Search Results - "Póo Argüelles, P"

Pitch perception deficits in nonverbal learning disability by Fernández-Prieto, I., Caprile, C., Tinoco-González, D., Ristol-Orriols, B., López-Sala, A., Póo-Argüelles, P., Pons, F., Navarra, J.

“…•Nonverbal learning disability patients present difficulties in spatial reasoning.•Difficulties in categorizing auditory frequencies are observed in NLD…”
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X‐Linked creatine transporter deficiency in two patients with severe mental retardation and autism by Póo‐Argüelles, P., Arias, A., Vilaseca, M. A., Ribes, A., Artuch, R., Sans‐Fito, A., Moreno, A., Jakobs, C., Salomons, G.

“…Summary We describe the first two unrelated Spanish patients with creatine transporter deficiency initially identified by brain proton magnetic resonance…”
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Prematuridad con parálisis cerebral y ceroidolipofuscinosis by Peña-Segura, J.L, Póo Argüelles, P, Lafuente Hidalgo, M, García Sánchez, V, Pérez Delgado, R, Monge Galindo, L, García Jiménez, M.C, Rebage Moisés, V, López Pisón, J

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P20.1 Long term outcome in haemolytic-uraemic syndrome: neurologic symptoms, neuroimaging, motor and neurocognitive performance by Martínez, A. Roche, Argüelles, P. Póo, Cucurella, M. Maristany, Plana, J. Campistol

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Valoración de la calidad de un programa de seguimiento del neurodesarrollo de prematuros de muy bajo peso al nacimiento by Agut Quijano, T, Conde Cuevas, N, Iriondo Sanz, M, Poo Argüelles, P, Ibáñez Fanes, M, Krauel Vidal, X

“…Resumen Introducción Los avances en la perinatología condicionan un aumento del número de recién nacidos de muy bajo peso (RNMBP) (<1.500 g) que sobreviven,…”
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The newborn infant at neurologic risk in the year 2000. Recommendations for the follow-up, incorporation of new instruments by Póo-Argüelles, P, Campistol-Plana, J, Iriondo-Sanz, M

“…Perinatal mortality has dropped markedly in recent years. However, there is still a considerable prevalence of neurological sequelas. Symptoms may present…”
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Prematurity with cerebral palsy and ceroid lipofuscinosis by Peña-Segura, J L, Argüelles, P Póo, Hidalgo, M Lafuente, Sánchez, V García, Delgado, R Pérez, Galindo, L Monge, Jiménez, M C García, Moisés, V Rebage, Pisón, J López

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Quality evaluation of a neuro-development follow-up program of very low birthweight infants by Agut Quijano, T, Conde Cuevas, N, Iriondo Sanz, M, Poo Argüelles, P, Ibáñez Fanes, M, Krauel Vidal, X

“…Advances in perinatology have been associated with improved survival of very low birth weight (VLBW;<1500 g) infants. These children have an increased risk of…”
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Periventricular leukomalacia: its retrospective diagnosis in children with spastic diplegia by Campistol Plana, J, Escofet Soteras, C, Póo Argüelles, P

“…Typical images of residual periventricular leukomalacia (PVL) have been searched for in a review of the CT scans of 135 children with spastic diplegia. Among…”
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Neurological follow-up of very low birth weight newborns at the age of two years (1998-1999) by Arce Casas, A, Iriondo Sanz, M, Krauel Vidal, J, Jiménez González, R, Campistol Plana, J, Poo Argüelles, P, Ibáñez, M

“…Because of improved obstetric and neonatal care, there is growing interest in the later outcome of very low birth weight newborns. The aim of this study was to…”
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Prematurity with cerebral palsy and ceroid lipofuscinosis by Peña-Segura, J L, Argüelles, P Póo, Hidalgo, M Lafuente, Sánchez, V García, Delgado, R Pérez, Galindo, L Monge, Jiménez, M C García, Moisés, V Rebage, Pisón, J López

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Seguimiento neurológico de recién nacidos menores de 1.500 gramos a los dos años de edad by Arce Casas, A., Iriondo Sanz, M., Krauel Vidal, J., Jiménez González, R., Campistol Plana, J., Poo Argüelles, P., Ibáñez, M.

“…Existe un interés creciente en el seguimiento de los recién nacidos de muy bajo peso al nacimiento con la mejoría de la asistencia obstétrica y neonatal…”
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Rabdomiólisis por varicela by Rodríguez Ferrán, L., Vernet Bori, A., Poo Argüelles, P., Fernández Álvarez, E., García Calatayud, J.

“…La primoinfección por virus de la varicela-zoster (VVZ) es muy frecuente durante la infancia y en pocos casos cursa con complicaciones. Las más frecuentes son…”
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Botulinum toxin in the treatment of spasticity in HIV-infected children affected with progressive encephalopathy by Noguera, Antoni, Perez-Duenas, Belen, Fortuny, Claudia, Lopez-Casas, Jesus, Poo-Arguelles, Pilar

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Varicella induced rhabdomyolysis by Rodríguez Ferrán, L, Vernet Bori, A, Poo Argüelles, P, Fernández Alvarez, E, García Calatayud, J

“…Primary varicella-zoster infection is very common during childhood and few patients develop complications. The most frequent complications are bacterial…”
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Embryonic pathology caused by maternal phenylketonuria. A cause of underdiagnosed mental retardation. A report of 8 cases by Campistol Plana, J, Arellano Pedrola, M, Poo Argüelles, P, Escofet Sotera, C, Pérez Olarte, P, Vilaseca Buscà, M A

“…Maternal phenylketonuria (MPKU) is characterized by intrauterine growth retardation, microcephaly, congenital malformations (mainly cardiac defects),…”
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Severe and mild forms of nemaline myopathy: a report of three cases by Colomer Oferil, J, López-Castillo, J, Poo Argüelles, P, Vila Torres, J, Fernández-Alvarez, E

“…Three new cases of two different forms of congenital nemaline myopathy are reported. Two of them represent a severe neonatal form. These cases were presented…”
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Peripheral neuropathy as a presenting form of Cockayne syndrome by Campistol Plana, J, Riverola de Veciana, A, Poo Argüelles, P, Colomer Oferil, J, Moreno Hernández, J

“…We report a clinical observation of an infant aged 5 months with Cockayne syndrome whose symptomatology included failure to thrive, microcephaly, peripheral…”
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Multicystic encephalomalacia in twin pregnancies by Sans Fito, A, Campistol Plana, J, Poo Argüelles, P, Krauel Vidal, J

“…Multicystic encephalomalacia (ME) is a rare entity in the pediatric age. In ME brain tissue in substituted by cavities of variable size. ME has different…”
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Metachromatic leukodystrophy. Late juvenile form. Review of 6 cases by Campistol Plana, J, Colomer Orefil, J, Poo Argüelles, P, Vernet Bori, A, Fernández Alvarez, E

“…Six cases of late infantile metachromatic leucodystrophy are presented. Behavioral changes and walking disturbances are the initial symptoms which tend to…”
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