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Items: 25

1.

Conversion from epoetin alfa to darbepoetin alfa for management of anaemia in a community chronic kidney disease centre: a retrospective cohort study.

Gobin J, Cernii A, McLean R, Finkelstein FO, Simon DB.

Clin Drug Investig. 2011;31(2):113-20. doi: 10.2165/11584460-000000000-00000.

PMID:
21067252
2.

Rare independent mutations in renal salt handling genes contribute to blood pressure variation.

Ji W, Foo JN, O'Roak BJ, Zhao H, Larson MG, Simon DB, Newton-Cheh C, State MW, Levy D, Lifton RP.

Nat Genet. 2008 May;40(5):592-599. doi: 10.1038/ng.118. Epub 2008 Apr 6.

3.

Metabolic lung disease: diffuse metastatic pulmonary calcifications with progression to calciphylaxis in end-stage renal disease.

Beyzaei A, Francis J, Knight H, Simon DB, Finkelstein FO.

Adv Perit Dial. 2007;23:112-7.

PMID:
17886615
4.

A one-year trial of in-center daily hemodialysis with an emphasis on quality of life.

Reynolds JT, Homel P, Cantey L, Evans E, Harding P, Gotch F, Wuerth D, Finkelstein S, Levin N, Kliger A, Simon DB, Finkelstein FO.

Blood Purif. 2004;22(3):320-8. Epub 2004 Jun 21.

PMID:
15256799
5.

Human hypertension caused by mutations in WNK kinases.

Wilson FH, Disse-Nicodème S, Choate KA, Ishikawa K, Nelson-Williams C, Desitter I, Gunel M, Milford DV, Lipkin GW, Achard JM, Feely MP, Dussol B, Berland Y, Unwin RJ, Mayan H, Simon DB, Farfel Z, Jeunemaitre X, Lifton RP.

Science. 2001 Aug 10;293(5532):1107-12.

6.

Mutations in the Na-Cl cotransporter reduce blood pressure in humans.

Cruz DN, Simon DB, Nelson-Williams C, Farhi A, Finberg K, Burleson L, Gill JR, Lifton RP.

Hypertension. 2001 Jun;37(6):1458-64.

PMID:
11408395
7.

Gitelman's syndrome revisited: an evaluation of symptoms and health-related quality of life.

Cruz DN, Shaer AJ, Bia MJ, Lifton RP, Simon DB; Yale Gitelman's and Bartter's Syndrome Collaborative Study Group.

Kidney Int. 2001 Feb;59(2):710-7.

8.

Bartter syndrome and focal segmental glomerulosclerosis: a possible link between two diseases.

Su IH, Frank R, Gauthier BG, Valderrama E, Simon DB, Lifton RP, Trachtman H.

Pediatr Nephrol. 2000 Sep;14(10-11):970-2.

PMID:
10975308
9.

Paracellin-1, a renal tight junction protein required for paracellular Mg2+ resorption.

Simon DB, Lu Y, Choate KA, Velazquez H, Al-Sabban E, Praga M, Casari G, Bettinelli A, Colussi G, Rodriguez-Soriano J, McCredie D, Milford D, Sanjad S, Lifton RP.

Science. 1999 Jul 2;285(5424):103-6.

10.

Mutations in Na(K)Cl transporters in Gitelman's and Bartter's syndromes.

Simon DB, Lifton RP.

Curr Opin Cell Biol. 1998 Aug;10(4):450-4. Review.

PMID:
9719864
11.

Ion transporter mutations in Gitelman's and Bartter's syndromes.

Simon DB, Lifton RP.

Curr Opin Nephrol Hypertens. 1998 Jan;7(1):43-7. Review.

PMID:
9442362
12.

Mutations in the chloride channel gene, CLCNKB, cause Bartter's syndrome type III.

