Francisco Barros Angueira

Determination and diagnostic value of CA9 mRNA in peripheral blood of patients with oral leukoplakia.

A. García, M. Sayáns, C. C. Petronacci, 2018 .

Severe neurological abnormalities in a young boy with impaired thyroid hormone sensitivity due to a novel mutation in the MCT8 gene

M. Castro‐Gago, L. Castro-Feijóo, J. Conde, 2017, Hormones.

The modifier effect of the BDNF gene in the phenotype of the WAGRO syndrome.

R. Rodríguez-López, E. G. Gómez, M. N. Estévez, 2013, Gene.

Three New Patients With Congenital Unilateral Facial Nerve Palsy due to Chromosome 22q11 Deletion

M. Castro‐Gago, Francisco Barros Angueira, J. Eirís Puñal, 2001, Journal of child neurology.

Alström syndrome caused by deletion in ALMS1 gene fixed in a Northern Pakistan recurrent haplotype

A. Amadoz, C. Monzó, G. Marcaida, 2017 .

Hereditary spastic paraplegia type 4: Description of a family with a new pathogenic SPAST gene variant, c.1156A > C (p.Asn386His)

B. Quintáns, D. A. G. Estévez, Francisco Barros Angueira, 2021, Neurology Perspectives.