Allan Meldgaard Lund
Clinical Professor
- 2024
- 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, , 2024, In: Journal of Inherited Metabolic Disease. 47, 2, p. 220-229 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
- 2023
- 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 journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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, , 2023, In: Journal of Inherited Metabolic Disease. 46, 2, p. 220-231Research output: Contribution to journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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 journal › Journal article › Research › peer-review
- 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 journal › Review › Research › peer-review
- 2022
- 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 journal › Journal article › Research › peer-review
- 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
- 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. 848-861Research output: Contribution to journal › Journal article › Research › peer-review
ID: 33844098
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Excellent response to asfotase alfa treatment in an adolescent patient with hypophosphatasia
Research output: Contribution to journal › Journal article › Research › peer-review
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11
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Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience
Research output: Contribution to journal › Journal article › Research › peer-review
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11
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Use of molecular genetic analyses in danish routine newborn screening
Research output: Contribution to journal › Journal article › Research › peer-review
Published