V. Sofia

STRUCTURAL ANOMALY OF LEFT LATERAL TEMPORAL LOBE IN EPILEPSY DUE TO MUTATED LGI1

M. Giannelli, M. Mascalchi, C. Tessa, 2007, Neurology.

Electroclinical features of a patient with GLUT1 deficiency syndrome and adult onset periodic weakness

M. Zappia, R. Barone, L. Giuliano, 2016, European journal of neurology.

Polipose adenomatosa familiar: a propósito de um caso clínico

V. Sofia, G. Teofilo, 2014 .

Further evidence that DDHD2 gene mutations cause autosomal recessive hereditary spastic paraplegia with thin corpus callosum

S. Zuchner, M. Muglia, M. Zappia, 2014, European journal of neurology.