Hemolysis

Emoglobinuria parossistica a frigore: è davvero così rara?

Esposto MP, Genesini S, Chinello M, Pezzella V, Bonetti E, Zaccaron A, Caddeo G, Vitale V, Guardo C, Cesaro S

2025/9 — pag. 231-235 — DOI

Paroxysmal Cold Haemoglobinuria (PCH) is considered the rarest form of autoimmune haemolytic anaemia (AIHA), although it is likely underdiagnosed. It is caused by biphasic haemolysins, known as Donath-Landsteiner antibodies, which bind to erythrocyte...

Ittero, pallore e urine scure: e se fosse un’anemia emolitica autoimmune?

Tessitore A, Putoto E, Romano F, Verzegnassi F, Barbi E, Cozzi G, Parodi E.

2022/7 — pag. 451-455 — DOI

The haemolytic crisis is a sudden reduction in the half-life of red blood cells. Consequently, it leads to massive destruction of red blood cells (haemolysis), which is more significant than the compensatory capacity of the bone marrow and results in...

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 ...

Alloimmunizzazione post-trasfusionale: terapia immunosoppressiva con rituximab e steroidi in una bambina affetta da drepanocitosi

E. Brivio, A. Cattoni, M. Pasetti

2014/9

Quando l’EBV arriva al fegato

Sara Lega, Martina Tubaro

2014/6

Una trasfusione “di troppo”

F. Sfriso, F. Visentin, G. Biddeci, T. Zangardi, S. Zanconato, S. Scanferla, S. Masiero

2013/10

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...

ß-talassemia (Parte prima)

G. Bartolozzi

2006/1

Un caso di malaria da Plasmodium Falciparum

S. Vaccher, F. Patarino, M. Lazzerini, E. Barbi

2005/5

Iperbilirubinemia neonatale

2001/4