W. Proesmans

发表

Patients with autosomal nephrogenic diabetes insipidus homozygous for mutations in the aquaporin 2 water-channel gene.

B. V. van Oost, P. Deen, L. Monnens, 1994, American journal of human genetics.

The complement system in hemolytic-uremic syndrome in childhood.

P. Lambert, L. Monnens, P. V. VAN MUNSTER, 1980, Clinical nephrology.

Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene.

C. Langman, N. Roslin, K. Morgan, 2001, Journal of the American Society of Nephrology : JASN.

Acute tubulo-interstitial nephritis and uveitis syndrome (TINU syndrome).

M. Praet, W. Proesmans, P. Vanhaesebrouck, 1985, Nephron.

Deletions of both alpha 5(IV) and alpha 6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumours.

C. Guyot, K. Dahan, K. Leppig, 1995, Human molecular genetics.

Recombinant Human Erythropoietin Increases Blood Pressure, Platelet Aggregability and Platelet Free Calcium Mobilisation in Uraemic Children: A Possible Link?

J. Vermylen, W. Proesmans, R. Damme-lombaerts, 1990, Thrombosis and Haemostasis.

Human complement factor H deficiency associated with hemolytic uremic syndrome.

M. Kazatchkine, G. Deschênes, V. Frémeaux-Bacchi, 1998, Journal of the American Society of Nephrology : JASN.

Deletions of both α5(IV) and α6(IV) collagen genes in Alport syndrome and in Alport syndrome associated with smooth muscle tumours

C. Guyot, K. Dahan, K. Leppig, 1995 .

Smooth muscle tumors associated with X-linked Alport syndrome: carrier detection in females.

K. Dahan, K. Leppig, J. Zhou, 1995, Kidney international.

Indomethacin therapy in Bartter syndrome.

L. Monnens, W. Proesmans, B. Muaka, 1977, Acta paediatrica Belgica.