Sérgia Soares

Pyruvate dehydrogenase complex deficiency: updating the clinical, metabolic and mutational landscapes in a cohort of Portuguese patients

I. Rivera, J. B. Vicente, E. Martins, 2020, Orphanet Journal of Rare Diseases.

Sodium Channel Myotonia and a Novel Gly701Asp Mutation in the SCN4A Gene: From an Ophthalmological Symptom to a Familial Disease

S. Pereira, Á. Mota, Sérgia Soares, 2020, Neuro-ophthalmology.

Pyruvate dehydrogenase complex deficiency: updating the clinical, metabolic and mutational landscapes in a cohort of Portuguese patients

I. Rivera, J. B. Vicente, E. Martins, 2020, Orphanet Journal of Rare Diseases.

Cerebral venous thrombosis in adolescence: Looking beyond the obvious

C. Melo, S. Gomes, R. Morais, 2022, International Journal of Pediatrics & Adolescent Medicine.

Rib osteomyelitis in a pediatric patient case report and literature review.

Sérgia Soares, Rui Almeida, Filipa Espada, 2012, The Pediatric infectious disease journal.

Pertussis with severe pulmonary hypertension in a newborn with good outcome - case report.

H. Guimarães, G. Rocha, I. Azevedo, 2008, Revista portuguesa de pneumologia.