Search Results - "Porta Ribera, R"

4CPS-136 Standard first day of life central parenteral nutrition, experience in real clinical practice by Bosch Peligero, M, Ginovart Galiana, G, Arias Martinez, A, Siles Baena, A, Ocaña Rico, M, Porta Ribera, R, Martín Val, A, Laguna Marmol, L, Terricabras Mas, E, Codina Jiménez, C, Quiñones Ribas, C

“…Background and ImportanceStandard parenteral nutrition (PN) solutions should generally be used over individualised PN solutions in the majority of paediatric…”
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Hiperbilirrubinemia neonatal prolongada asociada a una mutación del gen UGT1A1 by de la Fuente Juárez, A, Viñallonga Sardà, X, Capdevila Cogul, E, Porta Ribera, R

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Assessment of parental satisfaction in a neonatal unit by Capdevila Cogul, E, Sánchez Pozón, L, Riba García, M, Moriña Soler, D, Ríos Guillermo, J, Porta Ribera, R, Molina Morales, V

“…Parental satisfaction in a neonatal unit needs to be checked as a quality element in health care. 1/To measure how the severity of the newborn condition…”
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Monitoring neurodevelopment in children born as a result of using assisted reproduction techniques by Porta-Ribera, R, Trèmols, V, Munar-Mut, C, Boada-Palà, M, Ríos-Guillermo, J, Molina-Morales, V

“…In recent years a number of publications have reported a higher incidence of congenital defects or chromosome abnormalities linked to conventional in vitro…”
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Valoración de la satisfacción de los padres en una unidad neonatal by Capdevila Cogul, E, Sánchez Pozón, L, Riba García, M, Moriña Soler, D, Ríos Guillermo, J, Porta Ribera, R, Molina Morales, V

“…Resumen Introducción La satisfacción de los padres en una unidad neonatal (UN) debe ser evaluada como elemento de calidad asistencial. Objetivos 1/Determinar…”
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Prolonged neonatal hyperbilirubinemia associated with a UGT1A1 gene mutation by de la Fuente Juárez, A, Viñallonga Sardà, X, Capdevila Cogul, E, Porta Ribera, R

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Evolución perinatal de los niños nacidos por fecundación in vitro by Porta Ribera, R, Molina Morales, V, Boada Palà, M, Coroleu Lletget, V

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Síndrome de Aicardi-Goutières by de la Fuente Juárez, A, Sánchez Pozón, L, Muñoz Prades, A, Campistol Plana, J, Porta Ribera, R

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Perinatal progress of children born after in vitro fertilization by Ribera, R Porta, Morales, V Molina, Palà, M Boada, Lletget, V Coroleu

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Aicardi-Goutières syndrome by de la Fuente Juárez, A, Sánchez Pozón, L, Muñoz Prades, A, Campistol Plana, J, Porta Ribera, R

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Seguimiento posnatal del feto con pielectasia: un problema no resuelto by Baraibar Castelló, R., Porta Ribera, R.

“…El control posnatal del feto con pielectasia ha sido objeto de controversia en la bibliografía reciente. La definición de pielectasia, la necesidad de estudiar…”
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Postnatal followup of fetal pyelectasis: an unresolved problem by Baraibar Castelló R, Porta Ribera R

“…Postnatal followup of fetal pyelectasis is a controversial topic in recent literature. Questions such as the definition of pyelectasis, whether these neonates…”
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Traqueítis bacteriana por Haemophilus influenzae by Porta Ribera, R., Renom Llonch, M., Moreno Eguilaz, C., Cubells Fuentes, J.M.a, Viñas Doménech, L., Baraibar Castelló, R.

“…Se presenta un caso de traqueítis bacteriana en una niña de 6 años y medio. La forma clínica de presentación fue la de un crup intenso con fiebre alta y…”
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Bacterial tracheitis due to Haemophilus influenzae by Porta Ribera, R, Renom Llonch, M, Moreno Eguilaz, C, Cubells Fuentes, J, Viñas Doménech, L, Baraibar Castelló, R

“…We present a case of bacterial tracheitis in a 6.5 year old girl. Clinical signs and symptoms consisted of severe croup with high grade fever, which were…”
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Renovascular hypertension due to unilateral renal artery stenosis with hypokalemic alkalosis, the salt-losing syndrome and reversible hyperechogenicity of the contralateral kidney. A study of 2 infants by Castelló Girona, F, Yeste Fernández, D, Porta Ribera, R, Enríquez Cívicos, G

“…This report describes two infants with severe arterial hypertension secondary to unilateral renal artery stenosis which was manifested by polyuria, polydipsia,…”
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Prolonged neonatal hyperbilirubinemia associated with a UGT1A1 gene mutation by de la Fuente Juárez, A, Viñallonga Sardà, X, Capdevila Cogul, E, Porta Ribera, R

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Aicardi-Goutières syndrome by de la Fuente Juárez, A, Sánchez Pozón, L, Muñoz Prades, A, Campistol Plana, J, Porta Ribera, R

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