Search Results - "LOPEZ PISON, J"

Face recognition impairment in small for gestational age and preterm children by Perez-Roche, T., Altemir, I., Giménez, G., Prieto, E., González, I., López Pisón, J., Pueyo, V.

“…•Children born small for gestational age present worse immediate face recognition and delayed face memory compared with children born with an appropriate…”
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Functional progression of patients with neurological diseases in a tertiary paediatric intensive care unit: Our experience by Madurga Revilla, P, López Pisón, J, Samper Villagrasa, P, García Íñiguez, J P, Garcés Gómez, R, Domínguez Cajal, M, Gil Hernández, I

“…Neurological diseases explain a considerable proportion of admissions to paediatric intensive care units (PICU), and are a significant cause of morbidity and…”
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Congenital endplate acetylcholinesterase deficiency responsive to ephedrine by BESTUE-CARDIEL, M, SAENZ DE CABEZON-ALVAREZ, A, CAPABLO-LIESA, J. L, LOPEZ-PISON, J, PENA-SEGURA, J. L, MARTIN-MARTINEZ, J, ENGEL, A. G

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Melanosis neurocutánea by Giménez López, V, Monge Galindo, L, López Pisón, J, Zandueta Pascual, L, Clavero Montañés, N, Muñoz Mellado, A

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Telematic attention in a neuropediatrics consultation during the COVID-19 alarm state. Cross-sectional study and satisfaction survey by Carmen Marcén, G, López Pisón, J, Samper Villagrasa, P, Molina Herranz, D, Moreno Sanchez, A, Salinas Salvador, B

“…Crisis caused by the SARS-CoV-2 virus limit face-to-face consultation to the minimum necessary, this was a change toward telephone activity. To analyze the…”
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Changes in the demand for paediatric neurology care in a spanish tertiary care hospital over a 20-year period by Monge Galindo, L, López-Pisón, J, Samper Villagrasa, P, Peña Segura, J L

“…The purpose of this study is to determine the profile of the demand for paediatric neurology care in a Spanish tertiary hospital over the past 20 years. We…”
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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 by Ochoa-Gómez, L, López-Pisón, J, Fuertes-Rodrigo, C, Fernando-Martínez, R, Samper-Villagrasa, P, Monge-Galindo, L, Peña-Segura, J L, García-Jiménez, M C

“…We conducted a descriptive study of symptomatic epilepsy by age at onset in a cohort of patients who were followed up at a neuropaediatric department of a…”
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Congenital endplate acetylcholinesterase deficiency responsive to ephedrine by Bestue-Cardiel, M, Sáenz de Cabezón-Alvarez, A, Capablo-Liesa, J L, López-Pisón, J, Peña-Segura, J L, Martin-Martinez, J, Engel, A G

“…The authors describe two patients with congenital myasthenic syndrome (CMS) with end plate acetylcholinesterase (AChE) deficiency caused by mutations in the…”
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Disfunción autonómica paroxística desde el periodo neonatal y meduloblastoma by López Pisón, J, Monge Galindo, L, García Jiménez, M.C, Muñoz Albillos, M, Rodríguez-Vigil, C, Pérez Delgado, R

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Our experience with the aetiological diagnosis of global developmental delay and intellectual disability: 2006-2010 by López-Pisón, J, García-Jiménez, M C, Monge-Galindo, L, Lafuente-Hidalgo, M, Pérez-Delgado, R, García-Oguiza, A, Peña-Segura, J L

“…Global developmental delay (GDD) and intellectual disability (ID) are common reasons for consultation in paediatric neurology. Results from aetiological…”
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Monitorización continua de un protocolo: parálisis facial a frigore by Monge Galindo, L, Mateo Ferrando, A, López-Pisón, J, Martín Ruiz, N, Aznar, E, Pérez Delgado, R, García Mata, J.R, García Jiménez, M.C

“…Resumen Introducción La elaboración y revisión de protocolos de actuación neuropediátrica permite reducir la variabilidad de nuestra práctica médica, mejorando…”
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Angiomatosis leptomeníngea sin nevus facial y disminución del nivel de consciencia by Lafuente-Hidalgo, M, Pérez Delgado, R, López Pisón, J, Ranz Angulo, R, Monge Galindo, L, Peña Segura, J.L

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Distrofia miotónica. Nuestra experiencia de 18 años en consulta de Neuropediatría by Armendáriz-Cuevas, Y, López-Pisón, J, Calvo-Martín, M.T, Rebage Moisés, V, Peña-Segura, J.L

“…Resumen Introducción La distrofia miotónica es una enfermedad multisistémica autosómica dominante de expresividad variable. Se revisa nuestra experiencia de 18…”
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Hipertensión intracraneal benigna. Experiencia en 18 años by Monge Galindo, L, Pérez Delgado, R, López-Pisón, J, Olloqui-Escalona, A, García Íñiguez, J.P, Ruiz del Olmo Izuzquiza, I, Peña-Segura, J.L

“…Resumen Introducción Hay casos de hipertensión intracraneal (HTIC) transitoria, identificables en lactantes por abombamiento de fontanela y en niños mayores…”
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Síndrome de apnea central del sueño como primera manifestación de malformación de Chiari tipo I by Miralbés Terraza, S, García Oguiza, A, López Pisón, J, Sáenz Moreno, I, Jiménez Escobar, V, Peña Segura, J.L, Marco Rived, A

“…Introducción La malformación de Chiari tipo I consiste en el descenso de las amígdalas cerebelosas a través del foramen magno. Con frecuencia es asintomática,…”
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Déficit de cobalamina hereditario juvenil causado por mutaciones en el gen GIF by GARCIA JIMENEZ, M, BALDELLOU VAZQUEZ, A, MARTIN, M, PEREZ-LUNGMUS, G, LOPEZ PISON, J

“…Los errores congénitos del metabolismo de la cobalamina afectan a su absorción, transporte o metabolismo intracelular. La anemia megaloblástica hereditaria…”
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Prader-Willi and Angelman syndromes: 21 years of experience by Royo Pérez, D, Monge Galindo, L, López Pisón, J, Pérez Delgado, R, Lafuente Hidalgo, M, Peña Segura, J L, Miramar Gallart, M D, Rodriguez Valle, A, Calvo Martín, M T

“…Prader-Willi syndrome (PWS) and Angelman syndrome (AS) were the first syndromes in humans that were known to originate from the phenomenon of the genomic…”
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Prenatal encephalopathies of unknown origin. Our 19-years experience. To what extent must genetic and biochemical studies be carried out? by López Pisón, J, García Jiménez, M C, Lafuente Hidalgo, M, Pérez Delgado, R, Monge Galindo, L, Cabrerizo de Diago, R, Rebage Moisés, V, Peña Segura, J L, Baldellou Vázquez, A

“…We examine those prenatal encephalopathies with clinical or neuroimaging data of encephalopathy before the birth. They affect a significant number of children…”
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Epilepsy with onset between the ages of 3 and 12 months. Our experience gained over a 10-year period by Pérez-Delgado, R, Galve-Pradel, Z, López-Pisón, J, Soria-Marzo, A, García-Oguiza, A, Peña-Segura, J L

“…The prognosis of epilepsy is essentially determined by its aetiology and a poorer prognosis is generally associated with an early onset of the seizures. In…”
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Myotonic dystrophy. 18 years experience in a neuropaediatric clinic by Armendáriz-Cuevas, Y, López-Pisón, J, Calvo-Martín, M T, Moisés, V Rebage, Peña-Segura, J L

“…Myotonic dystrophy is a highly variable autosomic dominant inherited multisystemic disease. We review our 18 years experience with patients suffering from this…”
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