Emilia Servián‐Morilla

A <i> <scp>POGLUT</scp> 1 </i> mutation causes a muscular dystrophy with reduced Notch signaling and satellite cell loss

Emilia Servián‐Morilla, Hideyuki Takeuchi, Tom V. Lee et al. · EMBO Molecular Medicine · 2016 · 102 citations · Full text

Presenilin/γ-Secretase Regulates Neurexin Processing at Synapses

Carlos A. Saura, Emilia Servián‐Morilla, Francisco G. Scholl · PLoS ONE · 2011 · 71 citations · Full text

POGLUT1 biallelic mutations cause myopathy with reduced satellite cells, α-dystroglycan hypoglycosylation and a distinctive radiological pattern

Emilia Servián‐Morilla, Macarena Cabrera‐Serrano, Katherine Johnson et al. · Acta Neuropathologica · 2020 · 38 citations · Full text

Satellite Cells, Autoimmune Disease, Poglut1 Biallelic Mutations +4

Heterozygous <i>CAPN3</i> missense variants causing autosomal‐dominant calpainopathy in seven unrelated families

Laura González, Gianina Ravenscroft, Macarena Cabrera‐Serrano et al. · Neuropathology and Applied Neurobiology · 2020 · 35 citations

Altered myogenesis and premature senescence underlie human TRIM32-related myopathy

Emilia Servián‐Morilla, Macarena Cabrera‐Serrano, Eloy Rivas et al. · Acta Neuropathologica Communications · 2019 · 30 citations · Full text