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Long-term Tolvaptan Treatment of Autosomal Dominant Polycystic Kidney Disease in Korea

Kim HY, Lee SJ, Kim BK, Kim M, Bae EH, Ma SK, Kim SW

A 22-year-old male patient was diagnosed with autosomal dominant polycystic kidney disease (ADPKD). He received conservative treatment with an angiotensin-converting enzyme inhibitor. Two years later, oral therapy, consisting of 60...
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Autosomal Dominant Polycystic Kidney Desease Coexisting with Renal Dysplasia. First Case Described and Followed Since Prenatal Period

Truyols C

Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent hereditary renal disease and causes terminal chronic renal failure. ADPKD is characterized by bilateral multiple renal cysts, which are produced...
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Predictors and outcomes of laparoscopic nephrectomy in autosomal dominant polycystic kidney disease

Chen K, Tan YG, Tan D, Pek G, Huang HH, Sim SP

PURPOSE: Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease, and 20% of patients eventually require nephrectomies due to compressive symptoms or renal-related complications. Traditionally, nephrectomies...
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Femoral Neuropathy Secondary to Autosomal Dominant Polycystic Kidney Disease: A Case Report

Yoo J, Lim KB, Lee HJ, Kim J, You EC, Kang J

Compressive femoral neuropathy is a disabling condition accompanied by difficulty in hip flexion and knee extension. It may result from retroperitoneal hematoma or bleeding, or from complications associated with pelvic,...
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Esophageal Artery Pseudoaneurysm and Takayasu Arteritis in a Patient with Autosomal Dominant Polycystic Kidney Disease

Kim H, Yu Y, Shim KE, Kim JE, Koh J, Yoon JW, Ahn C, Oh YK

A 47-year-old female previously diagnosed with ADPKD visited the hospital due to sudden pain in her upper abdomen and back. Esophagogastroduodenoscopy, contrast-enhanced abdominal computed tomography (CT), and CT angiography identified...
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Obturator hernia in autosomal dominant polycystic kidney disease

Jung JH, Song JH, Ahn SH

No abstract available.
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Autosomal Dominant Polycystic Kidney Desease Coexisting with Renal Dysplasia. First Case Described and Followed Since Prenatal Period

Truyols C

Autosomal dominant polycystic kidney disease (ADPKD) is the most frequent hereditary renal disease and causes terminal chronic renal failure. ADPKD is characterized by bilateral multiple renal cysts, which are produced...
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Xp11.2 translocation renal cell carcinoma in the autosomal dominant polycystic kidney disease patient with preserved renal function

Huh H, Jo HA, Yi Y, Kim SH, Moon KC, Ahn C, Park HC

No abstract available.
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Hypokalemic Hypertension Leading to a Diagnosis of Autosomal Dominant Polycystic Kidney Disease

Vutthikraivit W, Assanatham M, Sriphrapradang C

Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited renal disease. Hypertension is common and occurs before decline in renal function. However, the coexistence of hypertension and hypokalemia...
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PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data

Entezam M, Khatami MR, Saddadi F, Ayati M, Roozbeh J, Keramatipour M

BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic renal disorder caused by mutation in 2 genes PKD1 and PKD2. Thus far, no mutation is identified in...
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Genetic diagnosis of autosomal dominant polycystic kidney disease: linkage analysis versus direct mutation analysis

Lee KB

No abstract available.
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Effect of Simultaneous Nephrectomy on Perioperative Blood Pressure and Graft Outcome in Renal Transplant Recipients with Autosomal Dominant Polycystic Kidney Disease

Jo HA, Park HC, Kim H, Han M, Jeong JC, Oh KH, Yang J, Jeon HJ, Koo TY, Ha J, Kwak C, Hwang YH, Ahn C

BACKGROUND: For various reasons, kidney transplant recipients with autosomal dominant polycystic kidney disease (ADPKD) often undergo native nephrectomy in preparation for the transplantation. Simultaneous nephrectomy can result in hypotensive events...
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A Case of Non ST Elevation Myocardial Infarction by Coronary Artery Focal Spasm in a Patient with Autosomal Dominant Polycystic Kidney Disease

Lee DW, Pyeon SI, Oh KJ, Park HJ, Chae CB, Choi JH, Kim JH

Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited renal disease. The main causes of death in ADPKD are cardiovascular disease as well as infections and neurological reasons....
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Recent Advances in the Management of Autosomal Dominant Polycystic Kidney Disease

Park H, Hwang YH

Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease. It is characterized by the dysregulated growth of kidney cysts, resulting in end-stage kidney failure. By identifying...
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Papillary Adenoma Identified in Removed Polycystic Kidneys during Kidney Transplantation in Autosomal Dominant Polycystic Kidney Disease Patient

Chai MH, Park H, Kim Y, Kim JS, Kim SH, Eom M, Yang JW, Han BG, Choi SO

Kidney transplantation is the preferred treatment in end stage renal disease for autosomal dominant polycystic kidney disease (ADPKD) patients. Removal of the native kidney is not usually recommended for ADPKD...
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Multiple Cardiovascular Manifestations in a Patient with Autosomal Dominant Polycystic Kidney Disease

Kang YR, Ahn JH, Kim KH, Choi YM, Choi J, Park JR

Autosomal dominant polycystic kidney disease (ADPKD) is a systemic disorder associated with various extrarenal complications. The major cardiovascular complications of ADPKD include valvulopathies and vascular ectasia. A 64-year-old man who...
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Autosomal Dominant Polycystic Kidney Disease Combined with Intracranial Aneurysm and Dilated Cardiomyopathy: A Case Report

Chung BM, Chong S, Lee WS, Hwang SN

Extrarenal manifestations of autosomal dominant polycystic kidney disease (ADPKD) include non-renal, various intracranial, and cardiac cysts. A 26-year-old man with presumed ADPKD was also diagnosed with hemoptysis and dyspnea. The...
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Cyst growth, polycystins, and primary cilia in autosomal dominant polycystic kidney disease

Lee SH, Somlo S

  • KMID: 2224270
  • Kidney Res Clin Pract.
  • 2014 Jun;33(2):73-78.
The primary cilium of renal epithelia acts as a transducer of extracellular stimuli. Polycystin (PC)1 is the protein encoded by the PKD1 gene that is responsible for the most common...
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A Case of Cystadenocarcinoma of the Pancreas in a Patient with Autosomal Dominant Polycystic Kidney Disease

Lee SY, Yang YJ, Jang DS, Lee YM, Na KR, Lee BS, Lee KW, Shin YT

  • KMID: 2079753
  • Korean J Nephrol.
  • 2007 Jul;26(4):465-468.
Polycystic kidney disease is an autosomal dominant disease that may be associated with liver and pancretic cysts. Mitral valve prolapse and intracranial berry aneurysms are also well-known manifestations of autosomal...
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A Case of Intramural Hematoma Coexisting with Autosomal Dominant Polycystic Kidney Disease and Intracranial Aneurysm

Kim MH, Lee DH, Yim SM, Choi SW, Choi YS, Kim JH, Park CS, Oh YS, Youn HJ, Chung WS, Hong SJ

  • KMID: 1509689
  • J Cardiovasc Ultrasound.
  • 2006 Mar;14(1):19-21.
Autosomal dominant polycystic kidney disease(ADPKD) is one of the most common hereditary diseases, and frequently has well defined extrarenal manifestations. Among the fatal vascular complications associated with ADPKD, ruptured intracerebral...
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