S. Freire

Leber hereditary optic neuropathy: Usefulness of next generation sequencing to study mitochondrial mutations on apparent homoplasmy

J. L. Siles, P. C. Salas, C. P. Milla, 2016 .

Neurofibromatosis type I: mutation spectrum of NF1 in spanish patients.

J. L. Siles, José Miguel Lezana Rosales, C. P. Milla, 2018 .

Omicron (BA.1) SARS-CoV-2 variant is associated with reduced risk of hospitalization and length of stay compared with Delta (B.1.617.2)

J. P. Almeida, E. Fernandes, J. Isidro, 2022, medRxiv.

Haemophagocytic Lymphohistiocytosis as a Complication of Israeli Spotted Fever

Diogo Cruz, S. Freire, Ana Gorgulho, 2022, European journal of case reports in internal medicine.