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Publikationer

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Kapitel i bog
2017

Mitochondrial Fatty Acid Oxidation Defects

W. Strauss, A., Andresen, B. S. & Bennett, M. J., 2017, Pediatric Endocrinology And Inborn Errors Of Metabolism. Sarafoglou, K., F. Hoffmann, G. & S. Roth, K. (red.). 2. udg. McGraw-Hill, s. 125-144

Publikation: Kapitel i bog/rapport/konference-proceedingKapitel i bogUndervisning

2009

Fatty-acid oxidation defects: Chapter 5

Strauss, A., Andresen, B. S. & Bennett, M., 2009, Pediatric Endocrinology and Metabolism. Sarafoglu, K. (red.). 1 udg. New York, USA: McGraw-Hill, s. 51-70 20 s.

Publikation: Kapitel i bog/rapport/konference-proceedingKapitel i bogForskning

When the genetic code is not enough - How sequence variations can affect pre-mRNA splicing and cause (complex) disease. Chapter 15.

Andresen, B. S. & Krainer, A., 2009, Genetics of Complex Human Diseases.. Al-Chalabi, A. & Alamassy, L. (red.). Cold Spring Harbor, New York, USA: Cold Spring Harbor Laboratory Press, s. 165-182 18 s.

Publikation: Kapitel i bog/rapport/konference-proceedingKapitel i bogForskning

1992

Characterization of medium-chain acyl-CoA dehydrogenase (MCAD) with a point mutation associated with MCAD deficiency

Bross, P., Jensen, T., Kräutle, F., Winter, V., Andresen, B. S., Engst, S., Bolund, L., Kølvraa, S., Ghisla, S. & Rasched, I., 1992, Characterization of medium-chain acyl-CoA dehydrogenase (MCAD) with a point mutation associated with MCAD deficiency. Bind 375. s. 473-8 6 s. (Progress in clinical and biological research).

Publikation: Kapitel i bog/rapport/konference-proceedingKapitel i bogForskning