Müller T - Search Results

1

Unique PABPN1 gene mutation in a large Bulgarian family with OPMD.

Mihaylova V, Müller T, Petrova I, Tournev I, Cherninkova S, Walter MC, Deschauer M. Mihaylova V, et al. Among authors: muller t. J Neurol. 2008 Apr;255(4):609-11. doi: 10.1007/s00415-008-0769-y. Epub 2008 Feb 19. J Neurol. 2008. PMID: 18274805 No abstract available.

2

Genetic heterogeneity in 30 German patients with oculopharyngeal muscular dystrophy.

Müller T, Deschauer M, Kolbe-Fehr F, Zierz S. Müller T, et al. J Neurol. 2006 Jul;253(7):892-5. doi: 10.1007/s00415-006-0126-y. Epub 2006 Apr 20. J Neurol. 2006. PMID: 16619122

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

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

5

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

6

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

7

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

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

[Familial mitochondrial chronic progressive external ophthalmoplegia. Five families with differing genetics].

Deschauer M, Müller T, Dreha S, Zierz S. Deschauer M, et al. Among authors: muller t. Nervenarzt. 2001 Feb;72(2):122-9. doi: 10.1007/s001150050724. Nervenarzt. 2001. PMID: 11256146 German.

10

Dilated cardiomyopathy may be an early sign of the C826A Fukutin-related protein mutation.

Müller T, Krasnianski M, Witthaut R, Deschauer M, Zierz S. Müller T, et al. Neuromuscul Disord. 2005 May;15(5):372-6. doi: 10.1016/j.nmd.2005.02.004. Neuromuscul Disord. 2005. PMID: 15833432

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