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今日，中南大学湘雅医院神经内科江泓教授团队与核医学科（PET中心）胡硕教授团队和北京大学第一医院儿科熊晖教授团队分别合作，在《Movement Disorders》以论著形式，分别发表了题为“Synaptic Loss in Spinocerebellar Ataxia Type 3 Revealed by SV2A Positron Emission Tomography”和“CAG Repea...
近日，中南大学湘雅医院动物实验中心高常青博士团队与中南大学湘雅医院神经内科郭纪锋教授团队合作在《Movement Disorders》（IF=9.698）以封面论著形式发表了题为“Sensitivity of Sniffer Dogs for a Diagnosis of Parkinson’s Disease: A Diagnostic Accuracy Study”的原创性研究，发现对帕金森病...
近日，中南大学湘雅医院神经内科江泓教授、唐北沙教授团队在关于遗传性共济失调的生物标志物研究中取得重要进展，以“Blood Neurofilament Light Chain in Genetic Ataxia: A Meta-Analysis”为题，在国际临床神经病学顶尖期刊《Movement Disorders》（IF=10.338）以原创论著形式发表。江泓教授为论文通讯作者，博士研究生彭林柳、...
首都医科大学宣武医院陈彪教授团队在《Movement Disorders》发文揭示老年人群葡萄糖脑苷脂酶基因（GBA）突变对帕金森病的影响（图）
首都医科大学宣武医院 陈彪教授 Movement Disorders 老年人群 葡萄糖脑苷脂酶基因 GBA 突变对帕金森病的影响
2020/7/29
2020年4月22日，首都医科大学宣武医院帕金森病研究团队在《Movement Disorders》上以论著形式正式发表了题为"Decreased Penetrance of Parkinson's Disease in Elderly Carriers of Glucocerebrosidase Gene L444P/R Mutations: A Community‐Based 10‐Year ...
首都医科大学宣武医院帕金森病影像学联盟吴涛团队在《Movement Disorders》发文揭示快速眼动睡眠行为障碍患者双侧黑质出现异常铁沉积（图）
帕金森病 吴涛团队 快速眼动睡眠行为障碍 宣武医院
2022/9/6
2019年 12月17 日，首都医科大学宣武医院帕金森病影像学联盟团队与哈尔滨工业大学(深圳)合作在《Movement Disorders》(影响因子8.061)上以论著形式在线发表了题为 “Quantitative evaluation of iron content in idiopathic rapid eye movement sleep behavior disorder”的论文。首次利...
Comparing Teaching Methods on Skin Disorders Using Standardized Patients Dressed in Moulage vs Paper Cases
Comparing Teaching Methods
2018/11/22
Objective. To determine whether using standardized patients dressed in moulage improves pharmacy students’ ability to assess skin disorders compared to using picture-based paper cases. To determine ph...
Proteomic analysis of FOXP proteins reveals interactions between cortical transcription factors associated with neurodevelopmental disorders
Neural development FOXP transcription factors common human regulate gene protein the FOXP2 gene
2018/3/5
FOXP transcription factors play important roles in neurodevelopment, but little is known about how their transcriptional activity is regulated. FOXP proteins cooperatively regulate gene expression by ...
New Window Into Brain Lets Researchers Study Brain Disorders（图）
New Window Into Brain Researchers Brain Disorders
2018/1/10
Until recently, the composition of brain tissue limited researchers' insights into the brain's neural circuitry and function.NSF-funded scientists developed a technique called CLARITY to chemically di...
Genomics Discovery Paves Way For Possible New Treatments Of Genetic Disorders,Diseases
Genomics Paves Way New Treatments Genetic Disorders Diseases
2017/10/24
NSF-funded researchers studying how a bacterium's immune system fights off viruses uncovered a powerful new gene-editing technique called CRISPR-Cas9.CRISPR-Cas9 acts like a pair of molecular-sized sc...
Next-gen sequencing identifies non-coding variation disrupting miRNA binding sites in neurological disorders
SCZ ASD
2017/8/28
Understanding the genetic factors underlying neurodevelopmental and neuropsychiatric disorders is a major challenge given their
prevalence and potential severity for quality of life. While large-scal...
LASER-SCANNER SURVEY OF STRUCTURAL DISORDERS: AN INSTRUMENT TO INSPECT THE HISTORY OF PARMA CATHEDRAL’S CENTRAL NAVE
Parma Cathedral Laser Scanner Structural Disorders Historical Monitoring Structural Analysis
2017/6/20
This paper presents the use of laser scanner derived data for the study of the structural disorders in the central nave of the Parma Cathedral. An accurate three-dimensional model of the entire nave w...
山东大学医学院医学遗传学课件（七年制） chromosome disorders。
山东大学医学院病理生理学课件 potassium disorders。
山东大学医学院病理生理学课件 water and electrolyte disorders
山东大学医学院 病理生理学 课件 water and electrolyte disorders
2017/4/18
山东大学医学院病理生理学课件 water and electrolyte disorders。
The Gordon Research Seminar on CAG Triplet Repeat Disorders
CAG Triplet Repeat Disorders new data
2017/3/7
Applications for this meeting must be submitted by May 6, 2017. Please apply early, as some meetings become oversubscribed (full) before this deadline. If the meeting is oversubscribed, it will be sta...