Gerth-Kahlert, Christina

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Journal Article

Gerull, Roland; Brauer, Viviane; Bassler, Dirk; Laubscher, Bernard; Pfister, Riccardo E; Nelle, Mathias; Müller, Beatrice; Roth-Kleiner, Matthias; Gerth-Kahlert, Christina; Adams, Mark (2018). Prediction of ROP Treatment and Evaluation of Screening Criteria in VLBW Infants-a Population Based Analysis. Pediatric research, 84(5), pp. 632-638. Nature Publishing Group 10.1038/s41390-018-0128-3

Gerull, Roland; Brauer, Viviane; Bassler, Dirk; Laubscher, Bernard; Pfister, Riccardo E; Nelle, Mathias; Müller, Béatrice; Gerth-Kahlert, Christina; Adams, Mark (2018). Incidence of retinopathy of prematurity (ROP) and ROP treatment in Switzerland 2006-2015: a population-based analysis. Archives of disease in childhood - fetal and neonatal edition, 103(4), F337-F342. BMJ Publishing Group 10.1136/archdischild-2017-313574

Bolognini, Ramona; Gerth-Kahlert, Christina; Abegg, Mathias; Bartholdi, Deborah; Mathis, Nicolas; Sturm, Veit; Gallati, Sabina; Schaller, André (2017). Characterization of two novel intronic OPA1 mutations resulting in aberrant pre-mRNA splicing. BMC medical genetics, 18(1), p. 22. BioMed Central 10.1186/s12881-017-0383-x

Tiwari, Amit; Bahr, Angela; Bähr, Luzy; Fleischhauer, Johannes; Zinkernagel, Martin; Winkler, Niklas; Barthelmes, Daniel; Berger, Lieselotte Erika; Gerth-Kahlert, Christina; Neidhardt, John; Berger, Wolfgang (2016). Next generation sequencing based identification of disease-associated mutations in Swiss patients with retinal dystrophies. Scientific Reports, 6(28755), p. 28755. Nature Publishing Group 10.1038/srep28755

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