Schulte-Mattler WJ - Search Results

1

Immune-mediated rippling muscle disease.

Schulte-Mattler WJ, Kley RA, Rothenfusser-Korber E, Böhm S, Brüning T, Hackemann J, Steinbrecher A, Düring MV, Voss B, Vorgerd M. Schulte-Mattler WJ, et al. Neurology. 2005 Jan 25;64(2):364-7. doi: 10.1212/01.WNL.0000149532.52938.5B. Neurology. 2005. PMID: 15668444

2

Autonomic involvement in tick-borne encephalitis (TBE): report of five cases.

Kleiter I, Steinbrecher A, Flügel D, Bogdahn U, Schulte-Mattler W. Kleiter I, et al. Eur J Med Res. 2006 Jun 30;11(6):261-5. Eur J Med Res. 2006. PMID: 16820340

3

Increased metabolic muscle fatigue is caused by some but not all mitochondrial mutations.

Schulte-Mattler WJ, Müller T, Deschauer M, Gellerich FN, Iaizzo PA, Zierz S. Schulte-Mattler WJ, et al. Arch Neurol. 2003 Jan;60(1):50-8. doi: 10.1001/archneur.60.1.50. Arch Neurol. 2003. PMID: 12533088

4

Autonomic and peripheral nervous system function in acute tick-borne encephalitis.

Neumann B, Schulte-Mattler W, Brix S, Pöschl P, Jilg W, Bogdahn U, Steinbrecher A, Kleiter I. Neumann B, et al. Brain Behav. 2016 May 5;6(8):e00485. doi: 10.1002/brb3.485. eCollection 2016 Aug. Brain Behav. 2016. PMID: 27247855 Free PMC article.

5

Borrelia burgdorferi myelitis presenting as a partial stiff man syndrome.

Martin R, Meinck HM, Schulte-Mattler W, Ricker K, Mertens HG. Martin R, et al. J Neurol. 1990 Feb;237(1):51-4. doi: 10.1007/BF00319670. J Neurol. 1990. PMID: 2319268

6

Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11).

Winner B, Uyanik G, Gross C, Lange M, Schulte-Mattler W, Schuierer G, Marienhagen J, Hehr U, Winkler J. Winner B, et al. Arch Neurol. 2004 Jan;61(1):117-21. doi: 10.1001/archneur.61.1.117. Arch Neurol. 2004. PMID: 14732628

7

Thin corpus callosum and amyotrophy in spastic paraplegia--case report and review of literature.

Winner B, Gross C, Uyanik G, Schulte-Mattler W, Lürding R, Marienhagen J, Bogdahn U, Windpassinger C, Hehr U, Winkler J. Winner B, et al. Clin Neurol Neurosurg. 2006 Oct;108(7):692-8. doi: 10.1016/j.clineuro.2005.06.007. Epub 2005 Aug 15. Clin Neurol Neurosurg. 2006. PMID: 16102895

8

Myopathy in Childhood Muscle-Specific Kinase Myasthenia Gravis.

Kirzinger L, Khomenko A, Schulte-Mattler W, Backhaus R, Platen S, Schalke B. Kirzinger L, et al. Pediatr Neurol. 2016 Dec;65:90-92. doi: 10.1016/j.pediatrneurol.2016.08.005. Epub 2016 Aug 20. Pediatr Neurol. 2016. PMID: 27697312

9

Chance or challenge, spoilt for choice? New recommendations on diagnostic and therapeutic considerations in hereditary transthyretin amyloidosis with polyneuropathy: the German/Austrian position and review of the literature.

Dohrn MF, Auer-Grumbach M, Baron R, Birklein F, Escolano-Lozano F, Geber C, Grether N, Hagenacker T, Hund E, Sachau J, Schilling M, Schmidt J, Schulte-Mattler W, Sommer C, Weiler M, Wunderlich G, Hahn K. Dohrn MF, et al. J Neurol. 2021 Oct;268(10):3610-3625. doi: 10.1007/s00415-020-09962-6. Epub 2020 Jun 4. J Neurol. 2021. PMID: 32500375 Free PMC article.

10

Linkage of proximal myotonic myopathy to chromosome 3q.

Ricker K, Grimm T, Koch MC, Schneider C, Kress W, Reimers CD, Schulte-Mattler W, Mueller-Myhsok B, Toyka KV, Mueller CR. Ricker K, et al. Neurology. 1999 Jan 1;52(1):170-1. doi: 10.1212/wnl.52.1.170. Neurology. 1999. PMID: 9921867

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