| LC control no. | sh 99004283 |
|---|---|
| LC classification | RC641.7.P37 |
| Topical heading | Paroxysmal hemoglobinuria |
| Variant(s) | Marchiafava-Micheli syndrome Paroxysmal cold hemoglobinuria Paroxysmal nocturnal hemoglobinuria |
| See also | Hemoglobinuria Myelodysplastic syndromes |
| Found in | Work cat.: 99-34956: Biro, D. One hundred days, 2000. MESH (Hemoglobinuria, Paroxysmal; also called paroxysmal nocturnal hemoglobinuria; x Marchiafava-Micheli syndrome) United States Health Information Network, June 2, 1999 (PNH ... somatic mutation ... X chromosome ... stem cell) On-line med. dict., June 2, 1999 (Paroxysmal cold hemoglobinuria) Purow, D.B. "Genetic instability and the etiology of somatic PIG-A mutations in paroxysmal nocturnal hemoglobinuria." Blood Cells, Molecules, & Disease: vol. 25 (5), p. 79-89 (PNH is a hematologic disorder characterized by acquired PIG-A gene mutations that lead to defective bioassembly of glycosylphosatidlyinositol (GPI) anchors and the absence of GPI-linked surface proteins) |
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