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Disease-Modifying Targets in Neurodegenerative Disorders: Paving the Way for Disease-Modifying Therapies examines specific neurodegenerative disorders in comprehensive chapters… Read more
SUSTAINABLE DEVELOPMENT
Save up to 30% on top Physical Sciences & Engineering titles!
Disease-Modifying Targets in Neurodegenerative Disorders: Paving the Way for Disease-Modifying Therapies examines specific neurodegenerative disorders in comprehensive chapters written by experts in the respective fields. Each chapter contains a summary of the disease management field, subsequently elaborating on the molecular mechanisms and promising new targets for disease-modifying therapies.
This overview is ideal for neuroscientists, biomedical researchers, medical doctors, and caregivers, not only providing readers with a summary of the way patients are treated today, but also offering a glance at the future of neurodegenerative disorder treatment.
Chapter 1: The multitude of therapeutic targets in neurodegenerative proteinopathies
Chapter 2: Synuclein misfolding as a therapeutic target
Chapter 3: Neuroinflammation as a therapeutic target in neurodegenerative diseases
Chapter 4A: Stem cells in neurodegeneration: mind the gap
Chapter 4B: The potential of stem cells in tackling neurodegenerative diseases
Chapter 5: Preclinical models of Alzheimer’s disease for identification and preclinical validation of therapeutic targets: from fine-tuning strategies for validated targets to new venues for therapy
Chapter 6: Parkinson’s disease
Chapter 7: Lewy body dementia
Chapter 8: Frontotemporal dementia
Chapter 9: From huntingtin gene to Huntington’s disease-altering strategies
Chapter 10: Amyotrophic lateral sclerosis: mechanisms and therapeutic strategies
VB
She was appointed Assistant Professor at the KU Leuven in 2003 and in 2007, as full-time Research Professor (BOF-ZAP). She is now Head of the Laboratory for Neurobiology and Gene Therapy. Her research focuses on disease modeling and therapy for Parkinson’s disease using viral vectors in cell culture and in vivo. The underlying rationale is that the generation of more relevant models in cells and in pre-clinical model brain will lead to a better insight into the molecular pathogenesis of PD and to the development of new therapeutic strategies and drugs.
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