Feistner H - Search Results

1

Mitochondrial tRNA(Cys) mutation A5823G in a patient with motor neuron disease and temporal lobe epilepsy.

Kirches E, Winkler K, Vielhaber S, Michael M, Warich-Kirches M, von Bossanyi P, Plate I, Kunz WS, Szibor R, Feistner H, Dietzmann K. Kirches E, et al. Among authors: feistner h. Pathobiology. 1999 Jul-Aug;67(4):214-8. doi: 10.1159/000028075. Pathobiology. 1999. PMID: 10738184

2

Mitochondrial DNA abnormalities in skeletal muscle of patients with sporadic amyotrophic lateral sclerosis.

Vielhaber S, Kunz D, Winkler K, Wiedemann FR, Kirches E, Feistner H, Heinze HJ, Elger CE, Schubert W, Kunz WS. Vielhaber S, et al. Among authors: feistner h. Brain. 2000 Jul;123 ( Pt 7):1339-48. doi: 10.1093/brain/123.7.1339. Brain. 2000. PMID: 10869047 Clinical Trial.

3

Laser-excited fluorescence studies of mitochondrial function in saponin-skinned skeletal muscle fibers of patients with chronic progressive external ophthalmoplegia.

Winkler K, Kuznetsov AV, Lins H, Kirches E, von Bossanyi P, Dietzmann K, Frank B, Feistner H, Kunz WS. Winkler K, et al. Among authors: feistner h. Biochim Biophys Acta. 1995 Dec 12;1272(3):181-4. doi: 10.1016/0925-4439(95)00085-2. Biochim Biophys Acta. 1995. PMID: 8541350 Free article.

4

Impairment of mitochondrial function in skeletal muscle of patients with amyotrophic lateral sclerosis.

Wiedemann FR, Winkler K, Kuznetsov AV, Bartels C, Vielhaber S, Feistner H, Kunz WS. Wiedemann FR, et al. Among authors: feistner h. J Neurol Sci. 1998;156(1):65-72. doi: 10.1016/s0022-510x(98)00008-2. J Neurol Sci. 1998. PMID: 9559989

5

Mitochondrial complex I deficiency in a female with multiplex arthrogryposis congenita.

Vielhaber S, Feistner H, Schneider W, Weis J, Kunz WS. Vielhaber S, et al. Among authors: feistner h. Pediatr Neurol. 2000 Jan;22(1):53-6. doi: 10.1016/s0887-8994(99)00097-1. Pediatr Neurol. 2000. PMID: 10669207

6

Defective mitochondrial oxidative phosphorylation in myopathies with tubular aggregates originating from sarcoplasmic reticulum.

Vielhaber S, Schröder R, Winkler K, Weis S, Sailer M, Feistner H, Heinze HJ, Schröder JM, Kunz WS. Vielhaber S, et al. Among authors: feistner h. J Neuropathol Exp Neurol. 2001 Nov;60(11):1032-40. doi: 10.1093/jnen/60.11.1032. J Neuropathol Exp Neurol. 2001. PMID: 11706933

7

Effect of creatine supplementation on metabolite levels in ALS motor cortices.

Vielhaber S, Kaufmann J, Kanowski M, Sailer M, Feistner H, Tempelmann C, Elger CE, Heinze HJ, Kunz WS. Vielhaber S, et al. Among authors: feistner h. Exp Neurol. 2001 Dec;172(2):377-82. doi: 10.1006/exnr.2001.7797. Exp Neurol. 2001. PMID: 11716561

8

Application of inhibitor titrations for the detection of oxidative phosphorylation defects in saponin-skinned muscle fibers of patients with mitochondrial diseases.

Kuznetsov AV, Winkler K, Kirches E, Lins H, Feistner H, Kunz WS. Kuznetsov AV, et al. Among authors: feistner h. Biochim Biophys Acta. 1997 Apr 12;1360(2):142-50. doi: 10.1016/s0925-4439(96)00072-5. Biochim Biophys Acta. 1997. PMID: 9128179 Free article.

9

Frontal-executive dysfunction in early onset cerebellar ataxia of Holmes' type.

Vielhaber S, Ebert AD, Feistner H, Herrmann M. Vielhaber S, et al. Among authors: feistner h. Clin Neurol Neurosurg. 2000 Jun;102(2):102-5. doi: 10.1016/s0303-8467(00)00068-8. Clin Neurol Neurosurg. 2000. PMID: 10817897

10

Primary carnitine deficiency: adult onset lipid storage myopathy with a mild clinical course.

Vielhaber S, Feistner H, Weis J, Kreuder J, Sailer M, Schröder JM, Kunz WS. Vielhaber S, et al. Among authors: feistner h. J Clin Neurosci. 2004 Nov;11(8):919-24. doi: 10.1016/j.jocn.2003.11.019. J Clin Neurosci. 2004. PMID: 15519880

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