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Clinical utility of chromosomal microarray analysis to detect copy number variants: Experience in a single tertiary hospital

Park HS, Kim A, Shin KS, Son BR

Purpose: To summarize the results of chromosomal microarray analysis (CMA) for copy number variants (CNVs) detection and clinical utility in a single tertiary hospital. Materials and Methods: We performed CMA in...
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Impact of Regional Emergency Medical Access on Patients’ Prognosis and Emergency Medical Expenditure

Kim Y, Lee TJ

Background: The purpose of this study was to examine the impact of the regional characteristics on the accessibility of emergency care and the impact of emergency medical accessibility on the...
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An Extensor Digitorum Muscle for Index Finger Originated from the Extensor Carpi Radialis Brevis

Kim J, Lee JH

The anomalous variations in the extensor carpi radialis brevis (ECRB) and extensor digitorum (ED) muscles of the forearm have been previously reported in the literature. The present article reported an...
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Complex Variations in Branching Pattern of the Axillary Artery and Hands with the Persistent Median Artery

Park JH, Kang SH, Baik TK, Woo RS, Song DY, Yoo HI

We report bilateral multiple variations in branching pattern of the axillary artery and superficial palmar arch of the hand in an 84-year-old Korean female cadaver. First, we identified an aberrant...
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Stafne bone cavity: a rare cadaveric case report

Iwanaga J, Wong TL, Kikuta S, Tubbs RS

The Stafne bone cavity (SBC), also called the static bone cavity, salivary inclusion cyst, latent cyst, and lingual bone defect is an asymptomatic bony defect that is commonly located inferior...
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Inter-rater agreement of Korean Triage and Acuity Scale between emergency physicians and nurses

Kim HI, Oh SB, Choi HJ

OBJECTIVE: The Korean Triage and Acuity Scale (KTAS) has been used in all emergency departments (EDs) since 2016. Medical personnel can provide the treatment priority based on the KTAS levels....
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Effects of Copy Number Variations on Developmental Aspects of Children With Delayed Development

Park KB, Nam KE, Cho AR, Jang W, Kim M, Park JH

OBJECTIVE: To determine effects of copy number variations (CNV) on developmental aspects of children suspected of having delayed development. METHODS: A retrospective chart review was done for 65 children who underwent...
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Insights of window-bsed mechanism approach to visualize composite bioData point in feature spaces

Daoud M

In this paper, we propose a window-based mechanism visualization approach as an alternative way to measure the seriousness of the difference among data-insights extracted from a composite biodata point. The...
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Report of an inferior rectal nerve variant arising from the S3 ventral ramus

Dupont G, Iwanaga J, Oskouian R, Tubbs RS

In surgical approaches to the perineum in general and anal region specifically, considering the possible variations of the inferior rectal nerve is important for the surgeon. Normally, the inferior rectal...
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Clinical anatomy of the nerve to the mylohyoid

Choi P, Iwanaga J, Dupont G, Oskouian R, Tubbs RS

The nerve to the mylohyoid (NM) originates from the mandibular division of the trigeminal nerve. The NM provides motor control to the mylohyoid and the anterior belly of the digastric....
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Pure 3D laparoscopy versus open right hemihepatectomy in a donor with type II and III portal vein variations

Park K, Shehta A, Lee JM, Hong SK, Yoon KC, Cho JH, Yi NJ, Lee KW, Suh KS

BACKGROUNDS/AIMS: Pure laparoscopic living donor right hemihepatectomy (PLDRH) has been performed in many experienced centers. However, portal vein variations still remain challenging thus disturbing the widespread of PLDRH in many...
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Right and left common carotid arteries arising from the branchiocephalic, a rare variation of the aortic arch

Panagouli , Tsoucalas , Papaioannou T, Fiska A, Venieratos D, Skandalakis P

The aortic arch may present a plethora of anatomical variations, which my cause a cluster of complications in interventional procedures in surgery and angiography. We present a rare case of...
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A rare double profunda femoris artery in a female cadaver

Tsoucalas , Panagouli , Fiska A, Troupis T, Venieratos D

The profunda femoris artery (PFA) represents the first and largest branch of the femoral artery in the thigh. A series of anatomical variations are reported, mostly concerning its point of...
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Impact of Time Delay in Processing Blood Sample on Next Generation Sequencing for Transcriptome Analysis

Lee JE, Jung SY, Shin SY, Kim YY

No abstract available.
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A cadaveric study on variations in branching pattern of external carotid artery

Devadas D, Pillay M, Sukumaran

Variations in the vascular anatomy of the carotid triangle have been reported in current scientific literature. The carotid arteries, being the major feeding arteries of the head and neck deserve...
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Copy Number Profiling of MammaPrintâ„¢ Genes Reveals Association with the Prognosis of Breast Cancer Patients

Fatima A, Tariq F, Malik MF, Qasim M, Haq F

PURPOSE: The MammaPrintâ„¢ gene signature, currently used in clinical practice, provides prognostic information regarding the recurrence and potential metastasis in breast cancer patients. However, the prognostic information of the 70...
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Next generation sequencing and array-based comparative genomic hybridization for molecular diagnosis of pediatric endocrine disorders

Fukami M, Miyado M

Next-generation sequencing (NGS) and array-based comparative genomic hybridization (array CGH) have enabled us to perform high-throughput mutation screening and genome-wide copy number analysis, respectively. These methods can be used for...
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Recognition of a rare intrathoracic rib with computed tomography: a case report

Abdollahifar MA, Abdi S, Bayat M, Masteri Farahani R, Abbaszadeh HA

One of the uncommon congenital variations is intrathoracic rib which a normal, a bifid, or an accessory rib lies within the thoracic cavity that is founded accidentally. Clinically, in most...
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Drosophila Homolog of Human KIF22 at the Autism-Linked 16p11.2 Loci Influences Synaptic Connectivity at Larval Neuromuscular Junctions

Park SM, Littleton , Park HR, Lee JH

Copy number variations at multiple chromosomal loci, including 16p11.2, have recently been implicated in the pathogenesis of autism spectrum disorder (ASD), a neurodevelopmental disease that affects 1~3% of children worldwide....
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Identification of a Copy Number Variation on Chromosome 20q13.12 Associated with Osteoporotic Fractures in the Korean Population

Park TJ, Hwang MY, Moon S, Hwang JY, Go MJ, Kim BJ

Osteoporotic fractures (OFs) are critical hard outcomes of osteoporosis and are characterized by decreased bone strength induced by low bone density and microarchitectural deterioration in bone tissue. Most OFs cause...
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