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Current Molecular Medicine|April 21, 2012
Neuroprotective strategies for the treatment of inherited photoreceptor degenerationD Trifunović, A Sahaboglu, J Kaur, et al.Investigative Ophthalmology & Visual Science|January 15, 1999
Phenotype in retinol deficiency due to a hereditary defect in retinol binding protein synthesisM W Seeliger, H K Biesalski, B Wissinger, et al.Journal of Neuroscience Methods|November 16, 2010
A new DTL-electrode holder for recording of electroretinograms in animalsA Schatz, G Willmann, H Enderle, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|May 10, 2006
Between and within: international perspectives on cancer and health disparitiesLovell A Jones, Janice A Chilton, Richard A Hajek, et al.Biochemical and Biophysical Research Communications|May 19, 1997
Mutation analysis of the ND6 gene in patients with Lebers hereditary optic neuropathyB Wissinger, D Besch, B Baumann, et al.Neurology|May 1, 1997
Color vision tests for early detection of antiepileptic drug toxicityA U Bayer, H J Thiel, E Zrenner, et al.The Annals of Otology, Rhinology, and Laryngology|August 30, 2021
Correlations of Radiographic and Endoscopic Observations in Subglottic StenosisAlexandra T Bourdillon, Michael A Hajek, Mitchel Wride, et al.Ophthalmology|February 1, 1987
Mutagenic potential of a 193-nm excimer laser on fibroblasts in tissue cultureJ Trentacoste, K Thompson, R K Parrish, et al.Head & Neck|October 9, 2015
Severe epistaxis due to aberrant vasculature in a patient with STAT-1 mutationMichael T Chang, Zachary G Schwam, Michael A Hajek, et al.Scandinavian Journal of Rheumatology|October 31, 2023
Physical activity in adults with and without rheumatoid arthritis: cross-sectional results from the Survey of Health, Ageing and Retirement in Europe (SHARE)M H Belau, F Flaßkamp, H Becher, et al.Pageof 36