Henrik Vestergaard

Henrik Vestergaard

Associate Professor


  1. 1997
  2. Published

    Identification of a common amino acid polymorphism in the p85alpha regulatory subunit of phosphatidylinositol 3-kinase : effects on glucose disappearance constant, glucose effectiveness, and the insulin sensitivity index. / Hansen, Torben; Andersen, C B; Echwald, Søren Morgenthaler; Urhammer, S A; Clausen, J O; Vestergaard, H; Owens, D; Hansen, L; Pedersen, O.

    In: Diabetes, Vol. 46, No. 3, 03.1997, p. 494-501.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Chromosomal mapping and mutational analysis of the coding region of the glycogen synthase kinase-3alpha and beta isoforms in patients with NIDDM. / Hansen, L; Arden, K C; Rasmussen, S B; Viars, C S; Vestergaard, H; Hansen, T; Møller, A M; Woodgett, J R; Pedersen, O.

    In: Diabetologia, Vol. 40, No. 8, 08.1997, p. 940-6.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Mutational analysis of the coding region of the uncoupling protein 2 gene in obese NIDDM patients : impact of a common amino acid polymorphism on juvenile and maturity onset forms of obesity and insulin resistance. / Urhammer, S A; Dalgaard, L T; Sørensen, T I; Møller, A M; Andersen, T; Tybjaerg-Hansen, A; Hansen, T; Clausen, J O; Vestergaard, H; Pedersen, O.

    In: Diabetologia, Vol. 40, No. 10, 10.1997, p. 1227-30.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Expression of protein-tyrosine phosphatases in the major insulin target tissues. / Norris, K; Norris, F; Kono, D H; Vestergaard, H; Pedersen, O; Theofilopoulos, A N; Møller, N P.

    In: FEBS letters, Vol. 415, No. 3, 06.10.1997, p. 243-8.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. 1999
  7. Published

    Alternative splicing of exon 17 and a missense mutation in exon 20 of the insulin receptor gene in two brothers with a novel syndrome of insulin resistance (congenital fiber-type disproportion myopathy). / Vorwerk, P; Christoffersen, C T; Müller, J; Vestergaard, H; Pedersen, O; De Meyts, P; Vestergaard, Henrik.

    In: Hormone Research, Vol. 52, No. 5, 1999, p. 211-20.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Low incidence rate of overt hypothyroidism compared with hyperthyroidism in an area with moderately low iodine intake. / Laurberg, P; Bülow Pedersen, I; Pedersen, K M; Vestergaard, H.

    In: Thyroid, Vol. 9, No. 1, 01.1999, p. 33-8.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Implications of compound heterozygous insulin receptor mutations in congenital muscle fibre type disproportion myopathy for the receptor kinase activation. / Klein, H H; Müller, R; Vestergaard, H; Pedersen, O.

    In: Diabetologia, Vol. 42, No. 2, 02.1999, p. 245-9.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published
  11. Published

    Studies of gene expression and activity of hexokinase, phosphofructokinase and glycogen synthase in human skeletal muscle in states of altered insulin-stimulated glucose metabolism. / Vestergaard, H.

    In: Danish Medical Bulletin (Print), Vol. 46, No. 1, 02.1999, p. 13-34.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Intact proinsulin and beta-cell function in lean and obese subjects with and without type 2 diabetes. / Røder, M E; Dinesen, B; Hartling, S G; Houssa, P; Vestergaard, H; Sodoyez-Goffaux, F; Binder, C.

    In: Diabetes Care. Supplement, Vol. 22, No. 4, 04.1999, p. 609-14.

    Research output: Contribution to journalJournal articleResearchpeer-review

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