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α-Galactosidase A Genotype N215S Induces a Specific Cardiac Variant of Fabry Disease.
Oder D, Liu D, Hu K, Üçeyler N, Salinger T, Müntze J, Lorenz K, Kandolf R, Gröne HJ, Sommer C, Ertl G, Wanner C, Nordbeck P. Oder D, et al. Among authors: muntze j. Circ Cardiovasc Genet. 2017 Oct;10(5):e001691. doi: 10.1161/CIRCGENETICS.116.001691. Circ Cardiovasc Genet. 2017. PMID: 29018006 Clinical Trial.
Value of the CHA2DS2-VASc score and Fabry-specific score for predicting new-onset or recurrent stroke/TIA in Fabry disease patients without atrial fibrillation.
Liu D, Hu K, Schmidt M, Müntze J, Maniuc O, Gensler D, Oder D, Salinger T, Weidemann F, Ertl G, Frantz S, Wanner C, Nordbeck P. Liu D, et al. Among authors: muntze j. Clin Res Cardiol. 2018 Dec;107(12):1111-1121. doi: 10.1007/s00392-018-1285-4. Epub 2018 May 24. Clin Res Cardiol. 2018. PMID: 29797054 Free PMC article.
Characterization of vertigo and hearing loss in patients with Fabry disease.
Köping M, Shehata-Dieler W, Schneider D, Cebulla M, Oder D, Müntze J, Nordbeck P, Wanner C, Hagen R, Schraven SP. Köping M, et al. Among authors: muntze j. Orphanet J Rare Dis. 2018 Aug 15;13(1):137. doi: 10.1186/s13023-018-0882-7. Orphanet J Rare Dis. 2018. PMID: 30111353 Free PMC article.
Association between Comorbidities and Progression of Transvalvular Pressure Gradients in Patients with Moderate and Severe Aortic Valve Stenosis.
Salinger T, Hu K, Liu D, Taleh S, Herrmann S, Oder D, Gensler D, Müntze J, Ertl G, Lorenz K, Frantz S, Weidemann F, Nordbeck P. Salinger T, et al. Among authors: muntze j. Cardiol Res Pract. 2018 Nov 11;2018:3713897. doi: 10.1155/2018/3713897. eCollection 2018. Cardiol Res Pract. 2018. PMID: 30534431 Free PMC article.
20 results