Preterm-born infants frequently suffer from an array of neurological damage, collectively
termed encephalopathy of prematurity (EoP). They also have an increased risk of presenting …

Duchenne muscular dystrophy (DMD) is a debilitating X-linked recessive skeletal muscle-
wasting disorder affecting 1 in 3,500–6,000 live-born males. Despite mutations in the dmd …

Background Duchenne's muscular dystrophy (DMD) is a severe type of hereditary,
neuromuscular disorder caused by a mutation in the dystrophin gene resulting in the …

Duchenne muscular dystrophy (DMD), the severest form of muscular dystrophy, is
characterized by progressive muscle weakness with fatal outcomes most often before the …

Dystrophin deficiency alters the sarcolemma structure, leading to muscle dystrophy, muscle
disuse, and ultimately death. Beyond limb muscle deficits, patients with Duchenne muscular …

Individuals with autism often experience gastrointestinal issues but the cause is unknown.
Many gene mutations that modify neuronal synapse function are associated with autism and …

Gastrointestinal (GI) dysfunction is an important, yet understudied condition associated with
Duchenne muscular dystrophy (DMD), with patients reporting bloating, diarrhea, and …

Arginine (Arg), as a basic amino acid, has been reported to be involved in regulation of gut
motility. However, the evidence is limited and the underlying mechanism is not fully …

目的探讨瓜氨酸对重症病人急性胃肠功能障碍的评估价值. 方法采用前瞻性研究方法, 选择ICU
及EICU 的重症病人113 例, 根据是否发生急性胃肠损伤(AGI) 分为AGI 组(n= 73) 和非AGI 组(n …

Intestinal macrophages are key resident immune cells in the gastrointestinal tract. Although
they play a macrophage-conventional role in recognizing and combatting pathogenic …