- Two Cases of Oculopharyngeal Muscular Dystrophy in One Family
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Suh MW, Lee KH, Rho JK, Myong HJ
- KMID: 2044096
- J Korean Neurol Assoc.
- 1984 Dec;2(2):208-216.
The authors encountered 2 siblings who showed progressive ophthalmoplegia and bulbar palsy. The patients were studied with various laboratory aids and thought to be as oculopharyngeal muscular dystrophy. The oculopharyngeal... -
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- A Case of Oculopharyngeal Muscular Dystrophy
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Kim MH, Chung SK, Park C
- KMID: 1949601
- J Korean Ophthalmol Soc.
- 1991 Dec;32(12):1153-1158.
Oculopharyngeal muscular dystrophy, one of the variants of chronic progressive external ophthalmoplegia, is a disorder characterized by progressive bilateral ptosis, immobility of the eyes and dysphagia. We have experienced a... -
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- A clinical study on Duchenne muscular dystrophy
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Yang MS, Chae SA, Kim KJ, Hwang YS
- KMID: 1691290
- J Korean Pediatr Soc.
- 1992 May;35(5):652-658.
No abstract available. -
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- Duchenne Muscular Dystrophy Complicated With Dilated Cardiomyopathy and Cerebral Infarction
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Song TJ, Cho H, Lee JB, Lee MJ, Seo KI, Kim SJ, Choi YC
- KMID: 2343363
- J Korean Neurol Assoc.
- 2009 Feb;27(1):82-84.
Duchenne muscular dystrophy, Cerebral infarction, Dilated cardiomyopathy -
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- A Clinical Study on Duchenne Muscular Dystrophy in Childhood
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Noh CI, Hwang YS
- KMID: 1676254
- J Korean Pediatr Soc.
- 1985 Jun;28(6):581-586.
No abstract available. -
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- Duchenne Type Muscular Dystrophy: Report of 8 Cases
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Hwang BY
- KMID: 2464372
- J Korean Orthop Assoc.
- 1970 Sep;5(3):149-153.
- doi: 10.4055/jkoa.1970.5.3.149
Clinical review has been made for 8 cases of Duchenne muscular dystrophy admitted to orthopedic Department during the time between 1964 and 1969. Duchenne type muscular dystrophy, (Duchenne, 1849), is... -
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- Carrier detection of duchenne muscular dystrophy with closelylinked RFLPs.
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Park GH, Park SH
- KMID: 1698794
- Korean J Phys Anthropol.
- 1991 Jun;4(1):53-61.
No abstract available. -
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- Facioscapulohumeral muscular dystrophy: report of two cases
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Choi CU, Kwon JU, Kwon H, Lee SH
- KMID: 1689199
- J Korean Orthop Assoc.
- 1991 Aug;26(4):1354-1358.
No abstract available. -
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- Early-Onset LMNA-Associated Muscular Dystrophy with Later Involvement of Contracture
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Lee Y, Lee JH, Park HJ, Choi YC
- KMID: 2392137
- J Clin Neurol.
- 2017 Oct;13(4):405-410.
- doi: 10.3988/jcn.2017.13.4.405
BACKGROUND AND PURPOSE: The early diagnosis of LMNA-associated muscular dystrophy is important for preventing sudden arrest related to cardiac conduction block. However, diagnosing early-onset Emery-Dreifuss muscular dystrophy (EDMD) with later... -
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- A Family of Oculopharyngeal Muscular Dystrophy and it's HLA Typing
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Yi SD, Park YC, Chung TH
- KMID: 1662008
- J Korean Neurol Assoc.
- 1986 Dec;4(2):266-272.
The authors presented a family whose 4 siblings had been suffered from oculopharyngeal muscular dystrophy of autoscmal recessive trend, with symptoms of progressive ptosis, external ophthalmoplegia, dysarthria, dysphagia and facial... -
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- A Case of the Oculopharyngeal Muscular Dystrophy
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Lee JB, Kim KC, Bum SG
- KMID: 2336426
- J Korean Ophthalmol Soc.
- 1987 Apr;28(2):489-494.
