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Yeungnam University Journal of Medicine

1984  to  Present  ISSN: 2384-0293

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Four Cases of Foreign Body in Lower Urinary Tract.

Jin Wook YOO ; Ki Hak MOON ; Hee Chang JUNG ; Tong Choon PARK

Yeungnam University Journal of Medicine.1998;15(2):391-396. doi:10.12701/yujm.1998.15.2.391

Foreign bodies in genitourinary tract are common and almost of then are within the bladder. These foreign bodies were inserted or applied for autoerotic, psychiatric, therapeutic, or no definite reasons by the patient. Foreign bodies(a thermometer and a piece of cloth) in the bladder were inserted as a mean of masturbation in two cases, and a cooper wire in the posterior urethra was introduced by iatrogenic causes in one case. In one case, four magnets were inserted into the bladder for the purpose of forceful penile erection. Clinical history, symptom, radiologic study, and endoscopic examination were required to diagnose foreign body. They were easily removed by endoscopic manipulation or open surgical procedure.
Foreign Bodies* ; Humans ; Male ; Masturbation ; Penile Erection ; Thermometers ; Urethra ; Urinary Bladder ; Urinary Tract*

Foreign Bodies* ; Humans ; Male ; Masturbation ; Penile Erection ; Thermometers ; Urethra ; Urinary Bladder ; Urinary Tract*

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A case of incontinentia pigmenti developed in a male newborn infant.

Min Jeong CHO ; Son Moon SHIN ; Han Ku MOON

Yeungnam University Journal of Medicine.1998;15(2):381-390. doi:10.12701/yujm.1998.15.2.381

Incontinentia pigmenti is characterized by irregular linear blisters with erythematous lesions which are developed from birth or later, verrucous papules on the extremities which are noted after a few weeks or months, and the appearnace of streaks, spots and swirls of hyperpigmentation. This disorder is known as a systemic disorder caused by a defect at the developmental stage of organs originated from ectoderm or mesoderm. We experienced an incontinentia pigmenti in a male newborn infant who did not have any family history and had cutaneous lesions, which were in bullous and verucous stages, ophthalmic problems, and neurologic abnormalities.
Blister ; Ectoderm ; Extremities ; Humans ; Hyperpigmentation ; Incontinentia Pigmenti* ; Infant, Newborn* ; Male* ; Mesoderm ; Parturition

Blister ; Ectoderm ; Extremities ; Humans ; Hyperpigmentation ; Incontinentia Pigmenti* ; Infant, Newborn* ; Male* ; Mesoderm ; Parturition

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Two Cases of Systemic Lupus Erythematosus with Cerebrovascular Involvement.

Bong Jun KIM ; Eun Young LEE ; Young Hoon HONG ; Ki Do PARK ; Young Doo SONG ; Choong Ki LEE ; Young Ran SHIM

Yeungnam University Journal of Medicine.1998;15(2):371-380. doi:10.12701/yujm.1998.15.2.371

Systemic lupus erythematosus(SLE) is an autoimmune disease which may affect many different organs and disclose various clinical manifestations. Recently central nervous system(CNS) involvement has been recognized as an increasingly significant contributor to morbidity and mortality of SLE. The clinical manifestations of CNS-lupus are highly variable and range from mild cognitive dysfunction, movement disorder, headache, psychosis to life-threatening stroke and coma. Among the neuropsychiatric disorders encountered in patients with SLE, cerebrovascular disease has been a relatively rare complication. The diagnosis and management of CNS-lupus is difficult because of the lack of useful diagnostic methods. If, cerebrovascular involvement is suspected, then aggressive treatment such as high dose steroid, immunosuppressive therapy, plasma exchange, may be required to reduce high mortality rate. We experienced 2 cases cerebrovascular disease occurring in SLE patients which presented with various neuropsychiatric manifestations. They were diagnosed as CNS-lupus by neuropsychiatric symptoms, brain MRI, and EEG, and showed good response to high dose steroid pulse therapy.
Autoimmune Diseases ; Brain ; Coma ; Diagnosis ; Electroencephalography ; Headache ; Humans ; Lupus Erythematosus, Systemic* ; Magnetic Resonance Imaging ; Mortality ; Movement Disorders ; Plasma Exchange ; Psychotic Disorders ; Stroke

Autoimmune Diseases ; Brain ; Coma ; Diagnosis ; Electroencephalography ; Headache ; Humans ; Lupus Erythematosus, Systemic* ; Magnetic Resonance Imaging ; Mortality ; Movement Disorders ; Plasma Exchange ; Psychotic Disorders ; Stroke

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A Clinicopathologic Review of Eight Cases of Chondroblastoma.

