Birth of two healthy girls following preimplantation genetic diagnosis and gestational surrogacy in a rapidly progressive autosomal dominant polycystic kidney disease case using tolvaptan

Míreanna Comhchosúla

• Co‐occurrence of neurofibromatosis type 1 and optic nerve gliomas with autosomal dominant polycystic kidney disease type 2
  le: Ramón Peces, et al.
  Foilsithe: (2020-08-01)
• Co‐occurrence of neurofibromatosis type 1 and optic nerve gliomas with autosomal dominant polycystic kidney disease type 2
  le: Peces, Ramón, et al.
  Foilsithe: (2020)
• Nephrotic Syndrome and Idiopathic Membranous Nephropathy Associated with Autosomal-Dominant Polycystic Kidney Disease
  le: Peces, Ramón, et al.
  Foilsithe: (2011)
• Rapamycin reduces kidney volume and delays the loss of renal function in a patient with autosomal-dominant polycystic kidney disease
  le: Peces, Ramón, et al.
  Foilsithe: (2009)
• Bilineal inheritance of type 1 autosomal dominant polycystic kidney disease (ADPKD) and recurrent fetal loss
  le: Peces, Ramón, et al.
  Foilsithe: (2008)