Medizinische Universität Graz Austria/Österreich - Forschungsportal - Medical University of Graz

Logo MUG-Forschungsportal

Gewählte Publikation:

SHR Neuro Krebs Kardio Lipid Stoffw Microb

Geser, F; Fellner, L; Haybaeck, J; Wenning, GK.
Development of neurodegeneration in amyotrophic lateral sclerosis: from up or down?
J Neural Transm (Vienna). 2020; Doi: 10.1007/s00702-020-02213-y
Web of Science PubMed FullText FullText_MUG

 

Co-Autor*innen der Med Uni Graz
Haybäck Johannes
Altmetrics:

Dimensions Citations:

Plum Analytics:

Scite (citation analytics):

Abstract:
Amyotrophic lateral sclerosis (ALS) is a fatal neurological disease associated with neurodegeneration and intracellular pathological 43-kDa transactive response sequence DNA-binding protein (TDP-43) positive inclusions. The various clinical symptoms, such as motor disorders and cognitive impairment, reflect the degeneration of certain areas of the nervous system. Since the discovery of the significance of pathological TDP-43 for human disease including ALS, there has been an increasing number of studies reporting on the distribution and severity of neurodegeneration. These have rekindled the old debate about whether the first or second motor neuron is the primary site of degeneration in ALS. To shed light on this question, the following is a review of the relevant neuropathological studies.

Find related publications in this database (Keywords)
Amyotrophic lateral sclerosis
Neurodegeneration
Pathological 43-kDa transactive response sequence DNA-binding protein (TDP-43)
Upper motor neuron
Lower motor neuron
© Med Uni Graz Impressum