Reticuloendothelial phagocytic function in human liver disease and its relationship to haemolysis

Arthropathy in hereditary haemochromatosis segregates with elevated erythrocyte mean corpuscular volume.

Scandinavian journal of rheumatology·2020

Concentrations of transferrin and carbohydrate-deficient transferrin in postmortem human brain from alcoholics.

Addiction biology·2016

Boron based separations for in situ recovery of L-erythrulose from transketolase-catalyzed condensation.

Biotechnology and bioengineering·2008

Patient-focused outcomes following detection in a hospital-based screening programme for C282Y haemochromatosis.

Internal medicine journal·2008

Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis.

Lancet (London, England)·2005

A novel mutation in ferroportin1 is associated with haemochromatosis in a Solomon Islands patient.

Gut·2003

Functional assessment of inherited myeloid neoplasm-associated SAMD9L germline variants via Monoallelic CRISPR modelling.

British journal of haematology·2026

First-line hetrombopag combined with immunosuppressive therapy for paediatric severe aplastic anaemia: A prospective randomized controlled trial.

British journal of haematology·2026

Sickle cell disease and commercial aviation. A retrospective analysis of in-flight and pre-flight medical events.

British journal of haematology·2026

LTB-TREAT: A validated international prognostic model for time to treatment in low tumour burden follicular lymphoma.

British journal of haematology·2026

Autoimmune neutropenia in children: Test cells versus beads and a role for pro-LL-37 and absolute neutrophil count.

British journal of haematology·2026

Real-world outcomes of ide-cel and cilta-cel in relapsed/refractory multiple myeloma: A nationwide, retrospective analysis in Austria.

British journal of haematology·2026

Prognostic Role of Blood Inflammatory Composite Biomarkers in Dvt After Lower Extremity Fractures.

The Iowa orthopaedic journal·2026

Pattern of blood utilization and blood wastage at blood bank of a tertiary care hospital in Lahore.

Pakistan journal of medical sciences·2026

RUNX1-IT1 and AK026392.1 long non-coding RNAs as early predictors of acute graft-versus-host disease following allogeneic hematopoietic stem cell transplantation in acute leukemia.

Caspian journal of internal medicine·2026

Coagulation potential of concomitant factor VIII administration in people with hemophilia A receiving emicizumab prophylaxis (CAGUYAMA study): a multicenter, open-label, nonrandomized clinical trial.

Research and practice in thrombosis and haemostasis·2026

Management and outcomes in patients with cryptogenic stroke and weakly positive antiphospholipid antibodies.

Research and practice in thrombosis and haemostasis·2026

Endoscopic combined intrarenal surgery for staghorn calculus in a horseshoe kidney with double collecting system: A case report.

Urology case reports·2026

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Reticuloendothelial phagocytic function in human liver disease and its relationship to haemolysis

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Arthropathy in hereditary haemochromatosis segregates with elevated erythrocyte mean corpuscular volume.

Concentrations of transferrin and carbohydrate-deficient transferrin in postmortem human brain from alcoholics.

Boron based separations for in situ recovery of L-erythrulose from transketolase-catalyzed condensation.

Patient-focused outcomes following detection in a hospital-based screening programme for C282Y haemochromatosis.

Use of community genetic screening to prevent HFE-associated hereditary haemochromatosis.

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