1.Effect of Antiandrogen on Calcitonin Gene-related Peptide mRNA Expression ofthe Rat Cremaster Nucleus.
Su Youn CHO ; Myung Sik SHIN ; Hee Jin LEE
Korean Journal of Urology 2000;41(3):430-434
No abstract available.
Animals
;
Calcitonin Gene-Related Peptide*
;
Calcitonin*
;
Rats*
;
RNA, Messenger*
2.DNA Profiling via Short Tandem Repeat Analysis by Using Serum Samples.
Ji Hyun LEE ; Hye Young LEE ; Sohee CHO ; Joo Youn CHO ; In Jin JANG ; Soong Deok LEE
Korean Journal of Legal Medicine 2013;37(4):220-223
Serum is free of cellular components. Because DNA is located in the nuclei or mitochondria of cells, serum could be assumed DNA free. Few previously published case reports to date have used serum for DNA typing. Here, we report on human genotyping via short tandem repeat (STR) analysis using serum as a sample, and discuss problems involved in the process.
DNA Fingerprinting*
;
DNA*
;
Humans
;
Microsatellite Repeats*
;
Mitochondria
3.Effect of obesity and age on the blood pressure.
Youn Jin KIM ; Young Hoon HAN ; Sang Wook PARK ; Byung Mann CHO ; Hyung Su SEOL ; Youn Jeong HEO
Journal of the Korean Academy of Family Medicine 1997;18(3):295-305
BACKGROUND: In recent years, the incidence of obesity increased in Koreans. The main cause suggested is the diet style of Korean changed to that of Western. It has been proved that obesity is a risk factor or an aggravating factor of hypertension and diabetes mellitus, cardiovascular disease, etc. Primary physician has been interested in the correlation of blood pressure with relative body weight and aging. The purpose of this study was to focus on the influence of age and relative body weight on blood pressure. METHODS: Subjects were collected from 2,068 adults who had received Adult Health Examination. That subjects were divided according to age, relative body weight and then the relation of blood pressure with age according to relative body weight and relation with relative body weight according to age were investigated. RESULTS: Systolic blood pressure increased significantly according to age in all male and female three weight groups and then increased significantly according to relative body weight in all male and female three age groups except male seventh decade group. Diastolic blood pressure increased significantly according to age in all male and female three weight groups except male obesity group and then increased significantly according to the relative body weight in all male and female three age groups except male and female seventh decade groups. Systolic blood pressure has higher correlation with age than relative body weight and diastolic blood pressure has higher correlation with relative body weight in male. In female, systolic and diastolic blood pressure have higher correlations with age. CONCLUSIONS: It can be suggested that blood pressure increase significantly according to aging process and relative body weight. These two factors have a little different effects to systolic and diastolic blood pressure according to sex. Relative body weight has more effect to diastolic blood pressure than systolic blood pressure in male.
Adult
;
Aging
;
Blood Pressure*
;
Body Weight
;
Cardiovascular Diseases
;
Diabetes Mellitus
;
Diet
;
Female
;
Humans
;
Hypertension
;
Incidence
;
Male
;
Obesity*
;
Risk Factors
4.A Clinicopathological Study of Chronic Cutaneous Lupus Erythematosus.
Tae Eun KWON ; Oh Sang KWON ; Jin Ho CHUNG ; Kwang Hyun CHO ; Jai Il YOUN
Korean Journal of Dermatology 1999;37(4):459-467
BACKGROUND: Chronic cutaneous lupus erythematosus(CCLE) is a well-known disease entity. But there has been no data about its clinical behavior and histopathologic features in Korea. OBJECTIVES: This study was conducted to elucidate the clinical, laboratory, and histopathologic features of CCLE, and the relationship between CCLE and SLE. MATERIALS AND METHODS: We investigated 48 cases of CCLE that visited the department of dermatology at the Seoul National University Hospital from January 1990 to June 1997. Medical records and biopsy slides were reviewed.
