Page last updated: 2024-11-08

alanine and Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis

alanine has been researched along with Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis in 2 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.

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Neeve, VC1
Samuels, DC1
Bindoff, LA1
van den Bosch, B1
Van Goethem, G1
Smeets, H1
Lombès, A1
Jardel, C1
Hirano, M1
Dimauro, S1
De Vries, M1
Smeitink, J1
Smits, BW1
de Coo, IF1
Saft, C1
Klopstock, T1
Keiling, BC1
Czermin, B1
Abicht, A1
Lochmüller, H1
Hudson, G1
Gorman, GG1
Turnbull, DM1
Taylor, RW1
Holinski-Feder, E1
Chinnery, PF1
Horvath, R1
Yamamoto, T1
Nanba, E1

Other Studies

2 other studies available for alanine and Alpers Diffuse Degeneration of Cerebral Gray Matter with Hepatic Cirrhosis

ArticleYear
What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?
    Brain : a journal of neurology, 2012, Volume: 135, Issue:Pt 12

    Topics: Adolescent; Adult; Age of Onset; Alanine; Child; Cohort Studies; Diffuse Cerebral Sclerosis of Schil

2012
A novel mutation (A246T) in exon 6 of the proteolipid protein gene associated with connatal Pelizaeus-Merzbacher disease.
    Human mutation, 1999, Aug-19, Volume: 14, Issue:2

    Topics: Alanine; Diffuse Cerebral Sclerosis of Schilder; Humans; Male; Myelin Proteolipid Protein; Point Mut

1999