1.The Relation of Family History and beta-Endorphin Levels in Alcohol Dependence.
Hee Yeon JEONG ; In Joon PARK ; Young Joon KWON
Journal of the Korean Society of Biological Psychiatry 1998;5(1):102-106
OBJECTIVES: To evaluated the relation of familial history of alcoholism and plasma level of beta-endorphin, ethanol, beta-endorphin, cortisol and blood glucose were compared in 48 male alcoholics and 29 normal controls. METHODS: Subjects are divided into two groups by family history of alcoholism. Blood samples were obtained before and after 0.75mg/kg of ethanol consumption a 7th admission day. RESULTS: 1) The ratio of family history positive to negative of the patient group was 2 to 1. 2) The age at admission of positive family history group was younger than negative groups. 3) There was no significant difference in change of plasma ethanol level among three groups. 4) There was no significant difference in change of plasma beta-endorphin level among three group. 5) There was no significant difference in change of plasma cortisol level among three groups. 6) There was no significant difference in change of fasting blood sugar level between two patients groups.
Alcoholics
;
Alcoholism*
;
beta-Endorphin*
;
Blood Glucose
;
Ethanol
;
Fasting
;
Humans
;
Hydrocortisone
;
Male
;
Plasma
2.Comparison of P300 between Schizophrenia and Bipolar Disorder.
In Joon PARK ; Hee Yeon JEONG ; Young Joon KWON
Journal of the Korean Society of Biological Psychiatry 2001;8(1):123-130
OBJECTIVE: Asymmetries in evoked potential P300 topography of schizophrenia and bipolar disorder are still controversial. The purpose of this study was to examine the difference in P300 topography between schizophrenia and bipolar disorder. METHOD: P300 was recorded from 16 schizophrenic, 15 bipolar manic, and 16 control subjects. All were right-handed. Subjects silently counted target stimuli(2.0kHz) among trains of standard stimuli(1.0 kHz). Averages were constructed from brain responses to target stimuli. RESULTS: 1) Schizophrenics displayed significantly smaller peak amplitude of P300 over Cz, Pz, T3 than controls. 2) Schizophrenics displayed significantly smaller peak amplitude of P300 over T3 than bipolar manics. 3) Schizophrenics displayed significantly smaller peak amplitude of P300 over T3 than their T4. 4) Schizophrenics displayed significantly delayed latency of P300 over T3 than bipolar manics. 5) Schizophrenics displayed significantly delayed latency of P300 over T3 than their T4. CONCLUSION: Left-sided P300 abnormality, especially left superior temporal gyrus, in schizophrenics, relative to bipolar manics and controls suggests that psychophysiological cause of schizophrenia and bipolar disorder is different and P300 asymmetry is specific to the psychophysiological cause of schizophrenia.
Bipolar Disorder*
;
Brain
;
Evoked Potentials
;
Schizophrenia*
4.Pre-and Postoperative Evaluation of Patent Ductus Arteriosus in Children.
In Hee PARK ; Jung Hee LEE ; In Joon SEOL ; Heung Jae LEE
Journal of the Korean Pediatric Society 1985;28(7):683-694
No abstract available.
Child*
;
Ductus Arteriosus, Patent*
;
Humans
5.A Case of Antipsychotic-Regression Syndrome in Haloperidol Treated Tourette's Syndrome.
Hee Yeon JEONG ; Hyun Ju CHO ; Young Joon KWON ; In Joon PARK ; Hyuk Hee JIN
Journal of the Korean Society of Biological Psychiatry 1998;5(1):134-137
Authors report a case of separation anxiety disorder, which developed as a side effect during haloperidol treatment of Tourette syndromes(TS). In this case, 14 years old boys developed attention deficit symptoms during his infancy. At 4th grade of primary school, he developed vocal tic, motor tic, and coprolalia. With 5mg/day of haloperidol treatment his symptoms of TS were subsided. During the treatment, he developed features of separation anxiety disorder, including dependence, pleading, clinging, and sadness. Symptoms of attention deficit and separation anxiety disorder were improved by 25mg/day of imipramine treatment. During haloperidol treatment of TS, careful observation may be needed whether separation anxiety disorder-like symptom develops.
Adolescent
;
Anxiety, Separation
;
Haloperidol*
;
Humans
;
Imipramine
;
Tics
;
Tourette Syndrome*
6.A Case of Leg Ulcer in Systemic Scleroderma Treated with Pinch Grafts.
Hyang Joon PARK ; Hee Chul EUN ; Yoo Shin LEE
Korean Journal of Dermatology 1984;22(4):427-430
The pinch graft is one type of skin graft and is indicated in small, chronic stubborn wounds or ulcers where cosmetic results are not paramount. It is a common procedure for the rapid healing of leg ulcers in countries where these are very common, such as in western society. However, it is an unfamiliar procedure to dermatologists in Korea where leg ulcers are quite rare. We treated a case of leg ulcer in systemic sclerosis using pinch grafts with satisfactory results. The pinch graft may be a useful treatment method for skin ulcers in dermatologic surgery under adverse conditions.
