- Patients with sickle cell disease, ranging from nearly asymptomatic to life-threatening
- Patients with different forms of thalassaemia
- Kernicterus in a G6PD deficient female infant
- Acquired alpha thalassaemia and myelodysplastic syndrome
- Paroxysmal nocturnal haemoglobinuria in a G6PD deficient patient
- The first case ever reported of homozygosity for an unstable haemoglobin
- Cases with long-term follow-up spanning decades, demonstrating disease progression, complications and therapeutic outcomes
