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Archives of Disease in Childhood|May 20, 1999
Anthropometry of patients with osteogenesis imperfectaA M Lund, J Müller, F Skovby
Human Mutation|January 1, 1997
(G586V) substitutions in the alpha 1 and alpha 2 chains of collagen I: effect of alpha-chain stoichiometry on the phenotype of osteogenesis imperfecta?A M Lund, F Skovby, M Schwartz
British Journal of Anaesthesia|May 1, 1980
A new nerve stimulator (Myotest)J Viby-Mogensen, P H Hansen, B C Jørgensen, et al.
Ugeskrift for Laeger|June 27, 2000
[Child abuse and osteogenesis imperfecta. How do we distinguish?]A M Lund, F Skovby, F U Knudsen
Ugeskrift for Laeger|November 24, 1998
[Shaken baby syndrome]A M Lund, G Sandgren, F U Knudsen
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1977
Dissociation of increases in levels of 3':5'-cyclic AMP and 3':5'-cyclic GMP from induction of ornithine decarboxylase by the tumor promoter 12-O-tetradecanoyl phorbol-13-acetate in mouse epidermis in vivoR A Mufson, E G Astrup, R C Simsiman, et al.
American Journal of Human Genetics|April 29, 1998
Identification of novel mutations in the ryanodine-receptor gene (RYR1) in malignant hyperthermia: genotype-phenotype correlationB M Manning, K A Quane, H Ording, et al.
Human Genetics|July 1, 1995
Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36H Eiberg, A M Lund, M Warburg, et al.
Nephron|September 8, 1998
Atraumatic loss of a kidney in a patient with alpha1-antitrypsin deficiencyE Randers, M Jønler, A M Lund, et al.
Acta Paediatrica (Oslo, Norway : 1992)|November 24, 1999
Bone mineral content and collagen defects in osteogenesis imperfectaA M Lund, C Mølgaard, J Müller, et al.
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