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Alison May

Cardiff University

34

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Legal talk : Socio-pragmatic aspects of legal questioning: police interviews, prosecutorial discourse and trial discourse

2020
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A recurring mutation in the respiratory complex 1 protein NDUFB11 is responsible for a novel form of X-linked sideroblastic anemia

2016 Blood
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Congenital sideroblastic anemia due to mutations in the mitochondrial HSP70 homologue HSPA9

2015 Blood
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EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies

2015 European Journal of Human Genetics
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Much Ado About Sweet Nothing by Alison May New Adult

2015
- Alison May
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X‐linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA‐binding site mutations

2014 American Journal of Hematology
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Mutations in TRNT1 cause congenital sideroblastic anemia with immunodeficiency, fevers, and developmental delay (SIFD)

2014 Blood
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(ALAS2) gene causes X-linked sideroblastic anemia A promoter mutation in the erythroid-specific 5-aminolevulinate synthase

2013
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A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD)

2013 Blood
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Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia

2011 Haematologica
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Citations (46)