Bettina Wabbels

Human TUBB3 Mutations Perturb Microtubule Dynamics, Kinesin Interactions, and Axon Guidance

Max A. Tischfield, Hagit Baris, Chen Wu et al. · Cell · 2010 · 589 citations · Full text

Axon Guidance, Protein Function, Molecular Biology +8

Lack of fundus autofluorescence to 488 nanometers from childhood on in patients with early-onset severe retinal dystrophy associated with mutations in RPE65

Birgit Lorenz, Bettina Wabbels, Erika Wegscheider et al. · Ophthalmology · 2004 · 160 citations

Ocular Disease, Retina, Photoreceptor Cell +8

A European randomised controlled trial of the addition of etoposide to standard vincristine and carboplatin induction as part of an 18-month treatment programme for childhood (≤16 years) low grade glioma – A final report

Astrid Gnekow, David Walker, Daniela Kandels et al. · European Journal of Cancer · 2017 · 141 citations · Full text

Longitudinal and cross-sectional study of patients with early-onset severe retinal dystrophy associated with RPE65 mutations

K. Paunescu, Bettina Wabbels, Markus N. Preising et al. · Graefe s Archive for Clinical and Experimental Ophthalmology · 2004 · 89 citations

Ocular Disease, Retina, Ophthalmology +7

Genotype-phenotype correlation and longitudinal course in ten families with Best vitelliform macular dystrophy

Bettina Wabbels, Markus N. Preising, Ulf Kretschmann et al. · Graefe s Archive for Clinical and Experimental Ophthalmology · 2006 · 86 citations · Full text

Ocular Disease, Mendelian Disorder, Ophthalmology +11