Pablo Llavona

CDHR1 mutations in retinal dystrophies

Katarína Štingl, Anja K. Mayer, Pablo Llavona et al. · Scientific Reports · 2017 · 51 citations · Full text

Multimodal assessment of choroideremia patients defines pre-treatment characteristics

Immanuel P. Seitz, Ahmad Zhour, Susanne Kohl et al. · Graefe s Archive for Clinical and Experimental Ophthalmology · 2015 · 45 citations

Clinical Evidence, Choroideremia Patients, Disease Assessment +3

The transcriptional regulator FUBP1 influences disease outcome in murine and human myeloid leukemia

Van T. Hoang, Divij Verma, Parimala Sonika Godavarthy et al. · Leukemia · 2019 · 30 citations

Hematological Malignancy, Chromatin, Transcriptional Regulation +10

Allelic Expression Imbalance in the Human Retinal Transcriptome and Potential Impact on Inherited Retinal Diseases

Pablo Llavona, Michele Pinelli, Margherita Mutarelli et al. · Genes · 2017 · 27 citations · Full text

Phenotypic spectrum of autosomal recessive retinitis pigmentosa without posterior column ataxia caused by mutations in the FLVCR1 gene

Laura Kuehlewein, Lüdger Schöls, Pablo Llavona et al. · Graefe s Archive for Clinical and Experimental Ophthalmology · 2019 · 15 citations

Posterior Column Ataxia, Mendelian Disorder, Genetic Disorder +8