S. Disse-Nicodème

Human Hypertension Caused by Mutations in WNK Kinases

Robert J. Unwin, Murat Gunel, Kazuhiko Ishikawa, 2001, Science.

Familial hyperkalemic hypertension: phenotypic analysis in a large family with the WNK1 deletion mutation.

X. Jeunemaître, D. Warnock, J. Achard, 2003, The American journal of medicine.

Multiple Promoters in the WNK1 Gene: One Controls Expression of a Kidney-Specific Kinase-Defective Isoform

X. Jeunemaître, P. Corvol, S. Disse-Nicodème, 2003, Molecular and Cellular Biology.

Familial hyperkalemic hypertension (Gordon syndrome): evidence for phenotypic variability in a study of 7 families.

X. Jeunemaître, D. Chauveau, J. Grünfeld, 2001, Advances in nephrology from the Necker Hospital.

Phenotypic And Genetic Heterogeneity Of Familial Hyperkalaemic Hypertension (Gordon Syndrome)

X. Jeunemaître, J. Achard, S. Disse-Nicodème, 2001, Clinical and experimental pharmacology & physiology.

Multiple Promoters in the WNK1 Gene: One Controls Expression of a Kidney-Specific Kinase-Defective Isoform

X. Jeunemaître, P. Corvol, S. Disse-Nicodème, 2003, Molecular and Cellular Biology.

Human Essential Hypertension: Role of the Genes of the Renin-Aldosterone System

X. Jeunemaître, P. Corvol, A. Gimenez-Roqueplo, 2002 .

A new locus on chromosome 12p13.3 for pseudohypoaldosteronism type II, an autosomal dominant form of hypertension.

X. Jeunemaître, J. Achard, P. Corvol, 2000, American journal of human genetics.

Genetic heterogeneity of familial hyperkalaemic hypertension

X. Jeunemaître, S. Disse-Nicodème, A. Houot, 2001, Journal of hypertension.