P. Saisawat

F. Hildebrandt, S. Heeringa, G. Chernin, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome.

F. Hildebrandt, S. Ashraf, V. Vega-Warner, 2014, Clinical journal of the American Society of Nephrology : CJASN.

COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness.

V. Pertegato, Y. Raphael, H. Prokisch, 2011, The Journal of clinical investigation.

ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling.

S. Levy, T. Hurd, O. Gribouval, 2013, The Journal of clinical investigation.

Whole exome resequencing distinguishes cystic kidney diseases from phenocopies in renal ciliopathies

S. Levy, N. Katsanis, T. Hurd, 2013, Kidney international.

Mapping of a new locus for congenital anomalies of the kidney and urinary tract on chromosome 8q24.

H. Chaib, F. Hildebrandt, B. Hoskins, 2010, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Mild recessive mutations in six Fraser syndrome-related genes cause isolated congenital anomalies of the kidney and urinary tract.

Friedhelm Hildebrandt, V. Tasic, F. Hildebrandt, 2014, Journal of the American Society of Nephrology : JASN.

Exome sequencing reveals cubilin mutation as a single-gene cause of proteinuria.

F. Hildebrandt, G. Chernin, S. Ashraf, 2011, Journal of the American Society of Nephrology : JASN.

Henoch-Schönlein purpura from vasculitis to intestinal perforation: A case report and literature review.

Nichanan Ruangwattanapaisarn, P. Saisawat, S. Treepongkaruna, 2016, World journal of gastroenterology.

Unusual cause of anemia in a child with end-stage renal disease: Answers

P. Saisawat, K. Praditpornsilpa, K. Pirojsakul, 2017, Pediatric nephrology (Berlin, West).

Waist-to-height-ratio is associated with sustained hypertension in children and adolescents with high office blood pressure

P. Saisawat, K. Pirojsakul, Witchuri Paksi, 2023, Frontiers in Cardiovascular Medicine.

Whole exome resequencing reveals recessive mutations in TRAP1 in individuals with CAKUT and VACTERL association

I. V. van Rooij, D. Tibboel, V. Tasic, 2013, Kidney international.