Literature DB >> 12365061

Gastrointestinal dysfunction in amyotrophic lateral sclerosis.

M Toepfer1, C Folwaczny, A Klauser, R L Riepl, W Müller-Felber, D Pongratz.   

Abstract

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder, characterized by progressive loss of motor neurons. However, ALS has been recognized to involve several non-motor systems. Subclinical involvement of the autonomic system (i.e. of cardial or sudomotor regulation) has been described in ALS. Gastrointestinal motor dysfunction can occur in amyotrophic lateral sclerosis, even if patients do not complain of gastrointestinal symptoms. New techniques in non-invasive evaluation of gastrointestinal function showed delayed gastric emptying and delayed colonic transit times in patients with ALS.

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Year:  1999        PMID: 12365061     DOI: 10.1080/146608299300079484

Source DB:  PubMed          Journal:  Amyotroph Lateral Scler Other Motor Neuron Disord        ISSN: 1466-0822


  24 in total

Review 1.  [Amyotrophic lateral sclerosis].

Authors:  R Gastl; A C Ludolph
Journal:  Nervenarzt       Date:  2007-12       Impact factor: 1.214

2.  Survey of current enteral nutrition practices in treatment of amyotrophic lateral sclerosis.

Authors:  May Zhang; Jane Hubbard; Stacy A Rudnicki; Carolyn S Johansen; Kate Dalton; Terry Heiman-Patterson; Dalles A Forshew; Anne-Marie Wills
Journal:  ESPEN J       Date:  2013-02-01

3.  Effects of Intraoperative Vagal Nerve Stimulation on the Gastrointestinal Microbiome in a Mouse Model of Amyotrophic Lateral Sclerosis.

Authors:  Megan M Haney; Aaron C Ericsson; Teresa E Lever
Journal:  Comp Med       Date:  2018-11-13       Impact factor: 0.982

4.  Amyotrophic lateral sclerosis and intestinal microbiota-toward establishing cause and effect.

Authors:  Marc Gotkine; Denise Kviatcovsky; Eran Elinav
Journal:  Gut Microbes       Date:  2020-06-05

Review 5.  Disorders of the enteric nervous system - a holistic view.

Authors:  Beate Niesler; Stefanie Kuerten; I Ekin Demir; Karl-Herbert Schäfer
Journal:  Nat Rev Gastroenterol Hepatol       Date:  2021-01-29       Impact factor: 46.802

Review 6.  Physiological changes in neurodegeneration - mechanistic insights and clinical utility.

Authors:  Rebekah M Ahmed; Yazi D Ke; Steve Vucic; Lars M Ittner; William Seeley; John R Hodges; Olivier Piguet; Glenda Halliday; Matthew C Kiernan
Journal:  Nat Rev Neurol       Date:  2018-03-23       Impact factor: 42.937

7.  Disease progression in a mouse model of amyotrophic lateral sclerosis: the influence of chronic stress and corticosterone.

Authors:  Jonathan A Fidler; Christopher M Treleaven; Ashley Frakes; Thomas J Tamsett; Mary McCrate; Seng H Cheng; Lamya S Shihabuddin; Brian K Kaspar; James C Dodge
Journal:  FASEB J       Date:  2011-08-29       Impact factor: 5.191

8.  Increased peripheral lipid clearance in an animal model of amyotrophic lateral sclerosis.

Authors:  Anissa Fergani; Hugues Oudart; Jose-Luis Gonzalez De Aguilar; Bastien Fricker; Frédérique René; Jean-François Hocquette; Vincent Meininger; Luc Dupuis; Jean-Philippe Loeffler
Journal:  J Lipid Res       Date:  2007-04-16       Impact factor: 5.922

9.  Autonomic system and amyotrophic lateral sclerosis.

Authors:  Ezequiel A Piccione; David M Sletten; Nathan P Staff; Phillip A Low
Journal:  Muscle Nerve       Date:  2015-03-31       Impact factor: 3.217

10.  Atypical familial amyotrophic lateral sclerosis with initial symptoms of pain or tremor in a Chinese family harboring VAPB-P56S mutation.

Authors:  Li Di; Hai Chen; Yuwei Da; Suobing Wang; Xin-Ming Shen
Journal:  J Neurol       Date:  2015-11-14       Impact factor: 4.849

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