Search Results - "Fitzsimons, Edward"
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Investigation and management of a raised serum ferritin
Published in British journal of haematology (01-05-2018)“…Summary Serum ferritin level is one of the most commonly requested investigations in both primary and secondary care. Whilst low serum ferritin levels…”
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2
Diagnosis and therapy of genetic haemochromatosis (review and 2017 update)
Published in British journal of haematology (01-05-2018)Get full text
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3
Serum ferritin values in primary care: are high values overlooked?
Published in Journal of clinical pathology (01-12-2010)“…To examine serum ferritin values in iron-replete patients in primary care and determine the action taken on those patients with very high values (>1000 μg/l)…”
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4
Improved detection of hereditary haemochromatosis
Published in Journal of clinical pathology (01-03-2015)“…There is high prevalence of hereditary haemochromatosis (HH) in North European populations, yet the diagnosis is often delayed or missed in primary care…”
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5
The management of pregnancy in paroxysmal nocturnal haemoglobinuria on long term eculizumab
Published in British journal of haematology (01-05-2010)“…Summary In Paroxysmal nocturnal haemoglobinuria (PNH), pregnancy is associated with increased maternal and foetal complications to such an extent that the…”
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Glasgow rangers lymphadenopathy
Published in British journal of haematology (01-03-2011)Get full text
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7
The chronic anaemia of rheumatoid arthritis: iron banking or blocking?
Published in The Lancet (British edition) (30-11-2002)“…Mysteries still remain regarding anaemia of chronic disease in rheumatoid arthritis. In particular, what is the explanation for the abnormalities of iron…”
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New horizons in iron deficiency anaemia in older adults
Published in Age and ageing (27-04-2020)“…Abstract Iron deficiency anaemia (IDA) is common in older adults and associated with a range of adverse outcomes. Differentiating iron deficiency from other…”
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Recurrence of allergic bronchopulmonary aspergillosis in the posttransplant lungs of a cystic fibrosis patient
Published in Chest (01-07-1997)“…Cystic fibrosis (CF) is an autosomal recessive disease of exocrine origin. Allergic bronchopulmonary aspergillosis (ABPA) is an immunologic disorder caused by…”
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Erythroblast iron metabolism in sideroblastic and sideropenic states
Published in Hematology (Luxembourg) (2002)“…Iron appears to exert self-regulatory control over erythroblast iron uptake, iron storage and its incorporation into haem. It does this via iron regulatory…”
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Incidental lymphocytosis. Cancer targets not as rational as testing
Published in BMJ (Online) (15-07-2009)Get full text
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12
The molecular basis of the sideroblastic anemias
Published in Current opinion in hematology (1996)“…The sideroblastic anemias display remarkable clinical and hematologic heterogeneity but share in common mitochondrial iron loading as evidence of unhinging…”
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13
Malignant and corticosteroid-dependent idiopathic anaphylaxis: successful responses to ketotifen
Published in Annals of allergy, asthma, & immunology (01-08-1997)“…Malignant idiopathic anaphylaxis refers to the most severe form of idiopathic anaphylaxis where defined episodes of idiopathic anaphylaxis are not controlled…”
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Erythroblast iron metabolism and serum soluble transferrin receptor values in the anemia of rheumatoid arthritis
Published in Arthritis and rheumatism (15-04-2002)“…Objectives We have investigated in vitro erythroblast iron metabolism in the anemia of rheumatoid arthritis (RA). We also have examined the results in relation…”
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Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation
Published in Blood (01-11-2000)“…The human protein ABC7 belongs to the adenosine triphosphate-binding cassette transporter superfamily, and its yeast orthologue, Atm1p, plays a central role in…”
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16
Development of a Laboratory Pathway to Assist the Diagnosis of Hereditary Haemochromatosis in Primary Care
Published in Blood (16-11-2012)“…Abstract 994 Hereditary Haemochromatosis (HH) is a common, treatable condition. It is autosomal recessive and usually associated with the C282Y mutation in the…”
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Human ABC7 transporter: gene structure and mutation causing X-linked sideroblastic anemia with ataxia with disruption of cytosolic iron-sulfur protein maturation
Published in Blood (01-11-2000)“…The human protein ABC7 belongs to the adenosine triphosphate-binding cassette transporter superfamily, and its yeast orthologue, Atm1p, plays a central role in…”
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18
Cancer targets not as rational as testing
Published in BMJ (Online) (18-07-2009)Get full text
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19
Open-label, Randomized Study of Pegfilgrastim vs. Daily Filgrastim as an Adjunct to Chemotherapy in Elderly Patients with Non-Hodgkin's Lymphoma
Published in Leukemia & lymphoma (01-09-2003)“…Pegfilgrastim is composed of the protein filgrastim to which a 20-kDa polyethylene glycol (PEG) is covalently bound at the N-terminal residue resulting in…”
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20
G. w. f hegel and the myth of total cinematic genius
Published 01-01-2012“…Since the early 1950s the concept of the individual cinematic genius has been widely accepted as a legitimate status of the successful auteur, and its most…”
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