Publications by authors named "Michael Graef"

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Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome.
Thushiha Logeswaran, Christoph Friedburg, Karoline Hofmann, Hakan Akintuerk, Saskia Biskup, Michael Graef

Am J Med Genet A· September 2017

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Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome.
Thushiha Logeswaran, Christoph Friedburg, Karoline Hofmann, Hakan Akintuerk, Saskia Biskup, Michael Graef

Am J Med Genet A· April 2017

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Retrobulbar Spot Sign Predicts Thrombolytic Treatment Effects and Etiology in Central Retinal Artery Occlusion.
Max Nedelmann, Michael Graef, Frank Weinand, Klaus-Heiko Wassill, Manfred Kaps

Stroke· August 2015

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Surgical outcomes in correction of Brown syndrome.
Yoonae A Cho, Soo Kim, Michael H Graef

Korean J Ophthalmol· March 2006

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