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Kidney diseases. Advances in diagnosis and treatment. III.Hereditary kidney diseases and others. Polycystic kidney disease.

机译：肾脏疾病。诊断和治疗进展。 III.Heredary肾脏疾病和其他人。多囊肾。

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1. Acquired cystic kidney disease: rapid progression from small to enlarged kidneys simulating adult polycystic kidney disease. [J] . Gagnon RF, Kintzen GM, Kaye M Clinical nephrology . 2000,第4期

机译：获得性胆囊性肾脏疾病：从小肾脏迅速发展为模拟成年多囊性肾脏疾病的肾脏。
2. Polycystic kidney disease: Promising new potential therapies for patients with autosomal dominant polycystic kidney disease. [J] . Ireland R Nature reviews. Nephrology . 2010,第8期

机译：多囊肾：常染色体显性遗传多囊肾患者有望获得新的治疗方法。
3. PKDB: Polycystic Kidney Disease Mutation Database--a gene variant database for autosomal dominant polycystic kidney disease. [J] . Gout AM, Martin NC, Brown AF, Human mutation . 2007,第7期

机译：PKDB：多囊肾疾病突变数据库-常染色体显性多囊肾疾病的基因变异数据库。
4. Detection and Segmentation of Kidneys from Magnetic Resonance Images in Patients with Autosomal Dominant Polycystic Kidney Disease [C] . Antonio Brunetti, Giacomo Donato Cascarano, Irio De Feudis, International conference on intelligent computing . 2019

机译：常染色体显性多囊性肾脏病患者的磁共振图像肾脏检测与分割
5. WNT signalling in kidney development and autosomal dominant polycystic kidney disease. [D] . Miller, Michelle. 2011

机译：WNT信号传导在肾脏发育和常染色体显性多囊肾疾病中。
6. Perrone RD Mouksassi M-S Romero K et al. Total kidney volume is a prognostic biomarker of renal function decline and progression to end-stage renal disease in patients with autosomal dominant polycystic kidney disease. Kidney Int Rep. 2017;2:442–450 [O] . 2018

机译：Perrone RDMouksassi M-SRomero K等。总肾脏体积是常染色体显性遗传性多囊肾患者肾功能下降和进展为终末期肾脏疾病的预后生物标志物。肾脏国际代表； 2017年； 2：442–450
7. Kidney diseases. Advances in diagnosis and treatment. III.Hereditary kidney diseases and others. Chronic pyelonephritis. [O] . 1996

机译：肾脏疾病。诊断和治疗进展。 III.Heredary肾脏疾病和其他人。慢性肾盂肾炎。
8. Inducing Somatic Pkd1 Mutations in Vivo in a Mouse Model of Autosomal-Dominant Polycystic Kidney Disease. [R] . Cebrian-Ligero, C. 2018

机译：在常染色体显性多囊肾病小鼠模型中体内诱导体细胞pkd1突变。

Kidney diseases. Advances in diagnosis and treatment. III.Hereditary kidney diseases and others. Polycystic kidney disease.

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