- Subperiosteal hematoma of the orbit associated with sinusitis
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Woo KI, Kim YD
- KMID: 1375110
- Korean J Ophthalmol.
- 1997 Dec;11(2):118-122.
- doi: 10.3341/kjo.1997.11.2.118
Subperiosteal hematoma of the orbit is a rare but well-recognized entity, usually caused by trauma. Two cases of subperiosteal hematoma associated with sinusitis are presented. A 44-year-old woman experienced the... -
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- Diagnostic and Therapeutic Significance of Sinoscopy in Maxillary Sinusitis
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Kim HN, Kim YM, Choi HS
- KMID: 692993
- Yonsei Med J.
- 1985 Jun;26(1):59-67.
- doi: 10.3349/ymj.1985.26.1.59
Sinoscopy as an endoscopic investigative method of examining the maxillary sinus offers the advantage of a direct local interpretation in contrast to the usual indirect methods. The beginning of sinoscopy... -
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- An Obscure Etiology for Headache: Sphenoid Sinus Disease
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Lee KJ, Yanagisawa K
- KMID: 1729549
- Yonsei Med J.
- 1988 Sep;29(3):209-218.
- doi: 10.3349/ymj.1988.29.3.209
No abstract available. -
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- The role of rhinosinusitis in severe asthma
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Jang AS
- KMID: 1780122
- Korean J Intern Med.
- 2013 Nov;28(6):646-651.
- doi: 10.3904/kjim.2013.28.6.646
The prevalence of asthma is approximately 5% to 10% in the general population. Of these, approximately 5% to 10% are severe asthmatics who respond poorly to asthmatic drugs, including high-dose... -
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- A Case of Odontogenic Orbital Cellulitis Causing Blindness by Severe Tension Orbit
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Park CH, Jee DH, La TY
- KMID: 1429218
- J Korean Med Sci.
- 2013 Feb;28(2):340-343.
- doi: 10.3346/jkms.2013.28.2.340
We report a very rare case of odontogenic orbital cellulitis causing blindness by severe tension orbit. A 41-yr old male patient had visited the hospital due to severe periorbital swelling... -
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- Cystic Fibrosis in Korean Children: A Case Report Identified by a Quantitative Pilocarpine Iontophoresis Sweat Test and Genetic Analysis
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Ahn KM, Park HY, Lee JH, Lee MG, Kim JH, Kang IJ, Lee SI
- KMID: 1781745
- J Korean Med Sci.
- 2005 Feb;20(1):153-157.
- doi: 10.3346/jkms.2005.20.1.153
Cystic fibrosis (CF) is inherited as an autosomal recessive trait, and the mutations in cystic fibrosis transmembrane conductance regulator (CFTR) gene contributes to the CF syndrome. Although CF is common... -
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