1.Clinical Competency for Directing of Registered Nurses's National Examination: focused on Fundamental, Medical-Surgical, Psychiatric, women's health, community, Pediatric, and Administrative Nursing.
Boon Han KIM ; SoYaJa KIM ; Jeong Seop LEE ; Young Ran TAK ; Hee Soon KIM ; Ee Soon CHOI ; Kyoung Rim SHIN ; Kyoung Sook CHOI ; Gui Boon KIM ; Gwang Joo KIM ; So Woo LEE ; Kem Soon KIM ; Sook Ja LEE ; Yun Hee KIM ; Kyoung Hea LEE ; Young Sook JEONG ; Ji Ho SONG ; Jeong Ho PAK
Journal of Korean Academy of Nursing 1998;28(4):1075-1087
For producing large numbers of professional nurses who could manage 21th century's human health, it is necessary to review the direction of registered nursed' national examination which evaluates the nursing education and is granted a licence. For adapting to social expectation of the nurse, we have to nurture the nurses' problem solving capability in clinical setting. Seven divisions of Korean Academy of Nursing suggested clinical competency according to their categories. This paper was presented in the workshop for setting up direction of registered nurses' national examination. We expect that this paper would be more refine and confirm through reviewing subdivisions' learning objectives and discussing clinical minimum level of competence contents with clinical leaders.
Education
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Education, Nursing
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Financing, Organized
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Humans
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Learning
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Mental Competency
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Nursing*
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Problem Solving
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Women's Health*
2.Loss of podocalyxin causes a novel syndromic type of congenital nephrotic syndrome.
Hee Gyung KANG ; Moses LEE ; Kyoung Boon LEE ; Michael HUGHES ; Bo Sang KWON ; Sangmoon LEE ; Kelly M MCNAGNY ; Yo Han AHN ; Jung Min KO ; Il Soo HA ; Murim CHOI ; Hae Il CHEONG
Experimental & Molecular Medicine 2017;49(12):e414-
Many cellular structures directly imply specific biological functions. For example, normal slit diaphragm structures that extend from podocyte foot processes ensure the filtering function of renal glomeruli. These slits are covered by a number of surface proteins, such as nephrin, podocin, podocalyxin and CD2AP. Here we report a human patient presenting with congenital nephrotic syndrome, omphalocele and microcoria due to two loss-of-function mutations in PODXL, which encodes podocalyxin, inherited from each parent. This set of symptoms strikingly mimics previously reported mouse Podxl(−/−) embryos, emphasizing the essential function of PODXL in mammalian kidney development and highlighting this patient as a human PODXL-null model. The results underscore the utility of current genomics approaches to provide insights into the genetic mechanisms of human disease traits through molecular diagnosis.