- Spinocerebellar Ataxia Type 8 Presenting as Ataxia without Definite Cerebellar Atrophy
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Eo YJ, Kim SK, Kim SH, Jang JW
- KMID: 2370974
- J Korean Neurol Assoc.
- 2017 Feb;35(1):55-57.
- doi: 10.17340/jkna.2017.1.15
No abstract available. -
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- A Case of Progressive Ataxia and Palatal Tremor
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Yong SW, Lee PH, Yeo SH, Lee JH
- KMID: 2185365
- J Korean Neurol Assoc.
- 2005 Aug;23(4):568-570.
Progressive ataxia and palatal tremor (PAPT) is a subgroup of symptomatic palatal tremors which is characterized by palatal tremor and idiopathic progressive cerebellar ataxia. Here, we report a 59 year-old-male... -
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- A Case of Early Onset Cerebellar Ataxia with Retained Tendon Reflexes
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Lee JB, Lee HY, Yang JS, Lim BK
- KMID: 2024068
- J Korean Pediatr Soc.
- 1997 Jan;40(1):129-133.
Early onset cerebellar ataxia with retained tendon reflexes is clinical syndrome characterized by progressive cerebelar ataxia of unknown etiology with an onset within the first two decades. This disorder was... -
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- A Case of Spinocerebellar Ataxia Type 7 with Torticollis
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Lee JG, Kim HS, Lee MS
- KMID: 2185774
- J Korean Neurol Assoc.
- 2003 Dec;21(6):663-666.
The spinocerebellar ataxia type 7 is an autosomal dominant neurodegenerative disorder with expansion of unstable CAG trinucleotide repeats in a gene on chromosome 3p, and is classified as autosomal dominant... -
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- Sporadic Congenital Oculomotor Apraxia Associated with Ataxia
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Hong S, Han S, Lee J
- KMID: 2207852
- J Korean Ophthalmol Soc.
- 2005 Aug;46(8):1368-1373.
PURPOSE: To evaluate the natural clinical course of sporadic congenital oculomotor apraxia associated with ataxia. METHODS: In a retrospective study from June 1994 to March 2004, 3 patients with sporadic... -
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- Craniocervical Segmental Dystonia in the Spinocerebellar Ataxia Type 2
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Roh JH, Koh SB, Kim JH, Lee DH, Park KW
- KMID: 1527874
- J Korean Neurol Assoc.
- 2007 May;25(2):232-235.
The spinocerebellar ataxia type 2 (SCA 2) is an autosomal dominant cerebellar ataxia that commonly presents with cerebellar ataxia, hyporeflexia, and slow saccades. Recent clinical series described movement disorder in... -
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- Cerebellar type Ataxia in Middle Cerebral Artery Territory Infarction
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Seo SW, Heo JH, Kim JH, Kim SM
- KMID: 2186019
- J Korean Neurol Assoc.
- 2001 Nov;19(6):671-673.
No abstract available. -
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- A case of ataxia telangiectasia
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Kang DW, Ahn SS, Jeon BS
- KMID: 2016258
- J Korean Neurol Assoc.
- 1997 Aug;15(4):895-899.
Ataxia telangiectasia is an autosomal recessive disorder characterized by progressive cerebellar degeneration, cancer predisposition, immune defects, radiosensitivity and genetic instability. Ataxia telangiectasia is rare and has not been reported in... -
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- Thalamic Ataxia in the Elderly
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Oh BC, Seo MW, Yang YJ
- KMID: 2188786
- J Korean Geriatr Soc.
- 1999 Sep;3(2):96-101.
Ataxia is one of the most serious neurological symptoms in elderly The clarification of the related anatomical structures are necessary for the understanding of pathophysiologic mechanisms of ataxia. We have... -
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- A Case of Friedreich's Ataxia with Optic Atrophy as an Initial Clinical Manifestation
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Heo JH, Bang OY, Moon JS, Sunwoo IN, Kim TS
- KMID: 2342453
- J Korean Neurol Assoc.
- 1994 Sep;12(3):562-565.
The incidence and the nature of visual involvement in Friedreich's ataxia who showed progressive visual impairment a few years before developing characteristic clinical manifestations of Friedreich's ataxia. The progress of... -
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- Early Onset Cerebellar Ataxia with Retained Tendon Reflexes Developed in Brothers: Report of two cases
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Park JM, Park TI, Park RW
- KMID: 2001916
- J Korean Acad Rehabil Med.
- 1997 Apr;21(2):461.
