Müller T - Search Results

1

Lactate increase and oxygen desaturation in mitochondrial disorders--evaluation of two diagnostic screening protocols.

Hanisch F, Müller T, Muser A, Deschauer M, Zierz S. Hanisch F, et al. Among authors: muller t. J Neurol. 2006 Apr;253(4):417-23. doi: 10.1007/s00415-006-0987-0. Epub 2006 Apr 20. J Neurol. 2006. PMID: 16619117

2

Increased metabolic muscle fatigue is caused by some but not all mitochondrial mutations.

Schulte-Mattler WJ, Müller T, Deschauer M, Gellerich FN, Iaizzo PA, Zierz S. Schulte-Mattler WJ, et al. Among authors: muller t. Arch Neurol. 2003 Jan;60(1):50-8. doi: 10.1001/archneur.60.1.50. Arch Neurol. 2003. PMID: 12533088

3

Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutation.

Deschauer M, Müller T, Wieser T, Schulte-Mattler W, Kornhuber M, Zierz S. Deschauer M, et al. Among authors: muller t. Arch Neurol. 2001 Nov;58(11):1885-8. doi: 10.1001/archneur.58.11.1885. Arch Neurol. 2001. PMID: 11708999

4

Phenotype of matrin-3-related distal myopathy in 16 German patients.

Müller TJ, Kraya T, Stoltenburg-Didinger G, Hanisch F, Kornhuber M, Stoevesandt D, Senderek J, Weis J, Baum P, Deschauer M, Zierz S. Müller TJ, et al. Ann Neurol. 2014 Nov;76(5):669-80. doi: 10.1002/ana.24255. Epub 2014 Sep 16. Ann Neurol. 2014. PMID: 25154462

5

Mitochondrial respiratory rates and activities of respiratory chain complexes correlate linearly with heteroplasmy of deleted mtDNA without threshold and independently of deletion size.

Gellerich FN, Deschauer M, Chen Y, Müller T, Neudecker S, Zierz S. Gellerich FN, et al. Among authors: muller t. Biochim Biophys Acta. 2002 Oct 3;1556(1):41-52. doi: 10.1016/s0005-2728(02)00305-5. Biochim Biophys Acta. 2002. PMID: 12351217 Free article.

6

Energetic depression caused by mitochondrial dysfunction.

Gellerich FN, Trumbeckaite S, Müller T, Deschauer M, Chen Y, Gizatullina Z, Zierz S. Gellerich FN, et al. Among authors: muller t. Mol Cell Biochem. 2004 Jan-Feb;256-257(1-2):391-405. doi: 10.1023/b:mcbi.0000009885.34498.e6. Mol Cell Biochem. 2004. PMID: 14977198 Review.

7

Mitochondrial changes in skeletal muscle in amyotrophic lateral sclerosis and other neurogenic atrophies.

Krasnianski A, Deschauer M, Neudecker S, Gellerich FN, Müller T, Schoser BG, Krasnianski M, Zierz S. Krasnianski A, et al. Among authors: muller t. Brain. 2005 Aug;128(Pt 8):1870-6. doi: 10.1093/brain/awh540. Epub 2005 May 18. Brain. 2005. PMID: 15901649

8

Late-onset mitochondrial myopathy with dystrophic changes due to a G7497A mutation in the mitochondrial tRNA(Ser(UCN)) gene.

Müller T, Deschauer M, Neudecker S, Zierz S. Müller T, et al. Acta Neuropathol. 2005 Oct;110(4):426-30. doi: 10.1007/s00401-005-1063-z. Epub 2005 Aug 25. Acta Neuropathol. 2005. PMID: 16133542

9

Between Wallenberg syndrome and hemimedullary lesion: Cestan-Chenais and Babinski-Nageotte syndromes in medullary infarctions.

Krasnianski M, Müller T, Stock K, Zierz S. Krasnianski M, et al. Among authors: muller t. J Neurol. 2006 Nov;253(11):1442-6. doi: 10.1007/s00415-006-0231-3. Epub 2006 Jun 14. J Neurol. 2006. PMID: 16775654

10

Pseudo-Popeye syndrome: extramedullary plasmacytoma manifesting in skeletal muscle.

Schneider I, Müller T, Stoltenburg G, Holzhausen HJ, Mawrin C, Hanisch F. Schneider I, et al. Among authors: muller t. Neurology. 2014 Feb 11;82(6):544-5. doi: 10.1212/WNL.0000000000000099. Neurology. 2014. PMID: 24514010 No abstract available.

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