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Phenotype of a Patient With a 1p36.11-p35.3 Interstitial Deletion Encompassing the AHDC1

Park HY, Kim M, Jang W, Jang DH

No abstract available.
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An experimental study on the effect of condylar osteoplasty with preservation of articular covered soft tissue on the healing process in rabbit

Jang DH, Lee DK, Kim SN

  • KMID: 1690245
  • J Korean Assoc Maxillofac Plast Reconstr Surg.
  • 1991 Nov;13(3):241-251.
No abstract available.
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Rhabdomyolysis with severe hypernatrenia

Yang CW, Jang DH, O KY, Lee KH, Park IS, Chang YS, Yoon YS, Bang BK

  • KMID: 1694971
  • Korean J Nephrol.
  • 1991 Dec;10(4):614-619.
No abstract available.
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Epidemiologic study of hemorrhagic fever with renal syndrome in Korean military: 1985-1990

Yang CW, Jang DH, Cho YH, Bang BK, Lee HW

  • KMID: 1698149
  • Korean J Intern Med.
  • 1992 Jun;42(6):802-808.
No abstract available.
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Novel Mutation (c.8725T>C) in Two Siblings With Late-Onset LAMA2-Related Muscular Dystrophy

Kim MW, Jang DH, Kang J, Lee S, Joo SY, Jang JH, Cho EH, Choi YC, Lee JH

No abstract available.
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Skin Infection Caused by Serratia marcescens in a Patient with Diabetes Mellitus

Lee DH, Jang DH, Park MY, Ahn J, Jung HJ

Serratia marcescens is an uncommon gram-negative bacterium strain that does not cause skin infections in healthy individuals. However, it is rarely reported as the causative agent of infection in immunosuppressed...
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A Case of Pheochromocytoma Presenting as Stress-Induced Cardiomyopathy with Large Left Ventricular Thrombus

Jang DH, Park J, Kang MS, Kim TH, Shin DH, Lee JH, Chae MJ

  • KMID: 2269267
  • Korean J Med.
  • 2014 Jul;87(1):77-80.
The clinical presentation of pheochromocytoma is variable. The classic symptoms are headache, diaphoresis, and tachycardia, with paroxysmal hypertension. Other less common cardiovascular manifestations, such as arrhythmias, angina pectoris, acute myocardial...
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Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3

Choi A, Oh JY, Kim M, Jang W, Jang DH

Patients with a duplication from 7q36 to the terminus or a deletion of 9p24 have been reported, whereas those harboring both mutations have not. Here, we report a patient with...
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Epizootiological study of theileriasis in Korea - Prevalence of the bovine theileriasis in relation to its vector, Haemaphysalis (Kaiseriana) longicornis Neumann. 1901

Jang DH

Investigations of some problems related to the bovine theileriasis and its vector have been undertaken in Korea. Owing to the nation-wide investment of dairy farming, hundreds of milk cattle were...
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A Case of Auricular Keloid Resulting from Conchal Cartilage Graft in Asian Rhinoplasty

Jang DH, Kim JS

When planning rhinoplasty, there are several options of grafts for augmentation, especially in relatively short and small Asian noses. Among such grafts, conchal cartilage is one of the most commonly...
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A Case of Cochlear Implantation in the Patient With Neurofibromatosis Type II Considering Magnetic Resonance Imaging

Jang DH, Chai MS, Shim HJ

Cochlear implantation is the treatment of choice for patients with profound sensorineural hearing loss. Neurofibromatosis type II is a multiple tumor syndrome caused by gene mutation, and MRI is necessary...
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Identification of a Heterozygous SPG11 Mutation by Clinical Exome Sequencing in a Patient With Hereditary Spastic Paraplegia: A Case Report

Oh JY, Do HJ, Lee S, Jang JH, Cho EH, Jang DH

Next-generation sequencing, such as whole-genome sequencing, whole-exome sequencing, and targeted panel sequencing have been applied for diagnosis of many genetic diseases, and are in the process of replacing the traditional...
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Scanning electron microscopic observations on the surface structure of the tick Boophilus microplus(Canestrini, 1887) female specimens

Kang YB, Jang DH

Boophilus microplus (Canestrini, 1887) female specimens were subjected to scanning electron microscopy for the observation of surface fine structures. Morphological characteristics observed were summarized as follows: The palpi were wider...
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Sonographic Findings of Polyneuropathy Associated With Cerebrotendinous Xanthomatosis: A Case Report

Yoon JY, Kim MW, Do HJ, Jang DH, Lee HW

Cerebrotendinous xanthomatosis is a rare autosomal recessive disease that involves multiple organs, including the peripheral nervous system. The present study is the first to report the ultrasonographic findings of peripheral...
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A description with scanning electron microscopy on the tick Ixodes persulcatus (Schulze, 1930 ) male and female specimens

Kang YB, Jang DH

The surface fine structures of Ixodes persulcatus (Schulze, 1930) male and female specimens were observed by means of a scanning electron microscope. A brief review on the biology of the...
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Comparison of Loudness Discomfort Level by the Testing Method in Adults With Normal Hearing and in Patients With Sensorineural Hearing Loss

Jang DH, Choi JH, Jeon SY, Kim KM, Kim DH, Han S, Park JH, Park KY, Choi HJ, Shim HJ, An YH

Background and Objectives There are several variations in the technique for measuring loudness discomfort levels (LDL). The aim of this study was to evaluate LDL by measuring pure tone and...
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A Case of Nasopharyngeal Tuberculosis Which Was Difficult to Differentiate From Sarcoidosis

Jang DH, Kim HC, Hong YO, Kim JS

Nasopharyngeal mass is a disease that can cause unilateral or bilateral nasal obstruction. Common diseases that can cause nasal obstruction include antrochoanal polyp, adenoid remnants, juvenile nasopharyngeal angiofibroma, and nasopharyngeal...
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Rehabilitation of spinal muscular atrophy: current consensus and future direction

Yi YG, Shin HI, Jang DH

Spinal muscular atrophy (SMA) is a neuromuscular disease that requires multidisciplinary medical care, including rehabilitation management. The emergence of a genetic therapy-based approach for SMA has markedly changed the disease...
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Takayasu's Disease in a Patient with Ulcerative Colitis

Chae MJ, Yu CW, Lee SY, Jang DH, Hyun JY, Jeong SJ, Kim MH

A 35-year-old Korean man with a 10-year history of ulcerative colitis (UC) presented with pain and swelling of the right neck. The patient was diagnosed with Takayasu's arteritis (TA) and...
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Correlation Between Vanishing White Matter Disease and Novel Heterozygous EIF2B3 Variants Using Next-Generation Sequencing: A Case Report

Hyun SE, Choi BS, Jang JH, Jeon I, Jang DH, Ryu JS

Vanishing white matter (VWM) disease is an autosomal recessive disorder that affects the central nervous system of a patient, and is caused by the development of pathogenic mutations in any...
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