• Publications
  • Influence
[Molecular analysis of glucose-6-dehydrogenase deficiency in Spain].
PURPOSE G6PD deficiency is the most frequent enzymopathy-producing genetic polymorphism in humans. Up to now, over 400 putative variants of G6PD have been distinguished on the basis of biochemicalExpand
  • 15
  • 1
Increase of enzyme activities following the in vitro peroxidation of normal human red blood cells.
Red blood cells (RBCs) from 15 normal human blood samples were incubated with different concentrations of hydrogen peroxide in sodium azide, and the effects of the peroxidation on several glycolyticExpand
  • 19
  • 1
Effects of a fish oil enriched diet on aspirin intolerant asthmatic patients: a pilot study.
The effect of a fish oil enriched diet containing about 3 g of eicosapentaenoic acid was studied in 10 patients with aspirin intolerant asthma. Subjects were studied during six weeks on a controlExpand
  • 62
Severe-glucose-6-phosphate dehydrogenase (G6PD) deficiency associated with chronic hemolytic anemia, granulocyte dysfunction, and increased susceptibility to infections: description of a new
Molecular, kinetic, and functional studies were carried out on erythrocytes and leukocytes in a Spanish male with G6PD deficiency, congenital nonspherocytic hemolytic anemia (CNSHA), and increasedExpand
  • 67
  • PDF
Pyrimidine 5′nucleotidase and several other red cell enzyme activities in β‐thalassaemia trait
Summary. The activity of 18 red blood cell (RBC) enzymes and reduced glutathione (GSH) content were measured in 70 normal subjects, in 50 heterozygous β‐thalassaemia carriers and in 50Expand
  • 20
A new approach to Hmb-backbone protection of peptides: Synthesis and reactivity of Nα-Fmoc-Nα-(Hmb)amino acids
Abstract The use of N -Fmoc- N -(Hmb)amino acids for the introduction of the Hmb backbone protection into peptides during solid-phase synthesis is described. An efficient two step synthesis of theseExpand
  • 25
Rapid detection of Spanish (delta beta)zero-thalassemia deletion by polymerase chain reaction.
delta beta-Thalassemia and hereditary persistence of fetal hemoglobin (HPFH) are inherited disorders characterized by the persistent synthesis of fetal hemoglobin (HbF) during adult life. The SpanishExpand
  • 16