ornithine and Familial Spastic Paraparesis, Htlv-1-Associated

ornithine has been researched along with Familial Spastic Paraparesis, Htlv-1-Associated in 1 studies

Research

Studies (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (100.00)18.2507
2000's0 (0.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Goto, I; Kobayashi, T; Shigeto, H; Yamada, T1

Other Studies

1 other study(ies) available for ornithine and Familial Spastic Paraparesis, Htlv-1-Associated

ArticleYear
[A case of hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome with spastic paraparesis and severe distal muscle atrophy of lower limbs].
    Rinsho shinkeigaku = Clinical neurology, 1992, Volume: 32, Issue:7

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Citrulline; Electromyography; Humans; Leg; Male; Muscular Atrophy; Ornithine; Paraparesis, Tropical Spastic; Spinal Cord; Syndrome

1992