Simultaneous measurement of ATP release and LTA does not potentiate platelet aggregation to epinephrine

по Lordkipanidzé, Marie, Lowe, Gillian C., Watson, Steve P.
Опубликовано 2013

Kikuchi-Fujimoto disease: a rare but important differential diagnosis for lymphadenopathy

по Srikantharajah, Mukunthan, Mahendra, Prem, Vydianath, Bindu, Lowe, Gillian C
Опубликовано 2014

A HaemSTAR is born; a trainee-led, UK-wide research network in haematology

по Nicolson, Phillip LR, Desborough, Michael JR, Hart, Daniel, Biss, Tina T, Lowe, Gillian C, Toh, Cheng-Hock
Опубликовано в: Clin Med (Lond) (2019)

Evaluation of a whole blood remote platelet function test for the diagnosis of mild bleeding disorders

по Dovlatova, Natalia, Lordkipanidzé, Marie, Lowe, Gillian C., Dawood, Ban, May, Jane, Heptinstall, Stan, Watson, Steve P., Fox, Susan C.
Опубликовано в: J Thromb Haemost (2014)

Microsatellite markers as a rapid approach for autozygosity mapping in Hermansky-Pudlak syndrome: Identification of the second HPS7 mutation in a patient presenting late in life

по Lowe, Gillian C., Guiu, Isabel Sánchez, Chapman, Oliver, Rivera, José, Lordkipanidzé, Marie, Dovlatova, Natalia, Wilde, Jonathan, Watson, Steve P., Morgan, Neil V.
Опубликовано 2013

Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel

по Dawood, Ban B., Lowe, Gillian C., Lordkipanidzé, Marie, Bem, Danai, Daly, Martina E., Makris, Mike, Mumford, Andrew, Wilde, Jonathan T., Watson, Steve P.
Опубликовано 2012

Mutation in GNE is associated with severe congenital thrombocytopenia

по Futterer, Jane, Dalby, Amanda, Lowe, Gillian C., Johnson, Ben, Simpson, Michael A., Motwani, Jayashree, Williams, Mike, Watson, Steve P., Morgan, Neil V.
Опубликовано в: Blood (2018)

Investigation of the contribution of an underlying platelet defect in women with unexplained heavy menstrual bleeding

по Lowe, Gillian C., Fickowska, Roksana, Al Ghaithi, Rashid, Maclachlan, Annabel, Harrison, Paul, Lester, Will, Watson, Steve P., Myers, Bethan, Clark, Justin, Morgan, Neil V.
Опубликовано в: Platelets (2018)

Rituximab prophylaxis to prevent thrombotic thrombocytopenic purpura relapse: outcome and evaluation of dosing regimens

по Westwood, John-Paul, Thomas, Mari, Alwan, Ferras, McDonald, Vickie, Benjamin, Sylvia, Lester, William A., Lowe, Gillian C., Dutt, Tina, Hill, Quentin A., Scully, Marie
Опубликовано в: Blood Adv (2017)

High-throughput platelet spreading analysis: a tool for the diagnosis of platelet-based bleeding disorders

по Khan, Abdullah O., Maclachlan, Annabel, Lowe, Gillian C., Nicolson, Phillip L.R., Ghaithi, Rashid Al, Thomas, Steven G., Watson, Steve P., Pike, Jeremy A., Morgan, Neil V.
Опубликовано в: Haematologica (2020)

Diversity and Impact of Rare Variants in Genes Encoding the Platelet G Protein-Coupled Receptors

по Jones, Matthew L., Norman, Jane E., Morgan, Neil V., Mundell, Stuart J., Lordkipanidzé, Marie, Lowe, Gillian C., Daly, Martina E., Simpson, Michael A., Drake, Sian, Watson, Steve P., Mumford, Andrew D.
Опубликовано в: Thromb Haemost (2015)

A comprehensive targeted next‐generation sequencing panel for genetic diagnosis of patients with suspected inherited thrombocytopenia

по Johnson, Ben, Doak, Rachel, Allsup, David, Astwood, Emma, Evans, Gillian, Grimley, Charlotte, James, Beki, Myers, Bethan, Stokley, Simone, Thachil, Jecko, Wilde, Jonathan, Williams, Mike, Makris, Mike, Lowe, Gillian C., Wallis, Yvonne, Daly, Martina E., Morgan, Neil V.
Опубликовано в: Res Pract Thromb Haemost (2018)

SLFN14 mutations underlie thrombocytopenia with excessive bleeding and platelet secretion defects

по Fletcher, Sarah J., Johnson, Ben, Lowe, Gillian C., Bem, Danai, Drake, Sian, Lordkipanidzé, Marie, Guiú, Isabel Sánchez, Dawood, Ban, Rivera, José, Simpson, Michael A., Daly, Martina E., Motwani, Jayashree, Collins, Peter W., Watson, Steve P., Morgan, Neil V.
Опубликовано в: J Clin Invest (2015)

Enrichment of FLI1 and RUNX1 mutations in families with excessive bleeding and platelet dense granule secretion defects

по Stockley, Jacqueline, Morgan, Neil V., Bem, Danai, Lowe, Gillian C., Lordkipanidzé, Marie, Dawood, Ban, Simpson, Michael A., Macfarlane, Kirsty, Horner, Kevin, Leo, Vincenzo C., Talks, Katherine, Motwani, Jayashree, Wilde, Jonathan T., Collins, Peter W., Makris, Michael, Watson, Steve P., Daly, Martina E.
Опубликовано 2013

Characterization of multiple platelet activation pathways in patients with bleeding as a high-throughput screening option: use of 96-well Optimul assay

по Lordkipanidzé, Marie, Lowe, Gillian C., Kirkby, Nicholas S., Chan, Melissa V., Lundberg, Martina H., Morgan, Neil V., Bem, Danai, Nisar, Shaista P., Leo, Vincenzo C., Jones, Matthew L., Mundell, Stuart J., Daly, Martina E., Mumford, Andrew D., Warner, Timothy D., Watson, Steve P.
Опубликовано 2014

Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects

по Johnson, Ben, Lowe, Gillian C., Futterer, Jane, Lordkipanidzé, Marie, MacDonald, David, Simpson, Michael A., Sanchez-Guiú, Isabel, Drake, Sian, Bem, Danai, Leo, Vincenzo, Fletcher, Sarah J., Dawood, Ban, Rivera, José, Allsup, David, Biss, Tina, Bolton-Maggs, Paula HB, Collins, Peter, Curry, Nicola, Grimley, Charlotte, James, Beki, Makris, Mike, Motwani, Jayashree, Pavord, Sue, Talks, Katherine, Thachil, Jecko, Wilde, Jonathan, Williams, Mike, Harrison, Paul, Gissen, Paul, Mundell, Stuart, Mumford, Andrew, Daly, Martina E., Watson, Steve P., Morgan, Neil V.
Опубликовано в: Haematologica (2016)