Living with the Unknown: Intolerance of Uncertainty in Parkinson's Disease [0.03%]
不知所带来的不安——帕金森病中的不确定性容忍度研究
Bradley McDaniels,Gregory M Pontone,Kuhan Pushparatnam et al.
Bradley McDaniels et al.
Background: Parkinson's disease (PD) is marked by pervasive uncertainty due to fluctuating motor and non-motor symptoms, variable treatment response, and an unpredictable clinical course. Intolerance of uncertainty (IU), ...
Severe Lower Limb and Abdominal Edema Associated with Subcutaneous Apomorphine Infusion [0.03%]
与皮下注射阿朴吗啡相关的严重下肢和腹部水肿
Guillaume Costentin,David Maltête
Guillaume Costentin
SEMA6B-Related Progressive Myoclonic Epilepsy Mimicking Angelman Syndrome [0.03%]
SEMA6B所致进行性肌阵挛性癫痫误诊为天使人综合征
Yasamin Mahjoub,Sangeetha Yoganathan,Christos Ganos
Yasamin Mahjoub
High Prevalence and Clinical Impact of Fibromyalgia in Functional Motor Disorder [0.03%]
功能运动障碍中纤维肌痛的高流行率和临床影响
Tereza Serranová,Lucia Nováková,Martin Jirásek et al.
Tereza Serranová et al.
Background: Fibromyalgia is characterized by widespread pain, fatigue, sleep and cognitive symptoms. It overlaps clinically with functional motor disorder (FMD), yet its prevalence and impact in FMD remain uncertain. ...
Parkinsonism in Childhood, a Clue to Autosomal Recessive ADCY5-Related Movement Disorder? [0.03%]
儿童帕金森综合征与ADCY5相关性染色体隐性运动障碍的关系研究？
Alexandra L DeArias,Peter E Morrison,Jennifer A Vermilion
Alexandra L DeArias
Background: Advances in genetic testing have allowed for refined phenotypic categorization of pediatric-onset genetic movement disorders. ADCY5-related movement disorder is among this group of conditions for which we have...
Phenotypic Exploration in Patients with Heterozygous Variant in AFG3L2 Gene: A Case-Series and Literature Review [0.03%]
AFG3L2基因杂合变异患者的表型探索：病例系列和文献综述
Sangeetha Yoganathan,Laura Tochen,Jacky Ganguly et al.
Sangeetha Yoganathan et al.
Background: Variants in AFG3-Like Matrix AAA Peptidase, Subunit 2 (AFG3L2) gene are associated with diverse clinical phenotypes. Here, we describe phenotypic findings of two unrelated children with de novo heterozygous va...
Sangeetha Yoganathan,Haya S AlFaris,Anika Menetrey et al.
Sangeetha Yoganathan et al.
Unilateral Oculomotor Apraxia and Pseudodystonia in Joubert Syndrome Associated With Novel CPLANE1 Variant [0.03%]
Joubert综合征伴新型CPLANE1变异的单侧动眼神经动眼 apraxia 和假性 dystonia
Joo Sung Park,Joo-Yeon Lee,Young Bae Sohn et al.
Joo Sung Park et al.
Mind the Gap: Predictors of Osteoporosis Treatment Following Fragility Fracture in Parkinsonism [0.03%]
谨防差距：帕金森综合征患者脆性骨折后开始接受骨质疏松症治疗的预测因素
Katie C Naylor,Emily J Henderson,Emma Tenison
Katie C Naylor
Background: Fracture risk is increased in Parkinson's yet this risk is often not addressed. Objectives: Our objective was to study the ...
"Doctor I Can't 'Tee' off, but I Can Walk 18 Holes on the Golf Course"-Indicates Orthostatic Tremor [0.03%]
“医生我不会‘打’高尔夫，但我可以走完18个洞”——体位性震颤的表现
Sangeeta Scotton,Francesca Magrinelli,Carla Cordivari et al.
Sangeeta Scotton et al.