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Items: 13

1.

NXY-059 for acute ischemic stroke.

Lees KR, Zivin JA, Ashwood T, Davalos A, Davis SM, Diener HC, Grotta J, Lyden P, Shuaib A, Hårdemark HG, Wasiewski WW; Stroke-Acute Ischemic NXY Treatment (SAINT I) Trial Investigators.

N Engl J Med. 2006 Feb 9;354(6):588-600.

2.

Clomethiazole acute stroke study (CLASS): results of a randomized, controlled trial of clomethiazole versus placebo in 1360 acute stroke patients.

Wahlgren NG, Ranasinha KW, Rosolacci T, Franke CL, van Erven PM, Ashwood T, Claesson L.

Stroke. 1999 Jan;30(1):21-8.

3.

Hypokinesia and rigidity as clinical manifestations of mitochondrial encephalomyopathy: report of three cases.

van Erven PM, Renier WO, Gabreëls FJ, Thijssen HO, Ruitenbeek W, Horstink MW.

Dev Med Child Neurol. 1989 Feb;31(1):81-91.

PMID:
2537772
4.

A mitochondrial encephalomyopathy with a partial cytochrome c oxidase deficiency of muscle.

Van Erven PM, Gabreëls FJ, Ruitenbeek W, Renier WO, Ter Laak HJ, Stadhouders AM.

J Neurol Neurosurg Psychiatry. 1988 May;51(5):704-8.

5.

Mitochondrial encephalomyopathy. Association with an NADH dehydrogenase deficiency.

van Erven PM, Gabreëls FJ, Ruitenbeek W, Renier WO, Fischer JC.

Arch Neurol. 1987 Jul;44(7):775-8.

PMID:
3593065
6.

Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brain.

van Erven PM, Gabreëls FJ, Ruitenbeek W, Renier WO, Lamers KJ, Sloof JL.

J Neurol. 1987 May;234(4):215-9.

PMID:
3612192
7.

Intravenous pyruvate loading test in Leigh syndrome.

Van Erven PM, Gabreëls FJ, Wevers RA, Doesburg WH, Ruitenbeek W, Renier WO, Lamers KJ.

J Neurol Sci. 1987 Feb;77(2-3):217-27.

PMID:
3819766
8.

Leigh syndrome, a mitochondrial encephalo(myo)pathy. A review of the literature.

van Erven PM, Cillessen JP, Eekhoff EM, Gabreëls FJ, Doesburg WH, Lemmens WA, Slooff JL, Renier WO, Ruitenbeek W.

Clin Neurol Neurosurg. 1987;89(4):217-30. Review.

PMID:
3319345
9.

Defect of NADH dehydrogenase in Leigh syndrome.

Van Erven PM, Fischer JC, Gabreëls FJ, Renier WO, Trijbels JM, Janssen AJ.

Acta Neurol Scand. 1986 Aug;74(2):167. No abstract available.

PMID:
3776463
10.

Disturbed oxidative metabolism in subacute necrotizing encephalomyelopathy (Leigh syndrome).

van Erven PM, Ruitenbeek W, Gabreëls FJ, Renier WO, Fischer JC, Janssen AJ.

Neuropediatrics. 1986 Feb;17(1):28-32.

PMID:
3008021
11.

Neurophysiological studies in the Leigh syndrome.

Van Erven PM, Colon EJ, Gabreëls FJ, Renier WO, Vingerhoets DM.

Brain Dev. 1986;8(6):590-5.

PMID:
3826550
12.

Subacute necrotizing encephalomyelopathy (Leigh syndrome) associated with disturbed oxidation of pyruvate, malate and 2-oxoglutarate in muscle and liver.

Van Erven PM, Gabreëls FJ, Ruitenbeek W, Den Hartog MR, Fischer JC, Renier WO, Trijbels JM, Slooff JL, Janssen AJ.

Acta Neurol Scand. 1985 Jul;72(1):36-42.

PMID:
4050316
13.

The Moya-Moya syndrome: a report of two children.

van Erven PM, Gabreëls FJ, Thijssen HO, Renier WO.

Clin Neurol Neurosurg. 1982;84(3):179-89.

PMID:
6295682

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