The Relation between Reading Skills and Eye Movement Patterns in Adolescent Readers: Evidence from a Regular Orthography von Krieber, Magdalena, Bartl-Pokorny, Katrin D, Pokorny, Florian B, Einspieler, Christa, Langmann, Andrea, Körner, Christof, Falck-Ytter, Terje, Marschik, Peter B

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Women Underrepresented on Editorial Boards of 60 Major Medical Journals von Amrein, Karin, MD, Langmann, Andrea, MD, Fahrleitner-Pammer, Astrid, MD, Pieber, Thomas R., MD, Zollner-Schwetz, Ines, MD

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Systemic and Ophthalmic Manifestations in Different Types of Refractive Errors in Patients with Down Syndrome von Ljubic, Antonela, Trajkovski, Vladimir, Stankovic, Branislav, Tojtovska, Biljana, Langmann, Andrea, Dimitrova, Galina, Jovanovic, Ivana, Tesic, Milorad

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Mutations in FRMD7 , a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus von Raymond, F Lucy, Gottlob, Irene, Tarpey, Patrick, Thomas, Shery, Sarvananthan, Nagini, Mallya, Uma, Lisgo, Steven, Talbot, Chris J, Roberts, Eryl O, Awan, Musarat, Surendran, Mylvaganam, McLean, Rebecca J, Reinecke, Robert D, Langmann, Andrea, Lindner, Susanne, Koch, Martina, Jain, Sunila, Woodruff, Geoffrey, Gale, Richard P, Degg, Chris, Droutsas, Konstantinos, Asproudis, Ioannis, Zubcov, Alina A, Pieh, Christina, Veal, Colin D, Machado, Rajiv D, Backhouse, Oliver C, Baumber, Laura, Constantinescu, Cris S, Brodsky, Michael C, Hunter, David G, Hertle, Richard W, Read, Randy J, Edkins, Sarah, O'Meara, Sarah, Parker, Adrian, Stevens, Claire, Teague, Jon, Wooster, Richard, Futreal, P Andrew, Trembath, Richard C, Stratton, Michael R

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Acute Bilateral Tonic Pupil in a Child von Brandner, Martina, Hubmann, Holger, Langmann, Andrea

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Extended optical treatment versus early patching with an intensive patching regimen in children with amblyopia in Europe (EuPatch): a multicentre, randomised controlled trial von Proudlock, Frank A, Hisaund, Michael, Maconachie, Gail, Papageorgiou, Eleni, Manouchehrinia, Ali, Dahlmann-Noor, Annegret, Khandelwal, Payal, Self, Jay, Beisse, Christina, Gottlob, Irene, Mellors, Ashleigh, Mallory, Lucy, Teli, Seema, Sheth, Viral, Langmann, Andrea, Bruce, Alison, Smith, Angie, Powell, Christine, Cross, Meriel, North, Lorraine, Abbott, Joseph, Mohan, Meyyammai, Kafil-Hussain, Namir, Joseph, Annie, Webb, Hilary, Redmill, Brian, Lawler, Carly, Sturm, Veit, Purohit, Ravi, Gupta, Mohit, Elliott, Sue, Mataftsi, Asimina, Hamada, Samer, Evans, Megan, Hatebur, Simone, Hussain, Shazia, Orr, Julie, Farooq, Shegufta, Osborne, Daniel, Begum, Farzana, Crofts, Catherine, Pausch, Franziska, Gaugl, Heike, Haug, Jennifer, Jones, Ruth, Steinmair, Karin, Sharma, Tina, Hillier, Stephanie, Dent, Michelle, Patel, Selina, Lienhart, Anna, Pennington, Emma, Maymond, Sian, Ludden, Siobhán, Zafeiropoulos, Parakevas, Asproudis, Ioannis, Tsironi, Evangelia, Scheitlin, Caroline, Chauhan, Monica, Toor, Sonia, Bennett, Carolyn, McPherson, Charlie, Ramm, Laura, Bibi, Mashal, Hussain, Hafsah, Samaddar, Julie, Shinh, Raadhika, Sarna, Sachi, Amlani, Kavita, Sauer, Wiebke, Kurt, Andrea, Chung-Crossley, Jenny, Ashraf, Nabila, Tailor, Vijay, Stewart, Catherine

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Acute concomitant esotropia in children von Schörkhuber, Marlene, Ivastinovic, Domagoj, Glatz, Wilfried, Schneider, Mona‐Regina, Lindner, Susanne, Langmann, Andrea

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The clinical and molecular genetic features of idiopathic infantile periodic alternating nystagmus von THOMAS, Mervyn G, CROSIER, Moira, LEROY, Bart P, MOORE, Anthony T, HUNTER, David G, HERTLE, Richard W, TARPEY, Patrick, LANGMANN, Andrea, LINDNER, Susanne, BRANDNER, Martina, GOTTLOB, Irene, LINDSAY, Susan, KUMAR, Anil, THOMAS, Shery, ARAKI, Masasuke, TALBOT, Chris J, MCLEAN, Rebecca J, SURENDRAN, Mylvaganam, TAYLOR, Katie

