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Significados de french settlement disease en inglés

ruso
спастическая спинальная параплегия
portugués
paraparesia espástica familiar
catalán
síndrome de strumpell-lorrain
español
paraplejia espástica familiar

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

Términos relacionados
paraplejia espástica familiar
Sinónimos
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