Dermatologic Surgical Procedures
;
Korea
;
Leg Ulcer*
;
Leg*
;
Scleroderma, Systemic*
;
Skin
;
Skin Ulcer
;
Transplants*
;
Ulcer
;
Wounds and Injuries
7.A Case fo Keratosis Palmaris et Plantaris Thost-Unna Type.
Eui Soo PARK ; Jung Hee SUH ; Joon Young SONG
Korean Journal of Dermatology 1979;17(3):229-233
A case of 17 years old male with KPP of Tbost-Unna Type is reported. The akin lesions were characterized by the presence of confluent, sharply demarcated hyperk eratotic plaques on the palmar and plantar surfaces. Hypercontraction of palms and soles and hyperhidro is of scalp, face, palms and soles were also noted. Roentogenologic study revealed secondary changes of osteoporosis, flexion deformity and osteoarthritis due to soft tissue contracture and phalangeal and metatarsal bones of hands and feet showed bony resorption with tapering appearance. Histalogic findings of palmar lesion showed excessive hyperkeratosis, parakeratosis and acantosis in the epidermis and no pathology was noted in the dermis and skin appendages, He was treated with hot water compress, 5% Salicylic acid ointment and vit. A and D for 2 months and favorable effect was noted. Authors reviewed relevant literature and made discussions also.
Adolescent
;
Betazole
;
Congenital Abnormalities
;
Contracture
;
Dermis
;
Epidermis
;
Foot
;
Hand
;
Humans
;
Keratoderma, Palmoplantar*
;
Keratosis*
;
Male
;
Metatarsal Bones
;
Osteoarthritis
;
Osteoporosis
;
Parakeratosis
;
Pathology
;
Salicylic Acid
;
Scalp
;
Skin
;
Water
8.Sources of Formalin: I. Formalin Concentration in Shampoos.
Hyang Joon PARK ; Hee Chul EUN ; Yoo Shin LEE
Korean Journal of Dermatology 1984;22(5):492-495
Formalin is a 37 5pg aqueous solution of formaldehyde gas and formaldehyde may be present in products as an active ingredient, preservative or contaminant. This contamination may be from the container, the package material or in situ formation by degradation of the formaldehyde releasers. The free formaldehyde content was determined in the 50 kinds of Korean shampoos by quantitative analysis recently described, the lutidine method, which is simple, rapid and used for colored products which cannot be analysed by the chrornotropic acid method. Formaldehyde has been found in 46 out of the 0 samples, i.e., 90g., and the concentration ranged from 0. 1 to 78. 6 pg/ml(0. 1 78. 6 ppm).
Formaldehyde*
9.Cloning and Expression of the Gene Encoding the 32-kDa Protein of Rickettsia typhi.
Kyung Hee PARK ; Myong Joon HAHN ; Jong Hyun KIM
Journal of the Korean Society for Microbiology 1997;32(4):399-404
The crystalline surface layer protein (SLP) and a 28-32 kDa antigen of Rickettsia typhi were known as strong immunogens. We previously reported a cloning and sequence analysis of the SLP gene of R. typhi (slpT) and showed that the open reading frame of this gene encodes both the SLP and a 32-kDa protein. Our study also showed that a 48-kDa protein reacted strongly with polyclonal antiserum of a patient with murine typhus. In this study, we produced three recombinant proteins (SLP, 32-kDa, and 48-kDa protein) in E. coli as fusion proteins with maltose binding proteins. The reactivity of these proteins with patients' sera was investigated.
Clone Cells*
;
Cloning, Organism*
;
Crystallins
;
Humans
;
Maltose-Binding Proteins
;
Open Reading Frames
;
Recombinant Proteins
;
Rickettsia typhi*
;
Rickettsia*
;
Sequence Analysis
;
Typhus, Endemic Flea-Borne
10.A Case of Hereditary Hemorrhagic Telangiectasia.
Hyarng Joon PARK ; Hee Chul EUN ; Yoo Shin LEE
Korean Journal of Dermatology 1983;21(4):415-419
Hereditary hemorrhagic telangiectasia (Osler-Weber-Rendu disease) is a familial disease that is characterized by delicate, ectatic vessels in the skin, mucous membrane and viscera. These patients have a generalized vascular derangement including pulmonary A-V fistula and angiomatosis. Episodes of hemorrhage in cornbination with a familial history and cutaneous telangiectasia are diagnostic. We preaented a typical case of hereditary hemorrhagic telangieetasia in a 3-year-old female who had. two episodes of hemoptysis and compatible telangiectatic skin lesion. Her pulmonary and hepatic angiornas were also proved by pulmonary and aortic angiography.
Angiography
;
Angiomatosis
;
Child, Preschool
;
Female
;
Fistula
;
Hemoptysis
;
Hemorrhage
;
Humans
;
Mucous Membrane
;
Skin
;
Telangiectasia, Hereditary Hemorrhagic*
;
Telangiectasis
;
Viscera