Amyotrophic lateral sclerosis (ALS) is a motor neuron disease involving both the upper and lower motor neurons in the brain stem and spinal cord. Although it is well known that various central nervous system disorders can produce a 'pseudo-infarction' pattern on the electrocardiogram, there have been no reports of this particular pattern in ALS patients. This report concerns an ALS patient who presented with an ECG pattern of S-T elevation followed by biphasic T and inverted T without any detectable myocardial abnormality . Data from the present case suggest that this pattern may be an inherent characteristic of ALS. Copyright (C) 2000 S. Karger AG. Basel
The literature on the involvement of the autonomic nervous system (ANS) in amyotrophic lateral scler...
The pseudopolyneuritic form of amyotrophic lateral sclerosis (ALS) is a subtype of ALS characterized...
AL amyloidosis is due to deposition of protein derived from immunoglobulin light chain fragments. It...
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, p...
The line distinguishing motor neuron diseases (MNDs) from motor neuropathies is sometimes blurred. A...
Abstract Introduction Amyotrophic lateral sclerosis is a rapidly progressive, fatal neurodegenerativ...
Amyotrophic lateral sclerosis (ALS) belongs to a group of disorders known as motor neuron diseases. ...
Amyotrophic lateral sclerosis (ALS) with atypical symptoms poses a diagnostic challenge to clinician...
Two patients in whom both the neurological examination and electromyography (EMG) were normal prior ...
Although the clinical hallmark of amyotrophic lateral sclerosis (ALS) is a progressive motor weaknes...
We examined the role of needle electromyography (EMG) of the rectus abdominis (RA) in assessing thor...
Copyright © 2020 by the American Clinical Neurophysiology SocietyAmyotrophic lateral sclerosis (ALS)...
BACKGROUND: In amyotrophic lateral sclerosis (ALS), the origin of fasciculations is disputed. We hyp...
The aim of this study was to investigate autonomic cardiac control in patients with amyotrophic late...
This thesis examines the pathophysiology of amyotrophic lateral sclerosis (ALS) and role of neurophy...
The literature on the involvement of the autonomic nervous system (ANS) in amyotrophic lateral scler...
The pseudopolyneuritic form of amyotrophic lateral sclerosis (ALS) is a subtype of ALS characterized...
AL amyloidosis is due to deposition of protein derived from immunoglobulin light chain fragments. It...
Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, p...
The line distinguishing motor neuron diseases (MNDs) from motor neuropathies is sometimes blurred. A...
Abstract Introduction Amyotrophic lateral sclerosis is a rapidly progressive, fatal neurodegenerativ...
Amyotrophic lateral sclerosis (ALS) belongs to a group of disorders known as motor neuron diseases. ...
Amyotrophic lateral sclerosis (ALS) with atypical symptoms poses a diagnostic challenge to clinician...
Two patients in whom both the neurological examination and electromyography (EMG) were normal prior ...
Although the clinical hallmark of amyotrophic lateral sclerosis (ALS) is a progressive motor weaknes...
We examined the role of needle electromyography (EMG) of the rectus abdominis (RA) in assessing thor...
Copyright © 2020 by the American Clinical Neurophysiology SocietyAmyotrophic lateral sclerosis (ALS)...
BACKGROUND: In amyotrophic lateral sclerosis (ALS), the origin of fasciculations is disputed. We hyp...
The aim of this study was to investigate autonomic cardiac control in patients with amyotrophic late...
This thesis examines the pathophysiology of amyotrophic lateral sclerosis (ALS) and role of neurophy...
The literature on the involvement of the autonomic nervous system (ANS) in amyotrophic lateral scler...
The pseudopolyneuritic form of amyotrophic lateral sclerosis (ALS) is a subtype of ALS characterized...
AL amyloidosis is due to deposition of protein derived from immunoglobulin light chain fragments. It...