Putting unstable hemoglobins on the map of London von Bain, BJ, Hann, A, Layton, DM

Volltext

RESULTS FROM A PHASE 2 STUDY OF MITAPIVAT IN ADULTS WITH NON–TRANSFUSION-DEPENDENT ALPHA- OR BETA-THALASSEMIA von Kuo, KH, Layton, DM, Lal, A, Al-Samkari, H, Bhatia, J, Tong, B, Lynch, M, Uhlig, K, Vichinsky, EP

Volltext

Voxelotor in sickle cell disease von Bain, BJ, Myburgh, J, Hann, A, Layton, DM

Volltext

Low serum haptoglobin and blood films suggest intravascular haemolysis contributes to severe anaemia in hereditary haemorrhagic telangiectasia von Thielemans, L, Layton, DM, Shovlin, CL

Volltext

ENERGIZE AND ENERGIZE-T: TWO PHASE 3, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDIES OF MITAPIVAT IN ADULTS WITH NON–TRANSFUSION-DEPENDENT OR TRANSFUSION-DEPENDENT ALPHA- OR... von Kuo, KH, Layton, DM, Al-Samkari, H, Kattamis, A, Sheth, S, Taher, A, Viprakasit, V, Chamberlain, CX, Czapla, L, Gheuens, S, Jiang, L, Lynch, M, Tong, B, Uhlig, K, Cappellini, MD

Volltext

Peripheral blood features of iron overload in post-splenectomy, type I congenital dyserythropoietic anemia von Dexter, D, Layton, DM, Kiritkumar, K, Bain, BJ

Volltext

Unusual inclusions in hemoglobin H disease post‐splenectomy von Spencer‐Chapman, Michael, Luqmani, Asad, Layton, D. Mark, Bain, Barbara J.

Volltext

P181 Pulmonary arteriovenous malformations, hereditary haemorrhagic telangiectasia and iron treatments von Shovlin, CL, Boother, EJ, Fung, CH, Bamford, KB, Layton, DM, Jackson, JE, Brownlow, S

Volltext

Hypoxaemia, sport and polycythaemia: a case from Imperial College London von Yasuda, W, Jackson, JE, Layton, DM, Shovlin, CL

Volltext

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 von 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

Volltext

LONG-TERM EFFICACY AND SAFETY OF THE ORAL PYRUVATE KINASE ACTIVATOR MITAPIVAT IN ADULTS WITH NON–TRANSFUSION-DEPENDENT ALPHA- OR BETA-THALASSEMIA von Kuo, KH, Layton, DM, Lal, A, Al-Samkari, H, Bhatia, J, Kosinski, PA, Tong, B, Lynch, M, Uhlig, K, Vichinsky, EP

Volltext

A statistical analysis of RNA folding algorithms through thermodynamic parameter perturbation von Layton, D. M., Bundschuh, R.

Volltext

Whole genome sequences discriminate hereditary hemorrhagic telangiectasia phenotypes by non-HHT deleterious DNA variants von Joyce, KE, Onabanjo, E, Brownlow, S, Nur, F, Olupona, K, Fakayode, K, Sroya, M, Thomas, GA, Ferguson, T, Redhead, J, Millar, CM, Cooper, N, Layton, DM, Boardman-Pretty, F, Caulfield, MJ, Genomics England Research Consortium, GE, Shovlin, CL

Volltext

Absence of CD47 in protein 4.2–deficient hereditary spherocytosis in man: an interaction between the Rh complex and the band 3 complex von Bruce, Lesley J., Ghosh, Sandip, King, May Jean, Layton, D. Mark, Mawby, William J., Stewart, Gordon W., Oldenborg, Per-Arne, Delaunay, Jean, Tanner, Michael J.A.

Volltext

Localization of a Gene for Familial Hemophagocytic Lymphohistiocytosis at Chromosome 9q21.3-22 by Homozygosity Mapping von Ohadi, Mina, Lalloz, Michel R.A., Sham, Pak, Zhao, Jinghua, Dearlove, Andrew M., Shiach, Caroline, Kinsey, Sally, Rhodes, Michael, Layton, D. Mark

Volltext

Protein 4.2 is critical to CD47-membrane skeleton attachment in human red cells von Dahl, Kris Noel, Parthasarathy, Ranganath, Westhoff, Connie M., Layton, D. Mark, Dennis Discher, E.

Volltext

Rapid Identification of Hemoglobin Variants by Electrospray Ionization Mass Spectrometry von Wild, B.J., Green, B.N., Cooper, E.K., Lalloz, M.R.A., Erten, S., Stephens, A.D., Layton, D.M.

Volltext

Characterization of erosion and failure processes of spark plugs after field service in natural gas engines von Lin, H.T., Brady, M.P., Richards, R.K., Layton, D.M.

Volltext

Predominance of the HLA-H Cys282Tyr mutation in Austrian patients with genetic haemochromatosis von Datz, Christian, Lalloz, Michel R.A., Vogel, Wolfgang, Graziadei, Ivo, Hackl, Franz, Vautier, Guy, Layton, D.Mark, Maier-Dobersberger, Theresia, Ferenci, Peter, Penner, Edward, Sandhofer, Friedrich, Bomford, Adrian, Paulweber, Bernhard

Volltext

Molecular analysis of the genotype-phenotype relationship in factor X deficiency von MILLAR, D. S, ELLISTON, L, CACHIA, P, PASI, K. J, LAYTON, D. M, COOPER, D. N, DEEX, P, KRAWCZAK, M, WACEY, A. I, REYNAUD, J, NIEUWENHUIS, H. K, BOLTON-MAGGS, P, MANNUCCI, P. M, REVERTER, J. C

Volltext