Joon Hyuk CHOI ; Hae Jeong CHOI ; Mi Jin KU ; Dae Hong SUH ; Duk Seop SHIN ; Kil Ho CHO

Yeungnam University Journal of Medicine.1998;15(2):359-370. doi:10.12701/yujm.1998.15.2.359

Eight cases of chondroblastoma were studied by analyzing the clinical and pathologic findings. The age of eight cases ranged from 17 to 38 years old(median age, 22.7 years old). The tumors developed in the femur (3 cases), patella (2 cases), tibia( 1 case), fibula (1 case), and ulna (1 case). The mean diameter of tumors was 4.0 cm (range, 1.5 to 8.0 cm). Grossly, tumors showed grayish brown solid area with foci of secondary aneurysmal bone cyst. Histologically, the tumor cells were round or polygonal in shape with nuclear groove. And there were chondroid differentiation(7 cases), mitosis(3 cases), calcific deposits(3 cases), secondary aneurysmal bone cyst(4 cases), hemosiderin deposits(4 cases), necrosis(3 cases), vascular invasion(1 caes) and foamy histiocytes and cholesterol cleft(1 cases). All cases showed no metastasis to lymph node and distant organ. Seven cases (87.5 %) were immunoreactive for S-100 protein. None were immunoreactive for cytokeratin.
Aneurysm ; Bone Cysts ; Cholesterol ; Chondroblastoma* ; Femur ; Fibula ; Hemosiderin ; Histiocytes ; Keratins ; Lymph Nodes ; Neoplasm Metastasis ; Patella ; S100 Proteins ; Ulna

Aneurysm ; Bone Cysts ; Cholesterol ; Chondroblastoma* ; Femur ; Fibula ; Hemosiderin ; Histiocytes ; Keratins ; Lymph Nodes ; Neoplasm Metastasis ; Patella ; S100 Proteins ; Ulna

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A case of primary antiphospholipid antibody syndrome showing vegetation on the mitral valve through echocardiography.

Seung Yeop LEE ; Seung Kwon PARK ; Sung Hwan YUN ; Yun Seok JUNG ; Hyen Jik KIM ; Sung Hwan LIM ; Jung Sang HAH ; Wook Nyeun KIM

Yeungnam University Journal of Medicine.1998;15(2):350-358. doi:10.12701/yujm.1998.15.2.350

Antiphospholipid antibody syndrome(APS) is a well-known clinical syndrome characterized by recurrent arterial or venous thromboses, recurrent fetal loss, thrombocytopenia, together with high titers of sustained anticardiolipin antibody(aCL) or lupus anticoagulant(LA). Although systemic lupus erythematosus(SLE) and APS may coexist, a high proportion of patients manifesting the APS do not suffer from classical lupus or other connective tissue disease. The patient has been defined as having a primary antiphospholipid antibody syndrome. We experienced one case of primary APS with recurrent fetal loss, recurrent cerebral infarctions, positive anticardiolipin antibody IgG and fluttering vegetation on the mitral valve, without other connective tissue diseases including SLE. Forty-three old female had 2 out of 11 criteria for the diagnosis of SLE, such as thrombocytopenia and positive antinuclear antibody, but did not meet whole criteria. The patient was treated with ticlopidine, and anticoagulant therapy was recommended.
Antibodies, Anticardiolipin ; Antibodies, Antinuclear ; Antibodies, Antiphospholipid* ; Antiphospholipid Syndrome* ; Cerebral Infarction ; Connective Tissue Diseases ; Diagnosis ; Echocardiography* ; Female ; Humans ; Immunoglobulin G ; Mitral Valve* ; Thrombocytopenia ; Ticlopidine ; Venous Thrombosis

Antibodies, Anticardiolipin ; Antibodies, Antinuclear ; Antibodies, Antiphospholipid* ; Antiphospholipid Syndrome* ; Cerebral Infarction ; Connective Tissue Diseases ; Diagnosis ; Echocardiography* ; Female ; Humans ; Immunoglobulin G ; Mitral Valve* ; Thrombocytopenia ; Ticlopidine ; Venous Thrombosis

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Indication of Bone Marrow Aspiration in Acute Idiopathic Thrombocytopenic Purpura in Children.

