E Sáez Pérez

Publications (7)0 Total impact

• Article: [Alloimmune neonatal neutropenia. Treatment with granulocyte colony- stimulating factor].

  P Cedena Romero, M Muro Brussi, L García Alonso, E Muñiz Díaz, L Cabanillas Vilaplana, E Sáez Pérez
  Anales espanoles de pediatria 12/1996; 45(5):536-8.
• Article: [Pseudohypoaldosteronism in a premature newborn infant].

  M J González González, M Muro Brussi, J Sarria Osés, L Cabanillas Vilaplana, F Uribarri Zarranz, E Sáez Pérez
  Anales espanoles de pediatria 06/1996; 44(5):517-9.
• Source

  Available from: José Martínez-Orgado

  Article: [Genital prolapse in a newborn infant].

  M R Vega Vega, E Fernández García, J Martínez Orgado, E Sáez Pérez, J García Aparicio, C Romeo Martínez
  Anales espanoles de pediatria 02/1993; 38(1):77-8.
• Article: [Prediction of complications in children of hypertensive mothers].

  J Martínez Orgado, E Sáez Pérez, J García Aparicio
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  ABSTRACT: The hypertensive disorders of pregnancy are a frequent cause of neonatal morbidity and mortality. 259 newborns of hypertensive women were study to establish the relationship between some maternal findings and the subsequent neonatal complications. The severity, early onset of hypertension, proteinuria and the gestation of 32 week or less, are related with special risk of small-for-date, anoxia, seizures and neutropenia. Preeclampsia was related with foetus more compromised. Also hyperuricemia, thrombocytopenia and cesarean section were light predictors of neonatal trouble. These findings can orientate the neonatologist to select the newborns prone to complications, watching them closely to start the treatment, if necessary, as soon as possible.
  Anales espanoles de pediatria 11/1991; 35(4):233-7.
• Article: [Choreoathetosis induced by diphenylhydantoin in and infant with CHARGE syndrome].

  J Martínez Orgado, J García Aparicio, L Cabanillas Vilaplana, E Sáez Pérez
  Anales espanoles de pediatria 11/1990; 33(4):384-6.
• Article: [Neonatal lactic acidosis caused by severe pyruvate carboxylase deficiency].

  B Merinero Cortés, J del Valle Martínez, C Pérez-Cerdá Silvestre, M J García Muñoz, M T Cortés Coto, J García Aparicio, E Sáez Pérez, M Ugarte Pérez
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  ABSTRACT: A new patient with neonatal lactic acidosis due to pyruvate carboxylase deficiency is described. Since birth he developed vomiting, hypothermia, lethargy, irritability, hypoglycemia and severe metabolic acidosis. During admission a progressive deterioration was observed. Despite different attempted therapies patient died at 4 1/2 months of age. High levels of plasma and urine lactate and pyruvate were detected. Enzymatic studies in cultures skin fibroblasts and postmortem tissues showed a severe deficiency of pyruvate carboxylase.
  Anales espanoles de pediatria 08/1988; 29(1):57-60.
• Article: [3 patients with maple syrup urine disease].

  B Merinero, J A del Valle, M J García, M J García Miguel, M I Barrio, J García Hortelano, E Morales, F González, J García Aparicio, E Sáez Pérez
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  ABSTRACT: Clinical manifestations, biochemistry and treatment of three patients with the inherited alteration of the so called maple syrup urine disease are presented. Diagnosis was based upon both detection of high concentrations of leucine, isoleucine, valine and their corresponding alpha-ketoacids in plasma and urine, and existence of a peculiar odor as well as an intense, progressive, neurological alteration. Considering the early onset of clinical symptoms, low protein tolerance and very reduced rate of leucine decarboxylation in cultured fibroblasts, the three patients exhibited grade I, classical type of this disease. None of them responded favorably to suprapharmacological doses of thiamine. Treatment of the patients is discussed and compared with that recommended in the literature.
  Anales espanoles de pediatria 12/1983; 19(5):393-400.