Schröder R - Search Results

1

Multisystem disorder and limb girdle muscular dystrophy caused by LMNA p.R28W mutation.

Türk M, Wehnert M, Schröder R, Chevessier F. Türk M, et al. Among authors: schroder r. Neuromuscul Disord. 2013 Jul;23(7):587-90. doi: 10.1016/j.nmd.2013.04.008. Epub 2013 Jun 6. Neuromuscul Disord. 2013. PMID: 23746545

2

Downstream effects of plectin mutations in epidermolysis bullosa simplex with muscular dystrophy.

Winter L, Türk M, Harter PN, Mittelbronn M, Kornblum C, Norwood F, Jungbluth H, Thiel CT, Schlötzer-Schrehardt U, Schröder R. Winter L, et al. Among authors: schroder r. Acta Neuropathol Commun. 2016 Apr 27;4(1):44. doi: 10.1186/s40478-016-0314-7. Acta Neuropathol Commun. 2016. PMID: 27121971 Free PMC article.

3

Compound heterozygous RYR1 mutations in a preterm with arthrogryposis multiplex congenita and prenatal CNS bleeding.

Brackmann F, Türk M, Gratzki N, Rompel O, Jungbluth H, Schröder R, Trollmann R. Brackmann F, et al. Among authors: schroder r. Neuromuscul Disord. 2018 Jan;28(1):54-58. doi: 10.1016/j.nmd.2017.09.009. Epub 2017 Sep 28. Neuromuscul Disord. 2018. PMID: 29169929

4

Perivascular hemosiderin deposits in human skeletal muscle tissue.

Delbridge C, Türk M, Agaimy A, Winterholler M, Schröder R. Delbridge C, et al. Among authors: schroder r. Neuromuscul Disord. 2018 Jun;28(6):538-539. doi: 10.1016/j.nmd.2018.04.004. Epub 2018 Apr 16. Neuromuscul Disord. 2018. PMID: 29724544 No abstract available.

5

Diaphragmatic dysfunction as the presenting symptom in neuromuscular disorders: A retrospective longitudinal study of etiology and outcome in 30 German patients.

Türk M, Weber I, Vogt-Ladner G, Schröder R, Winterholler M. Türk M, et al. Among authors: schroder r. Neuromuscul Disord. 2018 Jun;28(6):484-490. doi: 10.1016/j.nmd.2018.04.001. Epub 2018 Apr 9. Neuromuscul Disord. 2018. PMID: 29748118

6

Mutations of the LMNA gene can mimic autosomal dominant proximal spinal muscular atrophy.

Rudnik-Schöneborn S, Botzenhart E, Eggermann T, Senderek J, Schoser BG, Schröder R, Wehnert M, Wirth B, Zerres K. Rudnik-Schöneborn S, et al. Among authors: schroder r. Neurogenetics. 2007 Apr;8(2):137-42. doi: 10.1007/s10048-006-0070-0. Epub 2006 Nov 29. Neurogenetics. 2007. PMID: 17136397

7

C9ORF72-ALS: P62- and ubiquitin-aggregation pathology in skeletal muscle.

Türk M, Haaker G, Winter L, Just W, Nickel FT, Linker RA, Chevessier F, Schröder R. Türk M, et al. Among authors: schroder r. Muscle Nerve. 2014 Sep;50(3):454-5. doi: 10.1002/mus.24283. Muscle Nerve. 2014. PMID: 24817207 No abstract available.

8

Myofibrillar instability exacerbated by acute exercise in filaminopathy.

Chevessier F, Schuld J, Orfanos Z, Plank AC, Wolf L, Maerkens A, Unger A, Schlötzer-Schrehardt U, Kley RA, Von Hörsten S, Marcus K, Linke WA, Vorgerd M, van der Ven PF, Fürst DO, Schröder R. Chevessier F, et al. Among authors: schroder r. Hum Mol Genet. 2015 Dec 20;24(25):7207-20. doi: 10.1093/hmg/ddv421. Epub 2015 Oct 15. Hum Mol Genet. 2015. PMID: 26472074

9

Stroke in Duchenne Muscular Dystrophy: A Retrospective Longitudinal Study in 54 Patients.

Winterholler M, Holländer C, Kerling F, Weber I, Dittrich S, Türk M, Schröder R. Winterholler M, et al. Among authors: schroder r. Stroke. 2016 Aug;47(8):2123-6. doi: 10.1161/STROKEAHA.116.013678. Epub 2016 Jun 28. Stroke. 2016. PMID: 27354222

10

VCP-related multisystem proteinopathy presenting as early-onset Parkinson disease.

Regensburger M, Türk M, Pagenstecher A, Schröder R, Winkler J. Regensburger M, et al. Among authors: schroder r. Neurology. 2017 Aug 15;89(7):746-748. doi: 10.1212/WNL.0000000000004240. Epub 2017 Jul 19. Neurology. 2017. PMID: 28724584 No abstract available.

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