Simon DB[au] - Search Results

Year	Number of Results
1977	1
1978	1
1980	1
1982	3
1983	1
1996	4
1997	3
1998	2
1999	1
2000	1
2001	3
2004	1
2007	1
2008	1
2011	1
2024	0

1

Clinical spectrum of fascial inflammation.

Simon DB, Ringel SP, Sufit RL. Simon DB, et al. Muscle Nerve. 1982 Sep;5(7):525-37. doi: 10.1002/mus.880050707. Muscle Nerve. 1982. PMID: 6755243 Review. No abstract available.

2

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

Simon DB, Lifton RP. Simon DB, et al. Curr Opin Nephrol Hypertens. 1998 Jan;7(1):43-7. doi: 10.1097/00041552-199801000-00008. Curr Opin Nephrol Hypertens. 1998. PMID: 9442362 Review.

3

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

Simon DB, Lifton RP. Simon DB, et al. Curr Opin Cell Biol. 1998 Aug;10(4):450-4. doi: 10.1016/s0955-0674(98)80057-4. Curr Opin Cell Biol. 1998. PMID: 9719864 Review.

4

Neuropsychological findings in myotonic dystrophy.

Woodward JB 3rd, Heaton RK, Simon DB, Ringel SP. Woodward JB 3rd, et al. Among authors: simon db. J Clin Neuropsychol. 1982 Dec;4(4):335-42. doi: 10.1080/01688638208401141. J Clin Neuropsychol. 1982. PMID: 7174839

5

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

Simon DB, Lifton RP. Simon DB, et al. Am J Physiol. 1996 Nov;271(5 Pt 2):F961-6. doi: 10.1152/ajprenal.1996.271.5.F961. Am J Physiol. 1996. PMID: 8945989 Review.

6

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. Wilson FH, et al. Among authors: simon db. Science. 2001 Aug 10;293(5532):1107-12. doi: 10.1126/science.1062844. Science. 2001. PMID: 11498583

7

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

Simon DB, Lifton RP. Simon DB, et al. Adv Nephrol Necker Hosp. 1997;27:343-59. Adv Nephrol Necker Hosp. 1997. PMID: 9408455 Review. No abstract available.

8

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. Ji W, et al. Among authors: simon db. Nat Genet. 2008 May;40(5):592-599. doi: 10.1038/ng.118. Epub 2008 Apr 6. Nat Genet. 2008. PMID: 18391953 Free PMC article.

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. Simon DB, et al. Science. 1999 Jul 2;285(5424):103-6. doi: 10.1126/science.285.5424.103. Science. 1999. PMID: 10390358

10

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. Simon DB, et al. Nat Genet. 1996 Oct;14(2):152-6. doi: 10.1038/ng1096-152. Nat Genet. 1996. PMID: 8841184

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