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Ugeskrift for Laeger|March 4, 2006
[Vascular Ehlers-Danlos syndromes--biochemical and molecular-genetic investigations]Allan Meldgaard LundUgeskrift for Laeger|April 28, 2006
[Optimising treatment for people with rare diseases]Allan Meldgaard Lund, Flemming SkovbyUgeskrift for Laeger|January 14, 2003
[Treatment of inborn metabolic disorders]Allan Meldgaard Lund, Flemming SkovbyUgeskrift for Laeger|June 27, 2007
[Acute Addisonian crisis in a patient with systemic lupus erythematosus and secondary antiphospholipid syndrome]Anna Svarre Jakobsen, Veronica Basile Cvitanich, Bent Carsten KirkegaardUgeskrift for Laeger|January 14, 2003
[Diagnosis and acute treatment of inborn metabolic diseases in infants]Allan Meldgaard Lund, Ernst Christensen, Flemming SkovbyUgeskrift for Laeger|October 27, 2009
[Severe vitamin B12 deficiency in infants breastfed by vegans]Casper Roed, Flemming Skovby, Allan Meldgaard LundUgeskrift for Laeger|June 16, 2011
[Isovaleric acidaemia--a rare and serious defect in the metabolism of leucine]Ann-Britt Kiholm Lund, Allan Meldgaard LundJIMD Reports|January 17, 2017
Prevalence of Mucopolysaccharidosis Types I, II, and VI in the Pediatric and Adult Population with Carpal Tunnel Syndrome (CTS). Retrospective and Prospective Analysis of Patients Treated for CTSMette Borch Nørmark, Nanna Kjaer, Allan Meldgaard LundUgeskrift for Laeger|February 21, 2015
[Diagnostics and treatment of phenylketonuria]Allan Bayat, Libeth Birk Møller, Allan Meldgaard LundMolecular Genetics and Metabolism Reports|February 2, 2018
The impact of consanguinity on the frequency of inborn errors of metabolismRaja Majid Afzal, Allan Meldgaard Lund, Flemming SkovbyPageof 11