Anderson VE - Search Results

1

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns.

Singh NA, Charlier C, Stauffer D, DuPont BR, Leach RJ, Melis R, Ronen GM, Bjerre I, Quattlebaum T, Murphy JV, McHarg ML, Gagnon D, Rosales TO, Peiffer A, Anderson VE, Leppert M. Singh NA, et al. Among authors: anderson ve. Nat Genet. 1998 Jan;18(1):25-9. doi: 10.1038/ng0198-25. Nat Genet. 1998. PMID: 9425895

2

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum.

Singh NA, Westenskow P, Charlier C, Pappas C, Leslie J, Dillon J, Anderson VE, Sanguinetti MC, Leppert MF; BFNC Physician Consortium. Singh NA, et al. Among authors: anderson ve. Brain. 2003 Dec;126(Pt 12):2726-37. doi: 10.1093/brain/awg286. Epub 2003 Oct 8. Brain. 2003. PMID: 14534157

3

Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

Leppert M, Anderson VE, Quattlebaum T, Stauffer D, O'Connell P, Nakamura Y, Lalouel JM, White R. Leppert M, et al. Among authors: anderson ve. Nature. 1989 Feb 16;337(6208):647-8. doi: 10.1038/337647a0. Nature. 1989. PMID: 2918897

4

The discovery of epilepsy genes by genetic linkage.

Leppert M, Anderson VE, White R. Leppert M, et al. Among authors: anderson ve. Epilepsy Res Suppl. 1991;4:181-8. Epilepsy Res Suppl. 1991. PMID: 1815600 Review. No abstract available.

5

Genes for rare idiopathic generalized epilepsies: BFNC.

Singh N, Charlier C, Peiffer A, Stauffer D, Melis R, Enoch MA, Goldman D, Rogers S, Anderson VE, Leppert M. Singh N, et al. Among authors: anderson ve. Adv Neurol. 1999;79:341-50. Adv Neurol. 1999. PMID: 10514825 Review. No abstract available.

6

Seizure characteristics in chromosome 20 benign familial neonatal convulsions.

Ronen GM, Rosales TO, Connolly M, Anderson VE, Leppert M. Ronen GM, et al. Among authors: anderson ve. Neurology. 1993 Jul;43(7):1355-60. doi: 10.1212/wnl.43.7.1355. Neurology. 1993. PMID: 8327138

7

Andreas Rett and benign familial neonatal convulsions revisited.

Zimprich F, Ronen GM, Stögmann W, Baumgartner C, Stögmann E, Rett B, Pappas C, Leppert M, Singh N, Anderson VE. Zimprich F, et al. Among authors: anderson ve. Neurology. 2006 Sep 12;67(5):864-6. doi: 10.1212/01.wnl.0000234066.46806.90. Neurology. 2006. PMID: 16966552

8

dldhcri3 zebrafish exhibit altered mitochondrial ultrastructure, morphology, and dysfunction partially rescued by probucol or thiamine.

Lavorato M, Iadarola D, Remes C, Kaur P, Broxton C, Mathew ND, Xiao R, Seiler C, Nakamaru-Ogiso E, Anderson VE, Falk MJ. Lavorato M, et al. Among authors: anderson ve. JCI Insight. 2024 Aug 20;9(18):e178973. doi: 10.1172/jci.insight.178973. JCI Insight. 2024. PMID: 39163131 Free PMC article.

9

N-Glycosylation of MRS2 balances aerobic and anaerobic energy production by reducing rapid mitochondrial Mg²⁺ influx in conditions of high glucose or impaired respiratory chain function.

Peng M, Mathew ND, Anderson VE, Falk MJ, Nakamaru-Ogiso E. Peng M, et al. Among authors: anderson ve. bioRxiv [Preprint]. 2024 Jul 9:2024.07.09.602756. doi: 10.1101/2024.07.09.602756. bioRxiv. 2024. PMID: 39026824 Free PMC article. Preprint.

10

Randomized Trial of a Vascular Care Team vs Education for Patients With Peripheral Artery Disease.

Hess CN, Daffron A, Nehler MR, Morrison JT, Buchanan CE, Szarek M, Anderson VE, Cannon CP, Hsia J, Saseen JJ, Bonaca MP. Hess CN, et al. Among authors: anderson ve. J Am Coll Cardiol. 2024 Jun 25;83(25):2658-2670. doi: 10.1016/j.jacc.2024.04.034. J Am Coll Cardiol. 2024. PMID: 38897676 Clinical Trial.

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