Hypoglycemia Event Rates: A Comparison Between Real-World Data and Randomized Controlled Trial Populations in Insulin-Treated Diabetes von Elliott, Lisa, Fidler, Carrie, Ditchfield, Andrea, Stissing, Trine

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Hypoglycemia: An overview of fear of hypoglycemia, quality-of-life, and impact on costs von Fidler, Carrie, Elmelund Christensen, Torsten, Gillard, Samantha

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Mixed Treatment Comparison Meta-Analysis Evaluating the Relative Efficacy of Nucleos(t)ides for Treatment of Nucleos(t)ide-Naive Patients with Chronic Hepatitis B von Dakin, Helen, MSc, Fidler, Carrie, PhD, Harper, Christie, BSc RGN

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The value of fast-acting insulin aspart compared with insulin aspart for patients with diabetes mellitus treated with bolus insulin from a UK health care system perspective von Leelarathna, Lalantha, Ashley, Donna, Fidler, Carrie, Parekh, Witesh

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The role of the iron transporter ABCB7 in refractory anemia with ring sideroblasts von Boultwood, Jacqueline, Pellagatti, Andrea, Nikpour, Maryam, Pushkaran, Beena, Fidler, Carrie, Cattan, Helen, Littlewood, Tim J, Malcovati, Luca, Della Porta, Matteo G, Jädersten, Martin, Killick, Sally, Giagounidis, Aristoteles, Bowen, David, Hellström-Lindberg, Eva, Cazzola, Mario, Wainscoat, James S

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Narrowing and genomic annotation of the commonly deleted region of the 5q− syndrome von Boultwood, Jacqueline, Fidler, Carrie, Strickson, Amanda J., Watkins, Fiona, Gama, Susana, Kearney, Lyndal, Tosi, Sabrina, Kasprzyk, Arek, Cheng, Jan-Fang, Jaju, Rina J., Wainscoat, James S.

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Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Plasma von Lo, Y.M. Dennis, Hjelm, N. Magnus, Fidler, Carrie, Sargent, Ian L, Murphy, Michael F, Chamberlain, Paul F, Poon, Priscilla M.K, Redman, Christopher W.G, Wainscoat, James S

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Genome-wide analysis of copy number changes and loss of heterozygosity in myelodysplastic syndrome with del(5q) using high-density single nucleotide polymorphism arrays von Wang, Li, Fidler, Carrie, Nadig, Nandita, Giagounidis, Aristoteles, Della Porta, Matteo G, Malcovati, Luca, Killick, Sally, Gattermann, Norbert, Aul, Carlo, Boultwood, Jacqueline, Wainscoat, James S

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Gene expression profiling in the myelodysplastic syndromes using cDNA microarray technology von Pellagatti, Andrea, Esoof, Noor, Watkins, Fiona, Langford, Cordelia F., Vetrie, David, Campbell, Lisa J., Fidler, Carrie, Cavenagh, James D., Eagleton, Helen, Gordon, Peter, Woodcock, Barrie, Pushkaran, Beena, Kwan, Mark, Wainscoat, James S., Boultwood, Jacqueline

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Labour induction treatment guidelines across Europe: A review von Correa Astorquiza, Luis Guillermo, Jeapes, Catherine, Fidler, Carrie, Sugrue, Daniel, Murphy, Daniel, Watson, Marc

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Molecular Analysis of Cancer von Boultwood, Jacqueline, Fidler, Carrie

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Detection of Mammaglobin mRNA in the Plasma of Breast Cancer Patients von GAL, SHIRA, FIDLER, CARRIE, LO, Y. M. DENNIS, CHIN, KENNY, MOORE, JOHN, HARRIS, ADRIAN L., WAINSCOAT, JAMES S.

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Gene expression profiling of CD34+ cells in patients with the 5q− syndrome von Boultwood, Jacqueline, Pellagatti, Andrea, Cattan, Helen, Lawrie, Charles H., Giagounidis, Aristoteles, Malcovati, Luca, Porta, Matteo G. Della, Jädersten, Martin, Killick, Sally, Fidler, Carrie, Cazzola, Mario, Hellström‐Lindberg, Eva, Wainscoat, James S.

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Haploinsufficiency of RPS14 in 5q− syndrome is associated with deregulation of ribosomal‐ and translation‐related genes von Pellagatti, Andrea, Hellström‐Lindberg, Eva, Giagounidis, Aristoteles, Perry, Janet, Malcovati, Luca, Della Porta, Matteo G., Jädersten, Martin, Killick, Sally, Fidler, Carrie, Cazzola, Mario, Wainscoat, James S., Boultwood, Jacqueline

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Gene expression profiles of CD34+ cells in myelodysplastic syndromes: involvement of interferon-stimulated genes and correlation to FAB subtype and karyotype von Pellagatti, Andrea, Cazzola, Mario, Giagounidis, Aristoteles A.N., Malcovati, Luca, Porta, Matteo G. Della, Killick, Sally, Campbell, Lisa J., Wang, Li, Langford, Cordelia F., Fidler, Carrie, Oscier, David, Aul, Carlo, Wainscoat, James S., Boultwood, Jacqueline

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Cost Effectiveness of Tenofovir Disoproxil Fumarate for the Treatment of Chronic Hepatitis B from a Canadian Public Payer Perspective von Dakin, Helen, Sherman, Morris, Fung, Scott, Fidler, Carrie, Bentley, Anthony

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Transcription Mapping of the 5q− Syndrome Critical Region: Cloning of Two Novel Genes and Sequencing, Expression, and Mapping of a Further Six Novel cDNAs von Boultwood, Jacqueline, Fidler, Carrie, Strickson, Amanda J., Watkins, Fiona, Kostrzewa, Markus, Jaju, Rina J., Müller, Ulrich, Wainscoat, James S.

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The FOXP1 winged helix transcription factor is a novel candidate tumor suppressor gene on chromosome 3p von BANHAM, Alison H, BEASLEY, Nigel, WOOD, Katrina, CORDELL, Jacqueline L, CAMPO, Elias, FERNANDEZ, Pedro L, FIDLER, Carrie, GATTER, Kevin, JONES, Margaret, MASON, David Y, PRIME, John E, TROUGOUBOFF, Philippe

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A novel gene, NSD1, is fused to NUP98 in the t(5;11)(q35;p15.5) in de novo childhood acute myeloid leukemia von Jaju, Rina J., Fidler, Carrie, Haas, Oskar A., Strickson, Amanda J., Watkins, Fiona, Clark, Kevin, Cross, Nicholas C.P., Cheng, Jan-Fang, Aplan, Peter D., Kearney, Lyndal, Boultwood, Jacqueline, Wainscoat, James S.

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The HumanPOP2Gene: Identification, Sequencing, and Mapping to the Critical Region of the 5q- Syndrome von Fidler, Carrie, Wainscoat, James S., Boultwood, Jacqueline

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