Early onset cerebellar ataxia with retained tendon reflexes is distinctive clinical syndrome characterized by progressive cerebellar ataxia of unknown etiology with an onset within the first two decades. This disorder... -
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- Spinocerebellar Ataxia Type 2 with Only Clinical Feature of Memory Impairment: Case Report
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Joo J, Han SW, Ha SW, Han JH, Kim DE, Yang Y
- KMID: 1973685
- Dement Neurocogn Disord.
- 2014 Mar;13(1):16-19.
- doi: 10.12779/dnd.2014.13.1.16
Spinocerebellar ataxia (SCA) is one of a group of genetic disorders characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements.... -
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- Episodic Ataxia Type 2 with Downbeating Nystagmus Caused by Mutation in the CACNA1A: A Case Report
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Yun S, Chang YJ, Jung SC, Kwon JW, Lee GH, Lee CM, Song YM, Kim JI
- KMID: 1626918
- J Korean Neurol Assoc.
- 2005 Jun;23(3):399-401.
Episodic ataxia type 2 (EA 2) is a rare disorder characterized by intermittent episodes of ataxia with interictal nystagmus. The authors report a patient with EA 2, who presented with... -
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- Unilateral Parieto-Occipital Lobe Infarction Presenting with Optic Ataxia and Saccadic Abnormalties: A Case Report
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Jung SC, Lee CM
- KMID: 1603993
- J Korean Bal Soc.
- 2006 Dec;5(2):320-324.
Optic ataxia is characterized by an impaired visual control of the direction of arm reaching to a visual target, accompanied by defective hand orientation and grip formation. In humans, optic... -
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- A Case of Miller Fisher Syndrome (Variant of Guillain Barr'e Syndrome-Ophthalmoplegia, Ataxia, Areflexia)
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Hwang YM, Choi IS, Kim KH
- KMID: 1662490
- J Korean Neurol Assoc.
- 1983 Dec;1(2):85-88.
Miller Fisher syndrome is a syndrome of acute external ophthalmoplegia, ataxia and areflexia without significant motor or sensory deficit in the limbs and usually results in complete recovery without specific... -
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- Vestibular Dysfunction in Acute Cerebellar Ataxia
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Lee CM
- KMID: 1787780
- Res Vestib Sci.
- 2015 Mar;14(1):21-25.
- doi: 10.0000/rvs.2015.14.1.21
Acute cerebellar ataxia is described as a clinical syndrome of acute onset of cerebellar dysfunction with a good long-term prognosis. The pathogenesis of acute cerebellar ataxia remains unclear. A 55-year-old... -
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- Autosomal Dominant Cerebellar Ataxia Type II Associated with Optic Atrophy
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Kim IT, Shim SD
- KMID: 2205379
- J Korean Ophthalmol Soc.
- 1998 Oct;39(10):2494-2498.
Autosomal dominant cerebellar ataxia(ADCA) is an unusual, familial hereditary disorder that ha been called olivopontocerebellar atrophy. ADCA type II is usually accompanied with severely decreased visual acuity and cerebellar ataxia.... -
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- Dentatorubropallidoluysian Atrophy (DRPLA) With Comitant Esotropia
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Yoo JK, Koo YS, Kwon DY, Park MH, Park KW
- KMID: 2191932
- J Korean Neurol Assoc.
- 2009 Nov;27(4):428-431.
The possibility of a central origin should be considered for late-onset concomitant esotropia. Concomitant esotropia has been reported to occur with spinocerebellar ataxia types 1, 2, and 3, but not... -
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- Ataxia in Thalamic Stroke
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Yoon SS, Chang DI, Chung KC
- KMID: 2066045
- J Korean Neurol Assoc.
- 1996 Mar;14(1):69-73.
BACKGROUND & PURPOSE: Of thalamic stroke syndrome, according to previous reports, the syndrome of hemiataxia and hemisensory loss (thalamic ataxia syndrome) is known to have localizing value confined to the... -
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- Acetazolamide-responsive hereditary paroxysmal ataxia: report of a family
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Kim HJ, Jeon BS
- KMID: 1064969
- J Korean Med Sci.
- 1998 Apr;13(2):196-200.
- doi: 10.3346/jkms.1998.13.2.196
Hereditary paroxysmal ataxia is a rare dominantly inherited disorder characterized by recurrent attacks of cerebellar ataxia, dysarthria, and nystagmus. Each attack lasts from several minutes to few hours or... -
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