Haemochromatosis: a gene at last?

Increased leaf area index and efficiency drive enhanced production under elevated atmospheric [CO2 ] in a pine-dominated stand showing no progressive nitrogen limitation.

Global change biology·2024

Comment on "Mycorrhizal association as a primary control of the CO2 fertilization effect".

Science (New York, N.Y.)·2017

CD44 as a Potential Screening Marker for Preliminary Differentiation Between Congenital Dyserythropoietic Anemia Type II and Hereditary Spherocytosis.

Cytometry. Part B, Clinical cytometry·2016

The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis.

Genes and immunity·2015

Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2).

Annals of the rheumatic diseases·2014

Phase-contrast and magnification radiography at diagnostic X-ray energies using a pseudo-microfocus X-ray source.

The British journal of radiology·2014

CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.

Journal of medical genetics·2026

The British Society for Genetic Medicine guidance on managing incidental findings identified during rare disease genomic testing.

Journal of medical genetics·2026

Enrichment of an Ehlers-Danlos-like phenotype in women with the FMR1 premutation: a pilot study.

Journal of medical genetics·2026

Everolimus for the treatment of neuropsychological deficits in tuberous sclerosis complex: findings from the TRON multicentre randomised controlled trial.

Journal of medical genetics·2026

Single-cell transcriptomics identifies neural fate disruption and glial reprogramming caused by RARS2 deficiency.

Journal of medical genetics·2026

Unified genetic risk score for prostate cancer enables improved risk stratification for clinical decision-making.

Journal of medical genetics·2026

Early red blood cell transfusion burden, hemoglobin at first transfusion, and in-hospital mortality in patients supported with veno-arterial ECMO: a multicenter cohort study.

Annals of intensive care·2026

Large saccular aneurysms of the vertebrobasilar arteries with segmental chronic mural ectasia: A case report and review of management strategies.

Qatar medical journal·2026

Red blood cell subpopulation ratios identify samples at risk of dipstick-flow cytometry hematuria discordance in Sysmex UN-Series analyzers.

Practical laboratory medicine·2026

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Haemochromatosis: a gene at last?

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Increased leaf area index and efficiency drive enhanced production under elevated atmospheric [CO2 ] in a pine-dominated stand showing no progressive nitrogen limitation.

Comment on "Mycorrhizal association as a primary control of the CO2 fertilization effect".

CD44 as a Potential Screening Marker for Preliminary Differentiation Between Congenital Dyserythropoietic Anemia Type II and Hereditary Spherocytosis.

The genetic associations of acute anterior uveitis and their overlap with the genetics of ankylosing spondylitis.

Ankylosing spondylitis is associated with the anthrax toxin receptor 2 gene (ANTXR2).

Phase-contrast and magnification radiography at diagnostic X-ray energies using a pseudo-microfocus X-ray source.

CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.

The British Society for Genetic Medicine guidance on managing incidental findings identified during rare disease genomic testing.

Enrichment of an Ehlers-Danlos-like phenotype in women with the FMR1 premutation: a pilot study.

Everolimus for the treatment of neuropsychological deficits in tuberous sclerosis complex: findings from the TRON multicentre randomised controlled trial.

Single-cell transcriptomics identifies neural fate disruption and glial reprogramming caused by RARS2 deficiency.

Unified genetic risk score for prostate cancer enables improved risk stratification for clinical decision-making.

Early red blood cell transfusion burden, hemoglobin at first transfusion, and in-hospital mortality in patients supported with veno-arterial ECMO: a multicenter cohort study.

Large saccular aneurysms of the vertebrobasilar arteries with segmental chronic mural ectasia: A case report and review of management strategies.

Red blood cell subpopulation ratios identify samples at risk of dipstick-flow cytometry hematuria discordance in Sysmex UN-Series analyzers.

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Haemochromatosis: a gene at last?

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