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124 results

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Page 1
KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron.
Louis-Dit-Picard H, Barc J, Trujillano D, Miserey-Lenkei S, Bouatia-Naji N, Pylypenko O, Beaurain G, Bonnefond A, Sand O, Simian C, Vidal-Petiot E, Soukaseum C, Mandet C, Broux F, Chabre O, Delahousse M, Esnault V, Fiquet B, Houillier P, Bagnis CI, Koenig J, Konrad M, Landais P, Mourani C, Niaudet P, Probst V, Thauvin C, Unwin RJ, Soroka SD, Ehret G, Ossowski S, Caulfield M; International Consortium for Blood Pressure (ICBP); Bruneval P, Estivill X, Froguel P, Hadchouel J, Schott JJ, Jeunemaitre X. Louis-Dit-Picard H, et al. Among authors: delahousse m. Nat Genet. 2012 Mar 11;44(4):456-60, S1-3. doi: 10.1038/ng.2218. Nat Genet. 2012. PMID: 22406640
Blood CD9+ B cell, a biomarker of bronchiolitis obliterans syndrome after lung transplantation.
Brosseau C, Danger R, Durand M, Durand E, Foureau A, Lacoste P, Tissot A, Roux A, Reynaud-Gaubert M, Kessler R, Mussot S, Dromer C, Brugière O, Mornex JF, Guillemain R, Claustre J, Magnan A, Brouard S; COLT and SysCLAD Consortia. Brosseau C, et al. Am J Transplant. 2019 Nov;19(11):3162-3175. doi: 10.1111/ajt.15532. Epub 2019 Aug 21. Am J Transplant. 2019. PMID: 31305014 Free article.
Genetic heterogeneity of familial hyperkalaemic hypertension.
Disse-Nicodeme S, Desitter I, Fiquet-Kempf B, Houot AM, Stern N, Delahousse M, Potier J, Ader JL, Jeunemaitre X. Disse-Nicodeme S, et al. Among authors: delahousse m. J Hypertens. 2001 Nov;19(11):1957-64. doi: 10.1097/00004872-200111000-00005. J Hypertens. 2001. PMID: 11677360
Proteinuria and tubulointerstitial lesions in lupus nephritis.
Hill GS, Delahousse M, Nochy D, Mandet C, Bariéty J. Hill GS, et al. Among authors: delahousse m. Kidney Int. 2001 Nov;60(5):1893-903. doi: 10.1046/j.1523-1755.2001.00017.x. Kidney Int. 2001. PMID: 11703608 Free article.
Familial hyperkalemic hypertension (Gordon syndrome): evidence for phenotypic variability in a study of 7 families.
Disse-Nicodème S, Achard JM, Potier J, Delahousse M, Fiquet-Kempf B, Stern N, Blanchard A, Guilbaud JC, Niaudet P, Chauveau D, Dussol B, Berland Y, Dequiedt P, Ader JL, Paillard M, Grünfeld JP, Fournier A, Corvol P, Jeunemaitre X. Disse-Nicodème S, et al. Among authors: delahousse m. Adv Nephrol Necker Hosp. 2001;31:55-68. Adv Nephrol Necker Hosp. 2001. PMID: 11692471 No abstract available.
A clinicopathologic study of thrombotic microangiopathy in IgA nephropathy.
El Karoui K, Hill GS, Karras A, Jacquot C, Moulonguet L, Kourilsky O, Frémeaux-Bacchi V, Delahousse M, Duong Van Huyen JP, Loupy A, Bruneval P, Nochy D. El Karoui K, et al. Among authors: delahousse m. J Am Soc Nephrol. 2012 Jan;23(1):137-48. doi: 10.1681/ASN.2010111130. Epub 2011 Nov 3. J Am Soc Nephrol. 2012. PMID: 22052055 Free PMC article.
Antibody-mediated vascular rejection of kidney allografts: a population-based study.
Lefaucheur C, Loupy A, Vernerey D, Duong-Van-Huyen JP, Suberbielle C, Anglicheau D, Vérine J, Beuscart T, Nochy D, Bruneval P, Charron D, Delahousse M, Empana JP, Hill GS, Glotz D, Legendre C, Jouven X. Lefaucheur C, et al. Among authors: delahousse m. Lancet. 2013 Jan 26;381(9863):313-9. doi: 10.1016/S0140-6736(12)61265-3. Epub 2012 Nov 23. Lancet. 2013. PMID: 23182298
An open-label randomized controlled trial of low-dose corticosteroid plus enteric-coated mycophenolate sodium versus standard corticosteroid treatment for minimal change nephrotic syndrome in adults (MSN Study).
Rémy P, Audard V, Natella PA, Pelle G, Dussol B, Leray-Moragues H, Vigneau C, Bouachi K, Dantal J, Vrigneaud L, Karras A, Pourcine F, Gatault P, Grimbert P, Ait Sahlia N, Moktefi A, Daugas E, Rigothier C, Bastuji-Garin S, Sahali D; MSN Trial Investigators. Rémy P, et al. Kidney Int. 2018 Dec;94(6):1217-1226. doi: 10.1016/j.kint.2018.07.021. Epub 2018 Oct 29. Kidney Int. 2018. PMID: 30385039 Free article. Clinical Trial.
124 results