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Do we have to wait for a child to suffer a serious injury to suspect a hyperactivity/attention deficit disorder? A case-control study of patients admitted to PICU

Anales de pediatría (Barcelona, Spain : 2003), 2013-01, Vol.78 (1), p.67-68

2013

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Hypomyelinating leukodystrophy type 6. Clinical and neuroimaging key features in the detection of a new case

Revista de neurologiá, 2018-11, Vol.67 (9), p.339-342

2018

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A study of primary school teachers' knowledge of attention deficit hyperactivity disorder

Revista de neurologia, 2018-03, Vol.66 (S01), p.S121-S126

2018

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Provisional tic disorder or transient tic disorder?

Revista de neurologiá, 2019-04, Vol.68 (8), p.356-356

Eiris-Punal, J

2019

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Functional hemispherectomy: long-term follow-up in a series of five patients

Revista de neurologiá, 2018-03, Vol.66 (5), p.147-153

2018

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Retrospective analysis of the effect of a vagus nerve stimulator implanted in paediatric patients with refractory epilepsy

Revista de neurologiá, 2016-07, Vol.63 (1), p.11

2016

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Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes

Revista de neurologiá, 2015-09, Vol.61 (6), p.255-260

2015

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Clinical and genetic aspects of 22q13.3 deletion syndrome

Revista de neurologiá, 2007-09, Vol.45 (6), p.379

2007

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Current state of the attention deficit hyperactivity disorder approach in neuropediatrics

Revista de neurologia, 2017-02, Vol.64 (s01), p.S105-S109

2017

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Aicardi-Goutieres syndrome due to mutation of the IFIH1 gene with pontine involvement. A case report

Revista de neurologiá, 2016-10, Vol.63 (7), p.309-314

2016

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Estado actual del enfoque del trastorno por déficit de atención/hiperactividad en neuropediatría

Revista de neurologiá, 2017-02, Vol.64 (S01), p.S105

2017

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Myostatin Expression in Muscular Dystrophies and Mitochondrial Encephalomyopathies

Pediatric neurology, 2006-04, Vol.34 (4), p.281-284

2006

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Epileptic Disorder as the First Neurologic Manifestation of Blue Rubber Bleb Nevus Syndrome

Journal of child neurology, 2002-03, Vol.17 (3), p.219-222

2002

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Treatment of choline kinase beta deficiency with citicoline

Revista de neurologiá, 2018-07, Vol.67 (1), p.40-40

2018

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Long‐Term Treatment of Children with Epilepsy with Valproate or Carbamazepine May Cause Subclinical Hypothyroidism

Epilepsia (Copenhagen), 1999-12, Vol.40 (12), p.1761-1766

1999

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Abnormal growth in mitochondrial disease

Acta Paediatrica, 2010-06, Vol.99 (6), p.796-796

2010

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Usefulness of the Head‐Upright Tilt Test for Distinguishing Syncope and Epilepsy in Children

Epilepsia (Copenhagen), 2001-06, Vol.42 (6), p.709-713

2001

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Epilepsy and respiratory chain defects in children

Neuropediatrics, 2009-06, Vol.40 (3), p.152; author reply 152-152

2009

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Epidemiology of Pediatric Mitochondrial Respiratory Chain Disorders in Northwest Spain

Pediatric neurology, 2006-03, Vol.34 (3), p.204-211

2006

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Mixed hypotonia, neurological regression and atrophy of the cerebellum: manifestations that suggest infantile neuroaxonal dystrophy

Revista de neurologiá, 2003-07, Vol.37 (1), p.25-28

2003

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Neuropatía hereditaria con parálisis sensible a la presión (neuropatía tomacular). Estudio clínico, electrofisiológico y molecular de dos familias afectadas

Revista de neurologiá, 2000, Vol.31 (6), p.506

2000

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Importancia del diagnóstico precoz y el tratamiento temprano en el pronóstico de la aciduria glutárica tipo I

Anales de pediatría (Barcelona, Spain : 2003), 2008-09, Vol.69 (3), p.239-243

2008

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Congenital Hydranencephalic-Hydrocephalic Syndrome With Proliferative Vasculopathy: A Possible Relation With Mitochondrial Dysfunction

Journal of child neurology, 2001-11, Vol.16 (11), p.858-862

2001

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Debemos esperar a que un niño sufra un traumatismo grave para sospechar un trastorno por déficit de atención hiperactividad? Estudio de casos y controles en pacientes ingresados en la unidad de cuidados intensivos pediátricos

Anales de pediatría (Barcelona, Spain : 2003), 2013-01, Vol.78 (1), p.67-68

2013

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Pyruvate dehydrogenase deficit associated to the C515T mutation in exon 6 of the E1alpha gene

Revista de neurologiá, 2006-09, Vol.43 (6), p.341-345

2006

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Do we have to wait for a child to suffer a serious injury to suspect a hyperactivity/attention deficit disorder? A case-control study of patients admitted to PICU

Hypomyelinating leukodystrophy type 6. Clinical and neuroimaging key features in the detection of a new case

A study of primary school teachers' knowledge of attention deficit hyperactivity disorder

Provisional tic disorder or transient tic disorder?

Functional hemispherectomy: long-term follow-up in a series of five patients

Retrospective analysis of the effect of a vagus nerve stimulator implanted in paediatric patients with refractory epilepsy

Molecular characterisation and phenotypic description of two patients with reciprocal chromosomal aberrations in the region of the 3q29 microdeletion/microduplication syndromes

Clinical and genetic aspects of 22q13.3 deletion syndrome

Current state of the attention deficit hyperactivity disorder approach in neuropediatrics

Aicardi-Goutieres syndrome due to mutation of the IFIH1 gene with pontine involvement. A case report

Estado actual del enfoque del trastorno por déficit de atención/hiperactividad en neuropediatría

Myostatin Expression in Muscular Dystrophies and Mitochondrial Encephalomyopathies

Epileptic Disorder as the First Neurologic Manifestation of Blue Rubber Bleb Nevus Syndrome

Treatment of choline kinase beta deficiency with citicoline

Long‐Term Treatment of Children with Epilepsy with Valproate or Carbamazepine May Cause Subclinical Hypothyroidism

Abnormal growth in mitochondrial disease

Usefulness of the Head‐Upright Tilt Test for Distinguishing Syncope and Epilepsy in Children

Epilepsy and respiratory chain defects in children

Epidemiology of Pediatric Mitochondrial Respiratory Chain Disorders in Northwest Spain

Mixed hypotonia, neurological regression and atrophy of the cerebellum: manifestations that suggest infantile neuroaxonal dystrophy

Neuropatía hereditaria con parálisis sensible a la presión (neuropatía tomacular). Estudio clínico, electrofisiológico y molecular de dos familias afectadas

Importancia del diagnóstico precoz y el tratamiento temprano en el pronóstico de la aciduria glutárica tipo I

Congenital Hydranencephalic-Hydrocephalic Syndrome With Proliferative Vasculopathy: A Possible Relation With Mitochondrial Dysfunction

Debemos esperar a que un niño sufra un traumatismo grave para sospechar un trastorno por déficit de atención hiperactividad? Estudio de casos y controles en pacientes ingresados en la unidad de cuidados intensivos pediátricos

Pyruvate dehydrogenase deficit associated to the C515T mutation in exon 6 of the E1alpha gene

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