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A Case of Kartagener's Syndrome

Min YJ, Ahn CI, Cho SK, Cho JD

  • KMID: 1682701
  • J Korean Pediatr Soc.
  • 1988 Nov;31(11):1522-1526.
No abstract available.
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A Case of Kartagener's Syndrome Presenting as Respiratory and Right Heart Failures

Yang SC, Lee KS, Yoon HJ, Shin DH, Park SS, Lee JH, Park CK

  • KMID: 2317998
  • Tuberc Respir Dis.
  • 1996 Apr;43(2):251-256.
Kartagener's syndrome, a congenital disease transmitted as an autosomal recessive illness with a prevalence of approximately 1:20,000 persons, is characterized by the triple association of situs inversus, bronchiectasis, and sinusitis....
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Successful Role of Endoscopic Sinus Surgery in an Asthmatic Patient Associated with Kartagener's Syndrome

  • KMID: 1969536
  • Korean J Asthma Allergy Clin Immunol.
  • 2012 Jun;32(2):126-130.
BACKGROUND: Kartagener's syndrome is an autosomal recessive disorder characterized by bronchiectasis, chronic sinusitis and situs inversus. Chronic sinusitis in patients with Kartagener's syndrome can lead to exacerbation of bronchial asthma....
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A Case of Kartagener's Syndrome with Various Ultrastructural Defects

Lee SH, Park JH, Jang HS, Kim HS, Kang KW, Kim HC, Kwon KY

Kartagener's syndrome is an inherited condition characterized by triad of chronic paranasal sinusitis, situs inversus, and bronchiectasis. Since 1976, Afzelius found a lack of dynein arm in immotile spermatozoa by...
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Four Cases of Kartagener's Syndrome

Lee YC, Song HY, Lim ST, Kim HC, Lee HB, Lee YS, Rhee YK, Chung JM

Kartagener's syndrome is an autosomaly inherited recessive condition characterized by situs inversus, bronchiectasis, and chronic sinusitis. And recently it was recognized as a subclass of dyskinetic cilia syndrome which caused...
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A Case of Kartagener's syndrome combined with congenital nystagmus

Ryu JS, Jeong DW, Park YK, Kim KS

  • KMID: 2275683
  • Korean J Otolaryngol-Head Neck Surg.
  • 2001 Jun;44(6):657-661.
Primary ciliary dyskinesia results in characteristic clinical symptoms, including chronic pansinusitis, recurrent infections of the respiratory tract, and infertility. Kartagener's syndrome is clinically distinguishable by the presence of situs inversus...
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Total intravenous anesthesia for Kartagener's syndrome: A case report

Jo YY, Jung WS, Kim HS, Byen SH, Lee KC

  • KMID: 1742021
  • Anesth Pain Med.
  • 2012 Oct;7(4):317-319.
Kartagener's syndrome (KGS) is an autosomal recessive disorder which possible to link the occurrence of abnormal ciliary movement and abnormal position of the body organs. Considering the fact that airway...
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One case of Kartagener's syndrome with extracemtral microtubule in cilia

An CH, Choi JC, Lee BH, Park YB, Jee HS, Park SJ, Kim JY, Park IW, Choi BW, Hue SH

  • KMID: 1985265
  • Korean J Med.
  • 2000 Aug;59(2):230-234.
Kartagener's syndrome is an autosomal recessively inherited condition characterized by triad of situs inversus, bronchiectasis, and chronic sinusitis. And recently it was classified as a subclass of dyskinetic cilia syndrome,...
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Primary Ciliary Dyskinesia Associated with Kartagener's Syndrome

Byun EK, Cho YK, Song HJ, Lee HK, Lee JH, Sung SH, Kim YK, Chang JH

Primary ciliary dyskinesia is a genetic disorder of abnormal ciliary structure and function that leads to defective mucociliary clearance, resulting in sinopulmonary infection and infertility. Kartagener's syndrome is a subclass...
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Kartagener's syndrome with immunoglobulin G subclass deficiency

