WordNet

either of two bean-shaped excretory organs that filter wastes (especially urea) from the blood and excrete them and water in urine; "urine passes out of the kidney through ureters to the bladder"
relating to or evidencing dysplasia

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1. 先天性腎尿路異常（CAKUT）の概要 overview of congenital anomalies of the kidney and urinary tract cakut
2. 小児における腎嚢胞性疾患 renal cystic diseases in children
3. 嚢胞性腎疾患の胎児超音波診断 prenatal sonographic diagnosis of cystic renal disease
4. 先天性腎尿路異常（CAKUT）の評価 evaluation of congenital anomalies of the kidney and urinary tract cakut
5. 小児における常染色体劣性多発性嚢胞腎 autosomal recessive polycystic kidney disease in children

Renal cell carcinoma: translational aspects of metabolism and therapeutic consequences.

Yang OC, Maxwell PH, Pollard PJ.SourceCancer Biology and Metabolism Group, Henry Wellcome Building for Molecular Physiology, University of Oxford, Oxford, UK.
Kidney international.Kidney Int.2013 Oct;84(4):667-681. doi: 10.1038/ki.2013.245. Epub 2013 Jul 3.
The heterogeneity of renal cell carcinoma (RCC) poses a challenge for designing clinically applicable diagnostic and screening investigations, predictive and prognostic biomarkers, and targeted molecular therapies. Hereditary RCC syndromes harbor specific driver gene mutations, and their discoveries
PMID 23823604

Surmeli-Onay O, Yakarisik S, Korkmaz A, Akcoren Z, Yuce A, Runz H, Stampfer M, Yurdakok M.SourceDepartment of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey; Section of Neonatology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey. Electronic address: ozgeonay79@gmail.com.
Pediatrics and neonatology.Pediatr Neonatol.2013 Oct;54(5):344-347. doi: 10.1016/j.pedneo.2013.01.015. Epub 2013 Mar 11.
Niemann-Pick type C (NPC; OMIM 257219) disease is a neurodegenerative lysosomal storage disorder characterized by accumulation of unesterified cholesterol in the lysosomal/late endosomal system. This autosomal recessive disorder occurs in approximately 1/150,000 births. The broad clinical spectrum r
PMID 23597521

Khurana KK, Hillyer SP, Miocinovic R, Rhee AC, Haber GP.SourceGlickman Urological & Kidney Institute, Cleveland Clinic, Cleveland, OH. Electronic address: khurank@ccf.org.
Urology.Urology.2013 Sep 14. pii: S0090-4295(13)00999-0. doi: 10.1016/j.urology.2013.08.007. [Epub ahead of print]
PMID 24044917

Timing of renal replacement therapy initiation and choosing the optimal modality for pediatric patients with hypo/dysplastic kidney

本多貴実子,秋岡祐子,菅原典子,上田博章,藤井寛,近本裕子,服部元史
Nihon Shoni Jinzobyo Gakkai Zasshi 25(1), 1-5, 2012
… We retrospectively examined the timing of RRT initiation and choice of the modality in patients with hypo/dysplastic kidney, which is the major cause of end‐stage renal disease in children. … The mean time from the diagnosis of hypo/dysplastic kidney to the initiation of RRT was 6.7±3.7 years. …
NAID 130003346826

Retroperitoneoscopic Nephrectomy for Treatment of a Case of Left Single Ectopic Ureter Accompanied by Dysplastic Kidney

Hara Ryoei,Fujii Tomohiro,Jo Yoshimasa,Yokoyama Teruhiko,Miyaji Yoshiyuki,Nagai Atsushi
Acta Medica Okayama 65(5), 343-345, 2011-10
… Preoperative CT showed a contrasted dysplastic kidney of 1cm in the renal fossa and a left ureteral opening into the vagina. … Retroperitoneoscopic left nephrectomy was conducted with opening of the lateroconal fascia to enable identification of the dysplastic kidney. … This case shows that a retroperitoneal approach can be used in nephrectomy if the position of the kidney can be determined preoperatively. …
NAID 80022078066

Morphological and functional analyses of two infants with obstructive renal dysplasia

MIURA Kenichiro,SEKINE Takashi,NISHIMURA Riki,KANAMORI Yutaka,YANAGISAWA Atsuhiro,SAKAI Kiyohide,NAGATA Michio,IGARASHI Takashi
Clinical and experimental nephrology 15(4), 602-606, 2011-08-01
NAID 10029572082