The oculopharyngeal muscular dystrophy is a distinct, clinically well-defined myopathy of later life inherited in an autosomal dominant fashion with complete penetrance. Blepharoptosis, dysphagia, lower leg weakness are the most... -
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- A case of oculopharyngeal muscular dystrophy: electrophysiological review
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Kang SY, Yang SH, Song DH, Nam SH
- KMID: 1688120
- J Korean Acad Rehabil Med.
- 1991 Sep;15(3):377-383.
No abstract available. -
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- Clinical Implications of Pulmonary Function Test and Maximum Static Pressure in Duchenne Muscular Dystrophy
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Kang SW, Baek SK, Na YM, Moon JH, Kim TS
- KMID: 2136828
- J Korean Acad Rehabil Med.
- 1997 Oct;21(5):936-941.
Respiratory failure and pulmonary infection are the major causes of death in the Duchenne muscular dystrophy patients. The purposes of this study are to evaluate pulmonary function of Duchenne muscular... -
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- Correction of blepharoptosis in oculopharyngeal muscular dystrophy: cases in one family
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No authors listed
- KMID: 2204118
- J Korean Soc Plast Reconstr Surg.
- 1998 Oct;25(7):1353-1358.
Oculopharyngeal muscular dystrophy is a hereditary, autosomal dominant, slowly progressive disorder with middle age onset, major symptoms are ptosis and dysphagia mainly due to selectively involved levator palpebrae and the... -
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- Facioscapulohumeral Muscular Dystrophy Confirmedby D4Z4 Analysis
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Lee SC, Ki CS, Lee SH, Im HK, Koh SH, Lee KY, Lee YJ
- KMID: 2185082
- J Korean Neurol Assoc.
- 2008 Aug;26(3):292-294.
No abstract available. -
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- Significance of Immunohistochemical Study in Patients with Muscular Dystrophy
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Kim DS, Park KH, Nam SO, Lee CH, Park KJ
- KMID: 2343114
- J Korean Neurol Assoc.
- 2004 Dec;22(6):613-622.
BACKGROUND: For the differential diagnosis between the various subtypes of muscular dystrophy, the analysis of the protein expression pattern from the biopsied skeletal muscle tissue is essential. Authors performed the... -
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- Gene Therapy of Inherited Muscle Diseases
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Shin JH
- KMID: 1492122
- J Korean Soc Clin Neurophysiol.
- 2012 Dec;14(2):53-58.
For the last decades, molecular genetics has achieved great advances that the genes on the list of inherited muscle diseases are piling up. Those diseases of overlapping clinico-pathologic findings are... -
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- A Case of Becker Muscular Dystrophy Associated With Dilated Cardiomyopathy
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Lee JK, Jang JW, Im MK, Park KJ, Min YJ, Lee SA, Kim JJ, Park SW, Park SJ, Kim YH, Park JH, Lee JK
- KMID: 2080519
- Korean J Med.
- 1997 May;52(5):708-711.
Dilated cardiomyopaty is a rare occurrence in Hecker muscular dystropy. We report a case of Becken muscular dystrophy in 28 old man who presented with dyspnea, progressive muscle weakness, and... -
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- Ultrasound Findings in Duchenne Muscular Dystrophy Disease
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Na YM, Bae KJ, Kang SW, Kim MY, Kang BC
- KMID: 2323016
- J Korean Acad Rehabil Med.
- 1997 Jun;21(3):572-578.
The real-time ultrasonography is a simple, noninvasive procedure that is most suitable for application in pediatric practice. The ultrasonographic appearance of various disorders in children such as progressive muscular dystrophies,... -
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- Female Carriers of Duchenne Muscular Dystrophy
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Cho YN, Choi YC
- KMID: 1811003
- J Genet Med.
- 2013 Dec;10(2):94-98.
- doi: 10.5734/JGM.2013.10.2.94
Dystrophinopathy, caused by mutations in the DMD gene, presents with variable clinical phenotypes ranging from the severe Duchenne muscular dystrophy (DMD) to the milder Becker muscular dystrophy(BMD) forms. DMD is... -
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