Luísa Panadés‐de Oliveira

Bethlem myopathy: a series of 16 patients and description of seven new associated mutations

Luísa Panadés‐de Oliveira, Claudia Rodríguez-López, Diana Cantero et al. · Journal of Neurology · 2019 · 21 citations

Rare Diseases, Mendelian Disorder, Genetic Disorder +6

Persistent asymptomatic or mild symptomatic hyperCKemia due to mutations in ANO5: the mildest end of the anoctaminopathies spectrum

Luísa Panadés‐de Oliveira, Laura Bermejo‐Guerrero, Carlos Pablo de Fuenmayor‐Fernández de la Hoz et al. · Journal of Neurology · 2020 · 15 citations

Genetics, Pathology, Mildest End +3

Mood Disturbances, Anxiety, and Impact on Quality of Life in Patients Admitted to Epilepsy Monitoring Units

Rodrigo Rocamora, Beatriz Chavarría, E. Cebrián Pérez et al. · Frontiers in Neurology · 2021 · 15 citations · Full text

Stereo-electroencephalography–guided radiofrequency thermocoagulation in patients with MRI-negative focal epilepsy

Luísa Panadés‐de Oliveira, Carmen Pérez‐Enríquez, Ainara Barguilla et al. · Journal of neurosurgery · 2022 · 14 citations · Full text

A novel mutation in the mitochondrial MT-ND5 gene in a family with MELAS. The relevance of genetic analysis on targeted tissues

Luísa Panadés‐de Oliveira, Julio Montoya, Sonia Emperador et al. · Mitochondrion · 2019 · 10 citations