Fátima Furtado

发表

[Peutz-Jeghers syndrome: variability of gastrointestinal expression at pediatric age].

A. Marques, A. Lopes, A. Palha, 2004, Acta medica portuguesa.

LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance.

E. Bertini, A. Vanderver, R. Carrozzo, 2016, Brain : a journal of neurology.

Anatomical and physiological basis of continuous spike–wave of sleep syndrome after early thalamic lesions

A. Leal, J. Ferreira, J. P. Vieira, 2018, Epilepsy & Behavior.

Pharyngeal-cervical-brachial variant of Guillain-Barré syndrome: a rare cause of acute bulbar dysfunction in children

S. Quintas, A. Levy, F. Abecasis, 2014 .

Molecular and structural analyses of maple syrup urine disease and identification of a founder mutation in a Portuguese Gypsy community.

A. Amorim, E. Martins, L. Diogo, 2008, Molecular genetics and metabolism.