Results 31 to 40 of about 22,402 (256)

Clinical and epidemiological features of paroxysmal cold hemoglobinuria: a systematic review

open access: yesBlood Advances, 2023
Key Points • Among 230 reported cases, contemporary PCH has a median onset age of 5 years with no sex predilection.• PCH is associated with significant variability in DAT results, necessitating high clinical suspicion and DL testing.
J. Jacobs   +5 more
semanticscholar   +1 more source

A mutation in a functional Sp1 binding site of the telomerase RNA gene (hTERC) promoter in a patient with Paroxysmal Nocturnal Haemoglobinuria [PDF]

open access: yes, 2004
Background<br/><br/> Mutations in the gene coding for the RNA component of telomerase, hTERC, have been found in autosomal dominant dyskeratosis congenita (DC) and aplastic anemia.
Ulku, B.   +47 more
core   +2 more sources

Drowning Hemoglobinuria [PDF]

open access: yesBlood, 1953
Abstract 1. A case of hemoglobinemia and hemoglobinuria with recovery following incomplete drowning is presented. 2. The pathogenesis of the intravascular hemolysis is discussed.
openaire   +2 more sources

Long‐term safety and efficacy of ravulizumab in patients with paroxysmal nocturnal hemoglobinuria: 2‐year results from two pivotal phase 3 studies

open access: yesEuropean Journal of Haematology, 2022
The complement component 5 (C5) inhibitor ravulizumab demonstrated non‐inferiority to eculizumab following 26 weeks of treatment in complement inhibitor‐naïve and complement inhibitor‐experienced patients with paroxysmal nocturnal hemoglobinuria (PNH ...
A. Kulasekararaj   +10 more
semanticscholar   +1 more source

Consensus statement for diagnosis and treatment of paroxysmal nocturnal haemoglobinuria

open access: yesHematology, Transfusion and Cell Therapy, 2021
Paroxysmal nocturnal hemoglobinuria is a chronic, multi-systemic, progressive and life-threatening disease characterized by intravascular hemolysis, thrombotic events, serious infections and bone marrow failure.
Rodolfo D. Cançado   +8 more
doaj   +1 more source

The complement alternative pathway in paroxysmal nocturnal hemoglobinuria: From a pathogenic mechanism to a therapeutic target

open access: yesImmunological Reviews, 2022
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare clonal, not malignant, hematological disease characterized by intravascular hemolysis, thrombophilia and bone marrow failure.
A. Risitano   +3 more
semanticscholar   +1 more source

Spontaneous poisoning of cattle by onion (Allium cepa) in Brazil [PDF]

open access: yesPesquisa Veterinária Brasileira
: The state of Santa Catarina is the largest national producer of onions. The consumption of onion (Allium cepa) by domestic animals can cause hemolytic anemia and hyperhemoglobinemia of Heinz bodies in erythrocytes.
Gustavo Felipe G.P. Hugen   +7 more
doaj   +1 more source

Hemoglobinemia and Hemoglobinuria [PDF]

open access: yesThe American Journal of the Medical Sciences, 1912
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openaire   +2 more sources

Inhibition of C3 with pegcetacoplan results in normalization of hemolysis markers in paroxysmal nocturnal hemoglobinuria

open access: yesAnnals of Hematology, 2022
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired hematologic disorder characterized by complement-mediated hemolysis. C5 inhibitors (eculizumab/ravulizumab) control intravascular hemolysis but do not prevent residual extravascular hemolysis.
R. Wong   +16 more
semanticscholar   +1 more source

Exertional Hemoglobinuria

open access: yesThe Tohoku Journal of Experimental Medicine, 1975
A 16 years old boy had a typical exertional hemoglobinuria after walking with his new leather shoes on. The attacks of hemoglobinuria were associated with the appearance of an unstable hemoglobin in red cells. A slightly decreased fragility curve by 24 hr incubated red cells, the increase of autohemolysis and the appearance of heat labile hemoglobin ...
OHNO, YASUHICO   +6 more
openaire   +3 more sources

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