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

2

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: dietzmann k. J Inherit Metab Dis. 1998 Jun;21(4):400-8. doi: 10.1023/a:1005306725644. J Inherit Metab Dis. 1998. PMID: 9700597

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: dietzmann k. 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

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: dietzmann k. Mol Cell Biochem. 1998 Jun;183(1-2):87-96. doi: 10.1023/a:1006868130002. Mol Cell Biochem. 1998. PMID: 9655182

5

Expression of matrix metalloproteinases in a series of 12 meningiomas.

Kirches E, Grunewald J, von Bossanyi P, Szibor R, Plate I, Krüger S, Warich-Kirches M, Dietzmann K. Kirches E, et al. Among authors: dietzmann k. Clin Neuropathol. 2001 Jan-Feb;20(1):26-30. Clin Neuropathol. 2001. PMID: 11220692

6

Heterogeneous tissue distribution of a mitochondrial DNA polymorphism in heteroplasmic subjects without mitochondrial disorders.

Kirches E, Michael M, Warich-Kirches M, Schneider T, Weis S, Krause G, Mawrin C, Dietzmann K. Kirches E, et al. Among authors: dietzmann k. J Med Genet. 2001 May;38(5):312-7. doi: 10.1136/jmg.38.5.312. J Med Genet. 2001. PMID: 11333867 Free PMC article.

7

High frequency of mitochondrial DNA mutations in glioblastoma multiforme identified by direct sequence comparison to blood samples.

Kirches E, Krause G, Warich-Kirches M, Weis S, Schneider T, Meyer-Puttlitz B, Mawrin C, Dietzmann K. Kirches E, et al. Among authors: dietzmann k. Int J Cancer. 2001 Aug 15;93(4):534-8. doi: 10.1002/ijc.1375. Int J Cancer. 2001. PMID: 11477557

8

Comparison between mitochondrial DNA sequences in low grade astrocytomas and corresponding blood samples.

Kirches E, Krause G, Weis S, Mawrin C, Dietzmann K. Kirches E, et al. Among authors: dietzmann k. Mol Pathol. 2002 Jun;55(3):204-6. doi: 10.1136/mp.55.3.204. Mol Pathol. 2002. PMID: 12032233 Free PMC article.

9

Re-evaluation of the dysfunction of mitochondrial respiratory chain in skeletal muscle of patients with Parkinson's disease.

Winkler-Stuck K, Kirches E, Mawrin C, Dietzmann K, Lins H, Wallesch CW, Kunz WS, Wiedemann FR. Winkler-Stuck K, et al. Among authors: dietzmann k. J Neural Transm (Vienna). 2005 Apr;112(4):499-518. doi: 10.1007/s00702-004-0195-y. Epub 2004 Aug 3. J Neural Transm (Vienna). 2005. PMID: 15340872

10

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: dietzmann 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

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