中华神经科杂志
2016年 · 第49卷第07期
中华神经科杂志
After several years of preparation and revision, the highly anticipated "Chinese Guidelines for Clinical Application of Cerebrovascular Ultrasound" has finally been published[
Ultrasound technology is increasing in clinical application because of its real-time, portable, non-invasive, repeated examination and even long-range monitoring advantages. Even in the widespread application of advanced technologies such as computed tomography, magnetic resonance imaging and angiography, ultrasound can provide a lot of complementary information for it, so it occupies an important position in the diagnosis of nervous system diseases. At present, cerebrovascular ultrasound has expanded from the traditional transcranial Doppler ultrasound (TCD) to the application fields of detecting microembolus, detecting right-to-left shunt (RLS) of cardiac or pulmonary arteriovenous abnormalities, automatic regulation of cerebral blood flow and blood vessels, and clinical diagnosis and even treatment of central nervous system degenerative diseases and peripheral neuropathies.
Stroke has high incidence rate, high recurrence rate, high fatality and disability rate, and heavy disease burden, which has jumped to the first cause of death in China[
Susac syndrome, also known as microvascular disease of brain, retina and cochlea, is characterized by acute multiple encephalopathy, branch retinal artery occlusion (BRAO) and sensory deafness[
carotid artery stenting (CAS) has been widely used to prevent cerebral infarction in patients with carotid artery stenosis. Although the probability of intracranial hemorrhage is small, the mortality rate can be as high as 75%[
The human body is not only composed of human cells, but also the home of 100 billion microorganisms. Most of these microorganisms live in the human digestive tract, especially in the lower digestive tract (i.e. large intestine). The total number of genes of these microorganisms is about 150 times that of human genes, and they have an important impact on human health and diseases[
Duchenne muscular dystrophy (DMD) is a fatal X-linked recessive inherited myopathy, which is closely related to the protein deletion caused by the mutation of dystrophin gene on chromosome Xp21. However, myocyte membrane instability and mechanical damage caused by dystrophin deficiency do not fully explain the persistent skeletal muscle damage in DMD[
Because its ligand has not been discovered, the nuclear receptor Tlx is also known as the orphan nuclear receptor. It is not only the main regulator of nerve regeneration, but also plays an important role in the development of tumors. Its unique biological function gives Tlx the potential to be a therapeutic tool for many neurological disorders. We now review the biological functions and clinical application prospects of Tlx as follows.
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