Biopsy
;
Dermatology
;
Korea
;
Lupus Erythematosus, Cutaneous*
;
Medical Records
;
Seoul
5.Three Cases of Allopurinol Hypersensitivity Syndrome.
Hyeong Don BANG ; Jin Ho CHUNG ; Kwang Hyun CHO ; Jai Il YOUN
Korean Journal of Dermatology 1995;33(1):130-134
The allopurinol hypersensicivity syndrome is a rare, but life thereaning immunologic reaction of allopurinol therapy, characterized by multiple abnormalities such as fever, rash, decreased renal function, hepatocellular injury, leukocytosis, and eosinophila. It may require prolonged hospitalization and occasionally involves residual morbidity. Three patients developed erythematous skin eruption three to five weeks after beginning therapy with allopurinol. The clinical, laboratory, and histologic findings of these patients were compatible with a allopurinol hyperensitivity syndrome.
Abnormalities, Multiple
;
Allopurinol*
;
Exanthema
;
Fever
;
Hospitalization
;
Humans
;
Hypersensitivity*
;
Leukocytosis
;
Skin
6.A Case of Proliferating Trichilemmal Tumor Developing in the Public Area of a Patient Underdoing Hemodialysis.
Youn Jin KIM ; Ji Hyun KIM ; So Yun CHO ; Kyu Kwang WHANG ; Jeong Hee HAHM
Korean Journal of Dermatology 2000;38(5):676-678
No Abstract Available.
Humans
;
Renal Dialysis*
7.A Case of hereditary Angioedema.
Yong Suk LEE ; Jin Ho CHUNG ; Kwang Hyun CHO ; Jai Il YOUN
Korean Journal of Dermatology 1994;32(1):115-118
We report a case of hereditary angioedema in a 48-year old female patient. She experidenced facial edema and dyspnea 5 to 6 times for a year. Similar episodes developed on some members of her family, especially her sisters and father. We examined her and her sister's serum complement levels. The results showed decreased levels of C1 esterase inhibitor and C4, compared to normal levels. We treated the patient with danazol effectively.
Angioedemas, Hereditary*
;
Complement C1 Inhibitor Protein
;
Complement System Proteins
;
Danazol
;
Dyspnea
;
Edema
;
Fathers
;
Female
;
Humans
;
Middle Aged
;
Siblings
8.Red Blood Cell Transfusion in Autoimmune Hemolytic Anemia.
Youn Kyung KIL ; Young Jin CHOI ; Sung Ran CHO ; Hwi Jun KIM ; Hyun Ok KIM
Korean Journal of Clinical Pathology 1997;17(5):839-846
BACKGROUND: Autoimmune hemolytic anemias are characterized by autoantibodies recognizing antigens on the Individual's own red blood cells, resulting in immune- mediated hemolysis. Blood transfusions have been regarded as hazardous in patients with autoimmune hemolytic anemia (AIHA) because of potential intensification of hemolysis and a presumed high incidence of alloimmunization. METHODS: We examined the pretransfusion and posttransfusion hemoglobin levels in 6 patients with autoantibodies in their sera, which showed panagglutinations with all bloods tested in the compatibility testing. They received 'least' incompatible blood because of inability to find compatible blood. RESULTS: When we compared pretransfusion hemoglobin level with posttransfusion hemoglobin level, in 5 of 6 patients with AIHA, the hemoglobin levels were increased after red cell transfusion. 4 patient who did not respond to transfusion therapy initially had an increase in hemoglobin level after steroid treatment. Any signs or symptoms indicating hemolytic transfusion reaction were not observed ducting the transfusion period in all patients. CONCLUSIONS: The decision to transfuse in AIHA should consider multiple factors including the patient's clinical status, the potential benefit of transfusion, the potential response to other therapeutic modalities, but must never be regarded as contraindicated, even though the compatibility test may be strongly incompatible.
Anemia, Hemolytic*
;
Anemia, Hemolytic, Autoimmune
;
Autoantibodies
;
Blood Group Incompatibility
;
Blood Transfusion
;
Erythrocyte Transfusion*
;
Erythrocytes*
;
Hemolysis
;
Humans
;
Incidence
9.Red Blood Cell Transfusion in Autoimmune Hemolytic Anemia.
