- Two Cases of Probable Huntington's Disease
-
Lee HS, Baek SW, Kim SW
- KMID: 1957545
- J Korean Neurol Assoc.
- 1988 Dec;6(2):289-294.
Huntington's Disease (HD), an autosomal dominant disorder of mid-life onset, is characterized by progressive involuntary choreiform movement, psychological change and dementia. We present here two cases of Huntington's disease. One... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Huntington`s Disease
-
Lee SJ, Lee SB, Myung HJ
- KMID: 1662066
- J Korean Neurol Assoc.
- 1986 Jun;4(1):147-150.
Huntington's disease (HD), an autosomal dominant dominant disorder of mid-life onset, is characterized by progressive involuntary choreiform movement, psychological change and dementia. We present here one case of Huntington's disease,... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Huntington's Chorea
-
Chung JW, Lee BC, Kim JS
- KMID: 1957543
- J Korean Neurol Assoc.
- 1988 Dec;6(2):278-283.
This is a case report of 47 year-old male patient with Huntington's chorea. Huntington's chorea is a progressive neurodegenerative disorder with autosomal dominant inheritance. The first symptoms of Huntington's chorea... -
- CITED
-
- Close
- SHARE
-
- Close
- Huntington's chorea: two case reports
-
Lim OK, Lee SJ, Chon JS, Eoh H, Suk JH
- KMID: 1688119
- J Korean Acad Rehabil Med.
- 1991 Sep;15(3):372-376.
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Huntington's Disease Confirmed by Genetic and Pathological Study
-
Lyoo CH, Lee MS, Kim YJ, Suk SH, Yang KH, Song KS
- KMID: 2342560
- J Korean Neurol Assoc.
- 1996 Sep;14(3):725-737.
Huntington's disease is an autosomal dominantly inherited neurodegenerative disease, which is characterized by choreic movement and progressive dementia. A definite diagnosis of Huntington's disease cannot be made by clinical informations... -
- CITED
-
- Close
- SHARE
-
- Close
- Two Families with Huntington's Disease
-
Lim JK, Yi DD, Suh CK, Park YC, Byun YJ
- KMID: 2184398
- J Korean Neurol Assoc.
- 1989 Jun;7(1):172-177.
Huntington's disease(HD) is a neurcdegenerative disorder caused by a highly penetrant autosomal dominant genetic defect. It is characterized by adult onset progressive chorea, psychological change, and dementia with relentless deterioration.... -
- CITED
-
- Close
- SHARE
-
- Close
- Gene Analysis of Probable Huntington's Disease
-
Kim MH, Lee KW, Park KS, Jeon BS, Lee SB, Myung HJ
- KMID: 2342407
- J Korean Neurol Assoc.
- 1994 Jun;12(2):317-322.
Increased CAG repeats with full gene sequence (IT15) in Huntington's disease (HD) became known in 1993. We used polymerase chain reaction (PCR) in patients with clinically diagnosed Huntington's disease. After... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Huntington's Disease without Family History Who Has Diagnosed with CAG Repeat Expansion
-
Yun KW, Shin SJ, Park SS
- KMID: 2340189
- J Korean Neuropsychiatr Assoc.
- 1998 Jul;37(4):752-757.
We report a 48-year-old female with typical symptoms of Huntington's disease, including involuntary movement, cognitive dysfunction and psychiatric symptoms such as personality change, emotional instability, persecutory ideation and depression, but... -
- CITED
-
- Close
- SHARE
-
- Close
- Combined use of a double-lumen tube and Fogarty catheter to prevent the endobronchial spread of infection: a case report
-
Kim J, Lee H, Park H, Jeong CY
- KMID: 2360478
- Korean J Anesthesiol.
- 2016 Dec;69(6):619-622.
- doi: 10.4097/kjae.2016.69.6.619
Huntington's disease is a neurodegenerative disorder with an autosomal dominant inheritance pattern. Patients with Huntington's disease show an increased risk of aspiration pneumonia when the pharyngeal muscle is invaded. We... -
- CITED
-
- Close
- SHARE
-
- Close
- Hopping from One Cell to Another: Huntington's Disease Propagates
-
Park SM
- KMID: 2398419
- Exp Neurobiol.
- 2017 Dec;26(6):319-320.
- doi: 10.5607/en.2017.26.6.319
No abstract available. -
- CITED
-
- Close
- SHARE
-
- Close
- Anesthetic management of a patient with Huntington's chorea: A case report
-
Kang JM, Chung JY, Han JH, Kim YS, Lee BJ, Yi JW
- KMID: 1767338
- Korean J Anesthesiol.
- 2013 Mar;64(3):262-264.
- doi: 10.4097/kjae.2013.64.3.262
Huntington's chorea is a rare hereditary disorder of the nervous system. It is inherited as an autosomal dominant disorder and is characterized by progressive chorea, dementia and psychiatric disturbances. The... -
- CITED
-
- Close
- SHARE
-
- Close
- Animal Models of Neurodegenerative Diseases
-
Cho SR
- KMID: 1445606
- Brain Neurorehabil.
