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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
8
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pubmed:dateCreated |
1999-9-15
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pubmed:abstractText |
Hereditary spastic paraplegias (HSPs) are a heterogeneous group of neurodegenerative disorders characterized by progressive and predominant spasticity of the lower limbs, in which dominant, recessive, and X-linked forms have been described. While autosomal dominant HSP has been extensively studied, autosomal recessive HSP is less well known and is considered a rare condition.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0003-9942
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pubmed:author |
pubmed-author:AlvesCC,
pubmed-author:BarrosJJ,
pubmed-author:ChorãoRR,
pubmed-author:CoutinhoPP,
pubmed-author:GrimMM,
pubmed-author:GuimarãesJJ,
pubmed-author:HamriAA,
pubmed-author:HazanJJ,
pubmed-author:LoureiroJ LJL,
pubmed-author:LourençoEE,
pubmed-author:PaternotteCC,
pubmed-author:Prud'hommeJ FJF,
pubmed-author:RibeiroPP,
pubmed-author:SantosJ VJV,
pubmed-author:SilvaM CMC,
pubmed-author:ZemmouriRR
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pubmed:issnType |
Print
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pubmed:volume |
56
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
943-9
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:10448799-Adolescent,
pubmed-meshheading:10448799-Adult,
pubmed-meshheading:10448799-Aged,
pubmed-meshheading:10448799-Algeria,
pubmed-meshheading:10448799-Axons,
pubmed-meshheading:10448799-Child,
pubmed-meshheading:10448799-Child, Preschool,
pubmed-meshheading:10448799-Chromosomes, Human, Pair 16,
pubmed-meshheading:10448799-Chromosomes, Human, Pair 8,
pubmed-meshheading:10448799-Disability Evaluation,
pubmed-meshheading:10448799-Disease Progression,
pubmed-meshheading:10448799-Female,
pubmed-meshheading:10448799-Genetic Linkage,
pubmed-meshheading:10448799-Genetic Markers,
pubmed-meshheading:10448799-Humans,
pubmed-meshheading:10448799-Male,
pubmed-meshheading:10448799-Phenotype,
pubmed-meshheading:10448799-Portugal,
pubmed-meshheading:10448799-Risk Factors,
pubmed-meshheading:10448799-Severity of Illness Index,
pubmed-meshheading:10448799-Spastic Paraplegia, Hereditary,
pubmed-meshheading:10448799-X Chromosome
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pubmed:year |
1999
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pubmed:articleTitle |
Clinical heterogeneity of autosomal recessive spastic paraplegias: analysis of 106 patients in 46 families.
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pubmed:affiliation |
Department of Medicine, Hospital S. Sebastião, Santa Maria de Feira, Portugal.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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