Literature DB >> 26646612

[Amyotrophic lateral sclerosis. Multisystem degeneration].

A Hübers1, A C Ludolph1, A Rosenbohm1, E H Pinkhardt1, J H Weishaupt1, J Dorst2.   

Abstract

BACKGROUND: There is increasing evidence that amyotrophic lateral sclerosis (ALS) has to be regarded as multisystem degeneration rather than as purely a motor neuron disease, as it also includes various dnonmotor symptoms. This modern view has been confirmed by neuropathological and imaging findings.
OBJECTIVES: To review recent findings supporting the idea of multisystem degeneration and to describe the implications for diagnostics and therapy.
METHODS: A discussion of recent clinical, imaging, and neuropathological findings is presented.
RESULTS: Symptoms of ALS include not only motor symptoms but also cognitive impairment, oculomotor abnormalities, and extrapyramidal and sensory symptoms. As a neuropathological correlate, a systematic spreading of "transactive response DNA binding protein 43 kDa" (TDP-43) over functionally connected cortical structures has been described.
CONCLUSIONS: Nonmotor symptoms are regularly seen in ALS, although they usually do not dominate the clinical picture. Recent neuropathological findings offer new perspectives for diagnostics and therapy in ALS.

Entities:  

Keywords:  Amyotrophic lateral sclerosis; DNA-binding proteins; Motor neuron disease; Nervous system diseases; Protein TDP-43

Mesh:

Year:  2016        PMID: 26646612     DOI: 10.1007/s00115-015-0030-8

Source DB:  PubMed          Journal:  Nervenarzt        ISSN: 0028-2804            Impact factor:   1.214


  57 in total

1.  High-caloric food supplements in the treatment of amyotrophic lateral sclerosis: a prospective interventional study.

Authors:  Johannes Dorst; Joschka Cypionka; Albert C Ludolph
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2013-08-14       Impact factor: 4.092

2.  Percutaneous endoscopic gastrostomy in amyotrophic lateral sclerosis: a prospective observational study.

Authors:  Johannes Dorst; Luc Dupuis; Susanne Petri; Katja Kollewe; Susanne Abdulla; Joachim Wolf; Markus Weber; David Czell; Christian Burkhardt; Frank Hanisch; Stefan Vielhaber; Thomas Meyer; Gabriele Frisch; Dagmar Kettemann; Torsten Grehl; Bertold Schrank; Albert C Ludolph
Journal:  J Neurol       Date:  2015-01-25       Impact factor: 4.849

3.  The Edinburgh Cognitive and Behavioural Amyotrophic Lateral Sclerosis Screen: a cross-sectional comparison of established screening tools in a German-Swiss population.

Authors:  Dorothée Lulé; Christian Burkhardt; Susanne Abdulla; Sarah Böhm; Katja Kollewe; Ingo Uttner; Sharon Abrahams; Thomas H Bak; Susanne Petri; Markus Weber; Albert C Ludolph
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2014-10-08       Impact factor: 4.092

4.  Nutritional status is a prognostic factor for survival in ALS patients.

Authors:  J C Desport; P M Preux; T C Truong; J M Vallat; D Sautereau; P Couratier
Journal:  Neurology       Date:  1999-09-22       Impact factor: 9.910

Review 5.  Amyotrophic lateral sclerosis--a model of corticofugal axonal spread.

Authors:  Heiko Braak; Johannes Brettschneider; Albert C Ludolph; Virginia M Lee; John Q Trojanowski; Kelly Del Tredici
Journal:  Nat Rev Neurol       Date:  2013-11-12       Impact factor: 42.937

6.  Autosomal dominant frontotemporal lobar degeneration due to the C9ORF72 hexanucleotide repeat expansion: late-onset psychotic clinical presentation.