Youn Kyung KIL ; Young Jin CHOI ; Sung Ran CHO ; Hwi Jun KIM ; Hyun Ok KIM
Korean Journal of Clinical Pathology 1997;17(5):839-846
BACKGROUND: Autoimmune hemolytic anemias are characterized by autoantibodies recognizing antigens on the Individual's own red blood cells, resulting in immune- mediated hemolysis. Blood transfusions have been regarded as hazardous in patients with autoimmune hemolytic anemia (AIHA) because of potential intensification of hemolysis and a presumed high incidence of alloimmunization. METHODS: We examined the pretransfusion and posttransfusion hemoglobin levels in 6 patients with autoantibodies in their sera, which showed panagglutinations with all bloods tested in the compatibility testing. They received 'least' incompatible blood because of inability to find compatible blood. RESULTS: When we compared pretransfusion hemoglobin level with posttransfusion hemoglobin level, in 5 of 6 patients with AIHA, the hemoglobin levels were increased after red cell transfusion. 4 patient who did not respond to transfusion therapy initially had an increase in hemoglobin level after steroid treatment. Any signs or symptoms indicating hemolytic transfusion reaction were not observed ducting the transfusion period in all patients. CONCLUSIONS: The decision to transfuse in AIHA should consider multiple factors including the patient's clinical status, the potential benefit of transfusion, the potential response to other therapeutic modalities, but must never be regarded as contraindicated, even though the compatibility test may be strongly incompatible.
Anemia, Hemolytic*
;
Anemia, Hemolytic, Autoimmune
;
Autoantibodies
;
Blood Group Incompatibility
;
Blood Transfusion
;
Erythrocyte Transfusion*
;
Erythrocytes*
;
Hemolysis
;
Humans
;
Incidence
10.Two Cases of Transient Aplastic Crisis Associated with Human Parvovirus Bl9 Infection in Hereditary Spherocytosis and Hereditary Elliptocytosis.
Young Jin CHOI ; Youn Kyung KIL ; Sung Ran CHO ; Hwi Jun KIM ; Seung Ho BAICK
Korean Journal of Clinical Pathology 1997;17(5):694-702
Among the causes of pure red cell aplasia, human parvovirus B19 has been shown to be cytotoxic to erythroid progenitor cells in the bone marrow associated with chronic hemolytic anemia with rapidly dividing erythroids and persistently to be suppression of erythropoiesis in immunocompromised individuals related with failure to produce neutralizing antibody to the virus. In a patient with hereditary spherocytosis presenting acute onset of reticulocytopenia during hospitalization, who had shown severe anemia and prodromal symptoms including fever, fatigue and dizziness, infection of parvovirus Bl9 was proven by the presence of IgM and IgG antibodies to parvovirus Bl9, the detection of viral DNA using PCR technique in her serum and the decreased erythroid cells, especially late normoblasts in bone marrow, Also in the other who was diagnosed as hereditary elliptocytosis and complained of fever, headache, abdominal pain and diarrhea, an episode of reticulocytopenia and the nearly absence of late normoblasts in the bone marrow were observed. IgM antibodies to parvovirus Bl9 and the viral DNA were detected in her serum, too.
Abdominal Pain
;
Anemia
;
Anemia, Hemolytic
;
Antibodies
;
Antibodies, Neutralizing
;
Bone Marrow
;
Diarrhea
;
Dizziness
;
DNA, Viral
;
Elliptocytosis, Hereditary*
;
Erythroblasts
;
Erythroid Cells
;
Erythroid Precursor Cells
;
Erythropoiesis
;
Fatigue
;
Fever
;
Headache
;
Hospitalization
;
Humans*
;
Immunoglobulin G
;
Immunoglobulin M
;
Parvovirus B19, Human
;
Parvovirus*
;
Polymerase Chain Reaction
;
Prodromal Symptoms
;
Red-Cell Aplasia, Pure