Paroxysmal nocturnal haemoglobinuria. Experience over a 10 years period

Summary Introduction Paroxysmal nocturnal hemoglobinuria (PNH) is a hemolytic, clonal and acquired disorder of the hematopoietic stem cell with a deficiency of all glycophosphatidyl‐inositol (GPI) linked proteins. The aim of this retrospective study was to analyse haematological and biochemical data...

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Veröffentlicht in:	International journal of laboratory hematology 2014-04, Vol.36 (2), p.213-221
Hauptverfasser:	Canalejo, K., Riera Cervantes, N., Felippo, M., Sarandría, C., Aixalá, M.
Format:	Artikel
Sprache:	eng
Schlagworte:	Adolescent Adult Aged Aged, 80 and over Antigens, CD - metabolism Blood Cell Count Case-Control Studies Child Child, Preschool Clonal Evolution Erythrocyte Indices Female Flow Cytometry - methods Follow-Up Studies Hemoglobinuria, Paroxysmal - blood Hemoglobinuria, Paroxysmal - diagnosis hemolytic anemia Humans immunophenotypic analysis Immunophenotyping - methods Male Middle Aged PNH Retrospective Studies Young Adult
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