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Effect of prematurity and low birth weight in visual abilities and school performance

Research in developmental disabilities, 2016-12, Vol.59, p.451-457

2016

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Congenital endplate acetylcholinesterase deficiency responsive to ephedrine

Neurology, 2005-07, Vol.65 (1), p.144-146

2005

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Optic neuritis in paediatric patients: Experience over 27 years and a management protocol

Neurología (Barcelona, English ed. ), 2021-05, Vol.36 (4), p.253-261

2021

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A novel likely pathogenic variant in the H1-4 gene c.139G > C p.(Ala47Pro) associated with Rahman syndrome: a clinical report

Egyptian Journal of Medical Human Genetics, 2022-03, Vol.23 (1), p.50, Article 50

2022

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Be careful with familial unbalanced chromosome abnormalities

American journal of medical genetics. Part A, 2008-08, Vol.146A (15), p.2005-2007

2008

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Descriptive study of symptomatic epilepsy by age of onset in patients with a 3-year follow-up at the Neuropaediatric Department of a reference centre

Neurologia (Barcelona, Spain), 2017-09, Vol.32 (7), p.455

2017

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Our experience with the aetiological diagnosis of global developmental delay and intellectual disability: 2006-2010

Neurologia (Barcelona, Spain), 2014-09, Vol.29 (7), p.402

2014

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Congenital endplate acetylcholinesterase deficiency responsive to ephedrine

Neurology, 2005-07, Vol.65 (1), p.144

2005

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Angiomatosis leptomeníngea sin nevus facial y disminución del nivel de consciencia

Anales de pediatría (Barcelona, Spain : 2003), 2011, Vol.74 (5), p.347-349

2011

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Epilepsy with onset between the ages of 3 and 12 months. Our experience gained over a 10-year period

Revista de neurologiá, 2008-12, Vol.47 (11), p.561-565

2008

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Prematuridad con parálisis cerebral y ceroidolipofuscinosis

Anales de pediatría (Barcelona, Spain : 2003), 2010-11, Vol.73 (5), p.291-293

2010

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Síndrome de apnea central del sueño como primera manifestación de malformación de Chiari tipo I

Anales de pediatría (Barcelona, Spain : 2003), 2008-03, Vol.68 (3), p.277-281

2008

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Myotonic dystrophy. 18 years experience in a neuropaediatric clinic

Anales de pediatría (Barcelona, Spain : 2003), 2010-02, Vol.72 (2), p.133-138

2010

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Benign intracranial hypertension: experience over 18 years

Anales de pediatría (Barcelona, Spain : 2003), 2009-11, Vol.71 (5), p.400-406

2009

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Prematurity with cerebral palsy and ceroid lipofuscinosis

Anales de pediatría (Barcelona, Spain : 2003), 2010-11, Vol.73 (5), p.291

2010

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Optic neuritis in paediatric patients: experience over 27 years and a management protocol

Neurología (Barcelona, English ed. ), 2021-05, Vol.36 (4), p.253-261

2021

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Congenital infection by cytomegalovirus. A review of our 18 years' experience of diagnoses

Revista de neurologiá, 2009-04, Vol.48 (7), p.349-353

2009

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Valoración del cumplimiento de los criterios de calidad del protocolo de cefaleas en urgencias

Anales de pediatría (Barcelona, Spain : 2003), 2007-06, Vol.66 (6), p.630-631

2007

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Síndrome de duplicación MECP2 familiar

Revista de neurologiá, 2020, Vol.70 (8), p.309

2020

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Facial paralysis reported in a paediatric emergency department: actuation protocol reviewed and verified

Revista de neurologiá, 2007-08, Vol.45 (4), p.205-210

2007

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Our experience in the diagnosis of peroxisomal diseases with an abnormal fatty acid profile

Revista de neurologiá, 2008-07, Vol.47 (1), p.1-5

2008

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Neurofibromatosis 1 y cavernomatosis múltiple familiar en un lactante con sialorrea profusa episódica

Revista de neurologiá, 2019, Vol.69 (8), p.350

2019

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Changes in the demand for paediatric neurology care in a spanish tertiary care hospital over a 20-year period

Neurologia (Barcelona, Spain), 2014-01, Vol.29 (1), p.36

2014

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Retrospective diagnosis of congenital infection by cytomegalovirus in the case of one infant

Revista de neurologiá, 2005-06, Vol.40 (12), p.733-736

2005

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Atypical growth of an intracranial lipoma

Revista de neurologiá, 2022-11, Vol.75 (9), p.295

2022

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Effect of prematurity and low birth weight in visual abilities and school performance

Congenital endplate acetylcholinesterase deficiency responsive to ephedrine

Optic neuritis in paediatric patients: Experience over 27 years and a management protocol

A novel likely pathogenic variant in the H1-4 gene c.139G > C p.(Ala47Pro) associated with Rahman syndrome: a clinical report

Be careful with familial unbalanced chromosome abnormalities

Descriptive study of symptomatic epilepsy by age of onset in patients with a 3-year follow-up at the Neuropaediatric Department of a reference centre

Our experience with the aetiological diagnosis of global developmental delay and intellectual disability: 2006-2010

Congenital endplate acetylcholinesterase deficiency responsive to ephedrine

Angiomatosis leptomeníngea sin nevus facial y disminución del nivel de consciencia

Epilepsy with onset between the ages of 3 and 12 months. Our experience gained over a 10-year period

Prematuridad con parálisis cerebral y ceroidolipofuscinosis

Síndrome de apnea central del sueño como primera manifestación de malformación de Chiari tipo I

Myotonic dystrophy. 18 years experience in a neuropaediatric clinic

Benign intracranial hypertension: experience over 18 years

Prematurity with cerebral palsy and ceroid lipofuscinosis

Optic neuritis in paediatric patients: experience over 27 years and a management protocol

Congenital infection by cytomegalovirus. A review of our 18 years' experience of diagnoses

Valoración del cumplimiento de los criterios de calidad del protocolo de cefaleas en urgencias

Síndrome de duplicación MECP2 familiar

Facial paralysis reported in a paediatric emergency department: actuation protocol reviewed and verified

Our experience in the diagnosis of peroxisomal diseases with an abnormal fatty acid profile

Neurofibromatosis 1 y cavernomatosis múltiple familiar en un lactante con sialorrea profusa episódica

Changes in the demand for paediatric neurology care in a spanish tertiary care hospital over a 20-year period

Retrospective diagnosis of congenital infection by cytomegalovirus in the case of one infant

Atypical growth of an intracranial lipoma

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