A New Autosomal Recessive Form of Stickler Syndrome Is Caused by a Mutation in the COL9A1 Gene von Van Camp, Guy, Snoeckx, Rikkert L., Hilgert, Nele, van den Ende, Jenneke, Fukuoka, Hisakumi, Wagatsuma, Michio, Suzuki, Hiroaki, Erica Smets, R.M., Vanhoenacker, Filip, Declau, Frank, Van De Heyning, Paul, Usami, Shin-ichi

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Retinal Layer Location of Increased Retinal Thickness in Eyes with Subclinical and Clinical Macular Edema in Diabetes Type 2 von Bandello, Francesco, Tejerina, Amparo Navea, Vujosevic, Stela, Varano, Monica, Egan, Catherine, Sivaprasad, Sobha, Menon, Geeta, Massin, Pascale, Verbraak, Frank D., Lund-Andersen, Henrik, Martinez, Jose P., Jürgens, Ignasi, Smets, R.M. Erica, Coriat, Caroline, Wiedemann, Peter, Ágoas, Victor, Querques, Giuseppe, Holz, Frank G., Nunes, Sandrina, Alves, Dalila, Neves, Catarina, Santos, Torcato, Ribeiro, Luisa, Cunha-Vaz, José

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Benign intracranial hypertension as a cause of transient partial pituitary deficiency von De Paepe, Lutgarde, Abs, Roger, Verlooy, Jan, Clemens, Ann, Erica^Smets, R.M., Louis, Paul, Martin, Jean-Jacques

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