Sophia Aristodemou

Connexin32 Mutations Cause Loss of Function in Schwann Cells and Oligodendrocytes Leading to PNS and CNS Myelination Defects

Irene Sargiannidou, Natalie Vavlitou, Sophia Aristodemou et al. · Journal of Neuroscience · 2009 · 117 citations · Full text

Phase I/II open-label trial of intravenous allogeneic mesenchymal stromal cell therapy in adults with recessive dystrophic epidermolysis bullosa

Ellie Rashidghamat, Tendai Kadiyirire, Salma Ayis et al. · Journal of the American Academy of Dermatology · 2019 · 109 citations · Full text

Epithelial Inflammation Resulting from an Inherited Loss-of-Function Mutation in EGFR

Patrick Campbell, Penny E. Morton, Takuya Takeichi et al. · Journal of Investigative Dermatology · 2014 · 97 citations · Full text

Fibrosis, Epithelial Inflammation, Signaling Pathway +7

Safety and early efficacy outcomes for lentiviral fibroblast gene therapy in recessive dystrophic epidermolysis bullosa

Su M. Lwin, Farhatullah Syed, Wei‐Li Di et al. · JCI Insight · 2019 · 88 citations · Full text

Early Efficacy Outcomes, Immunology, Pathology +19

Mutations in GRHL2 Result in an Autosomal-Recessive Ectodermal Dysplasia Syndrome

Gabriela Petrof, Arti Nanda, Jake Davey Howden et al. · The American Journal of Human Genetics · 2014 · 59 citations · Full text