Kim KC, Park JH, Ban GY, Yoo HS, Shin YS, Park HS, Ye YM

Kartagener syndrome is characterized by the triad of situs inversus, bronchiectasis, and chronic paranasal sinusitis. Recurrent sinopulmonary infection, the major determinant for diagnosing immunodeficiency, is the most common clinical manifestation...
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Mycobacterium abscessus Lung Disease in a Patient with Kartagener Syndrome

Kim JH, Song WJ, Jun JE, Ryu DH, Lee JE, Jeong HJ, Jeong SH, Kang HK, Kim JS, Lee H, Chon HR, Jeon K, Kim D, Kim J, Koh WJ

Primary ciliary dyskinesia (PCD) is characterized by the congenital impairment of mucociliary clearance. When accompanied by situs inversus, chronic sinusitis and bronchiectasis, PCD is known as Kartagener syndrome. The main...
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Microtubular Dysfunction and Male Infertility

Gunes S, Sengupta P, Henkel R, Alguraigari A, Sinigaglia MM, Kayal M, Joumah A, Agarwal A

Microtubules are the prime component of the cytoskeleton along with microfilaments. Being vital for organelle transport and cellular divisions during spermatogenesis and sperm motility process, microtubules ascertain functional capacity of...
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Chemotaxis of Blood Neutrophils from Patients with Primary Ciliary Dyskinesia

Koh YY, Sun YH, Min YG, Chi JG, Kim CK

Primary ciliary dyskinesia is characterized by chronic upper and lower respiratory infections which are caused by the grossly impaired ciliary transport. Since the cilia and neutrophils both utilize microtubular system...
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A Case of Primary Ciliary Dyskinesia due to Radial Spokes Deficiency

Kim KB, Roh JL, Lee JK, Park SW

  • KMID: 1873965
  • Korean J Otolaryngol-Head Neck Surg.
  • 1998 Oct;41(10):1331-1334.
Primary ciliary dyskinesia encompasses a heterogenous group of inherited condition characterized by clinical, functional, and ultrastructural features. The transmission electronmicroscopic findings of nasal cilia in a 14-year old girl with...
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A Case of Brain Abscess in a Patient with Primary Mucociliary Transport Failure

Yoon SH, Lee HJ, Yi JS, Yang JH, Lee IW, Song KS, Kang JK

  • KMID: 1812854
  • J Korean Neurosurg Soc.
  • 2001 Dec;30(12):1430-1434.
The authors present a case of brain abscess in a patient with primary mucociliary transport failure. Primary mucociliary transport failure is unfamiliar term to neurosurgeon. It encompasses three hereditary disorders,...
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A Case of Primary Ciliary Dyskinesia

Kang SH, Kim JH, Kim H, Kim TH

Primary ciliary dyskinesia is a disease characterized by unexplained neonatal respiratory distress, otitis media, chronic sinusitis, and chronic bronchiectasis. In approximately half of cases, situs inversus totalis or other laterality...
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A novel compound heterozygous mutation in DNAH5 in a Korean neonate with primary ciliary dyskinesia

Lee NW, Jeong JE, Jang YY, Chung HL

Primary ciliary dyskinesia (PCD) is a genetically heterogeneous disease affecting motile cilia. A female neonate was hospitalized with respiratory distress 72 hours after birth and showed concurrent situs inversus. She...
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A Clinical Study on Primary Ciliary Dyskinesia

Park CW, Koh JS, Kim KR, Lee HS

  • KMID: 2274332
  • Korean J Otolaryngol-Head Neck Surg.
  • 1997 Aug;40(8):1079-1084.
BACKGROUND: Since ciliary dysfunction of the respiratory system impair mucosal ciliary clearance, it is associated with recurrent or persistent upper respiratory infections, chronic bronchitis, chronic sinusitis, recurrent pneumonia, recurrent otitis...
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Bronchiectasis in Children: 10-Year Experience at a Single Institution

Kim HY, Kwon JW, Seo J, Song YH, Kim BJ, Yu J, Hong SJ

PURPOSE: Bronchiectasis in children is still one of the most common causes of childhood mortality in developing countries. The aim of this study was to investigate the epidemiological characteristics, clinical...
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