Löscher WN - Search Results

1

Finsterer J, Löscher WN, Wanschitz J, Iglseder S. Finsterer J, et al. Among authors: loscher wn. J Neuromuscul Dis. 2021;8(1):1-23. doi: 10.3233/JND-200518. J Neuromuscul Dis. 2021. PMID: 32986679 Free PMC article. Review.

2

Influence of disposable, concentric needle electrodes on muscle enzyme and lactate serum levels.

Finsterer J, Mittendorfer B, Neuhuber W, Löscher WN. Finsterer J, et al. Among authors: loscher wn. J Electromyogr Kinesiol. 2002 Aug;12(4):329-37. doi: 10.1016/s1050-6411(02)00006-8. J Electromyogr Kinesiol. 2002. PMID: 12121689

3

Morvan's syndrome: clinical, laboratory, and in vitro electrophysiological studies.

Löscher WN, Wanschitz J, Reiners K, Quasthoff S. Löscher WN, et al. Muscle Nerve. 2004 Aug;30(2):157-63. doi: 10.1002/mus.20081. Muscle Nerve. 2004. PMID: 15266630

4

Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome.

Luoma PT, Luo N, Löscher WN, Farr CL, Horvath R, Wanschitz J, Kiechl S, Kaguni LS, Suomalainen A. Luoma PT, et al. Among authors: loscher wn. Hum Mol Genet. 2005 Jul 15;14(14):1907-20. doi: 10.1093/hmg/ddi196. Epub 2005 May 25. Hum Mol Genet. 2005. PMID: 15917273

5

Acute motor and sensory axonal neuropathy in Burkitt-like lymphoma.

Wanschitz J, Dichtl W, Budka H, Löscher WN, Boesch S. Wanschitz J, et al. Among authors: loscher wn. Muscle Nerve. 2006 Oct;34(4):494-8. doi: 10.1002/mus.20569. Muscle Nerve. 2006. PMID: 16671108

6

Clinical and electrophysiological features in Charcot-Marie-Tooth disease with mutations in the NEFL gene.

Miltenberger-Miltenyi G, Janecke AR, Wanschitz JV, Timmerman V, Windpassinger C, Auer-Grumbach M, Löscher WN. Miltenberger-Miltenyi G, et al. Among authors: loscher wn. Arch Neurol. 2007 Jul;64(7):966-70. doi: 10.1001/archneur.64.7.966. Arch Neurol. 2007. PMID: 17620486

7

Endothelial and myogenic differentiation of hematopoietic progenitor cells in inflammatory myopathies.

Hollemann D, Budka H, Löscher WN, Yanagida G, Fischer MB, Wanschitz JV. Hollemann D, et al. Among authors: loscher wn. J Neuropathol Exp Neurol. 2008 Jul;67(7):711-9. doi: 10.1097/NEN.0b013e31817d8064. J Neuropathol Exp Neurol. 2008. PMID: 18596542

8

Intrathecal anti-alphaB-crystallin IgG antibody responses: potential inflammatory markers in Guillain-Barré syndrome.

Wanschitz J, Ehling R, Löscher WN, Künz B, Deisenhammer F, Kuhle J, Budka H, Reindl M, Berger T. Wanschitz J, et al. Among authors: loscher wn. J Neurol. 2008 Jun;255(6):917-24. doi: 10.1007/s00415-008-0815-9. Epub 2008 Jul 11. J Neurol. 2008. PMID: 18712293

9

Identification and in silico analysis of 14 novel GJB1, MPZ and PMP22 gene mutations.

Miltenberger-Miltenyi G, Schwarzbraun T, Löscher WN, Wanschitz J, Windpassinger C, Duba HC, Seidl R, Albrecht G, Weirich-Schwaiger H, Zoller H, Utermann G, Auer-Grumbach M, Janecke AR. Miltenberger-Miltenyi G, et al. Among authors: loscher wn. Eur J Hum Genet. 2009 Sep;17(9):1154-9. doi: 10.1038/ejhg.2009.29. Epub 2009 Mar 4. Eur J Hum Genet. 2009. PMID: 19259128 Free PMC article.

10

Anti-alpha B-crystallin immunoreactivity in Guillain-Barré syndrome and chronic inflammatory demyelinating polyneuropathy.

Hegen H, Wanschitz J, Ehling R, Deisenhammer F, Löscher WN, Reindl M, Berger T. Hegen H, et al. Among authors: loscher wn. J Peripher Nerv Syst. 2010 Jun;15(2):150-2. doi: 10.1111/j.1529-8027.2010.00264.x. J Peripher Nerv Syst. 2010. PMID: 20626779 No abstract available.

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