Fluorescent Aerolysin (FLAER)‐based paroxysmal nocturnal hemoglobinuria (PNH) screening: a single center experience from India
Heterogeneity in the Molecular Pathogenesis of Paroxysmal Nocturnal Hemoglobinuria (PNH) Syndromes and Expansion Mechanism of a PNH Clone
Mutations in the PIG‐A gene causing partial deficiency of GPI‐linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuria
Three Years On: The Role of Pegcetacoplan in Paroxysmal Nocturnal Hemoglobinuria (PNH) since Its Initial Approval
PNH cells are as sensitive to T‐cell‐mediated lysis as their normal counterparts: implications for the pathogenesis of paroxysmal nocturnal haemoglobinuria