Schneider I - Search Results

1

Eosinophils in hereditary and inflammatory myopathies.

Schröder T, Fuchss J, Schneider I, Stoltenburg-Didinger G, Hanisch F. Schröder T, et al. Among authors: schneider i. Acta Myol. 2013 Dec;32(3):148-53. Acta Myol. 2013. PMID: 24803842 Free PMC article.

2

Respiratory function in late-onset Pompe disease patients receiving long-term enzyme replacement therapy for more than 48 months.

Schneider I, Hanisch F, Müller T, Schmidt B, Zierz S. Schneider I, et al. Wien Med Wochenschr. 2013 Jan;163(1-2):40-4. doi: 10.1007/s10354-012-0153-5. Epub 2012 Nov 19. Wien Med Wochenschr. 2013. PMID: 23160972

3

[Treatability of sporadic late onset nemaline myopathy].

Hanisch F, Schneider I, Müller T, Romeike BF, Stoltenburg G, Holzhausen HJ, Zierz S. Hanisch F, et al. Among authors: schneider i. Nervenarzt. 2013 Aug;84(8):955-61. doi: 10.1007/s00115-013-3825-5. Nervenarzt. 2013. PMID: 23836301 Review. German.

4

Mitochondrial abnormalities in myofibrillar myopathies.

Joshi PR, Hauburger A, Kley R, Claeys KG, Schneider I, Kress W, Stoltenburg G, Weis J, Vorgerd M, Deschauer M, Hanisch F. Joshi PR, et al. Among authors: schneider i. Clin Neuropathol. 2014 Mar-Apr;33(2):134-42. doi: 10.5414/NP300693. Clin Neuropathol. 2014. PMID: 24361111

5

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. Neurology. 2014 Feb 11;82(6):544-5. doi: 10.1212/WNL.0000000000000099. Neurology. 2014. PMID: 24514010 No abstract available.

6

Limb girdle muscular dystrophy type 2L presenting as necrotizing myopathy.

Schneider I, Stoltenburg G, Deschauer M, Winterholler M, Hanisch F. Schneider I, et al. Acta Myol. 2014 May;33(1):19-21. Acta Myol. 2014. PMID: 24843231 Free PMC article.

7

Long-term observation of incremental response and antibodies to voltage-gated calcium channels in patients with Lambert-Eaton myasthenic syndrome: two case reports.

Schneider I, Kornhuber ME, Hanisch F. Schneider I, et al. J Med Case Rep. 2015 Mar 14;9:59. doi: 10.1186/s13256-015-0524-9. J Med Case Rep. 2015. PMID: 25885033 Free PMC article.

8

Enzyme replacement therapy and antibodies in late-onset Pompe disease.

Schneider I, Deschauer M, Hanisch F. Schneider I, et al. Mol Genet Metab Rep. 2014 May 15;1:232-234. doi: 10.1016/j.ymgmr.2014.01.001. eCollection 2014. Mol Genet Metab Rep. 2014. PMID: 27896092 Free PMC article. No abstract available.

9

The p.S85C-mutation in MATR3 impairs stress granule formation in Matrin-3 myopathy.

Mensch A, Meinhardt B, Bley N, Hüttelmaier S, Schneider I, Stoltenburg-Didinger G, Kraya T, Müller T, Zierz S. Mensch A, et al. Among authors: schneider i. Exp Neurol. 2018 Aug;306:222-231. doi: 10.1016/j.expneurol.2018.05.012. Epub 2018 May 12. Exp Neurol. 2018. PMID: 29763601 No abstract available.

10

Associations between histogram analysis parameters derived from morphological sequences and histopathological tissue alterations in myositis and other myopathies: a preliminary study.

Meyer HJ, Schneider I, Emmer A, Kornhuber M, Surov A. Meyer HJ, et al. Among authors: schneider i. Clin Exp Rheumatol. 2021 Mar-Apr;39(2):304-309. doi: 10.55563/clinexprheumatol/a1cmel. Epub 2020 Jun 4. Clin Exp Rheumatol. 2021. PMID: 32573413

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