Authors:
Corydon, MJ
Vockley, J
Rinaldo, P
Rhead, WJ
Kjeldsen, M
Winter, V
Riggs, C
Babovic-Vuksanovic, D
Smeitink, J
De Jong, J
Levy, H
Sewell, AC
Roe, C
Matern, D
Dasouki, M
Gregersen, N
Citation: Mj. Corydon et al., Role of common gene variations in the molecular pathogenesis of short-chain acyl-CoA dehydrogenase deficiency, PEDIAT RES, 49(1), 2001, pp. 18-23
Authors:
Van Schilfgaarde, M
Van Ulsen, P
Van der Steeg, W
Winter, V
Eijk, P
Everts, V
Dankert, J
Van Alphen, L
Citation: M. Van Schilfgaarde et al., Cloning of genes of nontypeable Haemophilus influenzae involved in penetration between human lung epithelial cells, INFEC IMMUN, 68(8), 2000, pp. 4616-4623
Authors:
Andresen, BS
Christensen, E
Corydon, TJ
Bross, P
Pilgaard, B
Wanders, RJA
Ruiter, JPN
Simonsen, H
Winter, V
Knudsen, I
Schroeder, LD
Gregersen, N
Skovby, F
Citation: Bs. Andresen et al., Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoAdehydrogenase deficiency: Identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenasesin isoleucine and valine metabolism, AM J HU GEN, 67(5), 2000, pp. 1095-1103
Authors:
Bross, P
Pedersen, P
Winter, V
Nyholm, M
Johansen, BN
Olsen, RKJ
Corydon, MJ
Andresen, BS
Eiberg, H
Kolvraa, S
Gregersen, N
Citation: P. Bross et al., A polymorphic variant in the human electron transfer flavoprotein alpha-chain (alpha-T171) displays decreased thermal stability and is overrepresented in very-long-chain acyl-CoA dehydrogenase-deficient patients with mild childhood presentation, MOL GEN MET, 67(2), 1999, pp. 138-147
Authors:
Andresen, BS
Olpin, S
Poorthuis, BJHM
Scholte, HR
Vianey-Saban, C
Wanders, R
Ijlst, L
Morris, A
Pourfarzam, M
Bartlett, K
Baumgartner, ER
deKlerk, JBC
Schroeder, LD
Corydon, TJ
Lund, H
Winter, V
Bross, P
Bolund, L
Gregersen, N
Citation: Bs. Andresen et al., Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency, AM J HU GEN, 64(2), 1999, pp. 479-494