Won Duck KIM ; Jeong Ok HAH

Yeungnam University Journal of Medicine.2001;18(2):239-245. doi:10.12701/yujm.2001.18.2.239

BACKGROUND: Acute idiopathic thrombocytopenic purpura(ITP) is one of the common hematologic disorders in children. Bone marrow aspiration(BMA) is often performed in children with acute ITP to rule out leukemia, aplastic anemia or other hematologic diseases. However, whether BMA is needed in children with typical clinical and hematological features of acute ITP have been questioned. This study was performed to examine the proper indication of BMA in acute childhood ITP. MATERIALS AND METHODS: The medical records and BMA reports of children with the provisional diagnosis of acute ITP were reviewed from January 1984 to December 2000. Patients were divided into two groups, one with typical and another with atypical clinical and hematological features of acute ITP. Typical acute ITP group was characterized by the history of previous viral infection, well being appearance, no hepatosplenomegaly, no lymphadenopathy, normal Hb, WBC, neutrophil count and peripheral blood smear except thrombocytopenia. A platelet count of 50x109/L or lower was the cutoff level. RESULTS: Total 120 children with the provisional diagnosis of acute ITP were included. One hundred eighteen of them were confirmed to have acute ITP by BMAs. Of these, 66 had typical and 54 had atypical features. All of typical features and 52 of 54 with atypical features of acute ITP were confirmed to have acute ITP by BMAs. Two patients with atypical features of acute ITP were diagnosed as aplastic anemia and myelodyspalstic syndrome, respectively, by BMAs. CONCLUSION: This study concludes that BMA is not needed for the children with typical features of acute ITP but it is needed for the children with atypical features of acute ITP to rule out other hematologic disorders.
Anemia, Aplastic ; Bone Marrow* ; Child* ; Diagnosis ; Hematologic Diseases ; Humans ; Leukemia ; Lymphatic Diseases ; Medical Records ; Neutrophils ; Platelet Count ; Purpura, Thrombocytopenic, Idiopathic* ; Thrombocytopenia

Anemia, Aplastic ; Bone Marrow* ; Child* ; Diagnosis ; Hematologic Diseases ; Humans ; Leukemia ; Lymphatic Diseases ; Medical Records ; Neutrophils ; Platelet Count ; Purpura, Thrombocytopenic, Idiopathic* ; Thrombocytopenia

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A Study for Improvement of Erythropoietin Responsiveness in Hemodialysis Patients.

Jong Won PARK ; Jun Yeung DO ; Kyung Woo YOON

Yeungnam University Journal of Medicine.2001;18(2):226-238. doi:10.12701/yujm.2001.18.2.226

BACKGROUND: Anemia in chronic renal failure plays an important rolr in increasing morbidity of dialysis patients. The causes of the anemia are multifactorial. With using of erythropoietin(EPO), most of uremia-induced anemia can be overcome. However, about 10% of renal failure patients shows EPO-resistant anemia. Hyporesponsiveness to EPO has been realted to many factors: iron deficiency, aluminum intoxication, inflammations, malignancies and secondary hyperparathyroidism. So I evailuated the improvement of EPO responsiveness after correction of above several factors. MATERIALS AND METHODS: Seventy-two patients on hemodialysis over 6 months were treated with intravenous ascorbic acid(IVAA, 300 mg t.i.w. for 12 weeks). After administration of IVAA for 12 weeks,patients were classified into several groups according to iron status, serum aluminum levels and i-PTH levels. Indivisualized treatments were performed; increased iron supplement for absolute iron deficiency, active vitamin D3 for secondary hyperparathyroidism and desferrioxamine(DFO, 5 mg/kg t.i.w.) for aluminum intoxication or hyperferritinemia. RESULTS: 1) Results of IVAA therapy for 12 weeks on all patients(n=72) Hemoglobin levels at 2,4,6 week were significantly elevated compared to baseline. but those of hemoglobin at 8, 10, 12 week were not significantly different. 2) Result of IVAA therapy for 20 weeks on patients with 100 microgram/1< or =ferritin<500 microgram/1 and transferrin saturation(Tsat) below 30%(n=30) After treatment of IVAA for 12 weeks, patients were evaluated the response of therapy according to iron status. Patient with 100 microgram/1< or =ferritin?500 microgram/1 and Tsat below 30% showed the most effective response. These patients were treated further for 8 weeks. Hemoglobin levels at 2, 4 week were significantly increased compared to baseline with significantly reduced doses of EPO at 2, 4, 10, 12, 16, 20 week. Concomitantly significantly improvement of Tsat at 2, 6, 16, 20 week compared to baseline were identified. 3) Result of IVAA therapy for 12 weeks followed by DFO therapy for 8 weeks on patients with serume aluminum above 4 microgram/1(n=12) Hemoglobin levels were not significantly increased during IVAA therapy for 12 weeks but dosages of EPO were significantly decreased at 2, 4, 6, 8 week during DFO therapy compared to pre-treatment status. CONCLUSION: IVAA can be helpful for the treatment of the anemia caused by functional iron deficiency and can reduce the dosage of EPO for anemia correction. And administration of low dose DFO, in cases of increased serum aluminum level, can reduce the requirment of EPO.
Aluminum ; Anemia ; Ascorbic Acid ; Cholecalciferol ; Deferoxamine ; Dialysis ; Erythropoietin* ; Humans ; Hyperparathyroidism, Secondary ; Inflammation ; Iron ; Kidney Failure, Chronic ; Renal Dialysis* ; Renal Insufficiency ; Transferrin

