1.Receptors for murine monoclonal antibodies on the normal blood cells.
Joon Ki JUNG ; Myung Chul LEE ; Chang Soon KOH
Journal of the Korean Cancer Association 1993;25(2):252-260
No abstract available.
Antibodies, Monoclonal*
;
Blood Cells*
2.Congenital Hepatic Fibrosis with Caroli's Disease.
Yoon Jung KIM ; Soon Ae OAK ; In Chul LEE
Korean Journal of Pathology 1997;31(3):275-279
Congenital hepatic fibrosis is an inherited, congenital disorder of the liver, and is occasionally associated with cystic disease of the liver and kidney. We present a case of congenital hepatic fibrosis with Caroli's disease. A 21-year-old woman had suffered from an episodic fever with headaches for 3 years. In laboratory examination, the liver function test was within the normal limits. Esophageal varix was noted by an endoscopic examination. Hepatosplenomegaly and multiple dilated bile ducts were seen by abdominal CT scanning. An orthotopic whole liver transplantation was done. The liver was fibrotic and enlarged. Multiple cystically dilated intrahepatic ducts were noted. Microscopically, diffuse portal fibrosis and widening with proliferation of bile ductules were seen. Intrahepatic bile ducts were markedly dilated and tortuous. The liver cell cords were well preserved.
Bile
;
Bile Ducts
;
Bile Ducts, Intrahepatic
;
Caroli Disease*
;
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
;
Esophageal and Gastric Varices
;
Female
;
Fever
;
Fibrosis*
;
Headache
;
Humans
;
Kidney
;
Liver
;
Liver Function Tests
;
Liver Transplantation
;
Tomography, X-Ray Computed
;
Young Adult
3.A Case of Rieger's Syndrome Associated with Controlled Glaucoma.
Soon Kuk JUNG ; Sung Ki LEE ; Bong Chul KIM
Journal of the Korean Ophthalmological Society 1995;36(5):890-895
Rieger's syndrome is a rare autosomal dominant developmental anomaly characterized by ocular and systemic abnomalities. These disorders are typically bilateral and usually diagnosed at birth or in the childhood. The most common ocular defects are hypoplasia of the iris, a prominent Schwalbe's line with iris strands and corectopia. A large number of patients have glaucoma due to devel-opmental defects of the anterior chamber angle structure. The authors experienced a case of Rieger's syndrome which was found in 31-year-old female, who had characteristic ocular and other systemic abnormalities. Associated glaucoma was well controlled by filtering surgery.
Adult
;
Anterior Chamber
;
Atrophy
;
Edema
;
Female
;
Filtering Surgery
;
Frontal Lobe
;
Glaucoma*
;
Glioblastoma
;
Humans
;
Intracranial Pressure
;
Iris
;
Neurofibromatoses
;
Optic Atrophy
;
Optic Nerve
;
Optic Nerve Diseases*
;
Parturition
;
Skin
4.Anthelmintic effect of oxantel and oxantel/pyrantel tablets against intestinal nematode infections.
Soon Hyung LEE ; Chul Yong SONG ; Jung Kyoo LIM
The Korean Journal of Parasitology 1977;15(2):121-126
Present trial was carried out to evaluate the anthelmintic efficacy of oxantel/pyrantel tablets against intestinal nematode infections, and to determine the efficacy of oxantel tablels against Trichuris infection. A total of 34 subjects with the mixed infections were treated with oxantel/pyrantel tablets (100 mg/tablet each) in a single dose of 15 mg/kg body weight, and another group of 22 Trichuris infected cases received oxantel pamoate tablets (125 mg/tablet) in a single dose of 15 mg/kg. All stool examinations were done before the treatment and 3 weeks after the treatment. The cellophane thick smear (Kato's technique) and Stoll's dilution egg counting method were employed. The results of the trial were summarized as follows: The cure rates (egg negative conversion rates) and egg reduction rates for oxantel/pyrantel tablets were 85.3 percent and 97 percent in trichuriasis, 100 percent each in ascariasis and ancylostomiasis. The oxantel tablet treated group demonstrated a cure rate of 90.9 percent and an egg reduction rate of 96.3 percent in the treatment of Trichuris. There were no detectable objective and subjective side effects in this trial. Both oxantel/pyrantel and oxantel pamoate tablets were readily accepted and well tolerated.
parasitology-helminth-nematoda
;
Enterobius vermicularis
;
Ancylostoma duodenale
;
Trichuris trichiura
;
chemotherapy-oxantel/pyrante
;
oxantel pamoate
5.A Case Report of Congenital Hypoplastic Anemia.
Hyun Gi JUNG ; Tai Gyo WHANG ; In Soon PARK ; Chul Ho KIM ; Soon Yong LEE
Journal of the Korean Pediatric Society 1983;26(3):279-283
No abstract available.
Anemia, Hypoplastic, Congenital*
6.Molecular Evolution and Identification of Yersinia Species by 16S rDNA Analysis.
