A5103248739- Migraine and Headache Studies
- Trigeminal Neuralgia and Treatments
- Ophthalmology and Eye Disorders
- Sympathectomy and Hyperhidrosis Treatments
- Olfactory and Sensory Function Studies
- Renal Diseases and Glomerulopathies
- Neurosurgical Procedures and Complications
- Complementary and Alternative Medicine Studies
- Nicotinic Acetylcholine Receptors Study
- Fibromyalgia and Chronic Fatigue Syndrome Research
- Neurological Complications and Syndromes
- Cellular transport and secretion
- Biomedical Research and Pathophysiology
- Neuroscience of respiration and sleep
- Infrared Thermography in Medicine
- Social Media and Politics
- Media Studies and Communication
- Cardiovascular Syncope and Autonomic Disorders
The Affiliated Yongchuan Hospital of Chongqing Medical University
2011-2024
Chongqing Medical University
2011-2024
Huazhong University of Science and Technology
2019
Tongji Hospital
2019
Ohio University
2014
Migraine and metabolic syndrome have been reported to coexist a marked degree, especially in women migraine patients, but the relationship between these two conditions is still unclear. This study was performed evaluate association of headache characteristics its comorbidities with (MetS) components female patients.A total 142 who fulfilled criteria International Classification Headache Disorders 2nd edition were recruited neurological outpatient department China. The (analgesic use,...
This study aimed to analyze and classify the clinical features of headache in neurological outpatients. A cross-sectional was conducted consecutively from March May 2010 for among general outpatients attending First Affiliated Hospital Chongqing Medical University. Personal interviews were carried out a questionnaire used collect medical records. Diagnosis according International classification disorders, 2nd edition (ICHD-II). Headache patients accounted 19.5% neurology clinic total 843...
Background Recent genome‐wide association studies ( GWAS ) have identified 3 genetic variants that are strongly associated with migraine in E uropeans. The effect of these risk other populations is unknown. To further replicate the findings, we investigated rs2651899 (1p36.32, PRDM 16), rs10166942 (2q37.1, TRPM 8), and rs11172113 (12q13.3, LRP 1) for their C hinese H an population. Methods We performed a case–control study. Genomic DNA was collected from 608 unrelated individuals, including...
The aim of this study was to investigate the clinical characteristics cluster headache (CH) in a neurology outpatient population China.A cross-sectional survey conducted from June December 2011 tertiary care, university-affiliated hospital. All consecutive patients citing as their chief complaint were asked participate face-to-face interview with qualified specialist and complete detailed self-administered questionnaire. diagnosis CH made according International Classification Headache...
ObjectivesThe aim of this study was to investigate the clinical characteristics primary stabbing headache (PSH) and its prevalence in a neurology outpatient center at university hospital China.
Background and objective Migraine is characterized by recurrent headaches, frequently associated with nausea, photophobia, phonophobia; it highly prevalent linked to a heavy socioeconomic burden. While the prevalence of obesity in general population has increased recent years, no prior studies exist regarding relationship between body fat percentage (BF%) incidence severe headaches or migraine. In light this, we conducted this study address gap data. Methods We utilized data from National...
Headache is a common problem among the population, many factors may impact headache characteristics and medical consultation behaviors in different age groups. The purpose of this study was to evaluate clinical diagnosis treatment status headaches elderly patients hospitalized gerontologic department. Consecutive Department Gerontology eligible for were registered. All underwent comprehensive evaluation their whole health status, performed by three gerontologists initially. Then evaluated...
Oculocerebrorenal syndrome of Lowe is a rare X-linked disorder characterized by congenital cataract, mental retardation and proximal tubulopathy. The mutation OCRL1 gene localized at chromosome Xq26.1, encoding an inositol polyphosphate 5-phosphatase, responsible for the phenotypic characteristics this syndrome.