Simon DB, Bindra RS, Mansfield TA, Nelson-Williams C, Mendonca E, Stone R, Schurman S, Nayir A, Alpay H, Bakkaloglu A, Rodriguez-Soriano J, Morales JM, Sanjad SA, Taylor CM, Pilz D, Brem A, Trachtman H, Griswold W, Richard GA, John E, Lifton RP.

Nat Genet. 1997 Oct;17(2):171-8.

PMID:
9326936
13.

Multilocus linkage of familial hyperkalaemia and hypertension, pseudohypoaldosteronism type II, to chromosomes 1q31-42 and 17p11-q21.

Mansfield TA, Simon DB, Farfel Z, Bia M, Tucci JR, Lebel M, Gutkin M, Vialettes B, Christofilis MA, Kauppinen-Makelin R, Mayan H, Risch N, Lifton RP.

Nat Genet. 1997 Jun;16(2):202-5.

PMID:
9171836
14.

Mutations in renal ion transporters cause Gitelman's and Bartter's syndromes of inherited hypokalemic alkalosis.

Simon DB, Lifton RP.

Adv Nephrol Necker Hosp. 1997;27:343-59. Review. No abstract available.

PMID:
9408455
15.

The molecular basis of inherited hypokalemic alkalosis: Bartter's and Gitelman's syndromes.

Simon DB, Lifton RP.

Am J Physiol. 1996 Nov;271(5 Pt 2):F961-6. Review.

PMID:
8945989
16.

Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.

Simon DB, Karet FE, Rodriguez-Soriano J, Hamdan JH, DiPietro A, Trachtman H, Sanjad SA, Lifton RP.

Nat Genet. 1996 Oct;14(2):152-6.

PMID:
8841184
17.

Bartter's syndrome, hypokalaemic alkalosis with hypercalciuria, is caused by mutations in the Na-K-2Cl cotransporter NKCC2.

Simon DB, Karet FE, Hamdan JM, DiPietro A, Sanjad SA, Lifton RP.

Nat Genet. 1996 Jun;13(2):183-8.

PMID:
8640224
18.

Gitelman's variant of Bartter's syndrome, inherited hypokalaemic alkalosis, is caused by mutations in the thiazide-sensitive Na-Cl cotransporter.

Simon DB, Nelson-Williams C, Bia MJ, Ellison D, Karet FE, Molina AM, Vaara I, Iwata F, Cushner HM, Koolen M, Gainza FJ, Gitleman HJ, Lifton RP.

Nat Genet. 1996 Jan;12(1):24-30.

PMID:
8528245
19.

Practical management of neuromuscular diseases in the elderly.

Ringel SP, Simon DB.

Geriatrics. 1983 Jun;38(6):86-92. No abstract available.

PMID:
6852533
20.

Neuropsychological findings in myotonic dystrophy.

Woodward JB 3rd, Heaton RK, Simon DB, Ringel SP.

J Clin Neuropsychol. 1982 Dec;4(4):335-42.

PMID:
7174839
21.

Clinical spectrum of fascial inflammation.

Simon DB, Ringel SP, Sufit RL.

Muscle Nerve. 1982 Sep;5(7):525-37. Review. No abstract available.

PMID:
6755243
22.

Luetic meningitis with gumma.

Simon DB.

Neurology. 1982 May;32(5):573. No abstract available.

PMID:
7200217
23.

Unusual causes of stroke in a young adult.

Newman PE, Simon DB, Law RK, Earnest MP.

Arch Intern Med. 1980 Nov;140(11):1502-3. No abstract available.

PMID:
7436646
24.

Symptomatic osseous sarcoidosis with findings on bone scan.

Silver HM, Shirkhoda A, Simon DB.

Chest. 1978 Feb;73(2):238-41.

PMID:
145934
25.

Strontium-87m lung scans in pulmonary aspergillosis.

Rohatgi PK, Simon DB, Goldstein RA, Reba RC.

AJR Am J Roentgenol. 1977 Nov;129(5):879-82.

PMID:
410255

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