1.Epidemiology and Clinical Management of Traumatic Spine Injuries at a Major Government Hospital in Cambodia.
Jee Hye CHOI ; Paul J PARK ; Vuthy DIN ; Nang SAM ; Vycheth IV ; Kee B PARK
Asian Spine Journal 2017;11(6):908-916
STUDY DESIGN: Cross sectional study. PURPOSE: To characterize the pattern of injury, describe the current clinical management, and determine the outcomes in traumatic spine injury (TSI) patients presenting to a major government hospital in Phnom Penh, Cambodia. OVERVIEW OF LITERATURE: There is a paucity of literature on epidemiology or current clinical practices for TSIs in Cambodia. The findings from this study can thus serve as a valuable resource for future progress in treating TSIs in low-income countries. METHODS: This study was a cross-sectional study of TSI patients admitted to Preah Kossamak Hospital in Phnom Penh, Cambodia. Demographics, cause of spinal injury, spinal level of injury, surgical procedures and techniques, complications, and American Spinal Injury Association (ASIA) grades were recorded and analyzed. RESULTS: Eighty patients were admitted with TSI between October 2013 and June 2014. Falls from heights were the most common cause of TSI, followed by road traffic accidents. 78% of the admitted patients underwent at least one surgical procedure. Without intraoperative imaging, 4 patients (6%) had wrong level surgery, and 1 patient (2%) had misplacement of pedicle screws. Sacral decubitus ulcers were the most common non-surgically related complication. Antibiotics were administered to >90% of patients. There were no in-hospital mortalities. Of the 60 spinal cord injury (SCI) patients, 32% (19/60) showed improvement in their ASIA grade at the time of discharge, and 52% (31/60) showed no change. At follow-up, 32% (19/60) of SCI patients reported improvement, and 8% (5/60) reported no change. However, 36 SCI patients (60%) were lost to follow-up. CONCLUSIONS: Despite technological limitations, outcomes of TSI patients in Cambodia appear favorable with evidence of clinical improvement and low mortality.
Accidental Falls
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Accidents, Traffic
;
Anti-Bacterial Agents
;
Asia
;
Cambodia*
;
Cross-Sectional Studies
;
Demography
;
Epidemiology*
;
Follow-Up Studies
;
Global Health
;
Hospital Mortality
;
Humans
;
Intraoperative Complications
;
Lost to Follow-Up
;
Mortality
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Neurosurgical Procedures
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Pedicle Screws
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Pressure Ulcer
;
Spinal Cord Injuries
;
Spinal Injuries
;
Spine*
2.Serum Response Factor Is Essential for Prenatal Gastrointestinal Smooth Muscle Development and Maintenance of Differentiated Phenotype.
Chanjae PARK ; Moon Young LEE ; Paul J PARK ; Se Eun HA ; Robyn M BERENT ; Robert FUCHS ; Joseph M MIANO ; Laren S BECKER ; Kenton M SANDERS ; Seungil RO
Journal of Neurogastroenterology and Motility 2015;21(4):589-602
BACKGROUND/AIMS: Smooth muscle cells (SMCs) characteristically express serum response factor (SRF), which regulates their development. The role of SRF in SMC plasticity in the pathophysiological conditions of gastrointestinal (GI) tract is less characterized. METHODS: We generated SMC-specific Srf knockout mice and characterized the prenatally lethal phenotype using ultrasound biomicroscopy and histological analysis. We used small bowel partial obstruction surgeries and primary cell culture using cell-specific enhanced green fluorescent protein (EGFP) mouse lines to study phenotypic and molecular changes of SMCs by immunofluorescence, Western blotting, and quantitative polymerase chain reaction. Finally we examined SRF change in human rectal prolapse tissue by immunofluorescence. RESULTS: Congenital SMC-specific Srf knockout mice died before birth and displayed severe GI and cardiac defects. Partial obstruction resulted in an overall increase in SRF protein expression. However, individual SMCs appeared to gradually lose SRF in the hypertrophic muscle. Cells expressing low levels of SRF also expressed low levels of platelet-derived growth factor receptor alpha (PDGFRalphalow) and Ki67. SMCs grown in culture recaptured the phenotypic switch from differentiated SMCs to proliferative PDGFRalphalow cells. The immediate and dramatic reduction of Srf and Myh11 mRNA expression confirmed the phenotypic change. Human rectal prolapse tissue also demonstrated significant loss of SRF expression. CONCLUSIONS: SRF expression in SMCs is essential for prenatal development of the GI tract and heart. Following partial obstruction, SMCs down-regulate SRF to transition into proliferative PDGFRalphalow cells that may represent a phenotype responsible for their plasticity. These findings demonstrate that SRF also plays a critical role in the remodeling process following GI injury.
