Verónica Cantarín Extremera

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3. Ballock RT, Newton PO, Evans SJ, Estabrook M, Farnsworth CL, Bradley JS. A comparison of early versus late conversion from intravenous to oral therapy in the treatment of septic arthritis. J Pediatr Orthop. 2009;29: 636--42. 4. Pääkkönen M, Kallio MJ, Peltola H, Kallio PE. Pediatric septic hip with or without arthrotomy: Retrospective analysis of 62(More)
BACKGROUND CAPOS syndrome (cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss) is a rare disease that has been reported in 22 patients so far. In all cases, the mutation c.2452G>A (p.Glu818Lys) in the ATP1A3 gene was identified. Patients typically present at an early age with an acute-onset fever-induced episode of ataxia(More)
Cystic adenomatoid malformation of the lung is a rare malformation of the lung airway which often performed diagnosed in the prenatal period by ultrasound. Ultrasound monitoring should be performed during pregnancy to assess lung development. We report the case of a 4-year-old patient with prenatal diagnosis of cystic adenomatoid malformation of the lung,(More)
La enfermedad de Von Hippel Lindau (EVHL) es un síndrome tumoral multisistémico, de herencia autosómica dominante y penetrancia incompleta, que afecta a 1/36.000 personas. Se caracteriza por la presencia de hemangioblastomas retinianos o cráneo-espinales y lesiones viscerales (como en páncreas y riñón)1. La aciduria L-2-hidroxiglutárica (L2OHG) es una(More)
actualidad, se ha visto que la neuronectomía timpánica5 es la terapia quirúrgica con mayor efectividad y menor morbilidad siendo la parotidectomía total el último escalón terapéutico. La determinación rutinaria de poblaciones linfocitarias probablemente no resulte justificada ante el carácter benigno de esta patología. Aún así, dado que este es el primer(More)
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