Hypoxaemia, sport and polycythaemia: a case from Imperial College London

por Yasuda, Wakana, Jackson, James E, Layton, D Mark, Shovlin, Claire L
Publicado 2015

Whole genome sequences discriminate hereditary hemorrhagic telangiectasia phenotypes by non-HHT deleterious DNA variation

por Joyce, Katie E., Onabanjo, Ebun, Brownlow, Sheila, Nur, Fadumo, Olupona, Kike, Fakayode, Kehinde, Sroya, Manveer, Thomas, Geraldine A., Ferguson, Teena, Redhead, Julian, Millar, Carolyn M., Cooper, Nichola, Layton, D. Mark, Boardman-Pretty, Freya, Caulfield, Mark J., Shovlin, Claire L.
Publicado 2022

The Pyruvate Kinase Deficiency Global Longitudinal (Peak) Registry: rationale and study design

por Grace, Rachael F, van Beers, Eduard J, Vives Corrons, Joan-Lluis, Glader, Bertil, Glenthøj, Andreas, Kanno, Hitoshi, Kuo, Kevin H M, Lander, Carl, Layton, D Mark, Pospíŝilová, Dagmar, Viprakasit, Vip, Li, Junlong, Yan, Yan, Boscoe, Audra N, Bowden, Chris, Bianchi, Paola
Publicado 2023

Mutation of von Hippel–Lindau Tumour Suppressor and Human Cardiopulmonary Physiology

por Smith, Thomas G, Brooks, Jerome T, Balanos, George M, Lappin, Terence R, Layton, D. Mark, Leedham, Dawn L, Liu, Chun, Maxwell, Patrick H, McMullin, Mary F, McNamara, Christopher J, Percy, Melanie J, Pugh, Christopher W, Ratcliffe, Peter J, Talbot, Nick P, Treacy, Marilyn, Robbins, Peter A
Publicado 2006

Real-time national survey of COVID-19 in hemoglobinopathy and rare inherited anemia patients

por 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
Publicado 2020