E. Calado

E. Sellier, C. Cans, M. Torrioli, 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Síndrome do Nevus Linear Sebáceo

E. Calado, L. Gonçalves, 2003 .

Stereotypies in Rett syndrome

G. Oliveira, P. Maciel, P. Cabral, 2007, Neurology.

The "failures" of spina bifida transdisciplinary care.

E. Calado, C. Loff, 2002, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Interictal spike EEG source analysis in hypothalamic hamartoma epilepsy

A. Leal, J. P. Vieira, Eulália Calado, 2002, Clinical Neurophysiology.

Fractures in children and adolescents with spina bifida: the experience of a Portuguese tertiary‐care hospital

E. Calado, H. Marreiros, C. Loff, 2010, Developmental medicine and child 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.

Movement disorders in Rett syndrome: An analysis of 60 patients with detected MECP2 mutation and correlation with mutation type

G. Oliveira, P. Maciel, P. Cabral, 2008, Movement disorders : official journal of the Movement Disorder Society.

Origin of frontal lobe spikes in the early onset benign occipital lobe epilepsy (Panayiotopoulos syndrome)

A. I. Dias, A. Leal, J. Ferreira, 2008, Clinical Neurophysiology.

Protocadherin 19 mutations in girls with infantile-onset epilepsy

R. Guerrini, D. Mei, L. Parmeggiani, 2010, Neurology.

Analysis of the dynamics and origin of epileptic activity in patients with tuberous sclerosis evaluated for surgery of epilepsy

A. I. Dias, A. Leal, L. Tavora, 2008, Clinical Neurophysiology.

Atypical phenotype in two patients with LAMA2 mutations

S. Duarte, T. Evangelista, E. Bronze-da-Rocha, 2014, Neuromuscular Disorders.

[GNAO1: a new gene to consider on early-onset childhood dystonia].

S. Duarte, E. Calado, C. Marecos, 2018, Revista de neurologia.

Identification of novel genetic causes of Rett syndrome-like phenotypes

D. Pinto, G. Oliveira, A. Ameur, 2016, Journal of Medical Genetics.

Clinical and molecular findings in four new patients harbouring the mtDNA 8993T'C mutation

R. Carrozzo, A. Tessa, F. Santorelli, 2001, Journal of Inherited Metabolic Disease.

Epilepsy and cerebral palsy: characteristics and trends in children born in 1976-1998.

E. Sellier, C. Cans, M. Torrioli, 2012, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Identification of novel genetic causes of Rett syndrome-like phenotypes

D. Pinto, G. Oliveira, A. Ameur, 2016, Journal of Medical Genetics.

Atypical phenotype in two patients with LAMA2 mutations

S. Duarte, T. Evangelista, E. Bronze-da-Rocha, 2014, Neuromuscular Disorders.

Multiple surgeries in paediatric patients with myelomeningocele. Can we define quantitative and qualitative evolution patterns according to the level of spinal lesion?

E. Calado, H. Marreiros, C. Loff, 2010, Cerebrospinal Fluid Research.

N170 asymmetry as an index of inferior occipital dysfunction in patients with symptomatic occipital lobe epilepsy

A. Leal, P. Cabral, Ricardo Lopes, 2011, Clinical Neurophysiology.