Rivista di formazione e aggiornamento professionale del pediatra e del medico di base, fondata nel 1982. In collaborazione con l'Associazione Culturale Pediatri.
Login Abbonamenti Pubblicazioni Carrello Registrazione Perché registrarsi? Contatti

Anaemia emolitica

2 articoli — 2011-2015

EL Caso contributivo
Quando la sferocitosi incontra il chirurgo

C. Bibalo

2015/6

Summary Hereditary spherocytosis is a common inherited disorder that is characterized by anaemia, jaundice and splenomegaly. It is reported worldwide and is the most common inherited anaemia in individuals of northern European ancestry. Clinical ...

RI Problemi speciali
Il deficit di glucosio-6-fosfato deidrogenasi

M. Bramuzzo, S. Lega, I. Bruno

2011/10 — pag. 648-652

Glucose-6-phosphate dehydrogenase (G6PD) deficiency is an X-linked inherited disorder and it is the most common enzymatic defect in the world. G6PD is an enzyme involved in the genesis of NADPH which preserves the cells from oxidative stress. G6PD de...

Argomenti correlati
Neonatal Screening (123) Anemia (83) Splenomegaly (54) Jaundice, Neonatal (51) Neonatal jaundice (42) Ittero neonatale (39) Splenomegalia (36) Screening (31) Jaundice (30) Anemia emolitica (30) Anemia, Hemolytic (28) Splenectomy (19) Hemolysis (14) Spherocytosis, Hereditary (13) Splenectomia (12) Cholelithiasis (12) Oxidative Stress (11) Sferocitosi ereditaria (11) Hereditary spherocytosis (11) Glucosephosphate Dehydrogenase Deficiency (10)