- Evaluation of normal masseter muscles on ultrasonography
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Hwang HZ, Kim GT, Choi YS, Hwang EH
- KMID: 2013071
- Korean J Oral Maxillofac Radiol.
- 2008 Jun;38(2):73-79.
PURPOSE: To assess the internal echo intensity and morphological variability of masseter muscles on ultrasonography and to establish diagnostic criterion of estimation. MATERIALS AND METHODS: Participants consisted of 50 young adults (male... -
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- A Molecular Genetic Study with EcoRII Restriction Enzyme on the Steroidogenic Acute Regulatory Protein (StAR) Gene
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Oh PS, Hwang HZ, Jin DK, Shin JH, Lee H
- KMID: 2193691
- J Korean Soc Pediatr Endocrinol.
- 2000 Jun;5(1):115-120.
The molecular defect of congenital lipoid adrenal hyperplasia has been discovered to be in the transport of cholesterol into mitochondria due to defective regulatory protein called "Steroidogenic Acute Regulatory Protein... -
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- CAG Repeat Expansions in the Patients with Mood Disorder
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Sohn SE, Lim SW, Lee SY, Hwang HZ, Jin DK, Park JE, Kim DK, Kim E
- KMID: 2340441
- J Korean Neuropsychiatr Assoc.
- 2000 Mar;39(2):373-380.
OBJECTIVES: The genetic facotrs have been suggested for the etiology of mood disorders but the mode of inheritance is complex. Increased severity and an earlier onset of the bipolar and... -
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- The Molecular Genetic Study Using Automatic Sequence Analyzer on the Steroidogenic Acute Relulatory Protein(StAR) Gene
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Oh PS, Hwang HZ, Oh MR, Jeon KW, Ryu JS, Shin JH, Jin DK
- KMID: 2001540
- J Korean Soc Pediatr Endocrinol.
- 1997 Mar;2(1):109-115.
PURPOSE:The lesion of Congenital Lipoid Adrenal Hyperplasia has been suggested to be in the 1st step of steroidogenesis of conversion of cholesterol to pregnenolone by P450scc. In 1995, however, the... -
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- CAG Repeats of KCNN3 Gene in the Patients with Schizophrenia
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Kim DK, Lim SW, Koh HJ, Seo MY, Sohn SE, Lee S, Hwang HZ, Jin DK, Kim BL
- KMID: 2340605
- J Korean Neuropsychiatr Assoc.
- 2001 Sep;40(5):955-964.
OBJECTS:We investigated a possible association between the polymorphic trinucleotide repeat(TNR) expansion in neuronal potassium channel gene KCNN3 and schizophrenia. METHODS: CAG/CTG repeat distribution in KCNN3, CTG18.1 and ERDA1 was examined and... -
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- A study of trinucleotide repeat expansions in myotonic dystrophy
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Jin DK, Kim BJ, Lee KH, Lee MH, Oh PS, Jeon KW, Hwang HZ, Noh HW, Kim SJ, Yeo SH, Yu JS
- KMID: 2342590
- J Korean Neurol Assoc.
- 1997 Feb;15(1):90-98.
PURPOSE: The trinucleotide repeat expansion in the 3' untanslated resion of the gene is known to be the cause of myotonic dystrophy which is one of most common neurodegenerative disorder... -
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- A Study on the Relationship Between Genotype and Phenotype in Korean Patients with Congenital Adrenogenital Syndrome Caused by 21-hydroxylase Deficiency
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Jin DK, Kim JS, Song SM, Park SJ, Hwang HZ, On HY, Oh PS, Koh SW, Uhm MR, Lee DH, Shin JH, Han HS, Kim HS, Ko CW, Yoo HW, Lee JS, Kim DH
- KMID: 2199617
- J Korean Soc Endocrinol.
- 2000 Jun;15(2):237-247.
BACKGROUND: Congenital adrenal hyperplasia (CAH) results from an inherited defect in enzymatic steps required to synthesize cortisol from cholesterol. 21-hydroxylase deficiency accounts for 95% cases of CAH. It appears that... -
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