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2022
Gietzelt, Caroline 
ORCID: 0000-0002-9145-7385, Fricke, Julia, Neugebauer, Antje and Hedergott, Andrea
(2022).
Prism adaptation test before strabismus surgery in patients with decompensated esophoria and decompensated microesotropia.
Int. Ophthalmol., 42 (7).
S. 2195 - 2205.
DORDRECHT:
SPRINGER.
ISSN 1573-2630
2021
Hedergott, Andrea, Pink-Theofylaktopoulos, Ursula, Neugebauer, Antje and Fricke, Julia (2021). Tendon elongation with bovine pericardium in strabismus surgery-indications beyond Graves' orbitopathy. Graefes Arch. Clin. Exp. Ophthalmol., 259 (1). S. 145 - 156. NEW YORK: SPRINGER. ISSN 1435-702X
Volk, Alexander E., Hedergott, Andrea ORCID: 0000-0002-6398-3919, Preising, Markus, Rading, Sebastian, Fricke, Julia, Herkenrath, Peter, Nurnberg, Peter, Altmueller, Janine, von Ameln, Simon, Lorenz, Birgit, Neugebauer, Antje, Karsak, Meliha and Kubisch, Christian
(2021).
Biallelic mutations in l-dopachrome tautomerase (DCT) cause infantile nystagmus and oculocutaneous albinism.
Hum. Genet., 140 (8).
S. 1157 - 1169.
NEW YORK:
SPRINGER.
ISSN 1432-1203
2018
Hedergott, Andrea M., Wild, Dana, Fricke, Julia and Neugebauer, Antje (2018). Efficacy of Vertical Muscle Transpositions with and without Simultaneous Rectus Muscle Recession for Unilateral Sixth Nerve Palsy. Klinische Monatsblat. Augenheilkunde, 235 (10). S. 1096 - 1105. STUTTGART: GEORG THIEME VERLAG KG. ISSN 1439-3999
2017
Fazeli, Walid, Herkenrath, Peter, Stiller, Barbara, Neugebauer, Antje, Fricke, Julia, Lang-Roth, Ruth, Nuernberg, Gudrun, Thoenes, Michaela, Becker, Jutta, Altmueller, Janine, Volk, Alexander E., Kubisch, Christian ORCID: 0000-0003-4220-0978 and Heller, Raoul
(2017).
A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction.
Hum. Mol. Genet., 26 (20).
S. 4055 - 4067.
OXFORD:
OXFORD UNIV PRESS.
ISSN 1460-2083
2016
Bucher, Franziska, Fricke, Julia, Neugebauer, Antje, Cursiefen, Claus and Heindl, Ludwig M. (2016). Ophthalmological manifestations of Parry-Romberg syndrome. Surv. Ophthalmol., 61 (6). S. 693 - 702. NEW YORK: ELSEVIER SCIENCE INC. ISSN 1879-3304
2014
Beck, Bodo B., Phillips, Jennifer B., Bartram, Melte P., Wegner, Jeremy, Thoenes, Michaele, Pannes, Andrea, Sampson, Josephina, Heller, Raoul, Goebel, Heike, Koerber, Friederike, Neugebauer, Antje, Hedergott, Andrea, Nuernberg, Gudrun, Nuernberg, Peter, Thiele, Holger, Altmueller, Janine, Toliat, Mohammad R., Staubach, Simon, Boycott, Kym M., Valente, Enza Maria ORCID: 0000-0002-0600-6820, Janecke, Andreas R., Eisenberger, Tobias, Bergmann, Carsten, Tebbe, Lars, Wang, Yang, Wu, Yundong, Fry, Andrew M., Westerfield, Monte, Wolfrum, Uwe and Bolz, Hanno J.
(2014).
Mutation of POC1B in a Severe Syndromic Retinal Ciliopathy.
Hum. Mutat., 35 (10).
S. 1153 - 1163.
HOBOKEN:
WILEY.
ISSN 1098-1004
2013
Hauke, Jan, Schild, Andrea, Neugebauer, Antje, Lappa, Alexandra, Fricke, Julia, Fauser, Sascha, Roesler, Stefanie, Pannes, Andrea, Zarrinnam, Dirk, Altmueller, Janine, Motameny, Susanne, Nuernberg, Gudrun, Nuernberg, Peter, Hahnen, Eric and Beck, Bodo B. (2013). A Novel Large In-Frame Deletion within the CACNA1F Gene Associates with a Cone-Rod Dystrophy 3-Like Phenotype. PLoS One, 8 (10). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1932-6203
Schild, Andrea M., Thoenes, Julia, Fricke, Julia and Neugebauer, Antje (2013). Kestenbaum procedure with combined muscle resection and tucking for nystagmus-related head turn. Graefes Arch. Clin. Exp. Ophthalmol., 251 (12). S. 2803 - 2810. NEW YORK: SPRINGER. ISSN 1435-702X