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Journal of Inherited Metabolic Disease|March 6, 2007
Xanthurenic aciduria due to a mutation in KYNU encoding kynureninaseM Christensen, M Duno, A M Lund, et al.
The American Journal of Physiology|July 17, 1999
Effects of LPS on transport of indocyanine green and alanine uptake in perfused rat liverM Lund, L Kang, N Tygstrup, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Gly802Asp substitution in the pro alpha 2(I) collagen chain in a family with recurrent osteogenesis imperfecta due to paternal mosaicismA M Lund, M Schwartz, M Raghunath, et al.
Acta Neurologica Scandinavica. Supplementum|January 1, 1975
A double blind study of carbamazepine and diphenylhydantoin in temporal lobe epilepsyN Simonsen, P Z Olsen, V Kühl, et al.
Pediatric Research|June 13, 2018
Extreme neonatal hyperbilirubinemia, acute bilirubin encephalopathy, and kernicterus spectrum disorder in children with galactosemiaLaura F Bech, Mette Line Donneborg, Allan M Lund, et al.
Journal of Geriatric Oncology|July 2, 2024
Physical decline, falls, and hospitalization among vulnerable older patients in the trajectory of colorectal cancer treatmentCecilia M Lund, Dorte L Nielsen, Martin Schultz, et al.
Journal of Craniofacial Genetics and Developmental Biology|May 22, 1998
Dental manifestations of osteogenesis imperfecta and abnormalities of collagen I metabolismA M Lund, B L Jensen, L A Nielsen, et al.
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