Page last updated: 2024-11-08

alanine and Muscular Dystrophies, Limb-Girdle

alanine has been researched along with Muscular Dystrophies, Limb-Girdle 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.

Muscular Dystrophies, Limb-Girdle: A heterogenous group of inherited muscular dystrophy that can be autosomal dominant or autosomal recessive. There are many forms (called LGMDs) involving genes encoding muscle membrane proteins such as the sarcoglycan (SARCOGLYCANS) complex that interacts with DYSTROPHIN. The disease is characterized by progressing wasting and weakness of the proximal muscles of arms and legs around the HIPS and SHOULDERS (the pelvic and shoulder girdles).

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Fanin, M1
Nascimbeni, AC1
Fulizio, L1
Angelini, C1
Balci, B1
Uyanik, G1
Dincer, P1
Gross, C1
Willer, T1
Talim, B1
Haliloglu, G1
Kale, G1
Hehr, U1
Winkler, J1
Topaloğlu, H1

Other Studies

2 other studies available for alanine and Muscular Dystrophies, Limb-Girdle

ArticleYear
The frequency of limb girdle muscular dystrophy 2A in northeastern Italy.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:3

    Topics: Alanine; Arginine; Blotting, Western; Calpain; DNA Mutational Analysis; Family Health; Glutamine; Ha

2005
An autosomal recessive limb girdle muscular dystrophy (LGMD2) with mild mental retardation is allelic to Walker-Warburg syndrome (WWS) caused by a mutation in the POMT1 gene.
    Neuromuscular disorders : NMD, 2005, Volume: 15, Issue:4

    Topics: Adolescent; Adult; Alanine; Alleles; Child; DNA Mutational Analysis; Female; Humans; Intellectual Di

2005