Disease: Oligomeganephronic renal hypoplasia
- <em>PAX2</em> Mutation-Related Oligomeganephronia in a Young Adult Patient
- A new variant of the acrorenal syndrome associated with bilateral oligomeganephronic hypoplasia
- Abnormal renal development in the Os/+ mouse is intrinsic to the kidney
- Autosomal recessive acrorenal syndrome
- Focal sclerosis of hypertrophied glomeruli in solitary functioning kidneys of humans
- Glomerular hyperfiltration and hypertrophy in the rat hypoplastic kidney as a model of oligomeganephronic disease
- Monozygotic twins non-concordant for oligomeganephronic renal hypoplasia: artery-vein placental shunting as a possible pathogenetic mechanism
- Oligomeganephronic renal hypoplasia
- Oligomeganephronic renal hypoplasia
- Oligomeganephronic renal hypoplasia complicated by glomerulonephritis
- Oligomeganephronic renal hypoplasia in two siblings
- Oligomeganephronic renal hypoplasia with tapetoretinal degeneration. Report of one case with ultrastructural study of the renal biopsy
- PAX2 mutations in fetal renal hypodysplasia
- Renal disorders in the branchio-oto-renal syndrome
- Renal Hypoplasia, From Grossly Insufficient to Not Quite Enough: Consideration for Expanded Concepts Based Upon the Author's Perspective With Historical Review