No abstract available.
Tumor Lysis Syndrome*

No abstract available.
HL-60 Cells* ; Humans ; Mass Screening* ; Protein Kinases*

No abstract available.
Ascites* ; Pancreatitis, Chronic* ; Pleural Effusion*

BACKGROUND AND OBJECTIVES: Computed tomography of the temporal bone can provide otologists precise informations regarding the middle ear diseases. In this study, we aimed to measure the distance of mastoid antrum using the temporal bone CT for predicting the distance of mastoid depth during the mastoid surgery. MAERIALS AND METHODS: We analyzed normal ears of 88 patients who visited the Department of Otolaryngology, Chonnam University Hospital during the period between Aug. 1996 and Aug. 1997. These patients demonstrated unilateral chronic otitis media, temporal bone fracture, and traumatic facial nerve palsy. RESULTS: The mean distance of mastoid antrum was 11.45mm. The distance of mastoid antrum according to age distribution showed 7.75 mm in 0-4 year old group, 10.35 mm in 5-9 year old group, 10.71 mm in 10-14 year old group, 11.50 mm in 15-19 year old group, and 11.93 mm in over 20 year old group. The distance also differed between males and females, with 2.84 mm for male and 11.24 mm for female. CONCLUSION: For the group under 20 years old, the distance of mastoid antrum increased as the patient's age became older. Especially, the group who were between 5 to 9 years old showed marked increase in the distance, and the distance did not differ between male and female. The distance of the mastoid antrum of the Korean adults was 10.1-13.7 mm and it represents some difference when compared with that of Westerners.
Adult ; Age Distribution ; Child ; Ear ; Ear, Middle ; Facial Nerve ; Female ; Humans ; Jeollanam-do ; Male ; Mastoid* ; Otitis Media ; Otolaryngology ; Paralysis ; Temporal Bone* ; Young Adult

No abstract available.
Intellectual Disability ; Muscle Weakness ; Muscular Dystrophy, Duchenne*

No abstract available.
Autopsy* ; Cardiomyopathies* ; Humans ; Infant, Newborn*

No abstract available.
Humans ; Infant, Newborn*

Since the placenta is an organ composed of blood vessels, it is not surprising that its primary neoplasm would be a vascular tumor. Placental tumors, primary or secondary, have been known to interfere with placental function. Chorioangioma(primary tumor of the placenta), which is the most common of them, occurs with an incidence for clinically significant ranges from 1~2.8:10000 births. These tumors are benign and are not usually associated with clinical sequelae unless they are larger than 5cm in long diameter. About one third of the large chorioangiomas may be associated with the maternal and fetal complications. For diagnosis of these lesions, the ultrasonography was used. If the chorioangioma is suspected, color doppler study is informative to confirm the presence of the vascular channels. We reviewed ultrasonograms and clinical records of seven patients who had been diagnosed as placental chrioangioma. The appropriate diagnostic tests and treatment can then be initiated in order to prolong gestation and decrease fetal mortality and morbidity.
Blood Vessels ; Diagnosis ; Diagnostic Tests, Routine ; Fetal Mortality ; Hemangioma* ; Humans ; Incidence ; Parturition ; Placenta* ; Pregnancy ; Prenatal Diagnosis* ; Ultrasonography

The antigenic domain of the major surface protein (Nc-p43) of Neospora caninum was examined by polymerase chain reaction of its gene fragments and recombinant expression as GST fusion proteins. The fragments of Nc-p43 were as follow: a total open reading frame (OFR), T; OFR without signal sequence and C-terminal hydrophobic sequence, S; N-terminal 2/3 parts of S, A; C-terminal 2/3 parts, P; N-terminal 1/3 part, X; middle 1/3 part, Y; and C-terminal 1/3 part, Z, respectively. The DNA fragments were cloned into pGEX-4T vector. Recombinant plasmids transformed into Escherichia coli of BL21 pLysS (DE3) strain were induced to express GST or GST fused fragments of Nc-p43 such as 69 kDa protein for T, 66 kDa for S, 52 kDa for A, 53 kDa for P, and 40 kDa proteins for X, Y, and Z, respectively in SDS-PAGE. The Nc-p43 fragments of T, S, and P reacted with a bovine serum of neosporosis while those of A, X, Y, and Z together with GST did not in the western blot. These findings suggest that the antigenic domain of Nc-p43 of N. caninum may be localized in the C-terminal 2/3 parts. Together with A19 clone in SAG1 of Toxoplasma gondii (Nam et al., 1996), the P fragment of Nc-p43 could be used as efficient antigens to diagnose and differentiate those infections with both species.
Amino Acid Sequence ; Animals ; Base Sequence ; Biological Markers/analysis ; Blotting, Western ; Cells, Cultured ; Cercopithecus aethiops ; Coccidiosis/diagnosis ; Neospora/*immunology ; Protozoan Proteins/*analysis/genetics/immunology ; Reverse Transcriptase Polymerase Chain Reaction ; Support, Non-U.S. Gov't ; Vero Cells/parasitology

No abstract available.
Ectodermal Dysplasia*