Schlotter B - Search Results

1

[Noninvasive intermittent self-ventilation as a palliative measure in amyotrophic lateral sclerosis].

Schlamp V, Karg O, Abel A, Schlotter B, Wasner M, Borasio GD. Schlamp V, et al. Among authors: schlotter b. Nervenarzt. 1998 Dec;69(12):1074-82. doi: 10.1007/s001150050385. Nervenarzt. 1998. PMID: 9888144 German.

2

[New insights in pathogenesis and therapy of sporadic inclusion body myositis (s-IBM)].

Walter MC, Lochmüller H, Schlotter B, Reilich P, Müller-Felber W, Pongratz D. Walter MC, et al. Among authors: schlotter b. Nervenarzt. 2001 Feb;72(2):117-21. doi: 10.1007/s001150050723. Nervenarzt. 2001. PMID: 11256145 Review. German.

3

[50-year-old patient with rapid ataxia onset, generalized paresthesia and myoclonus].

Toepfer M, Müller-Felber W, Huber RM, Held E, Wekerle G, Unger J, Schlotter B, Pongratz D. Toepfer M, et al. Among authors: schlotter b. Internist (Berl). 1997 Apr;38(4):355-60. doi: 10.1007/s001080050048. Internist (Berl). 1997. PMID: 9213575 German. No abstract available.

4

High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study.

Walter MC, Lochmüller H, Toepfer M, Schlotter B, Reilich P, Schröder M, Müller-Felber W, Pongratz D. Walter MC, et al. Among authors: schlotter b. J Neurol. 2000 Jan;247(1):22-8. doi: 10.1007/s004150050005. J Neurol. 2000. PMID: 10701893 Clinical Trial.

5

Creatine monohydrate in myotonic dystrophy: a double-blind, placebo-controlled clinical study.

Walter MC, Reilich P, Lochmüller H, Kohnen R, Schlotter B, Hautmann H, Dunkl E, Pongratz D, Müller-Felber W. Walter MC, et al. Among authors: schlotter b. J Neurol. 2002 Dec;249(12):1717-22. doi: 10.1007/s00415-002-0923-x. J Neurol. 2002. PMID: 12529796 Clinical Trial.

6

A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin.

Abicht A, Stucka R, Karcagi V, Herczegfalvi A, Horváth R, Mortier W, Schara U, Ramaekers V, Jost W, Brunner J, Janssen G, Seidel U, Schlotter B, Müller-Felber W, Pongratz D, Rüdel R, Lochmüller H. Abicht A, et al. Among authors: schlotter b. Neurology. 1999 Oct 22;53(7):1564-9. doi: 10.1212/wnl.53.7.1564. Neurology. 1999. PMID: 10534268

7

[26-year-old female patient with elevated liver enzymes].

Martin K, Schlotter B, Müller-Höcker J, Loeschke K, Pongratz D, Folwaczny C. Martin K, et al. Among authors: schlotter b. Z Gastroenterol. 2002 Oct;40(10):885-90. doi: 10.1055/s-2002-35263. Z Gastroenterol. 2002. PMID: 12436356 German.

8

Phenotypic variability in two brothers with sarcotubular myopathy.

Müller-Felber W, Schlotter B, Töpfer M, Ketelsen UP, Müller-Höcker J, Pongratz D. Müller-Felber W, et al. Among authors: schlotter b. J Neurol. 1999 May;246(5):408-11. doi: 10.1007/s004150050374. J Neurol. 1999. PMID: 10399877 No abstract available.

9

Discrepant results for cardiac troponin T and troponin I in chronic myopathy, depending on instrument and assay generation.

Braun SL, Pongratz DE, Bialk P, Liem S, Schlotter B, Vogt W. Braun SL, et al. Among authors: schlotter b. Clin Chem. 1996 Dec;42(12):2039-41. Clin Chem. 1996. PMID: 8969648 No abstract available.

10

Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2P.

Reilich P, Schlotter B, Montagnese F, Jordan B, Stock F, Schäff-Vogelsang M, Hotter B, Eger K, Diebold I, Erdmann H, Becker K, Schön U, Abicht A. Reilich P, et al. Among authors: schlotter b. Neuromuscul Disord. 2021 Feb;31(2):123-133. doi: 10.1016/j.nmd.2020.11.011. Epub 2020 Nov 28. Neuromuscul Disord. 2021. PMID: 33414056

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