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Items: 7

1.

Thromboembolic events in Fabry disease and the impact of factor V Leiden.

Lenders M, Karabul N, Duning T, Schmitz B, Schelleckes M, Mesters R, Hense HW, Beck M, Brand SM, Brand E.

Neurology. 2015 Mar 10;84(10):1009-16. doi: 10.1212/WNL.0000000000001333. Epub 2015 Feb 6.

PMID:
25663229
2.

Cryptogenic stroke and small fiber neuropathy of unknown etiology in patients with alpha-galactosidase A -10T genotype.

Schelleckes M, Lenders M, Guske K, Schmitz B, Tanislav C, Ständer S, Metze D, Katona I, Weis J, Brand SM, Duning T, Brand E.

Orphanet J Rare Dis. 2014 Nov 26;9:178. doi: 10.1186/s13023-014-0178-5.

3.

Patients with Fabry disease after enzyme replacement therapy dose reduction versus treatment switch.

Weidemann F, Krämer J, Duning T, Lenders M, Canaan-Kühl S, Krebs A, Guerrero González H, Sommer C, Üçeyler N, Niemann M, Störk S, Schelleckes M, Reiermann S, Stypmann J, Brand SM, Wanner C, Brand E.

J Am Soc Nephrol. 2014 Apr;25(4):837-49. doi: 10.1681/ASN.2013060585. Epub 2014 Feb 20.

4.

Soluble adenylyl cyclase in vascular endothelium: gene expression control of epithelial sodium channel-α, Na+/K+-ATPase-α/β, and mineralocorticoid receptor.

Schmitz B, Nedele J, Guske K, Maase M, Lenders M, Schelleckes M, Kusche-Vihrog K, Brand SM, Brand E.

Hypertension. 2014 Apr;63(4):753-61. doi: 10.1161/HYPERTENSIONAHA.113.02061. Epub 2014 Jan 13.

PMID:
24420537
5.

Increased monocyte adhesion by endothelial expression of VCAM-1 missense variation in vitro.

Schmitz B, Vischer P, Brand E, Schmidt-Petersen K, Korb-Pap A, Guske K, Nedele J, Schelleckes M, Hillen J, Rötrige A, Simmet T, Paul M, Cambien F, Brand SM.

Atherosclerosis. 2013 Oct;230(2):185-90. doi: 10.1016/j.atherosclerosis.2013.07.039. Epub 2013 Jul 31.

6.

Tissue-specific differences in the regulation of KIBRA gene expression involve transcription factor TCF7L2 and a complex alternative promoter system.

Guske K, Schmitz B, Schelleckes M, Duning K, Kremerskothen J, Pavenstädt HJ, Brand SM, Brand E.

J Mol Med (Berl). 2014 Feb;92(2):185-96. doi: 10.1007/s00109-013-1089-y. Epub 2013 Sep 27.

PMID:
24072042
7.

Multifocal white matter lesions associated with the D313Y mutation of the α-galactosidase A gene.

Lenders M, Duning T, Schelleckes M, Schmitz B, Stander S, Rolfs A, Brand SM, Brand E.

PLoS One. 2013;8(2):e55565. doi: 10.1371/journal.pone.0055565. Epub 2013 Feb 5.

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