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L-2-hydroxyglutaric acidemia: a novel inherited neurometabolic disease.
Barth PG, Hoffmann GF, Jaeken J, Lehnert W, Hanefeld F, van Gennip AH, Duran M, Valk J, Schutgens RB, Trefz FK, et al. Barth PG, et al. Among authors: schutgens rb. Ann Neurol. 1992 Jul;32(1):66-71. doi: 10.1002/ana.410320111. Ann Neurol. 1992. PMID: 1642474
Peroxisomal disorders: a review.
Wanders RJ, Schutgens RB, Barth PG. Wanders RJ, et al. Among authors: schutgens rb. J Neuropathol Exp Neurol. 1995 Sep;54(5):726-39. doi: 10.1097/00005072-199509000-00016. J Neuropathol Exp Neurol. 1995. PMID: 7545216 Review.
The inborn errors of peroxisomal beta-oxidation: a review.
Wanders RJ, van Roermund CW, Schutgens RB, Barth PG, Heymans HS, van den Bosch H, Tager JM. Wanders RJ, et al. Among authors: schutgens rb. J Inherit Metab Dis. 1990;13(1):4-36. doi: 10.1007/BF01799330. J Inherit Metab Dis. 1990. PMID: 2109148 Review.
Delay in diagnosis of X-linked adrenoleukodystrophy.
van Geel BM, Assies J, Haverkort EB, Barth PG, Wanders RJ, Schutgens RB, Keyser A, Zwetsloot CP. van Geel BM, et al. Among authors: schutgens rb. Clin Neurol Neurosurg. 1993 Jun;95(2):115-20. doi: 10.1016/0303-8467(93)90004-z. Clin Neurol Neurosurg. 1993. PMID: 8344008
L-2-hydroxyglutaric aciduria and lactic acidosis.
Barth PG, Wanders RJ, Scholte HR, Abeling N, Jakobs C, Schutgens RB, Vreken P. Barth PG, et al. Among authors: schutgens rb. J Inherit Metab Dis. 1998 Jun;21(3):251-4. doi: 10.1023/a:1005316121584. J Inherit Metab Dis. 1998. PMID: 9686369 No abstract available.
205 results