Results 21 to 30 of about 53,574 (237)
Mapping aplastic anaemia hospital activity in England [PDF]
Bamidele Famokunwa +4 more
doaj +2 more sources
A 24-year-old primiparous woman was booked at 12 weeks' gestation. She had previously been diagnosed with acquired non-severe aplastic anaemia, 7 years previously.
A, Shetty, S Q, Anwar, S, Acharya
openaire +2 more sources
Aplastic anaemia: a review [PDF]
Aplastic anaemia is featured by bone marrow hypocellularity and peripheral pancytopenia and is a potentially fatal disease. In recent years, insight in it pathogenesis has increased.
Lugtenburg, P.J. (Pieternella) +1 more
core +1 more source
Background: Pancytopenia is a clinical outcome of various pathological conditions ranging from bone marrow suppression, bone marrow infiltration, infections, hypersplenism, haemolysis, and haematological malignancies.
Divendu Bhushan +3 more
doaj +1 more source
Neuroborreliosis in patient with aplastic anaemia secondary to therapy with ticlopidine [PDF]
Introduction. Aplastic anaemia is a rare but potentially fatal complication of treatment with ticlopidine. Case Outline. We present a 55-year-old male with aplastic anaemia which developed after 45 days of the therapy with 200 mg ticlopidine to ...
Čolović Milica +4 more
doaj +1 more source
Prevalence of Paroxysmal Nocturnal Haemoglobinuria Clone in Aplastic Anaemia: A Single Centre Study
Background: Flow cytometry assay for PNH clone is a compulsory routine test for all aplastic anaemia patients. Objective: To estimate the frequency of PNH clone in aplastic anaemia.
A. Q. M. Ashraful Haque +9 more
doaj +1 more source
Outcome of aplastic anaemia in children. A study by the severe aplastic anaemia and paediatric disease working parties of the European group blood and bone marrow transplant. [PDF]
This study analysed the outcome of 563 Aplastic Anaemia (AA) children aged 0-12 years reported to the Severe Aplastic Anaemia Working Party database of the European Society for Blood and Marrow Transplantation, according to treatment received.
Dufour, C. +42 more
core +1 more source
APLASTIC ANAEMIA IN CAPRINE FLUOROSIS [PDF]
The present work aimed to study the picture of anemia fllowing caprine fluorosis. The relation of such anemia to iron and copper levels was also discussed.
M.H. KARRAM, A.A. AMER, H.A. IBRAHIM
doaj +1 more source
Cancer incidence in relatives of British Fanconi Anaemia patients. [PDF]
BACKGROUND: Fanconi anemia (FA) is an autosomal recessive DNA repair disorder with affected individuals having a high risk of developing acute myeloid leukaemia and certain solid tumours. Thirteen complementation groups have been identified and the genes
Ball Jan +14 more
core +3 more sources
Using peripheral blood for determining B‐cell or T‐cell clonality is more reliable when we use cell‐free RNA (cfRNA) because cells release blood significantly more RNA than DNA. Next‐generation sequencing (NGS) of cfRNA allows us to evaluate fragment cfRNA and evaluate clonality reliably without the need for prior determination of the specific dominant
Adam Albitar +11 more
wiley +1 more source

