Estudio de hemoglobinopatías y del déficit de glucosa-6-fosfato deshidrogenasa en la población inmigrante subsahariana del centro y sur del Maresme (Cataluña)

Las Heras Manso, Germán; Juncà Piera, Jordi; Feliu Frasnedo, Evarist; Rovira Fernández, Joan Manel; García, Miguel Gil.
Med. clín (Ed. impr.) ; 131(1): 5-9, jun. 2008. tab
Artículo en Es | IBECS (España) | ID: ibc-66181

Documentos relacionados

  1. Molecular characterization of G6PD mutations reveals the high frequency of G6PD Aures in the Lao Theung population.
  2. Systematic literature review of the epidemiology of glycogen storage disease type 1a.
  3. Immunological features and complications in patients with glycogen storage disease 1b after living donor liver transplantation.
  4. Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants.
  5. Glycogen storage disease type I patients with hyperlipidemia have no signs of early vascular dysfunction and premature atherosclerosis.
  6. Glycemic control and complications in glycogen storage disease type I: Results from the Swiss registry.
  7. [A case report of glycogen storage disease type 1a].
  8. [Post-transfusion hemolytic reactions in regions endemic for the hereditary glucose-6-phosphate dehydrogenase deficiency].
  9. Assessment of auditory functions in patients with hepatic glycogen storage diseases.
  10. Clinical, pathological and molecular spectrum of patients with glycogen storage diseases in Pakistan.