Leo A. H. Monnens

Infantile Refsum disease: an inherited peroxisomal disorder

R. Wanders, R. Schutgens, B. Poll-The, 1987, European Journal of Pediatrics.

Nephrogenic diabetes insipidus: clinical symptoms, pathogenesis, genetics and treatment

N. Knoers, L. Monnens, Leo A. H. Monnens, 1992, Pediatric Nephrology.

New mutations in the AQP2 gene in nephrogenic diabetes insipidus resulting in functional but misrouted water channels.

P. Deen, N. Knoers, L. Monnens, 1997, Journal of the American Society of Nephrology : JASN.

Nephrogenic diabetes insipidus.

N. Knoers, Leo A. H. Monnens, 2012, Seminars in nephrology.

Hereditary isolated renal magnesium loss maps to chromosome 11q23.

F. Hildebrandt, L. P. Van den Heuvel, A. Reis, 1999, American journal of human genetics.

A variant of nephrogenic diabetes insipidus: V2 receptor abnormality restricted to the kidney

N. Knoers, L. Monnens, Leo A. H. Monnens, 1991, European Journal of Pediatrics.