Ellaway, C., Lund, A. M., Mori, M., Grünert, S. C., Scholl-Bürgi, S., Zöggeler, T., Oberhuber, R. & 3 others, Schneeberger, S., Müller, T. & Karall, D., 2024, In: Journal of Inherited Metabolic Disease. 47, 2, p. 220-229 10 p.

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

  3. Published

    MCAD deficiency in Denmark

    Andresen, B. S., Lund, Allan Meldgaard, Hougaard, D. M., Christensen, E., Gahrn, B., Christensen, M., Bross, P. G., Vested, A., Simonsen, H., Skogstrand, K., Olpin, S., Brandt, N. J., Skovby, F., Nørgaard-Pedersen, B. & Gregersen, N., 2012, In: Molecular Genetics and Metabolism. 106, 2, p. 175-88 14 p.

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

  4. 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

  5. Published

    Pyridoxine or pyridoxal-5-phosphate treatment for seizures in glycosylphosphatidylinositol deficiency: A cohort study

    Bayat, A., Aledo-Serrano, A., Gil-Nagel, A., Korff, C. M., Thomas, A., Boßelmann, C., Weber, Y., Gardella, E., Lund, Allan Meldgaard, de Sain-van der Velden, M. G. M. & Møller, R. S., 2022, In: Developmental Medicine and Child Neurology. 64, 6, p. 789-798 10 p.

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

  6. 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

  7. Published

    Kliniske aspekter af Marfans syndrom

    Belsing, T. Z., Lund, Allan Meldgaard, Søndergaard, Lars, Friis-Hansen, L. & Abildstrøm, S. Z., 2011, In: Ugeskrift for Laeger. 173, 5, p. 337-42 6 p.

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

  8. Published

    Molekylærbiologiske aspekter af Marfansyndromer

    Belsing, T. Z., Lund, Allan Meldgaard, Abildstrøm, S. Z., Søndergaard, Lars & Friis-Hansen, L., 2011, In: Ugeskrift for Laeger. 173, 5, p. 333-7 5 p.

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

  9. Published

    Normal Levels of Plasma Free Carnitine and Acylcarnitines in Follow-Up Samples From a Presymptomatic Case of Carnitine Palmitoyl Transferase 1 (CPT1) Deficiency Detected Through Newborn Screening in Denmark

    Borch, L., Lund, Allan Meldgaard, Wibrand, F., Christensen, E., Søndergaard, C., Gahrn, B., Hougaard, D. M., Andresen, B. S., Gregersen, N. & Olsen, R. K. J., 2011, In: JIMD Reports. 3, p. 11-15 5 p.

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

  10. Published

    Heterozygosity for an in-frame deletion causes glutaryl-CoA dehydrogenase deficiency in a patient detected by newborn screening: investigation of the effect of the mutant allele

    Bross, P. G., Frederiksen, J. B., Bie, A. S., Hansen, J., Palmfeldt, J., Nielsen, M. N., Duno, M., Lund, Allan Meldgaard & Christensen, E., 2012, In: Journal of Inherited Metabolic Disease. 35, 5, p. 787-96 10 p.

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

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