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Beate Schlotter

High-dose immunoglobulin therapy in sporadic inclusion body myositis: a double-blind, placebo-controlled study
2000 · M. C. Walter, H. Lochmüller, et al. · Journal of Neurology · 234
Hexosamine Biosynthetic Pathway Mutations Cause Neuromuscular Transmission Defect
2011 · Jan Senderek, Juliane S. Müller, et al. · The American Journal of Human Genetics · 173
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Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers
1998 · Afif Hentati, Karim Ouahchi, et al. · Neurogenetics · 171
Calf enlargement in neuromuscular diseases: a quantitative ultrasound study in 350 patients and review of the literature
1996 · Carl D. Reimers, Beate Schlotter, et al. · Journal of the Neurological Sciences · 124
A common mutation (ε1267delG) in congenital myasthenic patients of Gypsy ethnic origin
1999 · A. Abicht, R. Stucka, et al. · Neurology · 109
Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations
2011 · Velina Guergueltcheva, Juliane S. Müller, et al. · Journal of Neurology · 96
Creatine monohydrate in myotonic dystrophy
2002 · Maggie C. Walter, Peter Reilich, et al. · Journal of Neurology · 60
Mutation screening of the N-myc downstream-regulated gene 1 (NDRG1) in patients with Charcot-Marie-Tooth Disease
2003 · Michael Hunter, Rafaëlle Bernard, et al. · Human Mutation · 50
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Discrepant results for cardiac troponin T and troponin I in chronic myopathy, depending on instrument and assay generation
1996 · S L Braun, D E Pongratz, et al. · Clinical Chemistry · 26
Phenotypic variability in two brothers with sarcotubular myopathy
1999 · W. Müller-Felber, Beate Schlotter, et al. · Journal of Neurology · 24
Nichtinvasive intermittierende Selbstbeatmung (ISB) als Palliativmaßnahme bei amyotropher Lateralsklerose
1998 · V. Schlamp, O. Karg, et al. · Der Nervenarzt · 18
Der Einfluß von Muskelarbeit auf das Myosonogramm
2008 · C. Reimers, H. Lochmüller, et al. · Ultraschall in der Medizin - European Journal of Ultrasound · 9
Location matters – Genotype-phenotype correlation in LRSAM1 mutations associated with rare Charcot-Marie-Tooth neuropathy CMT2P
2020 · Peter Reilich, Beate Schlotter, et al. · Neuromuscular Disorders · 3
Neue Gesichtspunkte zur Pathogenese und Therapie der sporadischen Einschlusskörpermyositis (s-IBM)
2001 · M.C. Walter, H. Lochmüller, et al. · Der Nervenarzt · 3
26-jährige Patientin mit unklarer Transaminasen-Erhöhung
2002 · K Martin, B Schlotter, et al. · Zeitschrift für Gastroenterologie · 2
50jährige Patientin mit rasch einsetzender Ataxie, generalisierten Parästhesien und Myokloni
1997 · M. Toepfer, W. Müller-Felber, et al. · Der Internist · 1
P104 Neurophysiological follow-up of type-I-diabetics after pancreas and kidney transplantation
1996 · W. Müller-Felber, B. Schlotter, et al. · Electroencephalography and Clinical Neurophysiology
Works count: 17
Citation count: 1,103
H-index: 11
I10-index: 11
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