Michael Graef

Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome

B. Lorenz, C. Friedburg, D. Schranz, 2017, American journal of medical genetics. Part A.

Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome

B. Lorenz, C. Friedburg, D. Schranz, 2017, American journal of medical genetics. Part A.

Silicone intraocular lens implantation in children: preliminary results.

K. Jacobi, F. Jacobi, Michael Graef, 2000, Journal of cataract and refractive surgery.

Retrobulbar Spot Sign Predicts Thrombolytic Treatment Effects and Etiology in Central Retinal Artery Occlusion

M. Kaps, B. Lorenz, C. Tanislav, 2015, Stroke.