Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Schroeder, L. D."'
Autor:
Andresen, B. S., Christensen, E., Thomas Juhl Corydon, Bross, P., Pilgaard, B., Wanders, R. J. A., Ruiter, J. P. N., Simonsen, H., Winter, V., Knudsen, I., Schroeder, L. D., Gregersen, N., Skovby, F.
Publikováno v:
Andresen, B S, Christensen, E, Corydon, T J, Bross, P, Pilgaard, B, Wanders, R J A, Ruiter, J P N, Simonsen, H, Winter, V, Knudsen, I, Schroeder, L D, Gregersen, N & Skovby, F 2000, ' Isolated 2-methylbutyrylglycinuria caused by Short/Branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoAdehydrogenases in isoleucine and valine metabolism ', Am. J. Hum. Genet., nr. 67, s. 1095-1103 .
Aarhus University
Aarhus University
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::8757be27889afb64d1c8a9a0daa396d3
https://pure.au.dk/portal/da/publications/isolated-2methylbutyrylglycinuria-caused-by-shortbranchedchain-acylcoa-dehydrogenase-deficiency-identification-of-a-new-enzyme-defect-resolution-of-its-molecular-basis-and-evidence-for-distinct-acylcoadehydrogenases-in-isoleucine-and-valine-metabolism(72f0caf0-f7b7-11da-bee9-02004c4f4f50).html
https://pure.au.dk/portal/da/publications/isolated-2methylbutyrylglycinuria-caused-by-shortbranchedchain-acylcoa-dehydrogenase-deficiency-identification-of-a-new-enzyme-defect-resolution-of-its-molecular-basis-and-evidence-for-distinct-acylcoadehydrogenases-in-isoleucine-and-valine-metabolism(72f0caf0-f7b7-11da-bee9-02004c4f4f50).html
Autor:
Jones, S. P., Schroeder, L. D.
Publikováno v:
Journal of Aircraft. Jan/Feb2001, Vol. 38 Issue 1, p64. 5p. 1 Diagram, 4 Charts, 11 Graphs.
Akademický článek
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Akademický článek
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Autor:
Andresen BS; Research Unit for Molecular Medicine, Aarhus University Hospital, and Faculty of Health Science, Skejby Sygehus, DK 8200 Arhus N, Denmark. brage@biobase.dk, Christensen E, Corydon TJ, Bross P, Pilgaard B, Wanders RJ, Ruiter JP, Simonsen H, Winter V, Knudsen I, Schroeder LD, Gregersen N, Skovby F
Publikováno v:
American journal of human genetics [Am J Hum Genet] 2000 Nov; Vol. 67 (5), pp. 1095-103. Date of Electronic Publication: 2000 Sep 29.
Autor:
Andresen BS; Research Unit for Molecular Medicine, Aarhus University Hospital and Faculty of Health Science, Skejby Sygehus, Denmark. brage@biobase.dk, Corydon TJ, Wilsbech M, Bross P, Schroeder LD, Hindkjaer TF, Bolund L, Gregersen N
Publikováno v:
Mammalian genome : official journal of the International Mammalian Genome Society [Mamm Genome] 2000 Apr; Vol. 11 (4), pp. 275-80.
Autor:
Andresen BS; Research Unit for Molecular Medicine, Aarhus University Hospital, Denmark. brage@biobase.dk, Olpin S, Kvittingen EA, Augoustides-Savvopoulou P, Lindhout D, Halley DJ, Vianey-Saban C, Wanders RJ, Ijlst L, Schroeder LD, Bolund L, Gregersen N
Publikováno v:
Journal of inherited metabolic disease [J Inherit Metab Dis] 1999 May; Vol. 22 (3), pp. 281-5.
Autor:
Andresen BS; Research Unit for Molecular Medicine, Skejby Sygehus, DK 8200 Arhus N, Denmark, Germany. brage@biobase.dk, Olpin S, Poorthuis BJ, Scholte HR, Vianey-Saban C, Wanders R, Ijlst L, Morris A, Pourfarzam M, Bartlett K, Baumgartner ER, deKlerk JB, Schroeder LD, Corydon TJ, Lund H, Winter V, Bross P, Bolund L, Gregersen N
Publikováno v:
American journal of human genetics [Am J Hum Genet] 1999 Feb; Vol. 64 (2), pp. 479-94.