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Patient-specific surgical options for breast cancer-related lymphedema: technical tips

Kwon JG, Hong DW, Suh HP, Pak CJ, Hong JP

In order to provide a physiological solution for patients with breast cancer-related lymphedema (BCRL), the surgeon must understand where and how the pathology of lymphedema occurred. Based on each patient’s...
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Hospital Information Exchange System Using XML Document

Hong DW, Yoon JH, Namkung S

  • KMID: 2210365
  • J Korean Soc Med Inform.
  • 2001 Jun;7(2):1-16.
Recently many domestic hospitals computerize and automatize the process to manage their own medical data. These medical data should be shared among the departments in the hospital and be held...
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Atypical Thoracic Solitary Plasmacytoma

Kim DH, Yoo SD, Kim SM, Im SJ, Hong DW

  • KMID: 2391541
  • Ann Rehabil Med.
  • 2012 Oct;36(5):739-743.
Plasmacytoma is a rare disease, which afflicts 2 to 3 people per every 100,000 of the general population. Solitary plasmacytoma accounts for 5% of the plasma cell neoplasm. Solitary plasmacytoma...
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Characterization of H460R, a Radioresistant Human Lung Cancer Cell Line, and Involvement of Syntrophin Beta 2 (SNTB2) in Radioresistance

Im CN, Kim BM, Moon EY, Hong DW, Park JW, Hong SH

A radioresistant cell line was established by fractionated ionizing radiation (IR) and assessed by a clonogenic assay, flow cytometry, and Western blot analysis, as well as zymography and a wound...
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Efficacy of Ultrasonography Guided Stellate Ganglion Blockade in the Stroke Patients with Complex Regional Pain Syndrome

Yoo SD, Jung SS, Kim HS, Yun DH, Kim DH, Chon J, Hong DW

  • KMID: 2391525
  • Ann Rehabil Med.
  • 2012 Oct;36(5):633-639.
OBJECTIVE: To compare the efficacy of ultrasonography guided stellate ganglion block (US-SGB) with that of blind SGB in management of the stroke patients with complex regional pain syndrome (CRPS) type...
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Psychological characteristics of adult neurofibromatosis type 1 patients seeking elective surgery

Min K, Hong DW, Kim EK, Lee BH

Background Neurofibromatosis type 1 (NF1) is an autosomal dominant genetic disorder involving the nervous system characterized by the development of neurofibromas throughout the body. Patients with NF1 are also known...
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