Molecular genetics of human blood pressure variation : Cardiovascular medicineLIFTON, R. P.Science (Washington, D.C.). 1996, Vol 272, Num 5262, pp 676-680, issn 0036-8075Article

Finding genes that cause human hypertensionLIFTON, R. P; JEUNEMAITRE, X.Journal of hypertension. 1993, Vol 11, Num 3, pp 231-236, issn 0263-6352Article

Des mutations dans les transporteurs ioniques rénaux sont la cause des syndromes d'alcalose hypokaliémique héréditaire (syndromes de Gitelman et de Bartter) = Mutations of renal ionic transporters in the pathophysiology of hypokaliemic alcalosis hereditary syndrome (Gitelman and de Bartter syndromes)SIMON, D. B; LIFTON, R. P.Actualités néphrologiques Jean Hamburger. 1997, pp 323-336, issn 1168-1098Article

Les formes familiales de néphropathie à IgA études clinique et génétique = Familial IgA nephropathy : clinical trial and genetic studiesGHARAVI, A. G; SCOLARI, F; LIFTON, R. P et al.Actualités néphrologiques Jean Hamburger. 2002, pp 207-220, issn 1168-1098Article

Glucocorticoid-remediable aldosteronismDLUHY, R. G; LIFTON, R. P.The Journal of clinical endocrinology and metabolism. 1999, Vol 84, Num 12, pp 4341-4344, issn 0021-972XArticle

Glucocorticoid-remediable aldosteronismDLUHY, R. G; LIFTON, R. P.Endocrinology and metabolism clinics of North America. 1994, Vol 23, Num 2, pp 285-297, issn 0889-8529Article

The molecular basis of a hereditary form of hypertension, glucocorticoid-remediable aldosteronismLIFTON, R. P; DLUHY, R. G.Trends in endocrinology and metabolism. 1993, Vol 4, Num 2, pp 57-61, issn 1043-2760Article

Glucocorticoid-remediable aldosteronism (GRA) : diagnosis, variability of phenotype and regulation of potassium homeostasisDLUHY, R. G; LIFTON, R. P.Steroids. 1995, Vol 60, Num 1, pp 48-51, issn 0039-128XConference Paper

False positive mononucleosis screening test results associated with klebsiella hepatic abscessRIDKER, P. M; ENDERS, G. H; LIFTON, R. P et al.American journal of clinical pathology. 1990, Vol 94, Num 2, pp 222-223, issn 0002-9173Article

Absence of amiloride-sensitive sodium absorption in the airway of an infant with pseudohypoaldosteronismPRINCE, L. S; LAUNSPACH, J. L; GELLER, D. S et al.The Journal of pediatrics. 1999, Vol 135, Num 6, pp 786-789, issn 0022-3476Article

Intracranial aneurysm and hemorrhagic stroke in glucocorticoid-remediable aldosteronismLITCHFIELD, W. R; ANDERSON, B. F; WEISS, R. J et al.Hypertension (Dallas, Tex. 1979). 1998, Vol 31, Num 1, pp 445-450, issn 0194-911X, 2Conference Paper

Peptide block of constitutively activated Na⁺ channels in Liddle's diseaseISMAILOV, I. I; BERDIEV, B. K; FULLER, C. M et al.American journal of physiology. Cell physiology. 1996, Vol 39, Num 1, pp C214-C223, issn 0363-6143Article

The molecular basis of inherited hypokalemic alkalosis : Bartter's and Gitelman's syndromesSIMON, D. B; LIFTON, R. P; HEBERT, S. C et al.American journal of physiology. Renal, fluid and electrolyte physiology. 1996, Vol 40, Num 5, pp F957-F966, issn 0363-6127, 9 p.Article

Cloning of the NCX2 isoform of the plasma membrane Na⁺-Ca²⁺ exchangerZHAOPING LI; MATSUOKA, S; HRYSHKO, L. V et al.The Journal of biological chemistry (Print). 1994, Vol 269, Num 26, pp 17434-17439, issn 0021-9258Article

Exclusion of the Na⁺-H⁺ antiporter as a candidate gene in human essential hypertensionLIFTON, R. P; HUNT, S. C; WILLIAMS, R. R et al.Hypertension (Dallas, Tex. 1979). 1991, Vol 17, Num 1, pp 8-14, issn 0194-911X, 7 p.Article

The connecting tubule is the main site of the furosemide-induced urinary acidification by the vacuolar H⁺-ATPase. CommentaryCAPASSO, G; KOVACIKOVA, J; WINTER, C et al.Kidney international. 2006, Vol 70, Num 10, issn 0085-2538, 1674-1676,1706-1716 [14 p.]Article

Mutations in the gene encoding B1 subunit of H⁺-ATPase cause renal tubular acidosis with sensorineural deafnessKARET, F. E; FINBERG, K. E; HOFFBRAND, B. I et al.Nature genetics. 1999, Vol 21, Num 1, pp 84-90, issn 1061-4036Article

Localization of a gene for autosomal recessive distal renal tubular acidosis with normal hearing (rdRTA2) to 7q33-34KARET, F. E; FINBERG, K. E; NAYIR, A et al.American journal of human genetics. 1999, Vol 65, Num 6, pp 1656-1665, issn 0002-9297Article

Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type ii, to chromosomes 1q31-42 and 17p11-q21MANSFIELD, T. A; SIMON, D. B; MAYAN, H et al.Nature genetics. 1997, Vol 16, Num 2, pp 202-205, issn 1061-4036Article

Mutations in subunits of the epithelial sodium channel cause salt wasting with hyperkalaemic acidosis, pseudohypoaldosteronism type 1CHANG, S. S; GRUNDER, S; ROSSIER, B. C et al.Nature genetics. 1996, Vol 12, Num 3, pp 248-253, issn 1061-4036Article

Hypertension caused by a truncated epithelial sodium channel γ subunit: genetic heterogeneity of Liddle syndromeHANSSON, J. H; NELSON-WILLIAMS, C; SUZUKI, H et al.Nature genetics. 1995, Vol 11, Num 1, pp 76-82, issn 1061-4036Article

Mutations in the mineralocorticoid receptor gene cause autosomal dominant pseudohypoaldosteronism type IGELLER, D. S; RODRIGUEZ-SORIANO, J; VALLO BOADO, A et al.Nature genetics. 1998, Vol 19, Num 3, pp 279-281, issn 1061-4036Article

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type IIISIMON, D. B; BINDRA, R. S; RODRIGUEZ-SORIANO, J et al.Nature genetics. 1997, Vol 17, Num 2, pp 171-178, issn 1061-4036Article

Liddle's syndrome : Prospective genetic screening and suppressed aldosterone secretion in an extended kindredFINDLING, J. W; RAFF, H; HANSSON, J. H et al.The Journal of clinical endocrinology and metabolism. 1997, Vol 82, Num 4, pp 1071-1074, issn 0021-972XArticle

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K⁺ channel, ROMKSIMON, D. B; KARET, F. E; RODRIGUEZ-SORIANO, J et al.Nature genetics. 1996, Vol 14, Num 2, pp 152-156, issn 1061-4036Article