- The Effect of High-Dose Valsartan on Left Ventricular Function Following Primary Percutaneous Coronary Intervention
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Park TH
- KMID: 2177304
- J Cardiovasc Ultrasound.
- 2010 Sep;18(3):84-85.
- doi: 10.4250/jcu.2010.18.3.84
No abstract available. -
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- Serum Amino Acid Levels in Term and Preterm Neonates
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Youn YS, Kim SZ, Chang MY
- KMID: 2188581
- J Korean Soc Neonatol.
- 2006 May;13(1):90-96.
PURPOSE: This study was aimed to analyze the level of serum amino acids according to the sex, birth weight, gestational age in neonates. METHODS: Amino acid was measured by tandem... -
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- A Case of Maple Syrup Urine Disease Controlled by Peritoneal Dialysis and Diet
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Kim JW, Huh J, Park WI, Lee KJ, Lee HJ
- KMID: 1605948
- J Korean Pediatr Soc.
- 2001 Jan;44(1):94-98.
Maple syrup urine disease is an autosomal recessive disease caused by a deficiency of the branched-chain alpa-ketoacid dehydrogenase complex. The disease is often suspected because of the peculiar odor of... -
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- Studies of Enzymes in Hyman Skin Tissue
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Kim YP, Kahng JB
- KMID: 1920678
- Korean J Dermatol.
- 1976 Jun;14(2):115-121.
Gamma-glutamyl transpeptidase (GGTP) activity was measured in the homogenate of penile foreskin, using y-glutamyl-p-nitroanilide, as a substrate, and it was found that (GGTP) activity was present in the epidermis and... -
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- A Case of Maple Syrup Urine Disease
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Cho DH, Lee HM, Kim SY, Ra CS
- KMID: 1945759
- J Korean Pediatr Soc.
- 1997 Sep;40(9):1297-1302.
Maple syrup urine disease (MSUD) is an autosomal recessive disease caused by a deficiency in subunits of the branched-chain alpha-ketoacid dehydrogenase complex (BCKDH). The disease is characterized by the accumulation... -
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- SLC26A4 Mutations in Korean Population
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Kim BG
- KMID: 1963750
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2014 Nov;57(11):733-737.
- doi: 10.3342/kjorl-hns.2014.57.11.733
SLC26A4 mutations are common cause of congenital hearing loss in East Asia. The carrier frequency of SLC26A4 mutations is 1 in 75 in Korean populations. The SLC26A4 mutation spectrum varies... -
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- A Family with A Missense Mutation in the SCN5A Gene
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Shin CH, Kim NH, Kim KH, Yoo SS, Choi YB, Oh SK, Hong KM, Jeong JW, Paik MK
- KMID: 2029618
- Korean Circ J.
- 2003 Feb;33(2):150-154.
- doi: 10.4070/kcj.2003.33.2.150
Brugada syndrome, an autosomal dominantly inherited form of ventricular fibrillation, is characterized by ST-segment elevation in leads V1-3 and right bundle-branch block on surface electrocardiogram. It is caused by mutations... -
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- Hyperthyroidism Caused by a Mutation in the Thyrotropin Receptor Gene in Two Brothers
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Kim JH, Lee SS, Lim JS, Shin CH, Yang SW
- KMID: 1979735
- Korean J Pediatr.
- 2005 Mar;48(3):337-341.
Thyrotropin receptor(TSHR) mutations must be considered when congenital hyperthyroidism has persisted, but there has been no evidence for autoimmunity. TSHR mutations leading to constitutive activation of the thyroid gland were... -
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- Development of a novel vaccine against canine parvovirus infection with a clinical isolate of the type 2b strain
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Park SA, Park SY, Song CS, Choi IS, Kim HY, Lee JB, Lee NH
- KMID: 2278790
- Clin Exp Vaccine Res.
- 2012 Jul;1(1):70-76.
- doi: 10.7774/cevr.2012.1.1.70
PURPOSE: In spite of an extensive vaccination program, parvoviral infections still pose a major threat to the health of dogs. MATERIALS AND METHODS: We isolated a novel canine parvovirus (CPV) strain... -
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- A Case of Methylmalonic Acidemia in a 6-month-old Infant
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Cho SJ, Rho YI, Moon KR
- KMID: 2275147
- Korean J Pediatr Gastroenterol Nutr.
- 2001 Sep;4(2):249-255.
Methylmalonic acidemia is a rare congenital autosomal recessive metabolic disease. It is caused by blocking in the pathways of isoleucine, valine, threonine, methionine, cholesterol and odd-chain fatty acids to succinyl CoA, resulting... -
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- A Case of Maple Syrup Urine Disease Associated with Acrodermatitis Enteropathica-like Syndrome Due to Iisoleucine Deficinecy During Diet Therapy
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Moon KH, Gwon OS, Lee JI, Rho SW, Jeon SS, Seo SS
- KMID: 2335536
- J Korean Pediatr Soc.