Animals
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Blotting, Western
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Fluorescent Antibody Technique
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Gastrointestinal Tract
;
Heart
;
Humans
;
Mice
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Mice, Knockout
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Microscopy, Acoustic
;
Muscle Cells
;
Muscle, Smooth*
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Myocytes, Smooth Muscle
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Parturition
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Phenotype*
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Plastics
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Polymerase Chain Reaction
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Primary Cell Culture
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Receptors, Platelet-Derived Growth Factor
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Rectal Prolapse
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RNA, Messenger
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Serum Response Factor*
3.Exosomes as a Communication Tool Between the Lymphatic System and Bladder Cancer.
Rebekah J PARK ; Yeo Jin HONG ; Yifan WU ; Paul Myungchul KIM ; Young Kwon HONG
International Neurourology Journal 2018;22(3):220-224
No abstract available.
Exosomes*
;
Lymphatic System*
;
Urinary Bladder Neoplasms*
;
Urinary Bladder*
4.A Checklist of the Basidiomycetous Macrofungi and a Record of Five New Species from Mt. Oseo in Korea.
Won Dong LEE ; Hyun LEE ; Jonathan J FONG ; Seung Yoon OH ; Myung Soo PARK ; Ying QUAN ; Paul E JUNG ; Young Woon LIM
Mycobiology 2014;42(2):132-139
Basidiomycetous macrofungi play important roles in maintaining forest ecosystems via carbon cycling and the mobilization of nitrogen and phosphorus. To understand the impact of human activity on macrofungi, an ongoing project at the Korea National Arboretum is focused on surveying the macrofungi in unexploited areas. Mt. Oseo was targeted in this survey because the number of visitors to this destination has been steadily increasing, and management and conservation plans for this destination are urgently required. Through 5 field surveys of Mt. Oseo from April to October 2012, 116 specimens of basidiomycetous macrofungi were collected and classified. The specimens were identified to the species level by analyzing their morphological characteristics and their DNA sequence data. A total of 80 species belonging to 57 genera and 25 families were identified. To the best of our knowledge, this is the first study to identify five of these species-Artomyces microsporus, Hymenopellis raphanipes, Pholiota abietis, Phylloporus brunneiceps, and Sirobasidium magnum-in Korea.
Base Sequence
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Carbon
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Checklist*
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Ecosystem
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Human Activities
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Humans
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Korea
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Nitrogen
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Pholiota
;
Phosphorus
5.Delimitation of Russula Subgenus Amoenula in Korea Using Three Molecular Markers.
Myung Soo PARK ; Jonathan J FONG ; Hyun LEE ; Seung Yoon OH ; Paul Eunil JUNG ; Young Ju MIN ; Soon Ja SEOK ; Young Woon LIM
Mycobiology 2013;41(4):191-201
Distinguishing individual Russula species has been difficult due to extensive phenotypic plasticity and obscure morphological and anatomical discontinuities. Due to highly similar macroscopic features, such as the presence of a red-cap, species identification within the Russula subgenus Amoenula is particularly difficult. Three species of the subgenus Amoneula have been reported in Korea. We used a combination of morphology and three molecular markers, the internal transcribed spacer (ITS), 28S nuclear ribosomal large subunit (LSU), and RNA polymerase II gene (RPB2), for identification and study of the genetic diversity of Russula subgenus Amoenula in Korea. We identified only two species in Korea (R. mariae and R. violeipes); these two species were indistinguishable according to morphology and LSU, but were found to be reciprocally monophyletic species using ITS and RPB2. The markers, ITS, LSU, and RPB2, have been tested in the past for use as DNA barcoding markers, and findings of our study suggest that ITS and RPB2 had the best performance for the Russula subgenus Amoneula.
DNA
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Genetic Variation
;
Korea*
;
Plastics
;
RNA Polymerase II