Aluminum ; Anemia ; Ascorbic Acid ; Cholecalciferol ; Deferoxamine ; Dialysis ; Erythropoietin* ; Humans ; Hyperparathyroidism, Secondary ; Inflammation ; Iron ; Kidney Failure, Chronic ; Renal Dialysis* ; Renal Insufficiency ; Transferrin

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Change of Serum Levels of C-Reactive Protein After Coronary Angioplasty and Its Effects on Clinical Restenosis.

Jong Seon PARK ; Gu Ru HONG ; Chae Hoon LEE ; Dong Gu SHIN ; Young Jo KIM ; Bong Sup SHIM

Yeungnam University Journal of Medicine.2001;18(2):215-225. doi:10.12701/yujm.2001.18.2.215

BACKGROUND: There are many evidences that inflammation is an important determinant of the development of atherosclerosis and one of the systemic markers of inflammation, C-reactive protein(CRP), is associated with extent of coronary artery disease and risk of coronary events. We assessed the time response of CRP response after coronary angioplasty and it's influence on the clinical restenosis in angina patients. MATERIALS AND METHODS: Patients included 36 angina patients undergoing single vessel angioplasty. Levels of CRP were measured before and 12, 24, 48, and 72 hours after angioplasty. Clinical restenosis was assessed at 6 months after procedure. RESULTS: Baseline CRP level was 0.30+/-0.01 mg/dL in stable and 0.46+/-0.28 mg/dL in unstable angina patients(p<0.05). After angioplasty, CRP level was increased with peak at 24 hour and persisted to 72 hours after angioplasty. At 24 hour after angioplasty, the magnitude of CRP change was 0.32+/-0.31 mg/dL in stable and 0.79+/-0.73 mg/dL in unstable angina patient(p<0.05). The change of CRP level was not associated with troponin-T after angioplasty. In unstable angina patients, clinical restenosis was developed in 8% of patients with low baseline CRP levels and in 50% of those with high baseline CRP levels more than 0.6 mg/dL(p<0.05). CONCLUSION: In unstable angina patients, inflammatory response is more increased than stable angina patients, and increased inflammatory response effects on the restenosis after coronary angioplasty.
Angina, Stable ; Angina, Unstable ; Angioplasty* ; Atherosclerosis ; C-Reactive Protein* ; Coronary Artery Disease ; Humans ; Inflammation ; Troponin T

Angina, Stable ; Angina, Unstable ; Angioplasty* ; Atherosclerosis ; C-Reactive Protein* ; Coronary Artery Disease ; Humans ; Inflammation ; Troponin T

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A Lateral Cephalometric Study of Maxillofacial Morphologic Features in Class III Malocclusion Children.

