Not logged in.png)
Share.png)
SaveShare Save Corneal Infantile Myofibromatosis Caused by Novel Activating Imatinib-Responsive Variants in PDGFRB
Howaldt, Antonia; Lenglez, Sandrine; Velmans, Clara; Schultheis, Anne Maria; Clahsen, Thomas; Matthaei, Mario; Kohlhase, Juergen; Vokuhl, Christian; Buettner, Reinhard; Netzer, Christian; Demoulin, Jean -Baptiste; Cursiefen, Claus Share Save Share Save The novel role of lymphatic vessels in the pathogenesis of ocular diseasesClahsen, Thomas; Hadrian, Karina; Notara, Maria; Schlereth, Simona L.; Howaldt, Antonia; Prokosch, Verena; Volatier, Thomas; Hos, Deniz; Schroedl, Falk; Kaser-Eichberger, Alexandra; Heindl, Ludwig M.; Steven, Philipp; Bosch, Jacobus J.; Steinkasserer, Alexander; Rokohl, Alexander C.; Liu, Hanhan; Mestanoglu, Mert; Kashkar, Hamid; Schumacher, Bjorn; Kiefer, Friedemann; Schulte-Merker, Stefan; Matthaei, Mario; Hou, Yanhong; Fassbender, Sonja; Jantsch, Jonathan; Zhang, Wei; Enders, Philip; Bachmann, Bjorn; Bock, Felix; Cursiefen, Claus Share Save Share Save Correlation of Clinical Fibrillar Layer Detection and Corneal Thickness in Advanced Fuchs Endothelial Corneal DystrophyOezer, Orlando; Mestanoglu, Mert; Howaldt, Antonia; Clahsen, Thomas; Schiller, Petra; Siebelmann, Sebastian; Reinking, Niklas; Cursiefen, Claus; Bachmann, Bjoern; Matthaei, Mario Share Save Scheimpflug Backscatter Imaging of the Fibrillar Layer in Fuchs Endothelial Corneal DystrophyHribek, Agathe; Mestanoglu, Mert; Clahsen, Thomas; Reinking, Niklas; Frentzen, Falk; Howaldt, Antonia; Siebelmann, Sebastian; Bachmann, Bjoern O.; Cursiefen, Claus; Matthaei, Mario Share Save Adult Osteosclerotic Metaphyseal Dysplasia With Progressive Osteonecrosis of the Jaws and Abnormal Bone Resorption Pattern Due to a LRRK1 Splice Site MutationHowaldt, Antonia; Hennig, Anna Floriane; Rolvien, Tim; Roessler, Uta; Stelzer, Nina; Knaus, Alexej; Boettger, Sebastian; Zustin, Jozef; Geissler, Sven; Oheim, Ralf; Amling, Michael; Howaldt, Hans-Peter; Kornak, Uwe Share Save Sclerosing bone dysplasias with hallmarks of dysosteosclerosis in four patients carrying mutations in SLC29A3 and TCIRG1Howaldt, Antonia; Nampoothiri, Sheela; Quell, Lisa-Marie; Ozden, Ayse; Fischer-Zirnsak, Bjoern; Collet, Corinne; de Vernejoul, Marie-Christine; Doneray, Hakan; Kayserili, Hulya; Kornak, Uwe Share Save 
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
.png){kind=icon}
