- Stop Discussing New Medical Specialty Boards
-
Choung JT
- KMID: 2414033
- J Korean Med Sci.
- 2018 Jun;33(26):e205.
- doi: 10.3346/jkms.2018.33.e205
The Korean society is rapidly aging and the health care needs for aged people are increasing. In this context, some physicians claim to establish new medical specialty board (MSB) for... -
- CITED
-
- Close
- SHARE
-
- Close
- Reduction in Alpha Peak Frequency and Coherence on Quantitative Electroencephalography in Patients with Schizophrenia
-
Yeum TS, Kang UG
- KMID: 2414032
- J Korean Med Sci.
- 2018 Jun;33(26):e179.
- doi: 10.3346/jkms.2018.33.e179
BACKGROUND: The aim of the study was to examine the characteristics of alpha wave peak frequency, power, and coherence in patients with schizophrenia. METHODS: Thirty-one patients with schizophrenia and age- and... -
- CITED
-
- Close
- SHARE
-
- Close
- Why Geriatric Medicine Is Important for Korea: Lessons Learned in the United States
-
Won CW, Kim S, Swagerty D
- KMID: 2414029
- J Korean Med Sci.
- 2018 Jun;33(26):e175.
- doi: 10.3346/jkms.2018.33.e175
With the rapid increase in the number of Korean older adults, developing and integrating quality, expert older adult care in the Korean health care system will be essential and a... -
- CITED
-
- Close
- SHARE
-
- Close
- Plasma CRABP2 as a Novel Biomarker in Patients with Non-Small Cell Lung Cancer
-
Kim DJ, Kim WJ, Lim M, Hong Y, Lee SJ, Hong SH, Heo J, Lee HY, Han SS
- KMID: 2414031
- J Korean Med Sci.
- 2018 Jun;33(26):e178.
- doi: 10.3346/jkms.2018.33.e178
BACKGROUND: Lung cancer is the most common cause of cancer-related mortality worldwide. We previously reported the identification of a new genetic marker, cellular retinoic acid binding protein 2 (CRABP2), in... -
- CITED
-
- Close
- SHARE
-
- Close
- Multiplex Ligation-dependent Probe Amplification Analysis Subsequent to Direct DNA Full Sequencing for Identifying ATP7B Mutations and Phenotype Correlations in Children with Wilson Disease
-
Shim JO, Yang HR, Moon JS, Chang JY, Ko JS, Park SS, Seo JK
- KMID: 2414030
- J Korean Med Sci.
- 2018 Jun;33(26):e177.
- doi: 10.3346/jkms.2018.33.e177
BACKGROUND: Mutations in ATP7B cause Wilson disease (WD). However, direct DNA full sequencing cannot detect all mutations in patients with WD. Multiplex ligation-dependent probe amplification (MLPA) analysis is reportedly useful... -
- CITED
-
- Close
- SHARE
-
- Close
