Fast versus slow disease progression in amyotrophic lateral sclerosis–clinical and genetic factors at the edges of the survival spectrum-Reference-Cited by-同舟云学术

Fast versus slow disease progression in amyotrophic lateral sclerosis–clinical and genetic factors at the edges of the survival spectrum

Published:2022-11 Issue: Volume:119 Page:117-126
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Witzel Simon^ORCID,Wagner Matias,Zhao Chen,Kandler Katharina,Graf Elisabeth,Berutti Riccardo,Oexle Konrad,Brenner David,Winkelmann Juliane,Ludolph Albert C.

Funder

Deutsche Gesellschaft für Neurologie

Boehringer Ingelheim

Universität Ulm

Deutsche Forschungsgemeinschaft

Biogen

Teva Pharmaceutical Industries

Fondation Charcot

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference45 articles.

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1. Time from amyotrophic lateral sclerosis symptom onset to key disease milestones: analysis of data from a multinational cross-sectional survey;Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration;2023-12-29

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4. Nutritional and metabolic factors in amyotrophic lateral sclerosis;Nature Reviews Neurology;2023-07-27

5. A panel of TDP-43-regulated splicing events verify loss of TDP-43 function in amyotrophic lateral sclerosis brain tissue;2023-02-04