Allan Meldgaard Lund

Allan Meldgaard Lund

Clinical Professor

Member of:

  • Paediatrics


  1. 2024
  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 journalJournal articleResearchpeer-review

  3. 2023
  4. Published

    Adult patient diagnosed with NADSYN1 associated congenital NAD deficiency and analysis of NAD levels to be published in: European Journal of Medical Genetics

    Erbs, E., Brasen, C. L., Lund, Allan Meldgaard & Rasmussen, M., 2023, In: European Journal of Medical Genetics. 66, 3, 6 p., 104698.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    High yield on aetiology using a systematic diagnostic approach to paediatric acute liver failure, analysis of a nationwide cohort

    Nordmann Winther, T., Nielsen, A. Y., Lund, Allan Meldgaard, Larsen, F. S. & Jørgensen, M. H., 2023, In: Acta Paediatrica, International Journal of Paediatrics. 112, 5, p. 1082-1090 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Impact of the SARS-CoV-2 pandemic on the health of individuals with intoxication-type metabolic diseases—Data from the E-IMD consortium

    Mütze, U., Gleich, F., Barić, I., Baumgartner, M., Burlina, A., Chapman, K. A., Chien, Y. H., Cortès-Saladelafont, E., De Laet, C., Dobbelaere, D., Eysken, F., Gautschi, M., Santer, R., Häberle, J., Joaquín, C., Karall, D., Lindner, M., Lund, A. M., Mühlhausen, C., Murphy, E. & 8 others, Roland, D., Ruiz Gomez, A., Skouma, A., Grünert, S. C., Wagenmakers, M., Garbade, S. F., Kölker, S. & Boy, N., 2023, In: Journal of Inherited Metabolic Disease. 46, 2, p. 220-231

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Long-term safety and efficacy of velmanase alfa treatment in children under 6 years of age with alpha-mannosidosis: A phase 2, open label, multicenter study

    Guffon, N., Konstantopoulou, V., Hennermann, J. B., Muschol, N., Bruno, I., Tummolo, A., Ceravolo, F., Zardi, G., Ballabeni, A. & Lund, Allan Meldgaard, 2023, In: Journal of Inherited Metabolic Disease. 46, 4, p. 705-719 15 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    The impact of phenylalanine levels during pregnancy on birth weight and later development in children born to women with phenylketonuria

    Nielsen, M. R., Jørgensen, C., Ahring, K., Lund, Allan Meldgaard & Ørngreen, M. C., 2023, In: Journal of Inherited Metabolic Disease. 46, 4, p. 586-594 9 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    X-linked creatine transporter (SLC6A8) deficiency in females: Difficult to recognize, but a potentially treatable disease

    Mejdahl Nielsen, M., Petersen, E. T., Fenger, C. D., Ørngreen, M. C., Siebner, Hartwig Roman, Boer, V. O., Považan, M., Lund, Allan Meldgaard, Grønborg, S. W. & Hammer, T. B., 2023, In: Molecular Genetics and Metabolism. 140, 3, 9 p., 107694.

    Research output: Contribution to journalReviewResearchpeer-review

  10. 2022
  11. Published

    No effect of triheptanoin in patients with phosphofructokinase deficiency

    Raaschou-Pedersen, D. E., Madsen, K. L., Lokken, N., Storgaard, J. H., Quinlivan, R., Laforet, P., Lund, Allan Meldgaard, van Hall, Gerrit, Vissing, John & Orngreen, M., Apr 2022, In: Neuromuscular Disorders. 32, 4, p. 295-304 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. 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 journalJournal articleResearchpeer-review

  13. 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 journalJournal articleResearchpeer-review

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ID: 33844098