The beginnings of molecular medicine von Rees, David C.

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Update review of the acute porphyrias von Stein, Penelope E., Badminton, Michael N., Rees, David C.

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The 'rule of three' for fragment-based drug discovery: where are we now? von Jhoti, Harren, Williams, Glyn, Rees, David C., Murray, Christopher W.

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The role of ligand efficiency metrics in drug discovery von Hopkins, Andrew L., Keserü, György M., Leeson, Paul D., Rees, David C., Reynolds, Charles H.

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Sickle-cell disease von Rees, David C, Dr, Williams, Thomas N, PhD, Gladwin, Mark T, Prof

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Environmental determinants of severity in sickle cell disease von Tewari, Sanjay, Brousse, Valentine, Piel, Frédéric B, Menzel, Stephan, Rees, David C

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Recommendations regarding splenectomy in hereditary hemolytic anemias von Iolascon, Achille, Andolfo, Immacolata, Barcellini, Wilma, Corcione, Francesco, Garçon, Loïc, De Franceschi, Lucia, Pignata, Claudio, Graziadei, Giovanna, Pospisilova, Dagmar, Rees, David C, de Montalembert, Mariane, Rivella, Stefano, Gambale, Antonella, Russo, Roberta, Ribeiro, Leticia, Vives-Corrons, Jules, Martinez, Patricia Aguilar, Kattamis, Antonis, Gulbis, Beatrice, Cappellini, Maria Domenica, Roberts, Irene, Tamary, Hannah

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White matter integrity and processing speed in sickle cell anemia von Stotesbury, Hanne, Kirkham, Fenella J, Kölbel, Melanie, Balfour, Philippa, Clayden, Jonathan D, Sahota, Sati, Sakaria, Simrat, Saunders, Dawn E, Howard, Jo, Kesse-Adu, Rachel, Inusa, Baba, Pelidis, Maria, Chakravorty, Subarna, Rees, David C, Awogbade, Moji, Wilkey, Olu, Layton, Mark, Clark, Christopher A, Kawadler, Jamie M

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The Transfusion Alternatives Preoperatively in Sickle Cell Disease (TAPS) study: a randomised, controlled, multicentre clinical trial von Howard, Jo, Dr, Malfroy, Moira, BA, Llewelyn, Charlotte, PhD, Choo, Louise, PhD, Hodge, Renate, MSc, Johnson, Tony, PhD, Purohit, Shilpi, BSc, Rees, David C, FRCP, Tillyer, Louise, FRCP, Walker, Isabeau, FRCA, Fijnvandraat, Karin, PhD, Kirby-Allen, Melanie, MD, Spackman, Eldon, PhD, Davies, Sally C, Prof Dame, Williamson, Lorna M, FRCPath

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Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency von Bianchi, Paola, Fermo, Elisa, Glader, Bertil, Kanno, Hitoshi, Agarwal, Archana, Barcellini, Wilma, Eber, Stefan, Hoyer, James D., Kuter, David J., Maia, Tabita Magalhães, Mañu‐Pereira, Maria del Mar, Kalfa, Theodosia A., Pissard, Serge, Segovia, José‐Carlos, van Beers, Eduard, Gallagher, Patrick G., Rees, David C., van Wijk, Richard

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A gain of function variant in PIEZO1 (E756del) and sickle cell disease von Rooks, Helen, Brewin, John, Gardner, Kate, Chakravorty, Subarna, Menzel, Stephan, Hannemann, Anke, Gibson, John, Rees, David C

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Genome wide association study of silent cerebral infarction in sickle cell disease (HbSS and HbSC) von Brewin, John N, Rooks, Helen, Gardner, Kate, Senior, Harry, Morje, Mrinmayi, Patel, Hamel, Calvet, David, Bartolucci, Pablo, Thein, Swee-Lay, Menzel, Stephan, Rees, David C

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Real-time national survey of COVID-19 in hemoglobinopathy and rare inherited anemia patients von Telfer, Paul, De la Fuente, Josu, Sohal, Mamta, Brown, Ralph, Eleftheriou, Perla, Roy, Noémi, Piel, Frédéric B, Chakravorty, Subarna, Gardner, Kate, Velangi, Mark, Drasar, Emma, Shah, Farrukh, Porter, John B, Trompeter, Sara, Atoyebi, Wale, Szydlo, Richard, Anie, Kofi A, Ryan, Kate, Sharif, Joseph, Wright, Josh, Astwood, Emma, Nicolle, C Sarah, Webster, Amy, Roberts, David J, Lugthart, Sanne, Kaya, Banu, Awogbade, Moji, Rees, David C, Hollingsworth, Rob, Inusa, Baba, Howard, Jo, Layton, D Mark

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Long-term follow-up of givosiran treatment in patients with acute intermittent porphyria from a phase 1/2, 48-month open-label extension study von Sardh, Eliane, Balwani, Manisha, Rees, David C, Anderson, Karl E, Jia, Gang, Sweetser, Marianne T, Wang, Bruce

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Reduced GATA1 levels are associated with ineffective erythropoiesis in sickle cell anemia von El Hoss, Sara, Shangaris, Panicos, Brewin, John, Psychogyiou, Maria Eleni, Ng, Cecilia, Pedler, Lauren, Rooks, Helen, Gotardo, Érica M F, Gushiken, Lucas F S, Brito, Pâmela L, Nicolaides, Kypros H, Conran, Nicola, Rees, David C, Strouboulis, John

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Red blood cell mannoses as phagocytic ligands mediating both sickle cell anaemia and malaria resistance von Cao, Huan, Antonopoulos, Aristotelis, Henderson, Sadie, Wassall, Heather, Brewin, John, Masson, Alanna, Shepherd, Jenna, Konieczny, Gabriela, Patel, Bhinal, Williams, Maria-Louise, Davie, Adam, Forrester, Megan A., Hall, Lindsay, Minter, Beverley, Tampakis, Dimitris, Moss, Michael, Lennon, Charlotte, Pickford, Wendy, Erwig, Lars, Robertson, Beverley, Dell, Anne, Brown, Gordon D., Wilson, Heather M., Rees, David C., Haslam, Stuart M., Alexandra Rowe, J., Barker, Robert N., Vickers, Mark A.

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The significance of inadequate transcranial Doppler studies in children with sickle cell disease von Greenwood, Simon, Deane, Colin, Rees, Oliver L, Freedman, Ben, Kumar, Suresh, Ben Ramadan, Naser, Wilkinson, Sarah, Marais, Grant, Lord, Julie, Chakravorty, Subarna, Height, Susan E, Gardner, Kate, Rees, David C

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Precision Medicine and Sickle Cell Disease von El Hoss, Sara, El Nemer, Wassim, Rees, David C.

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A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia von Adeyemo, Titilope A, Ojewunmi, Oyesola O, Oyetunji, Idat A, Rooks, Helen, Rees, David C, Akinsulie, Adebola O, Akanmu, Alani S, Thein, Swee Lay, Menzel, Stephan

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Sickle Cell Disease von Piel, Frédéric B, Steinberg, Martin H, Rees, David C

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