Toward the harmonization of result presentation for the eosin‐5′‐maleimide binding test in the diagnosis of hereditary spherocytosis
Hunt, Linda, Greenwood, David, Heimpel, Hermann, Noel, Nigel, Whiteway, Alastair, King, May‐Jean
Published in Cytometry. Part B, Clinical cytometry (01.01.2015)
Published in Cytometry. Part B, Clinical cytometry (01.01.2015)
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Targeted next generation sequencing identifies a novel β-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis
Al-Riyami, Arwa Z, Iolascon, Achille, Al-Zadjali, Shoaib, Andolfo, Immacolata, Al-Mammari, Sahima, Manna, Francesco, Al Rawas, AbdulHakim, King, May-Jean, Russo, Roberta
Published in American journal of hematology (01.10.2017)
Published in American journal of hematology (01.10.2017)
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Monovalent cation leaks in human red cells caused by single amino-acid substitutions in the transport domain of the band 3 chloride-bicarbonate exchanger, AE1
C Robinson, Hannah, Lutz, Hans U, Harrison, Penny, Ficarella, Romina, King, May-Jean, Gore, Daniel M, Borgese, Franck, Goede, Jeroen S, Bruce, Lesley J, Ellory, J Clive, Guizouarn, Hélène, Stewart, Gordon W, Iolascon, Achille, Layton, D Mark, Coles, Suzanne E
Published in Nature genetics (01.11.2005)
Published in Nature genetics (01.11.2005)
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Using the eosin‐5‐maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis
King, May‐Jean, Telfer, Paul, MacKinnon, Heather, Langabeer, Lisa, McMahon, Corrina, Darbyshire, Philip, Dhermy, Didier
Published in Cytometry. Part B, Clinical cytometry (01.07.2008)
Published in Cytometry. Part B, Clinical cytometry (01.07.2008)
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Phenotype and mRNA Expression of Syncytiotrophoblast Microparticles Isolated from Human Placenta
Kumpel, Belinda, King, May-Jean, Sooranna, Suren, Jackson, Dave, Eastlake, Jane, Cheng, Rong, Johnson, Mark
Published in Annals of the New York Academy of Sciences (01.08.2008)
Published in Annals of the New York Academy of Sciences (01.08.2008)
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The diagnostic challenge of congenital dyserythropoietic anaemia: two cases of ‘CDA type II’
Dukka, Srivasavi, King, May-Jean, Hill, Quentin A
Published in Journal of clinical pathology (01.04.2014)
Published in Journal of clinical pathology (01.04.2014)
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Journal Article
Targeted next generation sequencing identifies a novel [beta]-spectrin gene mutation A2059P in two Omani children with hereditary pyropoikilocytosis
Al-Riyami, Arwa Z, Iolascon, Achille, Al-Zadjali, Shoaib, Andolfo, Immacolata, Al-Mammari, Sahima, Manna, Francesco, Al Rawas, AbdulHakim, King, May-Jean, Russo, Roberta
Published in American journal of hematology (01.10.2017)
Published in American journal of hematology (01.10.2017)
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Journal Article
Two different glycosyltransferase defects that result in GalNAc alpha-O-peptide (Tn) expression
King, M J, Chan, A, Roe, R, Warren, B F, Dell, A, Morris, H R, Bartolo, D C, Durdey, P, Corfield, A P
Published in Glycobiology (Oxford) (01.06.1994)
Published in Glycobiology (Oxford) (01.06.1994)
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Towards the harmonization of result presentation for the eosin-5’- maleimide (EMA) binding test in the diagnosis of hereditary spherocytosis: Feasibility of harmonizing EMA binding results
Hunt, Linda, Greenwood, David, Heimpel, Hermann, Noel, Nigel, Whiteway, Alastair, King, May-Jean
Published in Cytometry. Part B, Clinical cytometry (01.09.2014)
Published in Cytometry. Part B, Clinical cytometry (01.09.2014)
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