77 results match your criteria: "Hospital infantil de Cruces[Affiliation]"

Cases of hypomagnesaemia of hereditary renal origin represent at least three different congenital disorders of tubular reabsorption of magnesium (Mg). Isolated familial hypomagnesaemia has been reported in a heterogeneous group of patients and an autosomal dominant pattern of inheritance has often been found to be present. Familial hypokalaemia-hypomagnesaemia, inherited as an autosomal recessive trait, has been reported in 17 patients and we now describe 3 additional cases.

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A study to compare the effects of single oral doses of salbutamol (4 mg) and fenoterol (5 mg) was carried out in 22 asthmatic children aged 6-14 years. The patients received both drugs sequentially on two consecutive days within a week in a randomized, double-blind, crossover fashion. Peak expiratory flow rate, spirometry, flow-volume loops and whole body plethysmography were performed basally, at half-an-hour and hourly from 1 through 6 h.

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