A case report of crossed aphasia, grasping, and intermanual conflict with the left hand [0.03%]
交叉性失语症、抓握动作异常及左手相互手冲突的病例报告
Fuzuki Sakamoto,Yuhei Kodani,Katsuya Nakamura et al.
Fuzuki Sakamoto et al.
There are few reports describing the coexistence of alien hand syndrome (AHS) and crossed aphasia. The patient was a right-handed woman in her seventies. Following an infarction involving the medial right frontal lobe and the genu of the co...
Bimanual asymmetric exercises reduce pathological mirror movements after stroke: a case report with disconnectome mapping [0.03%]
卒中后病理镜像运动的治疗：一例双手不对称训练的病例报告及断连素绘图映射研究
Ken Ito,Shun Sawai,Hideki Nakano
Ken Ito
Involuntary mirror movements (MMs) may occur in the nonparetic hand after stroke events, accompanying voluntary movements of the paretic hand. These can interfere with unimanual dexterity and bimanual coordination, potentially impacting the...
Rhiannon MacKenzie-Phelan,Francis McGlone,Samantha Brooks et al.
Rhiannon MacKenzie-Phelan et al.
Direct electrical stimulation (DES) during awake craniotomy is the gold-standard for language mapping; however, conventional tasks (e.g. counting, object naming, reading) provide limited sensitivity to grammatical and sentence-level process...
Opsoclonus myoclonus syndrome in an HIV patient, following plasmodium falciparum infection [0.03%]
一名疟原虫感染后的HIV患者出现 opsoclonus-myoclonus 综合征
Ewodo Touna Hilaire Dominique,Kenmegne Caroline,Gams Massi Daniel et al.
Ewodo Touna Hilaire Dominique et al.
Opsoclonus myoclonus syndrome (OMS) is a rare inflammatory disease of the central nervous system characterized by ocular movements, ataxia, irritability, myoclonus, and sleep disturbances and is thought to result from variable etiologies. W...
A case of Joubert Syndrome and NPC1 mutation in a 7-year-old girl: presented with neuromotor developmental delay and ataxia [0.03%]
一名携带NPC1基因突变的7岁女童Joubert综合征病例报道：以神经运动发育迟缓和共济失调起病
B Diler Durgut,A Türkyılmaz
B Diler Durgut
Joubert Syndrome (JS) is a rare neurodevelopmental disorder characterized by cerebellar ataxia, oculomotor apraxia, and the characteristic "molar tooth sign" on brain MRI. Niemann - Pick Disease Type C (NPC) is an autosomal recessive lysoso...
Stimulation of the human periaqueductal gray induces threat bradycardia: a case report [0.03%]
人导水管周围灰质刺激诱发威胁性心动过缓的一项病例报告
Felix H Klaassen,Lycia D de Voogd,Anneloes M Hulsman et al.
Felix H Klaassen et al.
The ability to recognize and anticipate potential danger is crucial for survival across species. The midbrain periaqueductal gray (PAG) is implicated in regulating threat-anticipatory responses, including heart rate deceleration (threat bra...
Editorial Neurocase [0.03%]
神经病例期刊编辑部
Marc W Haut
Marc W Haut
Beyond motor impairment: investigating cognitive aspects of hereditary spastic paraplegia in a Greek case series [0.03%]
超越运动障碍：希腊病例系列中遗传性痉挛性截瘫的认知方面调查
Alex Malioukis,Dimitrios Kasselimis,Georgia Angelopoulou et al.
Alex Malioukis et al.
Hereditary spastic paraplegia (HSP) is a heterogeneous group of inherited disorders primarily characterized by progressive spasticity and lower extremity weakness. Traditionally associated with corticospinal tract dysfunction, HSP was long ...
Familial young-onset Parkinson's disease associated with SNCA gene duplication: a case series of three sisters from Turkey [0.03%]
土耳其三姐妹年轻帕金森病与SNCA基因重复的家系研究
Pervin Işeri,Enes Demiryurek
Pervin Işeri
SNCA gene duplications are a rare cause of autosomal dominant Parkinson's disease (PD), linked to early onset and cognitive or behavioral symptoms. Data from Turkey remain limited. To describe the clinical, cognitive, behavioral, and geneti...
Mixed primary progressive aphasia and alcohol use disorder: a case of detailed clinical phenotyping outperforming molecular imaging [0.03%]
详细临床表型优于分子影像的病例：混合性原发进行性失语和酒精使用障碍
Obiora Okoye,Cristiano Schaffer Aguzzoli,Petronilla Battista et al.
Obiora Okoye et al.
Primary progressive aphasia (PPA) refers to a group of clinically and pathologically heterogeneous syndromes characterized by progressive and relatively selective impairment in speech and language as the main cognitive domain in the early d...