Results 81 to 90 of about 86,213 (145)

Additional GPI-anchored glycoproteins on human platelets that are absent or deficient in paroxysmal nocturnal haemoglobinuria [PDF]

, 1993
In order to detect novel glycophosphatidylinositol (GPI)-anchored platelet proteins, human platelets were incubated with PI-specific phospholipase C (PI-PLC) and the supernatant was analysed by PAGE and silver-staining for additional protein bands.
Kenneth J. Clemetson, János Polgár, Daniela Gengenbacher, Polgár, János, Jeannine M. Clemetson, Clemetson, Kenneth J., Clemetson, Jeannine M., Gengenbacher, Daniela   +7 more
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Some observations in paroxysmal nocturnal haemglobinuraria and myelofibrosis [PDF]

, 1983
This thesis deals with some clinical and laboratory aspects o f two haematological disorders,namely paroxysmal nocturnal haemoglobinuria( PNH) and primary myelofibrosis (PMF).
Vellenga, Edo,, Vellenga, Edo
core  

An interesting case of atypical venous thrombosis with low red blood cells

Italian Journal of Medicine, 2019
Sex: F Age: 65 years. Recent abdominal colic. Petechial-like manifestations with painful discolored skin lesions (suggestive of dermal veins thromboses) on the chest and abdomen.
Giuseppe Chiariello, Raimondo Cavallaro, Giuseppe Covetti, Maria Carla Attilia Pisano, Antonella Schettini, Tiziana D'Aniello, Rossella Nappo, Emilio Aliberti, Arcangelo Iannuzzi   +8 more
doaj  

Lymphocyte characteristics and function in paroxysmal nocturnal haemoglobinuria

, 1983
In six patients with paroxysmal nocturnal haemoglobinuria (PNH) lymphocyte studies were performed to investigate whether the observed immunological dysfunction could be ascribed to a defect in lymphocytes as result of the PNH characteristics, or to an ...
E. Vellenga, M. R. Halie, C. G. M. Kallenberg, KALLENBERG, CGM, G. J. Ensing, Halie, MR, N. H. Mulder, Nieweg, HO, Vellenga, E, Ensing, GJ, Mulder, NH, T. H. The, The, TH, H. O. Nieweg   +13 more
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Consensus recommendations for optimising the diagnosis and treatment of paroxysmal nocturnal haemoglobinuria in Singapore

Annals, Academy of Medicine, Singapore
Introduction: Paroxysmal nocturnal haemoglobinuria (PNH) is a rare haematologic disease characterised by intravascular haemolysis, thrombophilia and bone marrow failure.
Yeow Tee Goh, Eng Soo Yap, Chuen Wen Tan, Daryl Tan, Yvonne Su Ming Loh, Yuh Shan Lee, Lip Leong Chong, Zi Yi Lim, Hein Than   +8 more
doaj   +1 more source

Trisomy 8 in a patient who responded to therapy with all-trans-retinoic acid and developed paroxysmal nocturnal haemoglobinuria

, 1997
Trisomy 8 is the most common numerical chromosomal abnormality in myelodysplastic syndromes (MDS). Paroxysmal nocturnal haemoglobinuria (PNH) is an aquired haemolytic anaemia, clonal in nature, due to somatic mutation. PNH may evolve to aplastic anaemia,
Meletis, J, Stavroyianni, N, Viniou, N, Yataganas, X, Michali, E, Andreopoulos, A, Vaiopoulos, G, Loukopoulos, D   +7 more
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The pathophysiology of paroxysmal nocturnal hemoglobinuria and treatment with eculizumab

, 2009
Richard Kelly1, Stephen Richards1, Peter Hillmen1, Anita Hill21Institute of Oncology, St. James’s University Hospital, Leeds, UK; 2Department of Haematology, Bradford Teaching Hospitals NHS Foundation Trust, Bradford, UKAbstract: Paroxysmal ...
Stephen Richards, Peter Hillmen, et al, Richard Kelly   +3 more
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A case report of CD4− CD8+ CD56− TCRγδ+ T-large granular lymphocytic leukaemia with severe aplastic anemia and a PNH clone

Annals of Hematology
T-large granular lymphocytic leukemia (T-LGLL) is a rare, indolent lymphoproliferative disorder of lymphocytes. Clonal expansion of T cells, driven by dysregulation of Fas-mediated apoptosis following activation, is a hallmark of this disease.
Yufei Du, Jinling Zhang, Shengyu Jin
doaj   +1 more source

Correction to: Pegcetacoplan: A Review in Paroxysmal Nocturnal Haemoglobinuria. [PDF]

Drugs, 2023
Heo YA.
europepmc   +1 more source

The immune response dis-regulation and the pathogenesis of hematopoietic disorders [PDF]

, 2008
Sica, Michela
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