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Cytoplasmic body myopathy revisited.
Schuelke M, Schwarz M, Stenzel W, Goebel HH. Schuelke M, et al. Among authors: stenzel w. Neuromuscul Disord. 2018 Nov;28(11):969-971. doi: 10.1016/j.nmd.2018.08.006. Epub 2018 Aug 30. Neuromuscul Disord. 2018. PMID: 30253894 No abstract available.
[Amyloidoses in neuropathology].
Prokop S, Stenzel W, Goebel HH, Heppner FL. Prokop S, et al. Among authors: stenzel w. Pathologe. 2009 May;30(3):193-6. doi: 10.1007/s00292-009-1131-6. Pathologe. 2009. PMID: 19340430 Review. German.
Pipestem capillaries in necrotizing myopathy revisited.
Schröder NW, Goebel HH, Brandis A, Ladhoff AM, Heppner FL, Stenzel W. Schröder NW, et al. Among authors: stenzel w. Neuromuscul Disord. 2013 Jan;23(1):66-74. doi: 10.1016/j.nmd.2012.09.001. Epub 2012 Oct 25. Neuromuscul Disord. 2013. PMID: 23102899
Juvenile autophagic vacuolar myopathy - a new entity or variant?
Stenzel W, Nishino I, von Moers A, Kadry MA, Glaeser D, Heppner FL, Goebel HH. Stenzel W, et al. Neuropathol Appl Neurobiol. 2013 Jun;39(4):449-53. doi: 10.1111/nan.12018. Neuropathol Appl Neurobiol. 2013. PMID: 23324055 No abstract available.
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticity.
Hirata H, Nanda I, van Riesen A, McMichael G, Hu H, Hambrock M, Papon MA, Fischer U, Marouillat S, Ding C, Alirol S, Bienek M, Preisler-Adams S, Grimme A, Seelow D, Webster R, Haan E, MacLennan A, Stenzel W, Yap TY, Gardner A, Nguyen LS, Shaw M, Lebrun N, Haas SA, Kress W, Haaf T, Schellenberger E, Chelly J, Viot G, Shaffer LG, Rosenfeld JA, Kramer N, Falk R, El-Khechen D, Escobar LF, Hennekam R, Wieacker P, Hübner C, Ropers HH, Gecz J, Schuelke M, Laumonnier F, Kalscheuer VM. Hirata H, et al. Among authors: stenzel w. Am J Hum Genet. 2013 May 2;92(5):681-95. doi: 10.1016/j.ajhg.2013.03.021. Epub 2013 Apr 25. Am J Hum Genet. 2013. PMID: 23623388 Free PMC article.
302 results