Bernhard Landwehrmeyer

Landwehrmeyer in 2022 Georg Bernhard Landwehrmeyer FRCP is a German neurologist and neuroscientist in the field of neurodegeneration primarily focusing on Huntington's disease. Landwehrmeyer is a professor of neurology at Ulm University Hospital. He was one of the founders of the European Huntington's Disease Network (EHDN) in 2004 and was chairman of its executive committee until 2014. Provided by Wikipedia
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  1. 1
    Fast-to-Slow Transition of Skeletal Muscle Contractile Function and Corresponding Changes in Myosin Heavy and Light Chain Formation in the R6/2 Mouse Model of Huntington's Disease.
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  2. 2
    How to Arrange Follow-Up Time-Intervals for Longitudinal Brain MRI Studies in Neurodegenerative Diseases
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  3. 3
    Research priorities for rare neurological diseases: a representative view of patient representatives and healthcare professionals from the European Reference Network for Rare Neurological Diseases
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  4. 4
    HAP40 protein levels are huntingtin-dependent and decrease in Huntington disease
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  5. 5
    Generation of three human iPSC lines from patients with Huntington’s disease with different CAG lengths and human control iPSC line from a healthy donor
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  6. 6
    Generation of two human iPSC lines from dermal fibroblasts of adult- and juvenile-onset Huntington's disease patients and two healthy donors
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  7. 7
    Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissues
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  8. 8
    Correction: Huntingtin HTT1a is generated in a CAG repeat-length-dependent manner in human tissues
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  9. 9
    Two-point magnitude MRI for rapid mapping of brown adipose tissue and its application to the R6/2 mouse model of Huntington disease.
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  10. 10
    Revisiting the Logan plot to account for non-negligible blood volume in brain tissue
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  11. 11
    An International Validation of a Clinical Tool to Assess Carers’ Quality of Life in Huntington’s Disease
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  12. 12
    Huntington disease alters the actionable information in plasma extracellular vesicles
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  13. 13
    Enroll-HD: An Integrated Clinical Research Platform and Worldwide Observational Study for Huntington's Disease
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  14. 14
    High-resolution respirometry of fine-needle muscle biopsies in pre-manifest Huntington's disease expansion mutation carriers shows normal mitochondrial respiratory function.
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  15. 15
    Bupropion for the treatment of apathy in Huntington's disease: A multicenter, randomised, double-blind, placebo-controlled, prospective crossover trial.
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  16. 16
    Symptomatic treatment options for Huntington’s disease (guidelines of the German Neurological Society)
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  17. 17
    Differential diagnosis of chorea (guidelines of the German Neurological Society)
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  18. 18
    Cellular Distribution of NMDA Glutamate Receptor Subunit mRNAs in the Human Cerebellum
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  19. 19
    Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy
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  20. 20
    Corrigendum: Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy
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