Wattjes MP - Search Results

1

Pathological consequences of VCP mutations on human striated muscle.

Hübbers CU, Clemen CS, Kesper K, Böddrich A, Hofmann A, Kämäräinen O, Tolksdorf K, Stumpf M, Reichelt J, Roth U, Krause S, Watts G, Kimonis V, Wattjes MP, Reimann J, Thal DR, Biermann K, Evert BO, Lochmüller H, Wanker EE, Schoser BG, Noegel AA, Schröder R. Hübbers CU, et al. Among authors: wattjes mp. Brain. 2007 Feb;130(Pt 2):381-93. doi: 10.1093/brain/awl238. Epub 2006 Sep 19. Brain. 2007. PMID: 16984901

2

Distinct neuromuscular phenotypes in myotonic dystrophy types 1 and 2 : a whole body highfield MRI study.

Kornblum C, Lutterbey G, Bogdanow M, Kesper K, Schild H, Schröder R, Wattjes MP. Kornblum C, et al. Among authors: wattjes mp. J Neurol. 2006 Jun;253(6):753-61. doi: 10.1007/s00415-006-0111-5. Epub 2006 Mar 6. J Neurol. 2006. PMID: 16511650

3

Different early pathogenesis in myotilinopathy compared to primary desminopathy.

Fischer D, Clemen CS, Olivé M, Ferrer I, Goudeau B, Roth U, Badorf P, Wattjes MP, Lutterbey G, Kral T, van der Ven PF, Fürst DO, Vicart P, Goldfarb LG, Moza M, Carpen O, Reichelt J, Schröder R. Fischer D, et al. Among authors: wattjes mp. Neuromuscul Disord. 2006 Jun;16(6):361-7. doi: 10.1016/j.nmd.2006.03.007. Epub 2006 May 8. Neuromuscul Disord. 2006. PMID: 16684602

4

Pattern of skeletal muscle involvement in primary dysferlinopathies: a whole-body 3.0-T magnetic resonance imaging study.

Kesper K, Kornblum C, Reimann J, Lutterbey G, Schröder R, Wattjes MP. Kesper K, et al. Among authors: wattjes mp. Acta Neurol Scand. 2009 Aug;120(2):111-8. doi: 10.1111/j.1600-0404.2008.01129.x. Epub 2008 Dec 22. Acta Neurol Scand. 2009. PMID: 19154541

5

Whole-body high-field MRI shows no skeletal muscle degeneration in young patients with recessive myotonia congenita.

Kornblum C, Lutterbey GG, Czermin B, Reimann J, von Kleist-Retzow JC, Jurkat-Rott K, Wattjes MP. Kornblum C, et al. Among authors: wattjes mp. Acta Neurol Scand. 2010 Feb;121(2):131-5. doi: 10.1111/j.1600-0404.2009.01228.x. Epub 2009 Dec 28. Acta Neurol Scand. 2010. PMID: 20047568

6

Innovative therapeutic concepts of progressive multifocal leukoencephalopathy.

Möhn N, Grote-Levi L, Hopfner F, Eiz-Vesper B, Maecker-Kolhoff B, Warnke C, Sühs KW, Wattjes MP, Höglinger GU, Skripuletz T. Möhn N, et al. Among authors: wattjes mp. J Neurol. 2022 May;269(5):2403-2413. doi: 10.1007/s00415-021-10952-5. Epub 2022 Jan 7. J Neurol. 2022. PMID: 34994851 Free PMC article. Review.

7

High field MR imaging and 1H-MR spectroscopy in clinically isolated syndromes suggestive of multiple sclerosis: correlation between metabolic alterations and diagnostic MR imaging criteria.

Wattjes MP, Harzheim M, Lutterbey GG, Bogdanow M, Schild HH, Träber F. Wattjes MP, et al. J Neurol. 2008 Jan;255(1):56-63. doi: 10.1007/s00415-007-0666-9. Epub 2007 Dec 20. J Neurol. 2008. PMID: 18080854 Clinical Trial.

8

Does high field MRI allow an earlier diagnosis of multiple sclerosis?

Wattjes MP, Harzheim M, Lutterbey GG, Hojati F, Simon B, Schmidt S, Schild HH, Barkhof F. Wattjes MP, et al. J Neurol. 2008 Aug;255(8):1159-63. doi: 10.1007/s00415-008-0861-3. Epub 2008 May 2. J Neurol. 2008. PMID: 18446305

9

SPG7 mutations in amyotrophic lateral sclerosis: a genetic link to hereditary spastic paraplegia.

Osmanovic A, Widjaja M, Förster A, Weder J, Wattjes MP, Lange I, Sarikidi A, Auber B, Raab P, Christians A, Preller M, Petri S, Weber RG. Osmanovic A, et al. Among authors: wattjes mp. J Neurol. 2020 Sep;267(9):2732-2743. doi: 10.1007/s00415-020-09861-w. Epub 2020 May 23. J Neurol. 2020. PMID: 32447552 Free PMC article.

10

Mild COVID-19 symptoms despite treatment with teriflunomide and high-dose methylprednisolone due to multiple sclerosis relapse.

Möhn N, Saker F, Bonda V, Respondek G, Bachmann M, Stoll M, Wattjes MP, Stangel M, Skripuletz T. Möhn N, et al. Among authors: wattjes mp. J Neurol. 2020 Oct;267(10):2803-2805. doi: 10.1007/s00415-020-09921-1. Epub 2020 May 28. J Neurol. 2020. PMID: 32494855 Free PMC article. No abstract available.

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