[Cutaneous larva migrans of native origin].
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Antinematodal Agents↗
Biomedical subjects
A Escobar Gallego
Publications and source records attributed to A Escobar Gallego.
[Familial hypercholesterolemia in a homozygote and LDL kinetics].
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Homozygote↗
[Homozygous familial hypercholesterolemia. Response to combined cholestyramine and lovastatin therapy].
Homozygous familiar hypercholesterolemia (FH) is a serious inherited disease caused by a genetic defect in the cell surface receptor that controls the degradation of low density lipoprotein (LDL). These patients often have myocardial infarction in their teens or early adulthood and are usually unresponsive to drugs. Recently it has been reported promising results using combined drugs regimens in patients with residual receptor activity. We report a new additional patient with receptor-defective homozygous FH treated with a combination of lovastatin and cholestyramine. The cholesterol levels were reduced in a 67% and there were adverse events related to treatment during a 7 month period of follow-up.
Child, Preschool↗
[Pseudohypoaldosteronism and obstructive uropathy].
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Humans↗
[Comparative study of human milk and adapted formulas].
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Carbohydrates↗