Winkler K - Search Results

1

mtDNA depletion and impairment of mitochondrial function in a case of a multisystem disorder including severe myopathy.

Kirches EJ, Winkler K, Warich-Kirches M, Szibor R, Wien F, Kunz WS, von Bossanyi P, Bajaj PK, Dietzmann K. Kirches EJ, et al. Among authors: winkler k. J Inherit Metab Dis. 1998 Jun;21(4):400-8. doi: 10.1023/a:1005306725644. J Inherit Metab Dis. 1998. PMID: 9700597

2

Detection of mitochondrial defects by laser fluorimetry.

Kunz WS, Winkler K, Kuznetsov AV, Lins H, Kirches E, Wallesch CW. Kunz WS, et al. Among authors: winkler k. Mol Cell Biochem. 1997 Sep;174(1-2):97-100. Mol Cell Biochem. 1997. PMID: 9309672

3

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: winkler k. Pathobiology. 1999 Jul-Aug;67(4):214-8. doi: 10.1159/000028075. Pathobiology. 1999. PMID: 10738184

4

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. 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.

5

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: winkler k. 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.

6

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: winkler k. J Neurol Sci. 1998;156(1):65-72. doi: 10.1016/s0022-510x(98)00008-2. J Neurol Sci. 1998. PMID: 9559989

7

Use of saponin-permeabilized muscle fibers for the diagnosis of mitochondrial diseases.

Kuznetsov AV, Wiedemann FR, Winkler K, Kunz WS. Kuznetsov AV, et al. Among authors: winkler k. Biofactors. 1998;7(3):221-3. doi: 10.1002/biof.5520070312. Biofactors. 1998. PMID: 9568252 Review. No abstract available.

8

Impaired mitochondrial oxidative phosphorylation in skeletal muscle of the dystrophin-deficient mdx mouse.

Kuznetsov AV, Winkler K, Wiedemann FR, von Bossanyi P, Dietzmann K, Kunz WS. Kuznetsov AV, et al. Among authors: winkler k. Mol Cell Biochem. 1998 Jun;183(1-2):87-96. doi: 10.1023/a:1006868130002. Mol Cell Biochem. 1998. PMID: 9655182

9

Loss of heteroplasmy in the displacement loop of brain mitochondrial DNA in astrocytic tumors.

Kirches E, Michael M, Woy C, Schneider T, Warich-Kirches M, Schneider-Stock R, Winkler K, Wittig H, Dietzmann K. Kirches E, et al. Among authors: winkler k. Genes Chromosomes Cancer. 1999 Sep;26(1):80-3. doi: 10.1002/(sici)1098-2264(199909)26:1<80::aid-gcc11>3.0.co;2-4. Genes Chromosomes Cancer. 1999. PMID: 10441009

10

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: winkler k. Brain. 2000 Jul;123 ( Pt 7):1339-48. doi: 10.1093/brain/123.7.1339. Brain. 2000. PMID: 10869047 Clinical Trial.

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