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Inclusion Body Myositis: A case report

Oh HI, Yoo YJ, Ahn SH, Chang SK

  • KMID: 2323614
  • J Korean Acad Rehabil Med.
  • 2000 Dec;24(6):1229-1234.
In 1971 inclusion body myositis was reported by Yunis and Samaha. This disease is similar with chronic multiple myositis clinically. Pathologically, inclusion body myositis is characterized by intracytoplasmic vacuole with...
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Inclusion body myositis: a case report

Park SH, Park HR

Inclusion body myositis is a rare myopathy that clinically resembles a chronic polymyositis and histopathologically is characterized by the presence of rimmed vacuoles containing ultrastructural cytoplasmic degradation products with filamentous...
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A Case of Inclusion Body Myositis

Moon JS, Sunwoo IN, Kim TS, Seo CK

  • KMID: 2065967
  • J Korean Neurol Assoc.
  • 1993 Mar;11(1):138-140.
Here we report a case of the classical inclusion body myositis. The muscle pathology in a 61-year-old male patient with slowly progressive proximal muscle weakness and atrophy revealed basophilic rimmed...
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Hypokalemia-Induced Rhabdomyolysis by Primary Aldosteronism Coexistent With Sporadic Inclusion Body Myositis

Lee JH, Kim E, Chon S

We describes a patient with hypokalemia-induced rhabdomyolysis due to primary aldosteronism (PA), who suffered from slowly progressive muscle weakness after laparoscopic adrenalectomy, and was later diagnosed with coexisting sporadic inclusion...
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Inclusion Body Myositis Distal Myopathy?

Kim SM, Lee HM, Song HK, Kim SY, Kwon KH, Lee BC, Ha CW, Chi JG

  • KMID: 1686782
  • J Korean Neurol Assoc.
  • 1993 Sep;11(3):427-433.
Inclusion body myositis (IBM) is a chronic inflammatory myopathy with characteristic rimmed vacuoles. Cytoplasmic and intranuclear filamentous inclusions in muscle speci men. The clinical features manifest male dominance with the...
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A Case of Incontinentia Pigmenti with Destructive Encephalopathy

Han JK, Choi JC, Park MK, Park KW, Eun BL, Chung JT, Lee DH

  • KMID: 2342736
  • J Korean Neurol Assoc.
  • 1998 Oct;16(5):739-742.
Becker muscular dystrophy is a X-linked recessive disease with the affected gene at locus Xp21, characterized by progressive muscular weakness. Without the definite family history, it has been known that...
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A Case of Polymyositis Treated with Intravenous Immunoglobulin

Lee JO, Oh JH, Lee SJ, Koh DK

  • KMID: 1829647
  • J Korean Pediatr Soc.
  • 1999 Dec;42(12):1735-1740.
Inflammatory myopathies are comprised of three major subsets, polymyositis, dermatomyositis and inclusion body myositis. Although their etiology is unclear, each group retains its characteristic clinical, immunopathologic features. In polymyositis, a...
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A Case of Mumps Virus Infection Associated with Severe Myositis

Kim SB, Heo JH, Hong SK, Shin JW, Kim IH, Pai HJ, Cho JH, Lee JY, Park JW

  • KMID: 2248237
  • Korean J Infect Dis.
  • 1999 Jun;31(3):239-242.
Myositis caused by mumps virus is very rare. Mumps virus has been suggested as a causative agent of inclusion body myositis, but there has been no definite evidence. We experienced...
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A case of rigid spine syndrome with rimmed vacuolar myopathy

Kim YD, Cho SJ, Sunwoo IN, Cho TY, Kim TS

  • KMID: 2342682
  • J Korean Neurol Assoc.
  • 1998 Jun;16(3):416-420.
Rigid spine syndrome (RSS) is a childhood onset muscle disorder characterized by: marked limitation of motility of cervical and lumbar spine with severe lordosis, contracture of limb joints, mild and...
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Effect of beta-amyloid Peptide on Fine Structure of Cardiac Myocytes in Culture

Sung EK, Lee YS, Sung HK, Park JH, Kim JY, Song IH, Lee YC

  • KMID: 2224560
  • Korean J Anat.
  • 2000 Aug;33(4):497-510.
Several predetermined concentrations of beta-amyloid peptide, (betaA) were administered to the rat cardiac myocyte cultures for three days to determine the effects of betaA. Stainings with congo red and crystal...
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