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The Journal of Spinal Cord Medicine
|
July 17, 2014
Who needs surgery for pediatric myelomeningocele? A retrospective study and literature review
Humberto Marreiros, Clara Loff, Eulália Calado
Developmental Medicine and Child Neurology
|
March 30, 2010
Fractures in children and adolescents with spina bifida: the experience of a Portuguese tertiary-care hospital
Humberto Marreiros, Luísa Monteiro, Clara Loff, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
July 16, 2008
Origin of frontal lobe spikes in the early onset benign occipital lobe epilepsy (Panayiotopoulos syndrome)
Alberto J R Leal, José C Ferreira, Ana I Dias, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
December 5, 2002
Interictal spike EEG source analysis in hypothalamic hamartoma epilepsy
Alberto J R Leal, Vitorina Passão, Eulália Calado, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
January 22, 2008
Analysis of the dynamics and origin of epileptic activity in patients with tuberous sclerosis evaluated for surgery of epilepsy
Alberto J R Leal, Ana I Dias, José P Vieira, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
April 3, 2007
Analysis of the generators of epileptic activity in early-onset childhood benign occipital lobe epilepsy
Alberto J R Leal, Sofia Nunes, Ana I Dias, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
June 23, 2010
N170 asymmetry as an index of inferior occipital dysfunction in patients with symptomatic occipital lobe epilepsy
Ricardo Lopes, Pedro Cabral, Nuno Canas, et al.
Epilepsy & Behavior : E&B
|
November 15, 2017
Anatomical and physiological basis of continuous spike-wave of sleep syndrome after early thalamic lesions
Alberto Leal, Eulália Calado, José P Vieira, et al.
Neuromuscular Disorders : NMD
|
February 19, 2014
Atypical phenotype in two patients with LAMA2 mutations
Joana Marques, Sofia T Duarte, Sónia Costa, et al.
Journal of Child Neurology
|
January 27, 2009
Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients
Mónica Santos, Teresa Temudo, Teresa Kay, et al.
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of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
The Journal of Spinal Cord Medicine
|
July 17, 2014
Who needs surgery for pediatric myelomeningocele? A retrospective study and literature review
Humberto Marreiros, Clara Loff, Eulália Calado
Developmental Medicine and Child Neurology
|
March 30, 2010
Fractures in children and adolescents with spina bifida: the experience of a Portuguese tertiary-care hospital
Humberto Marreiros, Luísa Monteiro, Clara Loff, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
July 16, 2008
Origin of frontal lobe spikes in the early onset benign occipital lobe epilepsy (Panayiotopoulos syndrome)
Alberto J R Leal, José C Ferreira, Ana I Dias, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
December 5, 2002
Interictal spike EEG source analysis in hypothalamic hamartoma epilepsy
Alberto J R Leal, Vitorina Passão, Eulália Calado, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
January 22, 2008
Analysis of the dynamics and origin of epileptic activity in patients with tuberous sclerosis evaluated for surgery of epilepsy
Alberto J R Leal, Ana I Dias, José P Vieira, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
April 3, 2007
Analysis of the generators of epileptic activity in early-onset childhood benign occipital lobe epilepsy
Alberto J R Leal, Sofia Nunes, Ana I Dias, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
June 23, 2010
N170 asymmetry as an index of inferior occipital dysfunction in patients with symptomatic occipital lobe epilepsy
Ricardo Lopes, Pedro Cabral, Nuno Canas, et al.
Epilepsy & Behavior : E&B
|
November 15, 2017
Anatomical and physiological basis of continuous spike-wave of sleep syndrome after early thalamic lesions
Alberto Leal, Eulália Calado, José P Vieira, et al.
Neuromuscular Disorders : NMD
|
February 19, 2014
Atypical phenotype in two patients with LAMA2 mutations
Joana Marques, Sofia T Duarte, Sónia Costa, et al.
Journal of Child Neurology
|
January 27, 2009
Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients
Mónica Santos, Teresa Temudo, Teresa Kay, et al.
Page
of 2