Results 101 to 110 of about 82,322 (154)

A Case Presenting with Acute Kidney Injury and Paroxysmal Nocturnal Hemoglobinuria

Turkish Journal of Nephrology, 2019
There may be different clinical presentations of kidney involvement in the course of paroxysmal nocturnal hemoglobinuria, within a spectrum of acute kidney injury, generally due to hemolysis, to chronic kidney disease.
Ezgi ÇOŞKUN YENİGÜN, Didem TURGUT, Simge BARDAK, Serhan PİŞKİNPAŞA, Nihal ÖZKAYAR, Eyüp KOÇ, Fatih DEDE   +6 more
doaj  

Anticomplement therapy

Biologics: Targets & Therapy, 2009
Prathit A Kulkarni1, Vahid Afshar-Kharghan21Baylor College of Medicine, Houston, Texas, USA; 2The University of Texas, M.D. Anderson Cancer Center, Houston, Texas, USAAbstract: The complement system is an important part of innate immunity; however, as ...
Prathit A Kulkarni, Vahid Afshar-Kharghan   +1 more
doaj  

Reversible renal failure in paroxysmal nocturnal hemoglobinuria.

, 2001
A Chinese patient with paroxysmal nocturnal hemoglobinuria (PNH) developed acute nonoliguric renal failure with intercurrent urinary tract infection and hemolysis. There was no evidence of renal vein thrombosis.
Chow, K. M., Li, P. K., Lai, F. M., Wang, A. Y., Tang, N. L., Chan, Y. L.   +5 more
core  

Paroxysmal nocturnal hemoglobinuria pnh

Hematology, Transfusion and Cell Therapy, 2020
Hanan Hamed
doaj   +1 more source

De novo smoldering paroxysmal nocturnal hemoglobinuria: a flow cytometric diagnosis

Haematologica, 1997
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, G Bautista, JL Steegmann, F Javier Penalver, R Cabrera, MN Fernandez   +5 more
doaj  

Multidisciplinary clinical management of paroxysmal nocturnal hemoglobinuria

, 2015
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare, acquired disease caused by clonal expansion of one or more hematopoietic stem cell (HSC) lines due to a somatic mutation of the phosphatidylinositol glycan anchor (PIG-A) gene located on Xp22.1.
Mete, Nihal Gokmen, Bilgir, Ferda, Bilgir, Oktay, Sahin, Fahri, Gokcay, Figen, Ozkan, Melda Comert, Oruc, Nevin, Sari, Ismail Hakan, Saydam, Güray, Guler, Ayse, Yilmaz, Mumtaz, Gurgun, Alev, Kayikcioglu, Meral, Ceylan, Cengiz   +13 more
core  

Paroxysmal nocturnal hemoglobinuria and eculizumab

Haematologica, 2010
Lucio Luzzatto, Antonio Maria Risitano, Rosario Notaro   +2 more
doaj   +1 more source

Paroxysmal Nocturnal Hemoglobinuria.

Annals of Internal Medicine, 1973
E, Polli, G, Sirchia, S, Ferrone, F, Mercuriali, A, Zanella   +4 more
openaire   +3 more sources

The irreplaceable image: Paroxysmal nocturnal hemoglobinuria

Haematologica, 1999
N Shahab, DC Doll
doaj  

Paroxysmal Nocturnal Hemoglobinuria in Children

Pediatric Drugs, 2007
Paroxysmal nocturnal hemoglobinuria (PNH), an acquired hematologic disorder characterized by intravascular hemolysis, nocturnal hemoglobinuria, thrombotic events, serious infections, and bone marrow failure, is very rare in children. PNH is caused by a somatic mutation of the phosphatidylinositol glycan (GPI) complementation class A (PIGA) gene ...
Heuvel-Eibrink, M.M. (Marry) van den, Van den Heuvel - Eibrink, Marry   +1 more
openaire   +4 more sources