Schneider I - Search Results

1

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

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

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.

5

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.

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

An integrative correlation of myopathology, phenotype and genotype in late onset Pompe disease.

Kulessa M, Weyer-Menkhoff I, Viergutz L, Kornblum C, Claeys KG, Schneider I, Plöckinger U, Young P, Boentert M, Vielhaber S, Mawrin C, Bergmann M, Weis J, Ziagaki A, Stenzel W, Deschauer M, Nolte D, Hahn A, Schoser B, Schänzer A. Kulessa M, et al. Among authors: schneider i. Neuropathol Appl Neurobiol. 2020 Jun;46(4):359-374. doi: 10.1111/nan.12580. Epub 2019 Oct 24. Neuropathol Appl Neurobiol. 2020. PMID: 31545528

10

Bi-allelic truncating mutations in VWA1 cause neuromyopathy.

Deschauer M, Hengel H, Rupprich K, Kreiß M, Schlotter-Weigel B, Grimmel M, Admard J, Schneider I, Alhaddad B, Gazou A, Sturm M, Vorgerd M, Balousha G, Balousha O, Falna M, Kirschke JS, Kornblum C, Jordan B, Kraya T, Strom TM, Weis J, Schöls L, Schara U, Zierz S, Riess O, Meitinger T, Haack TB. Deschauer M, et al. Among authors: schneider i. Brain. 2021 Mar 3;144(2):574-583. doi: 10.1093/brain/awaa418. Brain. 2021. PMID: 33459760

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