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Marfan syndrome
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Losartan
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Franken, R.
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Groenink, M.
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Hartog, A.W. den
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Berg, M.P. van den
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Mulder, B.J.M.
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Timmermans, J.
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Zwinderman, A.H.
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Scholte, A.J.
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Waard, V. de
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Pals, G.
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Radonic, T.
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Lutter, R.
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Spijkerboer, A.M.
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The effect of losartan therapy on ventricular function in Marfan patients with haploinsufficient or dominant negative FBN1 mutations
Beneficial Outcome of Losartan Therapy Depends on Type of FBN1 Mutation in Marfan Syndrome
The revised role of TGF-β in aortic aneurysms in Marfan syndrome
The Risk for Type B Aortic Dissection in Marfan Syndrome
Enhanced beneficial outcome of losartan therapy in Marfan patients with FBN1 haploinsufficiency mutations
The risk of type B aortic dissection in Marfan syndrome
Losartan reduces aortic dilatation rate in adults with Marfan syndrome: a randomized controlled trial
Clinical Features Differ Substantially Between Caucasian and Asian Populations of Marfan Syndrome
Aortic Disease in Patients with Marfan Syndrome: Aortic Volume Assessment for Surveillance
Circulating transforming growth factor-beta as a prognostic biomarker in Marfan syndrome
Aortic tortuosity predicts cardiovascular events in Marfan syndrome