Authors:  Daniela Galimberti; Chiara Fenoglio; Maria Serpente; Chiara Villa; Rossana Bonsi; Andrea Arighi; Giorgio G Fumagalli; Roberto Del Bo; Amalia C Bruni; Maria Anfossi; Alessandra Clodomiro; Chiara Cupidi; Benedetta Nacmias; Sandro Sorbi; Irene Piaceri; Silvia Bagnoli; Valentina Bessi; Alessandra Marcone; Chiara Cerami; Stefano F Cappa; Massimo Filippi; Federica Agosta; Giuseppe Magnani; Giancarlo Comi; Massimo Franceschi; Innocenzo Rainero; Maria Teresa Giordana; Elisa Rubino; Patrizia Ferrero; Ekaterina Rogaeva; Zhengrui Xi; Annamaria Confaloni; Paola Piscopo; Giuseppe Bruno; Giuseppina Talarico; Annachiara Cagnin; Francesca Clerici; Bernardo Dell'Osso; Giacomo P Comi; A Carlo Altamura; Claudio Mariani; Elio Scarpini
Journal:  Biol Psychiatry       Date:  2013-03-07       Impact factor: 13.382

7.  Extrapyramidal stiffness in patients with amyotrophic lateral sclerosis.

Authors:  Pierre-François Pradat; Gaelle Bruneteau; Elisabetta Munerati; François Salachas; Nadine Le Forestier; Lucette Lacomblez; Timothee Lenglet; Vincent Meininger
Journal:  Mov Disord       Date:  2009-10-30       Impact factor: 10.338

8.  Dyslipidemia is a protective factor in amyotrophic lateral sclerosis.

Authors:  L Dupuis; P Corcia; A Fergani; J-L Gonzalez De Aguilar; D Bonnefont-Rousselot; R Bittar; D Seilhean; J-J Hauw; L Lacomblez; J-P Loeffler; V Meininger
Journal:  Neurology       Date:  2008-01-16       Impact factor: 9.910

9.  Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72.

Authors:  Bradley F Boeve; Kevin B Boylan; Neill R Graff-Radford; Mariely DeJesus-Hernandez; David S Knopman; Otto Pedraza; Prashanthi Vemuri; David Jones; Val Lowe; Melissa E Murray; Dennis W Dickson; Keith A Josephs; Beth K Rush; Mary M Machulda; Julie A Fields; Tanis J Ferman; Matthew Baker; Nicola J Rutherford; Jennifer Adamson; Zbigniew K Wszolek; Anahita Adeli; Rodolfo Savica; Brendon Boot; Karen M Kuntz; Ralitza Gavrilova; Andrew Reeves; Jennifer Whitwell; Kejal Kantarci; Clifford R Jack; Joseph E Parisi; John A Lucas; Ronald C Petersen; Rosa Rademakers
Journal:  Brain       Date:  2012-03       Impact factor: 13.501

10.  Therapeutic modulation of eIF2α phosphorylation rescues TDP-43 toxicity in amyotrophic lateral sclerosis disease models.

Authors:  Hyung-Jun Kim; Alya R Raphael; Eva S LaDow; Leeanne McGurk; Ross A Weber; John Q Trojanowski; Virginia M-Y Lee; Steven Finkbeiner; Aaron D Gitler; Nancy M Bonini
Journal:  Nat Genet       Date:  2013-12-15       Impact factor: 38.330

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  2 in total

1.  Minimizing the Diagnostic Delay in Amyotrophic Lateral Sclerosis: The Role of Nonneurologist Practitioners.

Authors:  Martin Matharan; Stéphane Mathis; Sarah Bonabaud; Louis Carla; Antoine Soulages; Gwendal Le Masson
Journal:  Neurol Res Int       Date:  2020-05-11

Review 2.  RNA-Targeted Therapies and Amyotrophic Lateral Sclerosis.

Authors:  Stéphane Mathis; Gwendal Le Masson
Journal:  Biomedicines       Date:  2018-01-15
  2 in total

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