1.A case of combined hyperlipoproteinemia.
Young Bae KWON ; Sung Hee IHM ; Moon Ki CHOI ; Byung Tae KIM ; Yeon Bok JANG ; Sung Woo PARK
Journal of Korean Society of Endocrinology 1991;6(2):191-195
No abstract available.
Hyperlipoproteinemias*
2.A case of acute supprative thyroiditis.
Sai Hyun PAIK ; Jin Goo LEE ; Jae Myung YOU ; Dong Seop CHOI
Journal of Korean Society of Endocrinology 1991;6(2):187-190
No abstract available.
Thyroid Gland*
;
Thyroiditis*
3.Successful management of pheochromocytoma in early pregnancy.
Bo In JUNG ; Jae Woong CHOI ; Yeon Sun KIM ; Jin Iee CHUNG ; Moon Ho KANG
Journal of Korean Society of Endocrinology 1991;6(2):179-186
No abstract available.
Pheochromocytoma*
;
Pregnancy*
4.Pseudohypoparathyroidism type Ia and type II.
Moo Il KANG ; Young Bu PARK ; Young Gil LEE ; Sun Jip YOO ; Hyun Shik SON ; Kun Ho YOON ; Kwan Su HONG ; Kwang Woo LEE ; Ho Young SON ; Sung Ku KANG ; Beum Sageng KIM
Journal of Korean Society of Endocrinology 1991;6(2):170-178
No abstract available.
Pseudohypoparathyroidism*
5.Clinical aspexts on craniopharyngioma.
Jae Hee CHUNG ; Hyun Chul LEE ; Nae Choon YOO ; Yoon Sok CHUNG ; Seong Kil LIM ; Kyung Rae KIM ; Kap Bum HUH
Journal of Korean Society of Endocrinology 1991;6(2):163-169
No abstract available.
Craniopharyngioma*
6.Effect of fluoride and vandate on the osteoblast MC3T3-E1 function.
Jung Taek WOO ; Hyun Koo YOON ; Young Seol KIM ; Sung Woon KIM ; In Myung YANG ; Jin Woo KIM ; Kwang Won KIM ; Young Kil CHOI ; Kwang Sik SEO
Journal of Korean Society of Endocrinology 1991;6(2):157-162
No abstract available.
Fluorides*
;
Osteoblasts*
7.Diagnostic value of fine needle aspiration of thyroid nodules.
Sang Seok LEE ; Sun Ho KIM ; Jong Kwan KIM ; Phil Seok OH ; Jung Kyu LIM ; Chin Duk HUH ; Jang Shin SOHN
Journal of Korean Society of Endocrinology 1991;6(2):150-156
No abstract available.
Biopsy, Fine-Needle*
;
Thyroid Gland*
;
Thyroid Nodule*
8.Therapeutic effect of thyroid hormone suppressive therapy for benign thyroid nodule.
Young Deok CHO ; Dong Hwa SONG ; Kyo Il SEO ; Myung Hi YOO ; Guk Bae KIM
Journal of Korean Society of Endocrinology 1991;6(2):141-149
No abstract available.
Thyroid Gland*
;
Thyroid Nodule*
9.Changes in diurnal variation of thyrotropin secretion in nonthyroid- al illness and its mechanism.
Bo Youn CHO ; Min Ho SHONG ; Ka Hee YI ; Jae Joon KOH ; Kyung Soo KO ; Kyoung Soo PARK ; Seong Yeon KIM ; Hong Kyu LEE ; Chang Soon KOH ; Hun Ki MIN
Journal of Korean Society of Endocrinology 1991;6(2):133-140
No abstract available.
Thyrotropin*
10.Clinical Characteristics of 10 Cases of Korean Osteogenesis Imperfecta.
Hyoung Suk LEE ; Hyon J KIM ; Jae Hyun CHO ; Seong Won LEE ; Hyun A KIM ; Joon Hyuck CHOI ; Young Jun SONG ; Dae Jung KIM ; Kwan Woo LEE ; Yoon Sok CHUNG
Journal of Korean Society of Endocrinology 2003;18(5):496-503
Osteogenesis Imperfecta (OI) is a relatively rare hereditary disease, which is characterized by multiple bone fractures and spine scoliosis, due to the fragility of bone, and is often associated with blue sclerae, deafness and dentinogenesis imperfecta. Four types of OI can be distinguished, according to the clinical findings. Although mutations affecting type I collagen are responsible for the disease in most patients, the mechanism by which the genetic defects cause abnormal bone development remains to be fully understood. Here, the clinical characteristics of 10 OI patient cases are reported, with a review of the literature. All the cases, including 4 type I, 4 type III and 2 type IV, inherited OI as an autosomal dominant trait. All the subjects had multiple old fractures and decreased bone densities. In this study, the biochemical marker of bone formation, serum alkaline phosphatase, was found to be increased only in the pediatric OI patients, while the biochemical marker of bone resorption, urinary deoxypyridinoline, was increased in all cases. The mobility score was found to correlate with the severity of the type on diagnosis.
Alkaline Phosphatase
;
Biomarkers
;
Bone Density
;
Bone Development
;
Bone Resorption
;
Collagen Type I
;
Deafness
;
Dentinogenesis Imperfecta
;
Diagnosis
;
Fractures, Bone
;
Genetic Diseases, Inborn
;
Humans
;
Osteogenesis Imperfecta*
;
Osteogenesis*
;
Sclera
;
Scoliosis
;
Spine