A. Lichtenberger

Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.

A. Bakkaloğlu, F. Hildebrandt, J. Haas, 2004, Kidney international.

Comparison of spontaneous and ultraviolet-induced mutagenesis on naked SV40 DNA and SV40 virus.

A. Sarasin, F. Bourre, A. Lichtenberger, 1991, Mutation research.

No evidence for genotype/phenotype correlation in NPHS1 and NPHS2 mutations

F. Hildebrandt, R. Wiggins, A. Fuchshuber, 2004, Pediatric Nephrology.

Patients with mutations in NPHS2 (podocin) do not respond to standard steroid treatment of nephrotic syndrome.

A. Bakkaloğlu, A. Bagga, F. Hildebrandt, 2004, Journal of the American Society of Nephrology : JASN.

A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2.

H. Hennies, F. Hildebrandt, M. Wolf, 2003, Journal of the American Society of Nephrology : JASN.

NPHS2 mutation associated with recurrence of proteinuria after transplantation

F. Hildebrandt, D. Haffner, U. Querfeld, 2004, Pediatric Nephrology.