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신장내과박혜인 교수 사진

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전문센터 : 신장비뇨의학센터 홈페이지

진료과 : 신장내과 홈페이지

전문진료분야 : 급·만성 신장기능 저하의 진단 및 치료, 유전성 신질환의 진단 및 유전상담, 신장조직검사를 통한 사구체신염의 진단, 투석치료

전화 : 02-829-5107

이메일 : haynepark798@hallym.or.kr


(주간) 진료시간표 (2021-05-03 ~ 2021-05-08)

* 전화예약 : 1577-5587

전화 전화예약 ( 1577-5587)
의료진 진료시간표
진료시간
오전  센터진료   센터진료    
오후      센터진료    

학 력

내용 숨기기
한림대학교의과대학 학사 (2005)
한림대학교의과대학 석사 (2010)
서울대학교의과대학 박사 (2013)

면허 및 자격

내용 숨기기
의사면허 (2005)
내과전문의 (2010)
신장내과분과전문의 (2012)
투석전문의 (2012)

경 력

내용 숨기기
서울대학교병원 수련의 (2005~2010)
서울대학교병원 내과 임상강사 (2010~2013)
서울대학교병원 장기이식센터 임상강사 (2011~2012)
서울대학교병원 연구조교수 (2013~2014)
국군수도병원 신장내과 분과장 (2014~2018)
한림대학교강남성심병원 신장내과 부교수 (현재)

가입학회 및 활동

내용 숨기기
대한내과학회 정회원
대한신장학회 정회원
대한신장학회 대외협력위원 (2016~2018)

수상경력

내용 숨기기
한림대학교의과대학 총장상(성적우수) (2005)
국제군진외상학술대회 최우수 포스터상 (2017)

국내학회지 발표논문

내용 숨기기
1. Korean clinical practice guidelines for preventing the transmission of infections in hemodialysis facilities. Kidney Res Clin Pract 2018; 37(1): 8-19.

2. Xp11.2 translocation renal cell carcinoma in autosomal dominant polycystic kidney patient with preserved renal function. Korean J Intern Med 2017; 32(6): 1108-1111.

3. Middle East respiratory syndrome clinical practice guideline for hemodialysis facilities. Kidney Res Clin Pract 2017; 36(2): 111-116.

4. Recent advances in the management of autosomal dominant polycystic kidney disease. Korean J Med 2015; 89(2): 169-178.

5. Recurrent thrombotic events after catastrophic antiphospholipid syndrome. Korean J Intern Med 2012; 27(2): 232-234.

6. Lower residual renal function is a risk factor for depression and impaired health-related quality of life in Korean peritoneal dialysis patients. J Korean Med Sci 2012; 27(1): 64-71.

7. Transcatheter arterial embolization therapy for a massive polycystic liver in autosomal dominant polycystic kidney disease patients. J Korean Med Sci 2009; 24(1): 57-61.

국제학회지 발표논문

내용 숨기기
1. Diagnostic evaluation as a biomarker in patients with ADPKD. Adv Exp Med Biol 2016; 933:85-103.

2. Increased urinary angiotensinogen/creatinine ratio may be associated with reduced renal function in ADPKD. BMC Nephrol 2015; 16:86.

3. Identification of novel PKD1 and PKD2 mutations in Korean patients with autosomal dominant polycystic kidney disease. BMC Med Genet 2014;15:129.

4. Chronic asymptomatic pyuria precedes overt urinary tract infection and deterioration of renal function in autosomal dominant polycystic kidney disease. BMC Nephrol 2013; 14:1.

5. Urinary N-acetyl-beta-D glucosaminidase as a surrogate marker for renal function in autosomal dominant polycystic kidney disease: 1 year prospective cohort study. BMC Nephrol 2012; 13:93.

6. Depression and health-related quality of life in maintenance hemodialysis patients. Clin Nephrol 2010; 73(5): 374-380.

국내학회지 발표논문

내용 숨기기
1. Korean clinical practice guidelines for preventing the transmission of infections in hemodialysis facilities. Kidney Res Clin Pract 2018; 37(1): 8-19.

2. Xp11.2 translocation renal cell carcinoma in autosomal dominant polycystic kidney patient with preserved renal function. Korean J Intern Med 2017; 32(6): 1108-1111.

3. Middle East respiratory syndrome clinical practice guideline for hemodialysis facilities. Kidney Res Clin Pract 2017; 36(2): 111-116.

4. Recent advances in the management of autosomal dominant polycystic kidney disease. Korean J Med 2015; 89(2): 169-178.

5. Recurrent thrombotic events after catastrophic antiphospholipid syndrome. Korean J Intern Med 2012; 27(2): 232-234.

6. Lower residual renal function is a risk factor for depression and impaired health-related quality of life in Korean peritoneal dialysis patients. J Korean Med Sci 2012; 27(1): 64-71.

7. Transcatheter arterial embolization therapy for a massive polycystic liver in autosomal dominant polycystic kidney disease patients. J Korean Med Sci 2009; 24(1): 57-61.

국제학회지 발표논문

내용 숨기기
1. Diagnostic evaluation as a biomarker in patients with ADPKD. Adv Exp Med Biol 2016; 933:85-103.

2. Increased urinary angiotensinogen/creatinine ratio may be associated with reduced renal function in ADPKD. BMC Nephrol 2015; 16:86.

3. Identification of novel PKD1 and PKD2 mutations in Korean patients with autosomal dominant polycystic kidney disease. BMC Med Genet 2014;15:129.

4. Chronic asymptomatic pyuria precedes overt urinary tract infection and deterioration of renal function in autosomal dominant polycystic kidney disease. BMC Nephrol 2013; 14:1.

5. Urinary N-acetyl-beta-D glucosaminidase as a surrogate marker for renal function in autosomal dominant polycystic kidney disease: 1 year prospective cohort study. BMC Nephrol 2012; 13:93.

6. Depression and health-related quality of life in maintenance hemodialysis patients. Clin Nephrol 2010; 73(5): 374-380.