Woo Ill SOHN ; Ic Jun CHANG ; Jae Chul SONG ; Byung Rho CHIN

Yeungnam University Journal of Medicine.2001;18(2):208-214. doi:10.12701/yujm.2001.18.2.208

BACKGROUND: When we make treatment plan of class III malocclusion children, it is difficult to determine whether we treat it with orthognathic surgery or without orthognathic surgery. To determine that, we must consider many factors, such as cephalometric analysis, growth pattern, family history, and skeletal age. A Harvold cephalometric analysis is useful in determining the amount of discrepancy by comparing the maxillary unit length with mandibular unit length. We tried this study to help the decision of treatment planning in class III malocclusion children by comparison in class III malocclusion and normal occlusion children using a Harvold analysis. MATERIALS AND METHODS: The materials for this study consisted of 20 class III malocclusion children. Cephalometric tracing and measurements were performed by one investigator. The control group consisted of 18 normal occlusion children and lateral cephalograms were obtained from 8.5 to 14.5 years old children biannually. The relationships between class III malocclusion group and normal occlusion group were evaluated statistically. RESULTS: The lower anterior facial heights between two groups were not significantly different, although the lower anterior facial heights of class III malocclusion group was higher than those of normal occlusion group in all age groups. The Maxillary-mandibular unit length differences of class III malocclusion group were significantly higher than those of normal occlusion group(p < 0.05). CONCLUSION: A Harvold analysis was useful to make treatment planning for class III malocclusion children.
Child* ; Humans ; Malocclusion* ; Orthognathic Surgery ; Research Personnel

Child* ; Humans ; Malocclusion* ; Orthognathic Surgery ; Research Personnel

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Treatment Outcomes of Septoplasty with Turbinate Surgery in Septal Deviation with Chronic Hypertrophic Rhinitis.

Yong Dae KIM ; Bo Su SUH ; Gil Sung CHO ; Si Youn SONG ; Seok Keun YOON ; Kei Won SONG

Yeungnam University Journal of Medicine.2001;18(2):199-207. doi:10.12701/yujm.2001.18.2.199

BACKGROUND: Septoplasty with turbinate surgery is common surgical treatment in patients with septal deviation and chronic hypertrophic rhinitis. The aim of this study was to evaluation objective outcomes of septoplasty with turbinate surgery by analysis of subjective symptom score with objective acoustic rhinometric test before and after surgery, prospectively. MATERIALS AND METHODS: We reviewed 45 adult patients which were done septoplasty with bilateral turbinectomy or turbinoplasty and followed up at least 3 months by one rhinologist from November 1999 to April 2000, prospectively. We analyzed subjective symptom score, minimal cross-sectional area (MCA), C-notch cross-sectional area, and total volume of both nasal cavity before and after surgery. Correlation test was studied between symptom improvement and acoustic rhinometric results. RESULTS: Twenty nine cases were male and sixteen cases female. The average age was 26.9 year-old (range: 17 to 57 years). There was significantly improvement of symptom score in postoperative 3 months (p<0.05). There was significantly increased C-notch cross-sectional area and total volume in postoperative 3 months. Symptoms improvement were associated with acoustic rhinometric profiles, but, there was not significantly correlation. CONCLUSION: Septoplasty with turbinate surgery is considered to be effective for nasal obstruction in patients with septal deviation and turbinate hypertrophy. Acoustic rhinometric test is favorable objective test for evaluation of symptom improvement after septal surgery.
Acoustics ; Adult ; Female ; Humans ; Hypertrophy ; Male ; Nasal Cavity ; Nasal Obstruction ; Prospective Studies ; Rhinitis* ; Rhinometry, Acoustic ; Turbinates*

Acoustics ; Adult ; Female ; Humans ; Hypertrophy ; Male ; Nasal Cavity ; Nasal Obstruction ; Prospective Studies ; Rhinitis* ; Rhinometry, Acoustic ; Turbinates*

Country

Republic of Korea

Publisher

Yeungnam University College of Medicine

ElectronicLinks

http://synapse.koreamed.org/LinkX.php?code=1109YUJM

Editor-in-chief

Hosun Park

E-mail

Abbreviation

Yeungnam Univ J Med

Vernacular Journal Title

영남의대학술지

ISSN

2384-0293

EISSN

2384-0293

Year Approved

2007

Current Indexing Status

Currently Indexed

Start Year

1984

Description

Yeungnam University Journal of Medicine (http://yujm.yu.ac.kr), the official publication of Yeungnam University College of Medicine, is published twice a year, June and December. It covers all fields of medical science including clinical research and basic medical science. The journal aims to communicate new medical information between medical personnels and to help development of medicine and propagation of medical knowledge.

Current Title

Journal of Yeungnam Medical Science

Previous Title

Yeungnam University Journal of Medicine

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