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Significats de hsmn v en anglès

rus
спастическая спинальная параплегия
portuguès
paraparesia espástica familiar
català
síndrome de strumpell-lorrain
espanyol
paraplejia espástica familiar

Genetically and clinically heterogeneous group of neurodegenerative disorders characterized by progressive spasticity and hyperreflexia of the lower limbs.

Termes relacionats
síndrome de strumpell-lorrain
Sinònims
Examples for "hsp"
Examples for "hsp"
1
Genetic variations of the hsp genes were not associated with degree of bone loss.
Pubmed
2
Lastly, we observed dopaminergic neurons in wild type worms and in hsp-70 mutants following Mn treatment.
Pubmed
3
The importance of hsp-70 against Mn toxicity was then corroborated in dopaminergic neurons, where Mn neurotoxicity was aggravated.
Pubmed
4
The role of stress was proved by the HSP-60 positivity of CA.
Pubmed
5
HSP induction might be used to develop novel approaches in clinical transplantation.
Pubmed
1
Reactive oxygen species and damage of mitochondrial structure were considered as major factors to GC-1 spg cells apoptosis.
Pubmed
2
The Uni Stas rgds tq of Ger spg seized in ts cou at t outbk o hox as a clod incident.
Public Opinion
3
From a dorsal lateral joint of the medullary tube (spc) the spinal ganglia (spg) grow out between it and the horn-plate.
The Evolution of Man — Volume 1
4
Simon Property Group SPG.N Chief Financial Officer Stephen Sterrett said the No.
Reuters
5
In our view, SPG Land's financial and risk controls have weakened.
Reuters
1
For years, they had worked side by side in the FSP garden.
The sex lives of cannibals: adrift in the equatorial pacific
2
Results showed that the Foley catheter might not be effective for FSP.
Pubmed
3
Results suggested the possibility of differential effectiveness of FSP depending on catheter choice.
Pubmed
4
Later that afternoon, Ruiti, the FSP accountant, stopped by the house.
The sex lives of cannibals: adrift in the equatorial pacific
5
Only randomized controlled studies comparing FSP with IUI were included in this review.
Pubmed
1
Autosomal dominant hereditary spastic paraplegia is genetically heterogeneous, with at least five loci identified by linkage analysis.
Pubmed
2
Understanding the cellular functions of spatacsin will allow deciphering mechanisms of motor cortex dysfunction in autosomal-recessive hereditary spastic paraplegia.
Pubmed
3
SPG13, an autosomal dominant form of pure hereditary spastic paraplegia, was recently mapped to chromosome 2q24-34 in a French family.
Pubmed
4
Recently, mutations in spastin were identified in SPG4, the most common locus for dominant hereditary spastic paraplegia that was previously mapped to chromosome 2p22.
Pubmed
5
Purpose of review: Hereditary spastic paraplegias are a genetically heterogeneous group of diseases.
Pubmed