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The Moya-Moya syndrome: a report of two children.
van Erven PM, Gabreëls FJ, Thijssen HO, Renier WO. van Erven PM, et al. Clin Neurol Neurosurg. 1982;84(3):179-89. doi: 10.1016/0303-8467(82)90041-5. Clin Neurol Neurosurg. 1982. PMID: 6295682
Defect of NADH dehydrogenase in Leigh syndrome.
Van Erven PM, Fischer JC, Gabreëls FJ, Renier WO, Trijbels JM, Janssen AJ. Van Erven PM, et al. Acta Neurol Scand. 1986 Aug;74(2):167. doi: 10.1111/j.1600-0404.1986.tb04646.x. Acta Neurol Scand. 1986. PMID: 3776463 No abstract available.
Neurophysiological studies in the Leigh syndrome.
Van Erven PM, Colon EJ, Gabreëls FJ, Renier WO, Vingerhoets DM. Van Erven PM, et al. Brain Dev. 1986;8(6):590-5. doi: 10.1016/s0387-7604(86)80004-3. Brain Dev. 1986. PMID: 3826550
Intravenous pyruvate loading test in Leigh syndrome.
Van Erven PM, Gabreëls FJ, Wevers RA, Doesburg WH, Ruitenbeek W, Renier WO, Lamers KJ. Van Erven PM, et al. J Neurol Sci. 1987 Feb;77(2-3):217-27. doi: 10.1016/0022-510x(87)90124-9. J Neurol Sci. 1987. PMID: 3819766
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