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B. Schlotter · SciRah

Researcher profile · Semantic Scholar

B. Schlotter

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B. Schlotter — researcher profile on SciRah

h-index: 12
Works: 21
Citations: 1,194

Most-cited papers

High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study
M. Walter, Hanns Lochmüller, M. Toepfer, B. Schlotter +4 more
2000Journal of Neurology236 citations
Semantic Scholar
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers
A. Hentati, K. Ouahchi, M. Pericak-Vance, D. Nijhawan +9 more
1998Neurogenetics203 citations
Semantic Scholar
Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defect.
J. Senderek, J. Müller, M. Dusl, T. Strom +35 more
2011American Journal of Human Genetics181 citations Open access
Semantic Scholar
Calf enlargement in neuromuscular diseases: a quantitative ultrasound study in 350 patients and review of the literature.
C. D. Reimers, B. Schlotter, B. Eicke, T. Witt
1996Journal of Neurological Sciences122 citations
Semantic Scholar
Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations
V. Guergueltcheva, J. Müller, M. Dusl, J. Senderek +33 more
2012Journal of Neurology98 citations Open access
Semantic Scholar
A common mutation (ε1267delG) in congenital myasthenic patients of Gypsy ethnic origin
A. Abicht, R. Stucka, V. Karcagi, Á. Herczegfalvi +13 more
199996 citations Open access
Semantic Scholar
Creatine monohydrate in myotonic dystrophy
M. Walter, P. Reilich, H. Lochmüller, R. Kohnen +5 more
2002Journal of Neurology54 citations
Semantic Scholar
Mutation screening of the N‐myc downstream‐regulated gene 1 (NDRG1) in patients with Charcot‐Marie‐Tooth Disease
Michael Hunter, R. Bernard, E. Freitas, A. Boyer +15 more
2003Human Mutation51 citations Open access
Semantic Scholar
A common mutation (epsilon1267delG) in congenital myasthenic patients of Gypsy ethnic origin.
A. Abicht, R. Stucka, V. Karcagi, Á. Herczegfalvi +13 more
1999Neurology44 citations
Semantic Scholar
Creatine monohydrate in myotonic dystrophy: a double-blind, placebo-controlled clinical study.
M. Walter, P. Reilich, Hanns Lochmüller, R. Kohnen +5 more
2002Journal of Neurology41 citations
Semantic Scholar
Discrepant results for cardiac troponin T and troponin I in chronic myopathy, depending on instrument and assay generation.
S. Braun, D. Pongratz, P. Bialk, S. Liem +2 more
1996Clinical Chemistry29 citations Open access
Semantic Scholar
Phenotypic variability in two brothers with sarcotubular myopathy
W. Müller-Felber, B. Schlotter, M. Töpfer, U. Ketelsen +2 more
1999Journal of Neurology17 citations
Semantic Scholar
[Effect of muscular work on the myosonogram].
C. Reimers, Hanns Lochmüller, N. Goebels, B. Schlotter +1 more
2008Ultraschall in der Medizin8 citations
Semantic Scholar
[Noninvasive intermittent self-ventilation as a palliative measure in amyotrophic lateral sclerosis].
V. Schlamp, O. Karg, A. Abel, B. Schlotter +2 more
1998Der Nervenarzt5 citations
Semantic Scholar
[New insights in pathogenesis and therapy of sporadic inclusion body myositis (s-IBM)].
M. Walter, Hanns Lochmüller, B. Schlotter, P. Reilich +2 more
2001Der Nervenarzt3 citations
Semantic Scholar
Location matters - Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2P.
P. Reilich, B. Schlotter, F. Montagnese, B. Jordan +9 more
2020Neuromuscular Disorders2 citations
Semantic Scholar
[26-year-old female patient with elevated liver enzymes].
K. Martin, B. Schlotter, J. Müller-Höcker, K. Loeschke +2 more
2002Zeitschrift für Gastroenterologie - German Journal of Gastroenterology2 citations
Semantic Scholar
Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations Velina GuergueltchevaJuliane S. MullerMarina DuslJan SenderekAnders Oldfors • Christopher LindberghSusan MaxwellJaume ColomerCecilia Jimenez MallebreraAndres Nascimento • Juan J. VilchezNuria MuelasJanbernd KirschnerSha
V. Guergueltcheva, M. Dusl, B. Schlotter, B. Schoser +14 more
20120 citations
Semantic Scholar
[50-year-old patient with rapid ataxia onset, generalized paresthesia and myoclonus].
M. Toepfer, W. Müller-Felber, R. Huber, E. Held +4 more
1997Der Internist0 citations
Semantic Scholar
P104 Neurophysiological follow-up of type-I-diabetics after pancreas and kidney transplantation
W. Müller-Felber, B. Schlotter, M. Topfer, R. Landgraf +3 more
19960 citations
Semantic Scholar
in Chronic Myopathy, Depending on Instrument and Assay
C. Hall, Siegmund L. Braun, D. Pongratz, S. Liem +1 more
19960 citations
Semantic Scholar

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