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Phenotypical characteristics of idiopathic infantile nystagmus with and without mutations in FRMD7 von Thomas, Shery, Proudlock, Frank A., Sarvananthan, Nagini, Roberts, Eryl O., Awan, Musarat, McLean, Rebecca, Surendran, Mylvaganam, Anil Kumar, A. S., Farooq, Shegufta J., Degg, Chris, Gale, Richard P., Reinecke, Robert D., Woodruff, Geoffrey, Langmann, Andrea, Lindner, Susanne, Jain, Sunila, Tarpey, Patrick, Raymond, F. Lucy, Gottlob, Irene

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Biomechanical Analysis of X-Pattern Exotropia von Brandner, Martina, Buchberger, Michael, Kaltofen, Thomas, Haslwanter, Thomas, Hoerantner, Robert, Langmann, Andrea

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Kraniomandibuläre Dysfunktion und Asthenopie – Literaturübersicht mit Fallbeispielen von Brandner, Martina, Strobl, Viktoria, Bizjak, Bianca, Lindner, Susanne, Langmann, Andrea

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Reply von Brandner, Martina, Langmann, Andrea, Buchberger, Michael, Kaltofen, Thomas, Haslwanter, Thomas, Hoerantner, Robert

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Reply von Brandner, Martina, Langmann, Andrea, Buchberger, Michael, Kaltofen, Thomas, Haslwanter, Thomas, Hoerantner, Robert

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Reply von Brandner, Martina, Langmann, Andrea, Buchberger, Michael, Kaltofen, Thomas, Haslwanter, Thomas, Hoerantner, Robert

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Die Universitäts-Augenklinik Graz erreicht den Recognised for Excellence (R4E) Preis des European Foundation for Quality (EFQM) Modells von Langmann, Gerald, Granitz, Elke, Kohlhofer, Aloisia, Kreilinger, Alex, Gliebe, Wolfgang, Langmann, Andrea, Wedrich, Andreas

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Orbital Revision after Trauma von Feichtinger, Matthias, Ardjomand, Navid, Santler, Gert, Langmann, Andrea, Kärcher, Hans

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Diplopia as the Presenting Sign of Systemic Lupus Erythematosus: The Chameleon Diagnosis von Koch, Martina, Langmann, Andrea

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Beidseitige posttraumatische Abduzensparalyse von Bizjak, Bianca S., Lindner, Susanne, Frühwirth-Kaspar, Daniela, Gaugl, Heike, Lienhart, Anna, Steinmair, Karin, Langmann, Andrea

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Corrigendum: Mutations in FRMD7 , a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus von Tarpey, Patrick, Thomas, Shery, Sarvananthan, Nagini, Mallya, Uma, Lisgo, Steven, Talbot, Chris J, Roberts, Eryl O, Awan, Musarat, Surendran, Mylvaganam, McLean, Rebecca J, Reinecke, Robert D, Langmann, Andrea, Lindner, Susanne, Koch, Martina, Jain, Sunila, Woodruff, Geoffrey, Gale, Richard P, Degg, Chris, Droutsas, Konstantinos, Asproudis, Ioannis, Zubcov, Alina A, Pieh, Christina, Veal, Colin D, Machado, Rajiv D, Backhouse, Oliver C, Baumber, Laura, Constantinescu, Cris S, Brodsky, Michael C, Hunter, David G, Hertle, Richard W, Read, Randy J, Edkins, Sarah, O'Meara, Sarah, Parker, Adrian, Stevens, Claire, Teague, Jon, Wooster, Richard, Futreal, P Andrew, Trembath, Richard C, Stratton, Michael R, Raymond, F Lucy, Gottlob, Irene

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Erratum: Corrigendum: Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus von Tarpey, Patrick, Thomas, Shery, Sarvananthan, Nagini, Mallya, Uma, Lisgo, Steven, Talbot, Chris J, Roberts, Eryl O, Awan, Musarat, Surendran, Mylvaganam, McLean, Rebecca J, Reinecke, Robert D, Langmann, Andrea, Lindner, Susanne, Koch, Martina, Jain, Sunila, Woodruff, Geoffrey, Gale, Richard P, Degg, Chris, Droutsas, Konstantinos, Asproudis, Ioannis, Zubcov, Alina A, Pieh, Christina, Veal, Colin D, Machado, Rajiv D, Backhouse, Oliver C, Baumber, Laura, Constantinescu, Cris S, Brodsky, Michael C, Hunter, David G, Hertle, Richard W, Read, Randy J, Edkins, Sarah, O'Meara, Sarah, Parker, Adrian, Stevens, Claire, Teague, Jon, Wooster, Richard, Futreal, P Andrew, Trembath, Richard C, Stratton, Michael R, Raymond, F Lucy, Gottlob, Irene

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