S. Katzke

Mutations of FBN1 and genotype–phenotype correlations in Marfan syndrome and related fibrillinopathies

P. Robinson, T. Rosenberg, L. Neumann, 2002, Human mutation.

Net reclassification improvement with serial biomarkers and bed-sided spirometry to early predict the need of organ support during the early post-transplantation in-hospital stay in allogeneic HCT recipients

G. Ehninger, M. Bornhäuser, G. Höffken, 2018, Bone Marrow Transplantation.

Guillain-Barré syndrome and catecholamine therapy. A potential risk for developing takotsubo cardiomyopathy?

R. Strasser, K. Ibrahim, S. Quick, 2013, International journal of cardiology.

TGGE screening of the entire FBN1 coding sequence in 126 individuals with marfan syndrome and related fibrillinopathies

Flemming Skovby, Christian Hagemeier, P. Robinson, 2002, Human mutation.

Clustering of mutations associated with mild Marfan-like phenotypes in the 3' region of FBN1 suggests a potential genotype-phenotype correlation.

P. Robinson, T. Rosenberg, C. Nienaber, 2000, American journal of medical genetics.

Clinical Relevance of Computed Tomography Pulmonary Venography.

K. Zöphel, I. Platzek, G. Höffken, 2016, Heart, lung & circulation.

Classic, atypically severe and neonatal Marfan syndrome: twelve mutations and genotype–phenotype correlations in FBN1 exons 24–40

Flemming Skovby, Christian Hagemeier, P. Robinson, 2001, European Journal of Human Genetics.

Kardiologie up2date

D. Messroghli, T. Wengenmayer, H. Trentzsch, 2017 .