Stenzel W - Search Results

1

Pathophysiology of protein aggregation and extended phenotyping in filaminopathy.

Kley RA, Serdaroglu-Oflazer P, Leber Y, Odgerel Z, van der Ven PF, Olivé M, Ferrer I, Onipe A, Mihaylov M, Bilbao JM, Lee HS, Höhfeld J, Djinović-Carugo K, Kong K, Tegenthoff M, Peters SA, Stenzel W, Vorgerd M, Goldfarb LG, Fürst DO. Kley RA, et al. Among authors: stenzel w. Brain. 2012 Sep;135(Pt 9):2642-60. doi: 10.1093/brain/aws200. Brain. 2012. PMID: 22961544 Free PMC article.

2

Th2-M2 immunity in lesions of muscular sarcoidosis and macrophagic myofasciitis.

Preusse C, Goebel HH, Pehl D, Rinnenthal JL, Kley RA, Allenbach Y, Heppner FL, Vorgerd M, Authier FJ, Gherardi R, Stenzel W. Preusse C, et al. Among authors: stenzel w. Neuropathol Appl Neurobiol. 2015 Dec;41(7):952-63. doi: 10.1111/nan.12231. Epub 2015 May 19. Neuropathol Appl Neurobiol. 2015. PMID: 25711697

3

Kyphoscoliosis peptidase (KY) mutation causes a novel congenital myopathy with core targetoid defects.

Straussberg R, Schottmann G, Sadeh M, Gill E, Seifert F, Halevy A, Qassem K, Rendu J, van der Ven PF, Stenzel W, Schuelke M. Straussberg R, et al. Among authors: stenzel w. Acta Neuropathol. 2016 Sep;132(3):475-8. doi: 10.1007/s00401-016-1602-9. Epub 2016 Aug 2. Acta Neuropathol. 2016. PMID: 27484770 No abstract available.

4

JAK inhibitor improves type I interferon induced damage: proof of concept in dermatomyositis.

Ladislau L, Suárez-Calvet X, Toquet S, Landon-Cardinal O, Amelin D, Depp M, Rodero MP, Hathazi D, Duffy D, Bondet V, Preusse C, Bienvenu B, Rozenberg F, Roos A, Benjamim CF, Gallardo E, Illa I, Mouly V, Stenzel W, Butler-Browne G, Benveniste O, Allenbach Y. Ladislau L, et al. Among authors: stenzel w. Brain. 2018 Jun 1;141(6):1609-1621. doi: 10.1093/brain/awy105. Brain. 2018. PMID: 29741608

5

ANO5-related muscle diseases: From clinics and genetics to pathology and research strategies.

Christiansen J, Güttsches AK, Schara-Schmidt U, Vorgerd M, Heute C, Preusse C, Stenzel W, Roos A. Christiansen J, et al. Among authors: stenzel w. Genes Dis. 2022 Feb 14;9(6):1506-1520. doi: 10.1016/j.gendis.2022.01.001. eCollection 2022 Nov. Genes Dis. 2022. PMID: 36157496 Free PMC article. Review.

6

Nuclear actin aggregation is a hallmark of anti-synthetase syndrome-induced dysimmune myopathy.

Stenzel W, Preuße C, Allenbach Y, Pehl D, Junckerstorff R, Heppner FL, Nolte K, Aronica E, Kana V, Rushing E, Schneider U, Claeys KG, Benveniste O, Weis J, Goebel HH. Stenzel W, et al. Neurology. 2015 Mar 31;84(13):1346-54. doi: 10.1212/WNL.0000000000001422. Epub 2015 Mar 6. Neurology. 2015. PMID: 25746564 Free article.

7

Phosphorylated α-synuclein in skin nerve fibres differentiates Parkinson's disease from multiple system atrophy.

Zange L, Noack C, Hahn K, Stenzel W, Lipp A. Zange L, et al. Among authors: stenzel w. Brain. 2015 Aug;138(Pt 8):2310-21. doi: 10.1093/brain/awv138. Epub 2015 May 27. Brain. 2015. PMID: 26017579

8

Anti-Jo-1 antibody-positive patients show a characteristic necrotizing perifascicular myositis.

Mescam-Mancini L, Allenbach Y, Hervier B, Devilliers H, Mariampillay K, Dubourg O, Maisonobe T, Gherardi R, Mezin P, Preusse C, Stenzel W, Benveniste O. Mescam-Mancini L, et al. Among authors: stenzel w. Brain. 2015 Sep;138(Pt 9):2485-92. doi: 10.1093/brain/awv192. Epub 2015 Jul 21. Brain. 2015. PMID: 26198592

9

MORC2 mutation causes severe spinal muscular atrophy-phenotype, cerebellar atrophy, and diaphragmatic paralysis.

Schottmann G, Wagner C, Seifert F, Stenzel W, Schuelke M. Schottmann G, et al. Among authors: stenzel w. Brain. 2016 Dec;139(Pt 12):e70. doi: 10.1093/brain/aww252. Epub 2016 Oct 29. Brain. 2016. PMID: 27794525 No abstract available.

10

1st ENMC European meeting: The EURO-NMD pathology working group Recommended Standards for Muscle Pathology Amsterdam, The Netherlands, 7 December 2018.

Udd B, Stenzel W, Oldfors A, Olivé M, Romero N, Lammens M, Kusters B, Sewry C, Goebel HH, Evangelista T. Udd B, et al. Among authors: stenzel w. Neuromuscul Disord. 2019 Jun;29(6):483-485. doi: 10.1016/j.nmd.2019.03.002. Epub 2019 Mar 15. Neuromuscul Disord. 2019. PMID: 31101462 No abstract available.

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