Literature DB >> 17575020

Generalised sensory system abnormalities in amyotrophic lateral sclerosis: a European multicentre study.

K Pugdahl1, A Fuglsang-Frederiksen, M de Carvalho, B Johnsen, P R W Fawcett, A Labarre-Vila, R Liguori, W A Nix, I S Schofield.   

Abstract

BACKGROUND: Amyotrophic lateral sclerosis (ALS) is defined as a disease of the motor neurones, although several studies indicate involvement of the sensory nervous system. AIM: To evaluate the sensory nerve conduction studies (NCS) in 88 patients with ALS as part of a European multicentre study.
METHODS: Seven European clinical neurophysiologists examined consecutive series of ALS patients. The examinations were peer reviewed, and the diagnosis of ALS was confirmed clinically.
RESULTS: 20 (22.7%) patients with ALS had sensory NCS abnormalities in at least one nerve. Of those, 11 (12.5% of all patients) obtained an additional peer review diagnosis of electrophysiological polyneuropathy. There was no difference between the subgroups of patients with normal versus abnormal sensory NCS findings with respect to age, duration and region of onset.
CONCLUSION: The findings support previous reports of sensory involvement in ALS, and raise the question of whether patients with ALS with sensory nerve abnormalities represent a variant of ALS. ALS associated with generalised sensory system abnormalities may be consistent with degeneration of motor neurones and dorsal root ganglion cells.

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Year:  2007        PMID: 17575020      PMCID: PMC2117695          DOI: 10.1136/jnnp.2006.098533

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  24 in total

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Authors:  J M Shefner; H R Tyler; C Krarup
Journal:  Muscle Nerve       Date:  1991-12       Impact factor: 3.217

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Authors:  M Mondelli; A Rossi; S Passero; G C Guazzi
Journal:  Muscle Nerve       Date:  1993-02       Impact factor: 3.217

5.  Progressive sensory nerve dysfunction in amyotrophic lateral sclerosis: a prospective clinical and neurophysiological study.

Authors:  R Gregory; K Mills; M Donaghy
Journal:  J Neurol       Date:  1993-05       Impact factor: 4.849

6.  ESTEEM (European Standardised Telematic Tool to Evaluate EMG Knowledge-Based Systems and Methods): AIM Project A2010.

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Journal:  Comput Methods Programs Biomed       Date:  1994-10       Impact factor: 5.428

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Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-09       Impact factor: 10.154

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Journal:  Ann Neurol       Date:  1983-09       Impact factor: 10.422

10.  Morphometric comparison of the vulnerability of peripheral motor and sensory neurons in amyotrophic lateral sclerosis.

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Journal:  J Neuropathol Exp Neurol       Date:  1981-11       Impact factor: 3.685

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  30 in total

Review 1.  Neurological diseases and pain.

Authors:  David Borsook
Journal:  Brain       Date:  2011-11-08       Impact factor: 13.501

2.  Facial onset sensory motor neuronopathy: not always a slowly progressive disorder.

Authors:  Emanuele Barca; Massimo Russo; Anna Mazzeo; Carmen Terranova; Antonio Toscano; Paolo Girlanda
Journal:  J Neurol       Date:  2013-04-03       Impact factor: 4.849

3.  Sural nerve pathology in ALS patients: a single-centre experience.

Authors:  Marco Luigetti; Amelia Conte; Alessandra Del Grande; Giulia Bisogni; Angela Romano; Mario Sabatelli
Journal:  Neurol Sci       Date:  2011-12-28       Impact factor: 3.307

Review 4.  Molecular mechanisms underlying monosynaptic sensory-motor circuit development in the spinal cord.

Authors:  Fumiyasu Imai; Yutaka Yoshida
Journal:  Dev Dyn       Date:  2018-01-17       Impact factor: 3.780

5.  Degeneration of proprioceptive sensory nerve endings in mice harboring amyotrophic lateral sclerosis-causing mutations.

Authors:  Sydney K Vaughan; Zachary Kemp; Theo Hatzipetros; Fernando Vieira; Gregorio Valdez
Journal:  J Comp Neurol       Date:  2015-07-21       Impact factor: 3.215

6.  Circuit Dysfunction in SOD1-ALS Model First Detected in Sensory Feedback Prior to Motor Neuron Degeneration Is Alleviated by BMP Signaling.

Authors:  Aaron Held; Paxton Major; Asli Sahin; Robert A Reenan; Diane Lipscombe; Kristi A Wharton
Journal:  J Neurosci       Date:  2019-01-18       Impact factor: 6.167

7.  Sensory involvement in the SOD1-G93A mouse model of amyotrophic lateral sclerosis.

Authors:  Yan Su Guo; Dong Xia Wu; Hong Ran Wu; Shu Yu Wu; Cheng Yang; Bin Li; Hui Bu; Yue Sheng Zhang; Chun Yan Li
Journal:  Exp Mol Med       Date:  2009-03-31       Impact factor: 8.718

Review 8.  Electrodiagnosis in persons with amyotrophic lateral sclerosis.

Authors:  Nanette C Joyce; Gregory T Carter
Journal:  PM R       Date:  2013-03-21       Impact factor: 2.298

Review 9.  The management of amyotrophic lateral sclerosis.

Authors:  Julie Phukan; Orla Hardiman
Journal:  J Neurol       Date:  2009-02-17       Impact factor: 4.849

Review 10.  Amyotrophic lateral sclerosis.

Authors:  Lokesh C Wijesekera; P Nigel Leigh
Journal:  Orphanet J Rare Dis       Date:  2009-02-03       Impact factor: 4.123

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