Schröder R - Search Results

1

Camptocormia as the presenting symptom in sporadic late onset nemaline myopathy: a case report.

Türk M, Nagel AM, Roemer F, Schlötzer-Schrehardt U, Thiel CT, Winterholler M, Schröder R. Türk M, et al. Among authors: schroder r. BMC Musculoskelet Disord. 2019 Nov 20;20(1):553. doi: 10.1186/s12891-019-2942-0. BMC Musculoskelet Disord. 2019. PMID: 31747907 Free PMC article.

2

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

3

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

4

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

5

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.

6

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.

7

²³ Na MRI depicts early changes in ion homeostasis in skeletal muscle tissue of patients with duchenne muscular dystrophy.

Gerhalter T, Gast LV, Marty B, Martin J, Trollmann R, Schüssler S, Roemer F, Laun FB, Uder M, Schröder R, Carlier PG, Nagel AM. Gerhalter T, et al. Among authors: schroder r. J Magn Reson Imaging. 2019 Oct;50(4):1103-1113. doi: 10.1002/jmri.26681. Epub 2019 Feb 4. J Magn Reson Imaging. 2019. PMID: 30719784

8

Genetic analysis of VCP and WASH complex genes in a German cohort of sporadic ALS-FTD patients.

Türk M, Schröder R, Khuller K, Hofmann A, Berwanger C, Ludolph AC, Dekomien G, Müller K, Weishaupt JH, Thiel CT, Clemen CS. Türk M, et al. Among authors: schroder r. Neurobiol Aging. 2017 Aug;56:213.e1-213.e5. doi: 10.1016/j.neurobiolaging.2017.04.023. Epub 2017 May 3. Neurobiol Aging. 2017. PMID: 28551275

9

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

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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