Corticospinal tract damage in HHH syndrome: a metabolic cause of hereditary spastic paraplegia
Corticospinal tract damage in HHH syndrome: a metabolic cause of hereditary spastic paraplegia
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England: BioMed Central Ltd
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Language
English
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England: BioMed Central Ltd
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Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome is a rare disorder of urea cycle characterized by progressive pyramidal and cerebellar dysfunction, whose pathophysiology is not yet fully understood. Here we describe the spectrum of the long fibers involvement in HHH syndrome, attempting a correlation between clinical, electrophysi...
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Corticospinal tract damage in HHH syndrome: a metabolic cause of hereditary spastic paraplegia
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TN_cdi_doaj_primary_oai_doaj_org_article_3c89ffaf434c4e04b6270ebaa30a1423
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_3c89ffaf434c4e04b6270ebaa30a1423
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ISSN
1750-1172
E-ISSN
1750-1172
DOI
10.1186/s13023-019-1181-7
