L. Ortega-Moreno

Atypical course in individuals from Spanish families with benign familial infantile seizures and mutations in the PRRT2 gene

J. Serratosa, J. García-Peñas, P. Gómez-Garre, 2014, Epilepsy Research.

Human intestinal pro-inflammatory CD11chighCCR2+CX3CR1+ macrophages, but not their tolerogenic CD11c−CCR2−CX3CR1− counterparts, are expanded in inflammatory bowel disease

J. Gisbert, D. Bernardo, S. Fernández-Tomé, 2018, Mucosal Immunology.

Novel mutation in STXBP1 gene in a patient with non-lesional Ohtahara syndrome.

J. Serratosa, B. G. Giráldez, R. Guerrero‐López, 2016, Neurologia.

Molecular diagnosis of patients with epilepsy and developmental delay using a customized panel of epilepsy genes

J. Serratosa, B. G. Giráldez, V. Soto-Insuga, 2017, PloS one.

Uniparental disomy as a cause of spinal muscular atrophy and progressive myoclonic epilepsy: Phenotypic homogeneity due to the homozygous c.125C>T mutation in ASAH1

J. Serratosa, R. Guerrero‐López, J. Pardal-Fernández, 2015, Neuromuscular Disorders.

Human intestinal pro-inflammatory CD11chighCCR2+CX3CR1+ macrophages, but not their tolerogenic CD11c−CCR2−CX3CR1− counterparts, are expanded in inflammatory bowel disease

J. Gisbert, D. Bernardo, S. Fernández-Tomé, 2018, Mucosal Immunology.

Atypical course in individuals from Spanish families with benign familial infantile seizures and mutations in the PRRT2 gene

J. Serratosa, J. García-Peñas, P. Gómez-Garre, 2014, Epilepsy Research.