Disease: Polycystic kidneys- severe infantile with tuberous sclerosis
- A case of TSC2-PKD1 contiguous deletion syndrome: Clinical features and effective treatment for epilepsy
- Autosomal recessive and dominant polycystic kidney diseases
- Deletion of the TSC2 and PKD1 genes associated with severe infantile polycystic kidney disease--a contiguous gene syndrome
- Diagnosis and genotype-phenotype correlation in patients with PKD1/TSC2 contiguous gene deletion syndrome
- End-stage renal disease in tuberous sclerosis complex-polycystic kidney disease contiguous gene syndrome: epidemiology, clinical manifestations and implications for transplantation
- Loss of Tsc1, but not Pten, in renal tubular cells causes polycystic kidney disease by activating mTORC1
- Mammalian target of rapamycin inhibitors in a patient with polycystic kidney disease-1-tuberous sclerosis-2 contiguous gene syndrome
- Molecular analysis of TSC2/PKD1 contiguous gene deletion syndrome
- Polycystin-1 expression in PKD1, early-onset PKD1, and TSC2/PKD1 cystic tissue
- The ominous sequence in patients with tuberous sclerosis complex
- The renal lesion in syndromes of multiple congenital malformations. Cerebrohepatorenal syndrome; Jeune asphyxiating thoracic dystrophy; tuberous sclerosis; Meckel syndrome
- TSC2/PKD1 contiguous gene deletion syndrome
- TSC2/PKD1 Contiguous Gene Deletion Syndrome
- TSC2/PKD1 contiguous gene sÃndrome
- Tuberous sclerosis and infantile spasms
- Tuberous sclerosis complex and polycystic kidney disease contiguous gene syndrome with Moyamoya disease