A. Meldgaard Lund

Splenomegaly – Diagnostic validity, work-up, and underlying causes

F. Wibrand, O. B. Schaffalitzky de Muckadell, H. Frederiksen, 2017, PloS one.

Fabry disease in children: agalsidase‐beta enzyme replacement therapy

M. Ballegaard, U. Feldt-Rasmussen, A. Meldgaard Lund, 2013, Clinical genetics.

Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy

L. de Meirleir, J. Zeman, O. Bodamer, 2007, European Journal of Pediatrics.

Protein-losing enteropathy in a child with junctional epidermolysis bullosa and pyloric atresia.

T. Karlsmark, T. Kobayasi, A. Meldgaard Lund, 1995, Acta dermato-venereologica.

An overview of L‐2‐hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype–phenotype study

D. Zafeiriou, J. Celli, J. D. den Dunnen, 2010, Human mutation.