References in periodicals archive ?
Biochemical, pathologic, and clinical aspects of alcaptonuria, ochronosis and ochronotic arthropathy.
A 62-year-old male patient with unknown alcaptonuria was admitted to our institution (Fig.
Biochemical, pathologic and clinical aspects of alcaptonuria, ochronosis, and ochronotic arthropathy.
La conexion entre estos dos personajes se dio gracias al patron hereditario autosomico recesivo de la alcaptonuria. su trabajo en conjunto permitio desarrollar tambien lo que hoy se conoce como la formula de Hardy-Weinberg y la tabla de Punnett.
Other possible culprits include vitamin [B.sub.12] deficiency, malnutrition, alcaptonuria, porphyria, graft-versus-host disease, AIDS, Laugier-Hunziker syndrome, and Peutz-Jeghers syndrome.
His work uncovered alcaptonuria, the first such inborn error.