Visual form agnosia of line drawings and alexia and agraphia of Kanji after right fusiform gyrus and occipitotemporal lobe infarction [0.03%]
右半球距状回及枕颞叶梗塞后引起的线条图视觉性失认和 kanji 字词视盲与失写症
Yoshiko Kurosaki,Masakuni Nomura,Ryusaku Hashimoto
Yoshiko Kurosaki
A 69-year-old Japanese man presented with prosopagnosia, visual form agnosia for line drawings of objects, as well as alexia and agraphia for Kanji after infarction in the right fusiform gyrus and occipitotemporal lobe. In contrast, the ver...
Exercise effects on consolidation of speech and language training in post-stroke aphasia: a case report [0.03%]
运动对卒中后失语症患者言语和语言训练巩固效果的影响：一例报告
Taylor Hebert,Holly Bardutz,Maegan Mason et al.
Taylor Hebert et al.
Post-stroke aphasia severely impacts communication and quality of life. Aerobic exercise enhances learning and memory in healthy adults, with evidence suggesting benefits for verbal tasks. Research exploring its effects in stroke patients w...
Anterior temporal lobe, word comprehension, and physiology of atrophy in semantic primary progressive aphasia [0.03%]
语义性原发进行性失语的颞叶侧区、词汇理解及萎缩生理学
Jordan Q Behn,Elena Barbieri,M Marsel Mesulam et al.
Jordan Q Behn et al.
Peak focal atrophy in the anterior temporal lobe (ATL) highlights the critical role of this area for word comprehension in semantic variant primary progressive aphasia (svPPA). However, the assumption that peak atrophy sites are specific ma...
Supernumerary phantom limb appearing in association with motor intention or pain in the paralyzed upper limb: a case report [0.03%]
与运动意图或偏瘫上肢疼痛相关的多余幻肢：病例报告
Shunpei Katsuura,Hisaaki Ota,Sumio Ishiai
Shunpei Katsuura
We describe a case of supernumerary phantom limb (SPL) persisting into the chronic phase of a right putaminal hemorrhage. The individual, a forced right-handed female in her 40's, was admitted to the hospital 9 months after onset with clear...
Management of MOGAD in an immunosuppressed HIV-positive patient: the first case presenting with alexia without agraphia [0.03%]
免疫抑制 HIV 阳性患者MOGAD的管理：第一例表现为失读症但书写能力正常的病例
Özlem Totuk,Çiğdem Akalan,Serkan Demir
Özlem Totuk
Myelin oligodendrocyte glycoprotein antibody-associated disease (MOG AD) is a rare autoimmune demyelinating condition typically presenting with optic neuritis, transverse myelitis, or encephalitis. Its occurrence in immunocompromised indivi...
Islands of memory in H.M. and other patients with global episodic amnesia: a mini review [0.03%]
H.M.及其他患者全球情景记忆缺失患者的记忆岛：迷你综述
Francesca Baro,Konstantinos Priftis
Francesca Baro
We reviewed the performance of global episodic amnesic patient H.M. Although he was affected by severe anterograde and retrograde amnesia (i.e. global amnesia), he occasionally showed some "islands" of residual intact memory. Therefore, we ...
Multiple ischemic strokes in a patient treated with Lecanemab: a case report [0.03%]
仑尼克马布治疗患者的多发性缺血性卒中个案报告
Hajar Alammar,Mamadou Diallo,Daniel A Llano
Hajar Alammar
Amyloid-lowering therapy via administration of monoclonal antibodies against amyloid beta has been previously associated with the formation of cerebral edema and/or microhemorrhage. These changes are often picked up on MRI and referred to a...
Expanding the genetic spectrum of corticobasal syndrome: novel CCNF p.M394L variant from a South Asian cohort [0.03%]
来自南亚队列的新型CCNF p.M394L变异体扩展了皮质基底综合征的遗传谱系
Faheem Arshad,Gautham Arunachal Udupi,Akhitha Hk et al.
Faheem Arshad et al.
Corticobasal syndrome (CBS) is a rare neurodegenerative disorder characterized by asymmetric motor symptoms, cognitive impairment, and cortical dysfunction. While CCNF gene mutations have been reported in frontotemporal dementia (FTD) and a...
Differential confrontation-naming performance associated with Kanji or Kana representation in a single Broca's aphasia case [0.03%]
单个Broca失语症病例中与汉字或假名表征相关的命名差异性对抗现象
Koji Yamada,Kosei Hashimoto,Noriko Haruhara
Koji Yamada
This study centers on a 44-year-old right-handed Japanese male with moderate Broca's aphasia. During a confrontation-naming task (CNT) during therapy, the person expressed that it was "easier to speak when I recall (in my mind) the Kana (Hi...
Multimodal neuroimaging in a case of familial (G114V) juvenile Creutzfeldt-Jakob disease presenting with parkinsonism [0.03%]
一例以帕金森病表现为首发症状的家族性（G114V）青少年克雅病多模态神经影像研究
Claudia Pascovich,Ignacio Amorin,Andrés Damian et al.
Claudia Pascovich et al.
Creutzfeldt - Jakob disease (CJD) is a subacute spongiform encephalopathy characterised by rapidly progressive dementia and is difficult to diagnose antemortem. We present the case of a 21-year-old woman with a family history of early-onset...