- 2001 Apr;44(4):469-474.
Maple syrup urine disease(MSUD) is an autosomal recessive disorder involving the metabolism of the branched-chain amino acids(BCAA) such as leucine, isoleucine and valine. The disorder is due to a defect... -
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- ras Gene Mutations in Malignant Fibrous Histiocytoma
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Yoo J, Lee AW, Kang SJ, Kim BK
- KMID: 2275609
- Korean J Pathol.
- 2001 Jun;35(3):232-237.
BACKGROUND: ras gene mutations have been described in various human malignancies, suggesting that their activation may play a role in oncogenesis. However, there are few reports concerning ras gene alterations... -
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- The Amino Acid Compositions of Formula for Children with Inherited Metabolic Disorder
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Ryu KH, Kim JS, Lee EH, Kwon IS, Hahn SH
- KMID: 2335559
- J Korean Pediatr Soc.
- 2002 Jan;45(1):37-43.
PURPOSE: This study aimed to determine the amino acids composition, safety and efficacy of formulas recently developed by Korean dairy companies for children with inherited metabolic disorder. METHODS: The determination of... -
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- Drug Treatment of Herpes Simplex Infection
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Lee ES
- KMID: 2065034
- J Korean Med Assoc.
- 2008 Oct;51(10):942-948.
- doi: 10.5124/jkma.2008.51.10.942
Herpes simplex virus (HSV) is one of Herpesviridae family viruses which belong to DNA viruses. HSV-associated diseases are among the most widespread infections, affecting nearly 60% to 95% of human... -
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- Taste Thresholds of Phenylthiocarbamide and 6-n-Propylthiouracil and their Correlation with TAS2R38 Genotype
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Choi SY, Shin SH, Ye MK
- KMID: 2277159
- Korean J Otorhinolaryngol-Head Neck Surg.
- 2010 Sep;53(9):547-551.
- doi: 10.3342/kjorl-hns.2010.53.9.547
BACKGROUND AND OBJECTIVES: Phenylthiocarbamide (PTC) and its chemically related compound,6-n-propylthiouracil (PROP), both produce a taste that is extremely bitter to some subjects (tasters) but tasteless or only slightly bitter to... -
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- Methylenetetrahydrofolate Reductase(MTHFR) Gene Expression in Kawasaki Disease
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Choi HR, Joo AR, Kim HS, Sohn S, Hong YM
- KMID: 2037361
- Korean J Pediatr.
- 2004 Jul;47(7):774-778.
PURPOSE: Hyperhomocysteinemia is known as an independent risk factor for cardiovascular diseases such as atherosclesosis and myocardiac infarct. A common mutation in 5, 10-methylenetetrahydrofolate reductase(MTHFR) gene results in a valine... -
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- Association Study of Val158Met Polymorphism of Catechol-O-Methyltransferase Gene and Cognitive Markers in Schizophrenia
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Park HJ, Park DY, Cho EY, Kim NR, Jeun HO, Lee YS, Lee D, Hong KS
- KMID: 2341417
- J Korean Neuropsychiatr Assoc.
- 2008 Mar;47(2):126-133.
OBJECTIVES: Catechol-O-methyltransferase (COMT) gene has been identified as a positional and functional candidate gene of schizophrenia. Although specific mechanism of increasing schizophrenia susceptibility by this gene has not been well... -
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- Paper chromatographic study on the amino acids of some parasitic helminths
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Seo BS, Yoon JS, Lee SH
- KMID: 1384139
- Korean J Parasitol.
- 1964 Jun;2(1):91-96.
- doi: 10.3347/kjp.1964.2.1.91
Unidimensional and two dimensional paper choromatogram were prepared of 10 kinds of parastic helminths. Fourteen amino acids were identified from the acid hydrolysed tissue proteins of A. lumbricoides(cuticle and musculature),... -
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- Acute Arterial Thrombosis in Leg Associated with Hyperhomocysteinemia
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Jeong CH, Park KH, Jung SJ, Choi DR, Joo DH, Lee HI, Park SH, Yu YW, Park KH
- KMID: 2096246
- J Korean Surg Soc.
- 2005 Jan;68(1):78-82.
Herein, two cases of acute arterial thrombosis associated with hyperhomocysteinemia are reported. A 34-year old male patient without heart disease, was brought to hospital with an acute ischemic limb due... -
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- Genetic Susceptibilities of MCP-1 and CCR2 to the Risk for Korean Allergic Rhinitis Patients Using Polymorphism Study
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Lee JH, Choi TW, Oh CK, Park SY, Yoon SW, Oh GJ, Kim JJ
- KMID: 2276098
- Korean J Otolaryngol-Head Neck Surg.
- 2004 Feb;47(2):127-131.
BACKGROUND AND OBJECTIVES: A biallelic A/G polymorphism in the Monocyte chemotactic protein (MCP) -1 at position -2518 has been found to affect the level of MCP-1 expression. To investigate if... -
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