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Paroxysmal nocturnal hemoglobinuria

Known as: Hemoglobinuria, Paroxysmal Nocturnal, Nocturnal Paroxysmal Hemoglobinuria, PNH 
A rare disorder in which red blood cells are easily destroyed by certain immune system proteins. Symptoms include blood clots, and red or brownish… 
National Institutes of Health

Related topics

Related topics

8 relations
Cold paroxysmal hemoglobinuriaHematopoietic and Lymphoid CellHematopoietic and Lymphoid TissuePAROXYSMAL NOCTURNAL HEMOGLOBINURIA 1

Broader (2)

HemoglobinuriaHemoglobinuria, Paroxysmal

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2008
Highly Cited
2008
Long-term follow-up after radiofrequency catheter ablation for atrial fibrillation.
AIMS Data on long-term follow-up of patients who have undergone catheter ablation for atrial fibrillation (AF) are very limited… 
Highly Cited
2003
Highly Cited
2003
Sleep Organization in Children With Partial Refractory Epilepsy
Although it is currently known that sleep can influence epilepsy and epilepsy can influence sleep organization, few data have… 
Highly Cited
2000
Highly Cited
2000
Impaired growth and elevated fas receptor expression in PIGA(+) stem cells in primary paroxysmal nocturnal hemoglobinuria.
The genetic defect underlying paroxysmal nocturnal hemoglobinuria (PNH) has been shown to reside in PIGA, a gene that encodes an… 
Highly Cited
1995
Highly Cited
1995
Immunophenotypic analysis of reticulocytes in paroxysmal nocturnal hemoglobinuria.
The hematologic disorder paroxysmal nocturnal hemoglobinuria (PNH) occurs following an acquired somatic mutation in the Piga gene… 
Highly Cited
1995
Highly Cited
1995
Heterogeneous PIG-A mutations in different cell lineages in paroxysmal nocturnal hemoglobinuria.
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired clonal defect of hematopoietic stem cells in which affected cells are… 
Highly Cited
1994
Highly Cited
1994
Flow cytometric measurement of glycosylphosphatidyl-inositol-linked surface proteins on blood cells of patients with paroxysmal nocturnal hemoglobinuria.
Paroxysmal nocturnal hemoglobinuria (PNH) is an acquired disorder of hematopoiesis in which affected cells are deficient in… 
1991
1991
Assembly and deacetylation of N-acetylglucosaminyl-plasmanylinositol in normal and affected paroxysmal nocturnal hemoglobinuria cells.
Decay-accelerating factor (DAF) is anchored in cell membranes by a glycosyl-plasmanylinositol (GPI) moiety that is transferred to… 
Highly Cited
1985
Highly Cited
1985
Disease-associated loss of erythrocyte complement receptors (CR1, C3b receptors) in patients with systemic lupus erythematosus and other diseases involving autoantibodies and/or complement activation…
Although surface membrane density of complement receptor type one (CR1) on erythrocytes (E) is probably an inherited trait among… 
1985
1985
Bone marrow transplantation for paroxysmal nocturnal hemoglobinuria: eradication of the PNH clone and documentation of complete lymphohematopoietic engraftment
Paroxysmal nocturnal hemoglobinuria (PNH) involves the proliferation of an abnormal and possibly premalignant hematopoietic stem… 
Highly Cited
1965
Highly Cited
1965
THE ACTION OF TWO SULFHYDRYL COMPOUNDS ON NORMAL HUMAN RED CELLS. RELATIONSHIP TO RED CELLS OF PAROXYSMAL NOCTURNAL HEMOGLOBINURIA.
In the paper by G. Sirchia, S. Ferrone and F. Mercuriali: "The Action of Two Sulfhydryl Compounds on Normal Human Red Cells… 
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