Research output per year
Research output per year
Personal profile
Expertises
Inborn metabolic diseases; biochemical genetics
Main research areas
Inborn metabolic diseases; diagnostic methods in biochemical genetics
Current research
Mitochondrial and lysosomal diseases; diagnostic methods in biochemical genetics
Potential conflicts of interest
None
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Dive into the research topics where Flemming Wibrand is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
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Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease
Zheng, W-Q., Pedersen, S. V., Thompson, K., Bellacchio, E., French, C. E., Munro, B., Pearson, T. S., Vogt, J., Diodato, D., Diemer, T., Ernst, A., Horvath, R., Chitre, M., Ek, J., Wibrand, F., Grange, D. K., Raymond, L., Zhou, X-L., Taylor, R. W. & Ostergaard, E., 21 Feb 2022, In: Human Molecular Genetics. 31, 4, p. 523-534 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
5 Citations (Scopus) -
Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience
Effraimidis, G., Rasmussen, Å. K., Dunoe, M., Hasholt, L. F., Wibrand, F., Sorensen, S. S., Lund, A. M., Kober, L., Bundgaard, H., Yazdanfard, P. D. W., Oturai, P., Larsen, V. A., de Abreu, V. H. F., Enevoldsen, L. H., Kristensen, T., Svenstrup, K., Bille, M. B., Arif, F., Mogensen, M., Klokker, M., & 3 others, 2022, In: PLoS One. 17, 11, p. 1-18 18 p., e0277767.Research output: Contribution to journal › Journal article › Research › peer-review
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The impact of metabolic supply lines - and the patterns between them - on the development of distant metastases in 64 women with breast cancer
Abrahamsen, O., Balslev, E., Christensen, M., Wibrand, F., Budtz-Jørgensen, E. & Høgdall, E., Sep 2022, In: Oncology letters. 24, 3, p. 327 327.Research output: Contribution to journal › Journal article › Research › peer-review
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β-Galactosidase deficiency in the GLB1 spectrum of lysosomal storage disease can present with severe muscle weakness and atrophy
Pedersen, J. J., Duno, M., Wibrand, F., Hammer, C., Krag, T. & Vissing, J., Nov 2022, In: JIMD Reports. 63, 6, p. 540-545 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A novel homoplasmic mt-tRNAGlu m.14701C>T variant presenting with a partially reversible infantile respiratory chain deficiency
Lundquist, A. A., Farholt, S., Børresen, M. L., Dunø, M., Wibrand, F., Witting, N. & Østergaard, E., Oct 2021, In: European Journal of Medical Genetics. 64, 10, p. 104306 104306.Research output: Contribution to journal › Journal article › Research › peer-review