Page last updated: 2024-11-08

alanine and Gyrate Atrophy

alanine has been researched along with Gyrate Atrophy in 1 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

Gyrate Atrophy: Progressive, autosomal recessive, diffuse atrophy of the choroid, pigment epithelium, and sensory retina that begins in childhood.

Research Excerpts

ExcerptRelevanceReference
"Gyrate atrophy (GA) is a rare degenerative, hereditary disease characterized by markedly high serum ornithine levels resulting from the deficiency of ornithine-delta-amino transferase (OAT), a mitochondrial matrix enzyme."3.73Osteoporosis associated with gyrate atrophy: a case report. ( Ahmet, I; Serdar, KS, 2006)

Research

Studies (1)

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

Authors

AuthorsStudies
Ahmet, I1
Serdar, KS1

Other Studies

1 other study available for alanine and Gyrate Atrophy

ArticleYear
Osteoporosis associated with gyrate atrophy: a case report.
    Documenta ophthalmologica. Advances in ophthalmology, 2006, Volume: 113, Issue:1

    Topics: Adult; Alanine; Female; Fluorescein Angiography; Glutamic Acid; Gyrate Atrophy; Humans; Lysine; Orni

2006