1.Dermoscopic Findings in Onychomycosis.
Korean Journal of Medical Mycology 2017;22(1):50-51
No abstract available.
Dermoscopy
;
Mycoses
;
Onychomycosis*
2.S Antigen Specific Rat Helper T Cell Line Induced Experimental Autoimmune Uveoretinitis.
Youn Mun HA ; Soon Tae HO ; Jeong Je CHO ; Seung Min YOO
Korean Journal of Immunology 1997;19(2):181-188
No abstract available.
Adaptive Immunity
;
Animals
;
Cell Line*
;
Rats*
3.Production of monoclonal antibody to Epstein-Barr virus antigen.
Jeong Je CHO ; Soon Tae HO ; Seung Min YOO ; Youn Mun HA
Korean Journal of Immunology 1992;14(1):117-131
No abstract available.
Herpesvirus 4, Human*
4.Production of human monoclonal antibodies against tetanus toxoid using the Epstein-Barr virus transformation.
Seung Min YOO ; Jeong Je CHO ; Soon Tae HO ; Youn Mun HA
Korean Journal of Immunology 1993;15(2):139-146
No abstract available.
Antibodies, Monoclonal*
;
Herpesvirus 4, Human*
;
Humans*
;
Tetanus Toxoid*
;
Tetanus*
5.Onychopapilloma Presenting as Erythronychia and Leukonychia: Dermoscopic Features of Two Cases in Korea.
Minsoo KIM ; Gwanghyun JO ; Cheol LEE ; Je Ho MUN
Annals of Dermatology 2018;30(6):742-744
No abstract available.
Korea*
7.Pigmented Onychomatricoma Showing a Longitudinal Melanonychia: A Case Report and Brief Review of Literature.
Sung Cheol JUNG ; Tae Min LEE ; Minsoo KIM ; Gwanghyun JO ; Je Ho MUN
Annals of Dermatology 2018;30(5):637-639
No abstract available.
Nail Diseases
;
Nails, Malformed
;
Melanoma
;
Skin Neoplasms
8.Generation of monoclonal antibodies reactive to human interleukin 2(IL 2).
Youn Mun HA ; Jun Hyung LEE ; Seung Min YOO ; Jeong Je CHO ; Soon Tae HO ; Jae Kyung PARK ; Sang Yun NAM
Journal of the Korean Society for Microbiology 1993;28(4):313-319
No abstract available.
Antibodies, Monoclonal*
;
Humans*
;
Interleukins*
9.Effect of Human Immunoglobulin G in Pneumoconiotic Patients with Pneumonia.
Je Hyuk MUN ; Jin Suk CHUNG ; Kyoung Ah KIM ; Young LIM ; Ho Woo NAM ; Joong Soo HAN
Korean Journal of Occupational and Environmental Medicine 2002;14(2):134-142
OBJECTIVES: It is well known that pneumoconiotic patients experience impairments of macrophage function, as well as poor penetration of drugs into the fibrotic nodules and the immune system. Resultantly, pneumonia is frequently involved in pneumoconiotic patients and its treatment is not easy. Therefore, we conducted a clinical evaluation of immunoglobulin G which is known to be effective in severe infectious diseases. METHODS: We randomly selected 45 pneumoconiotic patients with pneumonia and classified them into 2 groups. The experimental group (IgG group) was scheduled to receive antibiotics and IgG (5 g I.V./day for 7 days). The control group was treated with antibiotics alone. Sputum gram stain (counts of WBCs and microorganisms), body temperature, arterial oxygen tension, and counts of peripheral venous blood leukocytes and band neutrophils were used as markers to assess the response effect therapy at time periods of 0, 2, 4, 6, and 8 days after completion of therapy. We compared the clinical scores between the two groups. RESULTS: The experimental IgG treated group was composed of 27 patients, and the control group comprised 18 patients. There was no statistical differences between two groups in terms of age, pneumoconiotic profusion, impairment degree of pulmonary function, or frequency of pathogen isolation in the sputum before medication. The experimental IgG treated group showed lower clinical scores as compared with the control group (p=0.083). CONCLUSIONS: These results suggest that IgG infusion with antibiotics will have an effect on pneumonia therapy in pneumoconiosis patients that are under 60 years and exhibit simple pneumoconiosis.
Anti-Bacterial Agents
;
Body Temperature
;
Communicable Diseases
;
Humans*
;
Immune System
;
Immunoglobulin G*
;
Immunoglobulins*
;
Leukocytes
;
Macrophages
;
Neutrophils
;
Oxygen
;
Pneumoconiosis
;
Pneumonia*
;
Sputum
10.May-Thurner Syndrome Treated with Endovascular Wall Stent.
You Sang YOON ; Je Hwan WON ; Ho CHOI ; Dong Mun SOH ; Cheol Joo LEE ; Hyung Tae KIM
The Korean Journal of Thoracic and Cardiovascular Surgery 2003;36(3):202-205
Deep vein thrombosis (DVT) is a common disease. However, May-Thurner syndrome, which is the cause of DVT, is an uncommon processes in which there is an impaired venous return due to compression of the left iliac vein by the overlying right common artery. This condition results in a left iliofemoral deep thrombosis and severe leg edema. It is, therefore, called iliac compression syndrome. Catheter-directed thrombolytic therapy of acute extensive iliofemoral DVT and balloon angioplasty with venous stenting are recommended. Two cases with history of left leg swelling are diagnosed as May-Thurner syndrome, which was demonstrated by venography. We successfully treated the patients with thrombolysis, balloon angioplasty, and stent insertion at the site of common iliac vein compression. Therefore, we report the cases with overall review of the literature.
Angioplasty, Balloon
;
Arteries
;
Edema
;
Humans
;
Iliac Vein
;
Leg
;
May-Thurner Syndrome*
;
Phlebography
;
Stents*
;
Thrombolytic Therapy
;
Thrombosis
;
Venous Thrombosis