Zobrazeno 1 - 6
of 6
pro vyhledávání: '"You Jin Jung"'
Publikováno v:
Dermatologic Surgery. 48:327-333
Numerous treatments for pigmentary disorders have been used with variable outcomes. Recently, a new radiofrequency (RF) device with minimal pulse duration has been introduced.The aim of this study was to evaluate the efficacy and safety of a pulsed-t
Autor:
Sun Young Choi, Jae Wan Park, Young Gue Koh, You Jin Jung, Yun Jung Huh, Eun Jung Ko, Kwang Ho Yoo, Joon Seok, Soo Yeon Kim, Mihn Sook Jue, Joo Yeon Ko, Beom Joon Kim
Publikováno v:
Dermatologic Therapy. 35
Various treatment methods are used for noninvasive body contouring. To evaluate the efficacy and safety of a newly designed cryolipolysis device using a three-dimensional cooling method for abdominal fat reduction. Twenty-five participants with clini
Publikováno v:
Archives of Pharmacal Research. 43:714-723
Factor VIII (FVIII) is a blood coagulation protein that circulates as a complex with von Willebrand factor (vWF) in the plasma. In the survey of inhibitors in plasma product exposed toddlers (SIPPET) study, plasma-derived FVIII containing vWF was les
Publikováno v:
Journal of cosmetic and laser therapy : official publication of the European Society for Laser Dermatology. 22(4-5)
Facial erythema from rosacea and acne is one of the most common problems encountered in dermatologic clinics. Effective therapeutic interventions for persistent erythema, which can cause patients frustration and psychological distress, are needed. Th
Publikováno v:
The Journal of Nursing Research
Background: Since the Omnibus Budget and Reconciliation Act was passed in South Korea in 1987, function-focused care (FFC) has been used in long-term care to achieve the highest possible levels of self-care and independence for older adults. However,
Autor:
Su Jin Kim, Sung Yoon Cho, Se Hyun Maeng, Chang-Seok Ki, You Jin Jung, Dong-Kyu Jin, Young Bae Sohn
Publikováno v:
Journal of human genetics. 58(3)
Prader–Willi syndrome (PWS) is a genetic disorder caused by the absence of expression of the paternal copy of maternally imprinted genes in chromosome region 15q11–13. The genetic subtypes of PWS are classified into deletion (∼70%), maternal un