Neudecker S - Search Results

1

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: neudecker s. Brain. 2005 Aug;128(Pt 8):1870-6. doi: 10.1093/brain/awh540. Epub 2005 May 18. Brain. 2005. PMID: 15901649

2

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: neudecker s. 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.

3

Babinski-Nageotte's syndrome and Hemimedullary (Reinhold's) syndrome are clinically and morphologically distinct conditions.

Krasnianski M, Neudecker S, Schluter A, Zierz S. Krasnianski M, et al. Among authors: neudecker s. J Neurol. 2003 Aug;250(8):938-42. doi: 10.1007/s00415-003-1118-9. J Neurol. 2003. PMID: 12928912

4

Typical facioscapulohumeral dystrophy phenotype in patients without FSHD 4q35 deletion.

Krasnianski M, Neudecker S, Eger K, Jakubiczka S, Zierz S. Krasnianski M, et al. Among authors: neudecker s. J Neurol. 2003 Sep;250(9):1084-7. doi: 10.1007/s00415-003-0158-5. J Neurol. 2003. PMID: 14504970

5

Atypical phenotypes in patients with facioscapulohumeral muscular dystrophy 4q35 deletion.

Krasnianski M, Eger K, Neudecker S, Jakubiczka S, Zierz S. Krasnianski M, et al. Among authors: neudecker s. Arch Neurol. 2003 Oct;60(10):1421-5. doi: 10.1001/archneur.60.10.1421. Arch Neurol. 2003. PMID: 14568813 Clinical Trial.

6

Rimmed vacuoles in facioscapulohumeral muscular dystrophy: a unique ultrastructural feature.

Neudecker S, Krasnianski M, Bahn E, Zierz S. Neudecker S, et al. Acta Neuropathol. 2004 Sep;108(3):257-9. doi: 10.1007/s00401-004-0894-3. Epub 2004 Jun 24. Acta Neuropathol. 2004. PMID: 15221332

7

Alfred Hauptmann, Siegfried Thannhauser, and an endangered muscular disorder.

Krasnianski M, Ehrt U, Neudecker S, Zierz S. Krasnianski M, et al. Among authors: neudecker s. Arch Neurol. 2004 Jul;61(7):1139-41. doi: 10.1001/archneur.61.7.1139. Arch Neurol. 2004. PMID: 15262752 No abstract available.

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. Among authors: neudecker s. 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

Yawning despite trismus in a patient with locked-in syndrome caused by a thrombosed megadolichobasilar artery.

Krasnianski M, Gaul C, Neudecker S, Behrmann C, Schlüter A, Winterholler M. Krasnianski M, et al. Among authors: neudecker s. Clin Neurol Neurosurg. 2003 Dec;106(1):44-6. doi: 10.1016/s0303-8467(03)00045-3. Clin Neurol Neurosurg. 2003. PMID: 14643917

10

Isolated bilateral blindness as the sole manifestation of transient ischaemic attacks.

Krasnianski M, Bau V, Neudecker S, Lindner A, Zierz S. Krasnianski M, et al. Among authors: neudecker s. Acta Ophthalmol Scand. 2006 Jun;84(3):415-8. doi: 10.1111/j.1600-0420.2006.00635.x. Acta Ophthalmol Scand. 2006. PMID: 16704710 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

52 results

Search Page

Filters