Allan Meldgaard Lund

Allan Meldgaard Lund

Clinical Professor

Member of:

  • Paediatrics


Publication year:
All
1 - 10 out of 52Page size: 10
  1. 1998
  2. Published

    Collagen-derived markers of bone metabolism in osteogenesis imperfecta

    Lund, Allan Meldgaard, Hansen, M., Kollerup, G. B., Juul, Anders, Teisner, B. & Skovby, F., 1998, In: Acta Paediatrica. 87, 11, p. 1131-7 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  3. Published

    Dental manifestations of osteogenesis imperfecta and abnormalities of collagen I metabolism

    Lund, Allan Meldgaard, Jensen, B. L., Nielsen, L. A. & Skovby, F., 1998, In: Journal of craniofacial genetics and developmental biology. 18, p. 30-37

    Research output: Contribution to journal › Journal article › Research › peer-review

  4. 2004
  5. Published

    On the neurotoxicity of glutaric, 3-hydroxyglutaric, and trans-glutaconic acids in glutaric acidemia type 1

    Lund, Trine Meldgaard, Christensen, E., Kristensen, Anders Skov, Schousboe, Arne & Lund, Allan Meldgaard, 2004, In: Journal of Neuroscience Research. 77, 1, p. 143-7 5 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  6. 2007
  7. Published

    Preserved fertility in a non-mosaic Klinefelter patient with a mutation in the fibroblast growth factor receptor 3 gene: case report

    Juul, Anders, Aksglaede, L., Lund, Allan Meldgaard, Duno, M., Skakkebæk, Niels Erik & Rajpert-De Meyts, E., 2007, In: Human Reproduction. 22, 7, p. 1907-11 5 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  8. 2008
  9. Published

    Identification of two new mutations in the TAT gene in a Danish family with tyrosinaemia type II

    Pasternack, S. M., Betz, R. C., Brandrup, F., Gade, E. F., Clemmensen, O., Lund, Allan Meldgaard, Christensen, E. & Bygum, A., 2008, In: British Journal of Dermatology. 160, 3, p. 704-6 2 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  10. 2009
  11. Published

    Highly variable clinical phenotype of carbamylphosphate synthetase 1 deficiency in one family: an effect of allelic variation in gene expression?

    Klaus, V., Vermeulen, T., Minassian, B., Israelian, N., Engel, K., Lund, Allan Meldgaard, Roebrock, K., Christensen, E. & Häberle, J., 2009, In: Clinical Genetics. 76, 3, p. 263-9 6 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  12. Published

    Svaer vitamin B12-mangel hos spaedbørn brysternaeret af veganere

    Roed, C., Skovby, F. & Lund, Allan Meldgaard, 2009, In: Ugeskrift for læger. 171, 43, p. 3099-101 2 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  13. 2010
  14. Published

    OBSL1 mutations in 3-M syndrome are associated with a modulation of IGFBP2 and IGFBP5 expression levels

    Huber, C., Fradin, M., Edouard, T., Le Merrer, M., Alanay, Y., Da Silva, D. B., David, A., Hamamy, H., van Hest, L., Lund, Allan Meldgaard, Michaud, J., Oley, C., Patel, C., Rajab, A., Skidmore, D. L., Stewart, H., Tauber, M., Munnich, A. & Cormier-Daire, V., 1 Jan 2010, In: Human Mutation. 31, 1, p. 20-6 7 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  15. Published

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

    Steenweg, M. E., Jakobs, C., Errami, A., van Dooren, S. J. M., Adeva Bartolomé, M. T., Aerssens, P., Augoustides-Savvapoulou, P., Baric, I., Baumann, M., Bonafé, L., Chabrol, B., Clarke, J. T. R., Clayton, P., Coker, M., Cooper, S., Falik-Zaccai, T., Gorman, M., Hahn, A., Hasanoglu, A., King, M. D. & 31 others, de Klerk, H. B. C., Korman, S. H., Lee, C., Lund, Allan Meldgaard, Mejaski-Bosnjak, V., Pascual-Castroviejo, I., Raadhyaksha, A., Rootwelt, T., Roubertie, A., Ruiz-Falco, M. L., Scalais, E., Schimmel, U., Seijo-Martinez, M., Suri, M., Sykut-Cegielska, J., Trefz, F. K., Uziel, G., Valayannopoulos, V., Vianey-Saban, C., Vlaho, S., Vodopiutz, J., Wajner, M., Walter, J., Walter-Derbort, C., Yapici, Z., Zafeiriou, D. I., Spreeuwenberg, M. D., Celli, J., den Dunnen, J. T., van der Knaap, M. S. & Salomons, G. S., 1 Apr 2010, In: Human Mutation. 31, 4, p. 380-90 11 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  16. Published

    Clinical and biochemical monitoring of patients with fatty acid oxidation disorders

    Lund, Allan Meldgaard, Skovby, F., Vestergaard, H., Christensen, M. & Christensen, E., 1 Oct 2010, In: Journal of Inherited Metabolic Disease. 33, 5, p. 495-500 6 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

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ID: 33844098