Türk M - Search Results

1

Plectin-related scapuloperoneal myopathy with treatment-responsive myasthenic syndrome.

Argente-Escrig H, Schultheis D, Kamm L, Schowalter M, Thiel C, Türk M, Clemen CS, Muelas N, Castañón MJ, Wiche G, Herrmann H, Vilchez JJ, Schröder R. Argente-Escrig H, et al. Among authors: turk m. Neuropathol Appl Neurobiol. 2021 Feb;47(2):352-356. doi: 10.1111/nan.12652. Epub 2020 Aug 23. Neuropathol Appl Neurobiol. 2021. PMID: 32757300 No abstract available.

2

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. 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

3

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. Muscle Nerve. 2014 Sep;50(3):454-5. doi: 10.1002/mus.24283. Muscle Nerve. 2014. PMID: 24817207 No abstract available.

4

VCP and PSMF1: Antagonistic regulators of proteasome activity.

Clemen CS, Marko M, Strucksberg KH, Behrens J, Wittig I, Gärtner L, Winter L, Chevessier F, Matthias J, Türk M, Tangavelou K, Schütz J, Arhzaouy K, Klopffleisch K, Hanisch FG, Rottbauer W, Blümcke I, Just S, Eichinger L, Hofmann A, Schröder R. Clemen CS, et al. Among authors: turk m. Biochem Biophys Res Commun. 2015 Aug 7;463(4):1210-7. doi: 10.1016/j.bbrc.2015.06.086. Epub 2015 Jun 15. Biochem Biophys Res Commun. 2015. PMID: 26086101 Free article.

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: turk m. 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

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: turk m. Stroke. 2016 Aug;47(8):2123-6. doi: 10.1161/STROKEAHA.116.013678. Epub 2016 Jun 28. Stroke. 2016. PMID: 27354222

7

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. 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

8

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: turk m. Neurology. 2017 Aug 15;89(7):746-748. doi: 10.1212/WNL.0000000000004240. Epub 2017 Jul 19. Neurology. 2017. PMID: 28724584 No abstract available.

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: turk m. 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

Perivascular hemosiderin deposits in human skeletal muscle tissue.

Delbridge C, Türk M, Agaimy A, Winterholler M, Schröder R. Delbridge C, et al. Among authors: turk m. 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.

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