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Significados de amyotrophic lateral sclerosis en inglés

ruso
боковой амиотрофический склероз
portugués
esclerose amiotrófica lateral
catalán
malaltia de lou gehrig
español
esclerosis lateral
Wikidata

Neurodegenerative disease characterized by progressive muscular paralysis.

Términos relacionados
esclerosis lateral
Uso de amyotrophic lateral sclerosis en inglés
1
No increase was found in patients with amyotrophic lateral sclerosis.
Pubmed
2
A challenging aspect of amyotrophic lateral sclerosis research is the heterogeneous nature of the disease.
Pubmed
3
Lou Gehrig's disease ( amyotrophic lateral sclerosis, or ALS) can also result in this syndrome.
Human
4
These features may be beneficial in phase II trials in amyotrophic lateral sclerosis and other fields.
Pubmed
5
There was Hodgkin's disease, leukemia, amyotrophic lateral sclerosis.
Catch-22
6
Conclusion: The findings suggest that it is possible to identify different illness trajectories in amyotrophic lateral sclerosis.
Pubmed
7
We also revealed several notable associations between myeloid marker expression and clinical features in amyotrophic lateral sclerosis.
Pubmed
8
A pyramidal syndrome associated with biopsy-proven chronic neurogenic atrophy led to the diagnosis of amyotrophic lateral sclerosis.
Pubmed
9
The 49-year-old former businessman was diagnosed with amyotrophic lateral sclerosis (ALS) just over a year ago.
Reuters
10
Methods: Eighteen patients with amyotrophic lateral sclerosis attending a Neurology Department in northern Italy participated in the study.
Pubmed
11
Background: Cognitive disorders have been described in amyotrophic lateral sclerosis, but usually after the diagnosis has ben established.
Pubmed
12
The etiology of motor neuron degeneration in amyotrophic lateral sclerosis (ALS) remains to be better understood.
Pubmed
13
Our data suggest that oligodendroglial dysfunction may be a contributor to motor neuron degeneration in amyotrophic lateral sclerosis.
Pubmed
14
This study demonstrates that patients with amyotrophic lateral sclerosis with distinct clinical features have differential myeloid cell signatures.
Pubmed
15
The system was tested on a 58-year-old woman in the late stages of amyotrophic lateral sclerosis, or ALS.
Reuters
16
In normal controls and in patients with other neurological disorders including amyotrophic lateral sclerosis, neither lectin stained motor neurons.
Pubmed