alanine has been researched along with Myotonic Disorders 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.
Myotonic Disorders: Diseases characterized by MYOTONIA, which may be inherited or acquired. Myotonia may be restricted to certain muscles (e.g., intrinsic hand muscles) or occur as a generalized condition.
| Excerpt | Relevance | Reference |
|---|---|---|
| "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 | 2 (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 |
| Bouhours, M | 1 |
| Sternberg, D | 1 |
| Davoine, CS | 1 |
| Ferrer, X | 1 |
| Willer, JC | 1 |
| Fontaine, B | 1 |
| Tabti, N | 1 |
2 other studies available for alanine and Myotonic Disorders
| 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 |
Functional characterization and cold sensitivity of T1313A, a new mutation of the skeletal muscle sodium channel causing paramyotonia congenita in humans.
Topics: Adult; Alanine; Amino Acid Substitution; Cell Line; Cold Temperature; Electrophysiology; Female; Hum | 2004 |