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Meanings of strümpell-lorrain disease in 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.

      Related terms
      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