alanine has been researched along with Decreased Muscle Tone 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.
Excerpt | Relevance | Reference |
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"We report a male with late infantile glycogen storage disease type II (Pompe's disease) who presented at 12 months of age with muscular hypotonia and developmental delay." | 5.31 | L-alanine supplementation in late infantile glycogen storage disease type II. ( Bodamer, OA; Haas, D; Hermans, MM; Hoffmann, GF; Reuser, AJ, 2002) |
"We report a male with late infantile glycogen storage disease type II (Pompe's disease) who presented at 12 months of age with muscular hypotonia and developmental delay." | 1.31 | L-alanine supplementation in late infantile glycogen storage disease type II. ( Bodamer, OA; Haas, D; Hermans, MM; Hoffmann, GF; Reuser, AJ, 2002) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Bodamer, OA | 1 |
Haas, D | 1 |
Hermans, MM | 1 |
Reuser, AJ | 1 |
Hoffmann, GF | 1 |
1 other study available for alanine and Decreased Muscle Tone
Article | Year |
---|---|
L-alanine supplementation in late infantile glycogen storage disease type II.
Topics: Administration, Oral; Alanine; Cardiomyopathies; Dietary Supplements; Glycogen Storage Disease Type | 2002 |