"Neuromuscular Diseases" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A general term encompassing lower MOTOR NEURON DISEASE; PERIPHERAL NERVOUS SYSTEM DISEASES; and certain MUSCULAR DISEASES. Manifestations include MUSCLE WEAKNESS; FASCICULATION; muscle ATROPHY; SPASM; MYOKYMIA; MUSCLE HYPERTONIA, myalgias, and MUSCLE HYPOTONIA.
Descriptor ID |
D009468
|
MeSH Number(s) |
C10.668
|
Concept/Terms |
Foley-Denny-Brown Syndrome- Foley-Denny-Brown Syndrome
- Foley Denny Brown Syndrome
- Syndrome, Foley-Denny-Brown
- Fasciculation-Cramp Syndrome, Benign
- Benign Fasciculation-Cramp Syndrome
- Benign Fasciculation-Cramp Syndromes
- Fasciculation Cramp Syndrome, Benign
- Fasciculation-Cramp Syndromes, Benign
- Cramp-Fasciculation Syndrome
- Cramp Fasciculation Syndrome
- Cramp-Fasciculation Syndromes
- Syndrome, Cramp-Fasciculation
- Syndromes, Cramp-Fasciculation
Oppenheim Disease- Oppenheim Disease
- Oppenheim's Disease
- Oppenheims Disease
- Amyotonia Congenita
|
Below are MeSH descriptors whose meaning is more general than "Neuromuscular Diseases".
Below are MeSH descriptors whose meaning is more specific than "Neuromuscular Diseases".
This graph shows the total number of publications written about "Neuromuscular Diseases" by people in this website by year, and whether "Neuromuscular Diseases" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
---|
2018 | 1 | 0 | 1 |
2023 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Neuromuscular Diseases" by people in Profiles.
-
Closing the Gap - Detection of 5q-Spinal Muscular Atrophy by Short-Read Next-Generation Sequencing and Unexpected Results in a Diagnostic Patient Cohort. J Neuromuscul Dis. 2023; 10(5):835-846.
-
Targeted sequencing with expanded gene profile enables high diagnostic yield in non-5q-spinal muscular atrophies. Hum Mutat. 2018 09; 39(9):1284-1298.
-
Early effects in vitro of the muscular dysgenesis mutation on nervous tissue in the mouse. Muscle Nerve. 1984 Mar-Apr; 7(3):179-93.