Andresen BS - Search Results

1

Normal Levels of Plasma Free Carnitine and Acylcarnitines in Follow-Up Samples from a Presymptomatic Case of Carnitine Palmitoyl Transferase 1 (CPT1) Deficiency Detected Through Newborn Screening in Denmark.

Borch L, Lund AM, Wibrand F, Christensen E, Søndergaard C, Gahrn B, Hougaard DM, Andresen BS, Gregersen N, Olsen RK. Borch L, et al. Among authors: andresen bs. JIMD Rep. 2012;3:11-5. doi: 10.1007/8904_2011_35. Epub 2011 Sep 22. JIMD Rep. 2012. PMID: 23430868 Free PMC article.

2

[That is eliminating nursing in the care of the mentally handicapped].

Andresen B, Christensen EH. Andresen B, et al. Sygeplejersken. 1978 Mar 1;78(9):16-7. Sygeplejersken. 1978. PMID: 246614 Danish. No abstract available.

3

Expression of wild-type and mutant medium-chain acyl-CoA dehydrogenase (MCAD) cDNA in eucaryotic cells.

Jensen TG, Andresen BS, Bross P, Jensen UB, Holme E, Kølvraa S, Gregersen N, Bolund L. Jensen TG, et al. Among authors: andresen bs. Biochim Biophys Acta. 1992 Oct 13;1180(1):65-72. doi: 10.1016/0925-4439(92)90028-l. Biochim Biophys Acta. 1992. PMID: 1382617

4

Two novel nonradioactive polymerase chain reaction-based assays of dried blood spots, genomic DNA, or whole cells for fast, reliable detection of Z and S mutations in the alpha 1-antitrypsin gene.

Andresen BS, Knudsen I, Jensen PK, Rasmussen K, Gregersen N. Andresen BS, et al. Clin Chem. 1992 Oct;38(10):2100-7. Clin Chem. 1992. PMID: 1394999

5

Molecular analysis of medium-chain acyl-CoA dehydrogenase deficiency: a diagnostic approach.

Gregersen N, Winter V, Kølvraa S, Andresen BS, Bross P, Blakemore A, Curtis D, Bolund L. Gregersen N, et al. Among authors: andresen bs. Prog Clin Biol Res. 1992;375:441-52. Prog Clin Biol Res. 1992. PMID: 1438387 Review. No abstract available.

6

[Medium chain acyl-CoA dehydrogenase (MCAD) deficiency: a life-threatening defect of fatty acid oxidation].

Gregersen N, Winter V, Andresen BS, Kølvraa S, Christensen E, Petersen BN, Bolund LA. Gregersen N, et al. Among authors: andresen bs. Ugeskr Laeger. 1992 Feb 17;154(8):483-8. Ugeskr Laeger. 1992. PMID: 1539377 Review. Danish.

7

Internalization, lysosomal degradation and new synthesis of surface membrane CD4 in phorbol ester-activated T-lymphocytes and U-937 cells.

Petersen CM, Christensen EI, Andresen BS, Møller BK. Petersen CM, et al. Among authors: andresen bs. Exp Cell Res. 1992 Jul;201(1):160-73. doi: 10.1016/0014-4827(92)90360-k. Exp Cell Res. 1992. PMID: 1612121

8

The most common mutation causing medium-chain acyl-CoA dehydrogenase deficiency is strongly associated with a particular haplotype in the region of the gene.

Kølvraa S, Gregersen N, Blakemore AI, Schneidermann AK, Winter V, Andresen BS, Curtis D, Engel PC, Pricille D, Rhead W, et al. Kølvraa S, et al. Among authors: andresen bs. Hum Genet. 1991 Aug;87(4):425-8. doi: 10.1007/BF00197161. Hum Genet. 1991. PMID: 1679031

9

Specific diagnosis of medium-chain acyl-CoA dehydrogenase (MCAD) deficiency in dried blood spots by a polymerase chain reaction (PCR) assay detecting a point-mutation (G985) in the MCAD gene.

Gregersen N, Blakemore AI, Winter V, Andresen B, Kølvraa S, Bolund L, Curtis D, Engel PC. Gregersen N, et al. Clin Chim Acta. 1991 Nov 9;203(1):23-34. doi: 10.1016/0009-8981(91)90153-4. Clin Chim Acta. 1991. PMID: 1769118

10

Characterization of a disease-causing Lys329 to Glu mutation in 16 patients with medium-chain acyl-CoA dehydrogenase deficiency.

Gregersen N, Andresen BS, Bross P, Winter V, Rüdiger N, Engst S, Ghisla S, Christensen E, Kelly D, Strauss AW, et al. Gregersen N, et al. Among authors: andresen bs. J Inherit Metab Dis. 1991;14(3):314-6. doi: 10.1007/BF01811691. J Inherit Metab Dis. 1991. PMID: 1770781 No abstract available.

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