WordNet
- (medicine) any disturbance in the functioning of an organ or body part or a disturbance in the functioning of a social group; "erectile dysfunction"; "sexual relationship dysfunction" (同)disfunction
- relating to or associated with the cerebellum; "cerebellar artery"
PrepTutorEJDIC
- 機能障害,機能不全
UpToDate Contents
全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.
- 1. 成人における小脳性運動失調の概要 overview of cerebellar ataxia in adults
- 2. 腫瘍随伴性小脳変性症 paraneoplastic cerebellar degeneration
- 3. ウェルニッケ脳症 wernicke encephalopathy
- 4. 脊髄小脳変性症 the spinocerebellar ataxias
- 5. 遺伝性運動失調の概要 overview of the hereditary ataxias
English Journal
- Ocular motor disorders.
- Willard A, Lueck CJ.Author information Department of Neurology, The Canberra Hospital and Australian National University, Canberra, Australia.AbstractPURPOSE OF REVIEW: Studying eye movements can provide insight into how the normal brain works, how diseases affect eye movements, and how eye movement abnormalities can be used to study diseases and/or their treatments. In this review, we concentrate on recent studies looking at abnormalities of saccades in various diseases.
- Current opinion in neurology.Curr Opin Neurol.2014 Feb;27(1):75-82. doi: 10.1097/WCO.0000000000000054.
- PURPOSE OF REVIEW: Studying eye movements can provide insight into how the normal brain works, how diseases affect eye movements, and how eye movement abnormalities can be used to study diseases and/or their treatments. In this review, we concentrate on recent studies looking at abnormalities of sac
- PMID 24300789
- Genetics of dizziness: cerebellar and vestibular disorders.
- Requena T, Espinosa-Sanchez JM, Lopez-Escamez JA.Author information aOtology and Neurotology Group CTS495, Human DNA Variability Department, GENYO. Centre for Genomics and Oncological Research (GENyO), Pfizer/University of Granada/Andalusian Regional Government, PTS Granada bDepartment of Otolaryngology, Hospital San Agustin, Linares, Jaen cDepartment of Otolaryngology, Hospital de Poniente, El Ejido, Almería, Spain.AbstractPURPOSE OF REVIEW: Recent advances in next generation sequencing techniques (NGS) are increasing the number of novel genes associated with cerebellar and vestibular disorders. We have summarized clinical and molecular genetics findings in neuro-otolology during the last 2 years.
- Current opinion in neurology.Curr Opin Neurol.2014 Feb;27(1):98-104. doi: 10.1097/WCO.0000000000000053.
- PURPOSE OF REVIEW: Recent advances in next generation sequencing techniques (NGS) are increasing the number of novel genes associated with cerebellar and vestibular disorders. We have summarized clinical and molecular genetics findings in neuro-otolology during the last 2 years.RECENT FINDINGS: Whol
- PMID 24275721
- Affective communication deficits associated with cerebellar degeneration.
- Heilman KM, Leon SA, Burtis DB, Ashizawa T, Subramony SH.Author information a Department of Neurology , University of Florida College of Medicine , Gainesville , FL , USA.AbstractThe cerebellum has extensive connections with the frontal lobes. Cerebellar injury has been reported to induce frontal-executive cognitive dysfunction and blunting of affect. We examined a patient with idiopathic cerebellar degeneration with impaired family relationships attributed to an "emotional disconnection." Examination revealed ataxia, dysmetria, and adiadochokinesia more severe on the left and frontal-executive dysfunction; memory and cognitive functions were otherwise normal. Testing of emotional communication included assessments of emotional semantic knowledge, emotional prosody, and emotional facial expressions. Comprehension was normal but expression was severely impaired. Cerebellar dysfunction can cause a defect in facial and prosodic emotional communication.
- Neurocase.Neurocase.2014 Feb;20(1):18-26. doi: 10.1080/13554794.2012.713496. Epub 2012 Sep 28.
- The cerebellum has extensive connections with the frontal lobes. Cerebellar injury has been reported to induce frontal-executive cognitive dysfunction and blunting of affect. We examined a patient with idiopathic cerebellar degeneration with impaired family relationships attributed to an "emotional
- PMID 23020242
Japanese Journal
- 橋本脳症の臨床スペクトラムと病態
- 神経治療学 33(1), 27-31, 2016
- NAID 130005152228
- てんかん性脳波異常を伴う反復発作性運動失調症2型の一家系
- 臨床神経学 56(4), 260-264, 2016
- NAID 130005149743
- てんかん性脳波異常を伴う反復発作性運動失調症2型の一家系
- 臨床神経学 advpub(0), 2016
- NAID 130005142041
Related Pictures
★リンクテーブル★
| リンク元 | 「cerebellar disease」「cerebellar disorder」「小脳機能不全」 |
| 拡張検索 | 「transient traumatic cerebellar dysfunction」 |
| 関連記事 | 「dysfunction」「cerebellar」 |
「cerebellar disease」
「cerebellar disorder」
「小脳機能不全」
「transient traumatic cerebellar dysfunction」
「dysfunction」
- n.
- vi
- 機能不全に陥る
- 関
- barrier、damage、difficulty、disorder、disturbance、foe、functional disorder、functional impairment、hindrance、hypofunction、impair、impairment、impediment、incompetence、insufficiency、lesion、malfunction、obstacle、stun
「cerebellar」
- adj.
- 小脳の、小脳性の