Sang In CHUNG ; Chul Soon CHOI ; Won Yong KIM ; Mi Ok SONG ; Chul Min PARK ; Ki Jung KIM ; In Hwan YU
Journal of the Korean Society for Microbiology 1999;34(4):337-345
Sequence information from the ribosomal RNA molecule can be used as a molecular clock. Therefore, 16S rRNA sequences have become a widely used tool in bacterial systematics, bacterial typing and studies of the composition of micro-organisms in environmental samples. Consequently, the databases are continuously updated with new 16S rRNA sequence information from different species. This in turn facilitates the identification of new isolates, which is important for the diagnosis of various infectious diseases in research. To development differential identification technique in the Yersinia species, the 16S rDNA for total 17 serotypes of Y. pseudotuberculosis type strains and one of Y. enterocolitica wild strain were amplified by polymerase chain reaction and cloned into pGEM-T vector, partially sequenced and analyzed. The 16S rDNA nucleotide sequence homologies among Yersinia strains were ranged 100% to 93.6%. Phylogenetic tree generated from 16S rDNA sequencing data showed different phyletic line that could be readily separated from each serotypes and other enteric bacterium.
Bacterial Typing Techniques
;
Base Sequence
;
Classification
;
Clone Cells
;
Communicable Diseases
;
Diagnosis
;
DNA, Ribosomal*
;
Evolution, Molecular*
;
Polymerase Chain Reaction
;
RNA, Ribosomal
;
Yersinia*
7.A Case of Congenital Hypoprothrombinemia.
Jong Kwang LEE ; Hae Won CHEON ; Jung Hwa LEE ; Kwang Chul LEE ; Soon Kyum KIM
Journal of the Korean Pediatric Society 1994;37(3):422-428
Congenital hypoprothrombinemia is a rare congenital coagulation defect. The clinical signs are manifestation of generalized tendency such as; mucosal bleeding, hypermenorrhea and post tooth extraction hemorrage. It is associated with prolongation of PT and PTT with normal thrombin time and decreased serum prothrombin level. A case with congenital hypoprothrombinemia was experienced by the authors. A 36 days old male baby was admitted with palor skin and vomiting started one day before admission. Right side brain parenchymal hemorrhage and left shift of lateral ventricle were on brain CT scan. Prologation of prothrombin time and partial prothrombin time with decreased serum prothrombin level were resulted. Serum factor I, V, VII, VIII, IX and X were within normal level. We report a case congenital hypoprothrombinemia with a brief review of relaed literatures.
Brain
;
Female
;
Fibrinogen
;
Hemorrhage
;
Humans
;
Hypoprothrombinemias*
;
Lateral Ventricles
;
Male
;
Menorrhagia
;
Prothrombin
;
Prothrombin Time
;
Skin
;
Thrombin Time
;
Tomography, X-Ray Computed
;
Tooth Extraction
;
Vomiting
8.Effect on body weight control through behavior, diet, exercise therapy in obese patients.
Hye Soon PARK ; Young Sun JUNG ; En Su SHIN ; Myung Wha KIM ; Chul Jun KIM
Journal of the Korean Academy of Family Medicine 1993;14(4):250-257
No abstract available.
Body Weight*
;
Diet*
;
Exercise Therapy*
;
Humans
9.A study on T cell subsets and natural killer(NK) cells of peripheral blood in patients with various cancer.
Jin Yeong HAN ; Soon Ho KIM ; Han Chul SON ; Eun Yup LEE ; Jung Man KIM
Korean Journal of Clinical Pathology 1991;11(1):183-195
No abstract available.
Humans
;
T-Lymphocyte Subsets*
10.Santonin-kainic acid complex as a mass chemotherapeutic of Ascaris lumbricoides control in Korea.
Soon Hyung LEE ; Se Chul KANG ; Jong Ho AHN ; Jung Woo LEE ; Han Jong RIM
The Korean Journal of Parasitology 1972;10(2):79-85
Santonin-kainic acid complex was evaluated as a chemotherapeutic of the mass treatment of the Ascaris lumbricoides infection in Korea. The results could be summarized as follows: The negative conversion rate was 82.9% in average in 4 treated groups. Some variations of negative conversion rate among the treated groups were noticed. The egg reduciton rate was 97.7% in average and the results were rather uniform among the three evaluated groups. By the analysis of egg reduction, it seems that the lightly infected cases whose E.P.G. were under 5,000 were resistant to treatment with the less reduced egg output. After the treatment with this complex, the number of egg discharged cases were reduced to 1.84% and the average number of discharge eggs per incompletely treated or untreated cases were reduced to 12.5% compared with the level of before-treatment egg output. The successive observations of the pattern of worm expulsion after drug intake was made. The worms were mostly expelled in the stool within 3 days, and 58.9% of total expelled worms were collected within 24-hour stool. The minimum length of the immature worms expelled was 7.6cm. Among the 659 Ascaris collected in the first-day stool from 91 rural people, 8.5% were in the range of 7.6-12.2 cm-long, immature worms. The sex ratio, male: female= 0.69: 1.
parasitology-helminth-nematoda
;
Ascaris lumbricoides
;
chemotherapy
;
Santonin
;
kainic acid