Bulbo-Spinal Atrophy, X-Linked
"Bulbo-Spinal Atrophy, X-Linked" 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.
An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.
MeSH Number(s)
C10.228.854.468.399
C10.574.500.175
C10.574.562.500.374
C10.668.467.500.186
C16.320.322.076
Concept/Terms
Bulbo-Spinal Atrophy, X-Linked- Bulbo-Spinal Atrophy, X-Linked
- Atrophies, X-Linked Bulbo-Spinal
- Atrophy, X-Linked Bulbo-Spinal
- Bulbo Spinal Atrophy, X Linked
- Bulbo-Spinal Atrophies, X-Linked
- X-Linked Bulbo-Spinal Atrophies
- Spinal And Bulbar Muscular Atrophy, X-Linked 1
- Spinal And Bulbar Muscular Atrophy, X Linked 1
- X-Linked Bulbo-Spinal Atrophy
- X Linked Bulbo Spinal Atrophy
- X-linked Bulbospinal Muscular Atrophy
- X linked Bulbospinal Muscular Atrophy
- Bulbospinal Muscular Atrophy, X-linked
- Bulbospinal Muscular Atrophy, X linked
- Kennedy Spinal and Bulbar Muscular Atrophy
- Spinal and Bulbar Muscular Atrophy
- Kennedy Syndrome
- Syndrome, Kennedy
- Kennedy Disease
- Disease, Kennedy
Below are MeSH descriptors whose meaning is more general than "Bulbo-Spinal Atrophy, X-Linked".
- Diseases [C]
- Nervous System Diseases [C10]
- Central Nervous System Diseases [C10.228]
- Spinal Cord Diseases [C10.228.854]
- Muscular Atrophy, Spinal [C10.228.854.468]
- Bulbo-Spinal Atrophy, X-Linked [C10.228.854.468.399]
- Neurodegenerative Diseases [C10.574]
- Heredodegenerative Disorders, Nervous System [C10.574.500]
- Bulbo-Spinal Atrophy, X-Linked [C10.574.500.175]
- Motor Neuron Disease [C10.574.562]
- Muscular Atrophy, Spinal [C10.574.562.500]
- Bulbo-Spinal Atrophy, X-Linked [C10.574.562.500.374]
- Neuromuscular Diseases [C10.668]
- Motor Neuron Disease [C10.668.467]
- Muscular Atrophy, Spinal [C10.668.467.500]
- Bulbo-Spinal Atrophy, X-Linked [C10.668.467.500.186]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Genetic Diseases, X-Linked [C16.320.322]
- Bulbo-Spinal Atrophy, X-Linked [C16.320.322.076]
Below are MeSH descriptors whose meaning is more specific than "Bulbo-Spinal Atrophy, X-Linked".
This graph shows the total number of publications written about "Bulbo-Spinal Atrophy, X-Linked" by people in Harvard Catalyst Profiles by year, and whether "Bulbo-Spinal Atrophy, X-Linked" was a major or minor topic of these publication.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2013 | 1 | 0 | 1 |
| 2014 | 1 | 0 | 1 |
| 2016 | 1 | 0 | 1 |
| 2018 | 1 | 0 | 1 |
Below are the most recent publications written about "Bulbo-Spinal Atrophy, X-Linked" by people in Profiles.
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Side chain to main chain hydrogen bonds stabilize a polyglutamine helix in a transcription factor. Nat Commun. 2019 05 02; 10(1):2034.
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Safety, tolerability, and preliminary efficacy of an IGF-1 mimetic in patients with spinal and bulbar muscular atrophy: a randomised, placebo-controlled trial. Lancet Neurol. 2018 12; 17(12):1043-1052.
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Beyond motor neurons: expanding the clinical spectrum in Kennedy's disease. J Neurol Neurosurg Psychiatry. 2018 08; 89(8):808-812.
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Sequence Context Influences the Structure and Aggregation Behavior of a PolyQ Tract. Biophys J. 2016 06 07; 110(11):2361-2366.
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Sexual Reassignment Fails to Prevent Kennedy's Disease. J Neuromuscul Dis. 2016 03 03; 3(1):121-125.
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Brain MR diffusion tensor imaging in Kennedy's disease. Neuroradiol J. 2015 Apr; 28(2):126-32.
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Pearls & Oy-sters: HyperCKemia with limb-girdle weakness: Think beyond myopathies. Neurology. 2014 Dec 09; 83(24):e209-12.
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Tongue pressure as a novel biomarker of spinal and bulbar muscular atrophy. Neurology. 2014 Jan 21; 82(3):255-62.
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Postural leg tremor in X-linked spinal and bulbar muscular atrophy. J Clin Neurosci. 2014 May; 21(5):799-802.
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Current status of treatment of spinal and bulbar muscular atrophy. Neural Plast. 2012; 2012:369284.