Results 101 to 110 of about 32,733 (212)
Model-Informed Precision Dosing of Eculizumab in Patients with Paroxysmal Nocturnal Hemoglobinuria.
Contains fulltext : 322381.pdf (Publisher’s version ) (Open Access)BACKGROUND AND OBJECTIVE: Eculizumab is an expensive therapeutic monoclonal antibody inhibiting complement C5 and approved for various indications, including the rare ...
Heuvel, L.P.W.J. van den +5 more
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Key Clinical Message Haploidentical hematopoietic stem cell transplantation (HSCT) with posttransplant cyclophosphamide is an alternative treatment for aplastic anemia–paroxysmal nocturnal hemoglobinuria (PNH) syndrome with poor prognostic factors ...
Kazuki Sakurai +6 more
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© 2021 The Author(s).Paroxysmal nocturnal hemoglobinuria was studied using dual-beam optical tweezers. Force measurements show a moderate change between disease and healthy states.
Soysal, Kaan Batu +6 more
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De novo smoldering paroxysmal nocturnal hemoglobinuria: a flow cytometric diagnosis
An asymptomatic 26-year-old woman with mild macrocytic anemia (11.6 g Hb/dl) was studied. All biochemical parameters, bone marrow histology and cytogenetics were normal. The Ham's and sucrose tests were negative.
R Fores +5 more
doaj
The frequency of HLA class I alleles in Japanese patients with bone marrow failure
The frequencies of the HLA-B*4002 and HLA-A*0206 alleles in patients with aplastic anemia (AA) (n=32; 21.9%) and paroxysmal nocturanl hemoglobinuria (PNH) (n=24; 22.9%), respectively, were significantly different from those in controls (n=371; 8.6 ...
T Shichishima +4 more
doaj
Paroxysmal nocturnal hemoglobinuria and thrombosis
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare acquired clonal hematopoiesis disorder caused by a somatic mutation in the PIGA (phosphatidylinositol glycan, class A) gene, resulting in deficiency of glycosylphosphatidylinositol (GPI)anchored ...
A. R. Khisamieva +12 more
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Paroxysmal Nocturnal Hemoglobinuria: Diagnostic Challenges in Pediatric Patient
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, life-threatening hematologic stem cell disorder characterized by hemoglobinuria, thrombosis, and tendency for bone marrow failure.
Anna Sechser Perl +3 more
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Paroxysmal nocturnal hemoglobinuria is a rare, acquired disease associated with hemolytic anemia, bone marrow failure, thrombosis, and, frequently, poor quality of life.
Khursigara, Gus +12 more
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Acute tubular necrosis in a patient with paroxysmal nocturnal hemoglobinuria
Acute renal failure (ARF) is a well-recognized complication of paroxysmal nocturnal hemoglobinuria (PNH). The predominant mechanism is intravascular hemolysis resulting in massive hemoglobinuria ARF.
Rushika L Lanarolle +3 more
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The immune response dis-regulation and the pathogenesis of hematopoietic disorders [PDF]
Sica, Michela
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