- 2011 Mar;4(1):30-34.
- doi: 10.12786/bn.2011.4.1.30
Animal models of human diseases are essentially required to investigate the pathophysiological mechanisms of the diseases, and to test potential therapies for the clinics. However, neurodegenerative diseases including Parkinson's disease... -
- CITED
-
- Close
- SHARE
-
- Close
- Psychosis, Treatment Emergent Extrapyramidal Events, and Subsequent Onset of Huntington's Disease: A Case Report and Review of the Literature
-
Xu C, Yogaratnam J, Tan N, Sim K
- KMID: 2348480
- Clin Psychopharmacol Neurosci.
- 2016 Aug;14(3):302-304.
- doi: 10.9758/cpn.2016.14.3.302
Huntington's disease (HD) is an autosomal dominant neurodegenerative disease characterized by a triad of progressive motor dysfunction, cognitive decline and psychiatric disturbances. The hallmark of HD is the distinctive choreiform... -
- CITED
-
- Close
- SHARE
-
- Close
- Therapeutic Approaches for Inhibition of Protein Aggregation in Huntington's Disease
-
Kim S, Kim KT
- KMID: 2009023
- Exp Neurobiol.
- 2014 Mar;23(1):36-44.
- doi: 10.5607/en.2014.23.1.36
Huntington's disease (HD) is a late-onset and progressive neurodegenerative disorder that is caused by aggregation of mutant huntingtin protein which contains expanded-polyglutamine. The molecular chaperones modulate the aggregation in early... -
- CITED
-
- Close
- SHARE
-
- Close
- A Case of Huntington's Disease with Generalized Seizure and Prominent Family History of the Disease
-
Kim JS, Park EJ, Hong SC, Han JH, Lee SP
- KMID: 2340535
- J Korean Neuropsychiatr Assoc.
- 2001 Jan;40(1):162-167.
Huntington's disease(HD), an autosomal dominant disorder, is characterized by progressive involuntary choreiform movement, psychiatric symptoms, and dementia. We experienced a 44-year-old male HD patient with prominent family history of the... -
- CITED
-
- Close
- SHARE
-
- Close
- PET studies in Alzheimer Disease and Other Degenerative Dementias
-
Jeong Y, Na DL
- KMID: 1516895
- Korean J Nucl Med.
- 2003 Feb;37(1):13-23.
Neurodegenerative disorders cause a variety of dementia including Alzheimer disease, frontotemporal dementia, dementia with Lewy bodies, corticobasal degeneration, progressive supranuclear palsy, and Huntington's disease. PET scan is useful for early... -
- CITED
-
- Close
- SHARE
-
- Close
- Diagnosis of Huntington's disease with Polymerase Chain Reaction
-
Kim BJ, Park KW, Lee DH
- KMID: 2342521
- J Korean Neurol Assoc.
- 1996 Jun;14(2):502-510.
Huntington's disease is an autosomal dominant neurodegenerative disorder that usually begins in mid-life and is characterized by a progression of involuntary choreiform movements, personality change, and dementia. 4 specific unstable... -
- CITED
-
- Close
- SHARE
-
- Close
- Therapeutic Strategies in Huntington's Disease
-
Kanazawa I
- KMID: 1980460
- J Clin Neurol.
- 2006 Dec;2(4):213-224.
- doi: 10.3988/jcn.2006.2.4.213
This article provides an overview of the therapeutic strategies, from ordinary classical drugs to the modern molecular strategy at experimental level, for Huntington's disease. The disease is characterized by choreic... -
- CITED
-
- Close
- SHARE
-
- Close
- Cortical Axonal Secretion of BDNF in the Striatum Is Disrupted in the Mutant-huntingtin Knock-in Mouse Model of Huntington's Disease
-
Park H
- KMID: 2416249
- Exp Neurobiol.
- 2018 Jun;27(3):217-225.
- doi: 10.5607/en.2018.27.3.217
Deficient BDNF signaling is known to be involved in neurodegenerative diseases such as Huntington's disease (HD). Mutant huntingtin (mhtt)-mediated disruption of either BDNF transcription or transport is thought to be... -
- CITED
-
- Close
- SHARE
-
- Close
- Exosome-Based Delivery of miR-124 in a Huntington's Disease Model
-
Lee ST, Im W, Ban JJ, Lee M, Jung KH, Lee SK, Chu K, Kim M
- KMID: 2367608
- J Mov Disord.
- 2017 Jan;10(1):45-52.
- doi: 10.14802/jmd.16054
OBJECTIVE: Huntington's disease (HD) is a genetic neurodegenerative disease that is caused by abnormal CAG expansion. Altered microRNA (miRNA) expression also causes abnormal gene regulation in this neurodegenerative disease. The... -
- CITED
-
- Close
- SHARE
-
- Close
