Allan Meldgaard Lund

Allan Meldgaard Lund

Clinical Professor

Member of:

  • Paediatrics


  1. 2015
  2. 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 journalReviewResearchpeer-review

  3. 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 proceedingBook chapterResearchpeer-review

  4. 2012
  5. Published

    Adherence issues in inherited metabolic disorders treated by low natural protein diets

    MaCdonald, A., van Rijn, M., Feillet, F., Lund, Allan Meldgaard, Bernstein, L., Bosch, A. M., Gizewska, M. & van Spronsen, F. J., 2012, In: Annals of Nutrition and Metabolism. 61, 4, p. 289-95 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Alu-Alu Recombination Underlying the First Large Genomic Deletion in GlcNAc-Phosphotransferase Alpha/Beta (GNPTAB) Gene in a MLII Alpha/Beta Patient

    Coutinho, F., da Silva Santos, L., Lacerda, L., Quental, S., Wibrand, F., Lund, Allan Meldgaard, Johansen, K. B., Prata, M. J. & Alves, S., 2012, In: JIMD Reports. 4, p. 117-124 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Arvelige stofskiftesygdomme

    Lund, Allan Meldgaard & Skovby, F., 2012, Medicinsk genetik. Nørby, S. & Jensen, P. K. A. (eds.). 2 ed. København: FADL's Forlag, p. 201-218

    Research output: Chapter in Book/Report/Conference proceedingBook chapterResearchpeer-review

  8. Published

    Biochemical screening of 504,049 newborns in Denmark, the Faroe Islands and Greenland - Experience and development of a routine program for expanded newborn screening

    Lund, Allan Meldgaard, Hougaard, D. M., Simonsen, H., Andresen, B. S., Christensen, M., Dunø, M., Skogstrand, K., Olsen, R. K. J., Jensen, U. G., Cohen, A., Larsen, N. B., Saugmann-Jensen, P., Gregersen, N., Brandt, N. J., Christensen, E., Skovby, F. & Nørgaard-Pedersen, B., 2012, In: Molecular Genetics and Metabolism. 107, 3, p. 281-93 13 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    CTD og Færinger i Danmark

    Rasmussen, J. & Lund, Allan Meldgaard, 2012, In: Maanedsskrift for Praktisk Laegegerning. 4, April

    Research output: Contribution to journalJournal articleResearch

  10. Published

    Heparan sulfate and dermatan sulfate derived disaccharides are sensitive markers for newborn screening for mucopolysaccharidoses types I, II and III

    de Ruijter, J., de Ru, M. H., Wagemans, T., Ijlst, L., Lund, Allan Meldgaard, Orchard, P. J., Schaefer, G. B., Wijburg, F. A. & van Vlies, N., 2012, In: Molecular Genetics and Metabolism. 107, 4, p. 705-10 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  11. 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 journalJournal articleResearchpeer-review

  12. Published

    Karnitintransporterdefekt er en arvelig sygdom med høj hyppighed på Færøerne

    Poulsen, S. D., Lund, Allan Meldgaard, Christensen, E. & Skovby, F., 2012, In: Ugeskrift for Laeger. 174, 18, p. 1217-9 3 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

ID: 33844098