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Spastic paraplegia 3, autosomal dominant

Known as: strumpell's disease, SPG3, Spastic Paraplegia 3 
National Institutes of Health

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Related topics

7 relations
Autosomal dominant inheritanceGenetic HeterogeneityLower limb muscle weaknessScoliosis, unspecified

Broader (1)

Spastic Paraplegia, Hereditary

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Increased epithelial-free areas in thymuses with altered EphB-mediated thymocyte–thymic epithelial cell interactions
Epithelial-free areas, present in both thymic cortex and medulla, have been studied in WT and EphB-deficient mice that have… 
2015
2015
Atlastin Mediated Endoplasmic Reticulum Network Formation In Hereditary Spastic Paraplegia
The endoplasmic reticulum is an extensive multifunctional membrane bound organelle present in all eukaryotic cells. It houses a… 
2010
2010
exclusively males in a large pedigree (HSP) linked to locus SPG4 affects almost Autosomal dominant (AD) pure spastic paraplegia
http://jmg.bmj.com/content/39/12/e77.full.html Updated information and services can be found at: These include: References http… 
Review
2010
Review
2010
Studies on hereditary spastic paraplegia proteins
The hereditary spastic paraplegias (HSPs) are a clinically and genetically diverse group of inherited neurological disorders that… 
2009
2009
SPG3 英語を苦手とする学生のためのプレゼンテーション : 「街頭インタビュー」(Speaking,国際交流「新」時代における大学英語教育カリキュラム刷新)
2009
2009
The gene responsible for hereditary spastic paraplegia SPG3A encodes atlastin-1 (ATL), a dynamin-like GTPase
  • 2009
  • Corpus ID: 207861208
The gene responsible for hereditary spastic paraplegia SPG3A encodes atlastin-1 (ATL), a dynamin-like GTPase expressed in brain… 
2009
2009
A novel SPG3A mutation in an Italian patient with Hereditary Spastic Paraplegia
2006
2006
Mutation analysis of spastin (SPG4) and atlastin (SPG3A) in hereditary spastic paraplegia
2004
2004
Novel Mutation in the SPG 3 A Gene in an African American Family With an Early Onset of Hereditary Spastic Paraplegia
Patients: Complete neurological examination and genetic analysis were performed on 6 affected members of a small African American… 
1963
1963
[FAMILIAL SPASTIC PARAPLEGIA OF THE TYPE STRUMPELL-LORRAIN IN 3 SISTERS DAUGHTERS OF A CONSANGUINOUS MARRIAGE].