Zobrazeno 1 - 10
of 181
pro vyhledávání: '"Jo Howard"'
Autor:
Beatrice Nussberger, Soraia Barbosa, Mark Beaumont, Mathias Currat, Sébastien Devillard, Marco Heurich, Jo Howard-McCombe, Federica Mattucci, Carsten Nowak, Claudio Sebastián Quilodrán, Helen Senn, Paulo Célio Alves, EUROWILDCAT Consortium, Malte Götz, Pablo Ferreras, Dominik Fischer, Luisa Fischer, Lorenzo Frangini, René Janssen, Saskia Jerosch, Andrew Kitchener, Miha Krofel, Jarmila Krojerová-Prokešová, Johannes Lang, József Lanszki, Jenny MacPherson, Dime Melovski, Johan Michaux, Despina Migli, Marc Moes, Pedro Monterroso, Carolina Nogueira, Henryk Okarma, Dominique Pontier, Joe Premier, Héctor Ruiz-Villar, Ferran Sayol, Vinciane Schockert, Lara Semple, Andrea Sforzi, Olaf Simon, Magda Sindičić, Anil Soyumert, Arianna Spada, Sabrina Streif, Manfred Trinzen
Publikováno v:
Frontiers in Ecology and Evolution, Vol 11 (2023)
Preserving natural genetic diversity and ecological function of wild species is a central goal in conservation biology. As such, anthropogenic hybridization is considered a threat to wild populations, as it can lead to changes in the genetic makeup o
Externí odkaz:
https://doaj.org/article/c7cdd555093b49e09cd44c4e5863fdf8
Autor:
Georgina McAllister, Sandra Bhatasara, Priscilla Claeys, Jo Howard, Stefanie Lemke, Katherine McKinnon, Nina Isabella Moeller
Publikováno v:
Frontiers in Sustainable Food Systems, Vol 7 (2023)
Externí odkaz:
https://doaj.org/article/044e8e7287544864826ff8ecc82d7f65
Autor:
Hanne Stotesbury, Jamie M. Kawadler, Jonathan D. Clayden, Dawn E. Saunders, Anna M. Hood, Melanie Koelbel, Sati Sahota, David C. Rees, Olu Wilkey, Mark Layton, Maria Pelidis, Baba P. D. Inusa, Jo Howard, Subarna Chakravorty, Chris A. Clark, Fenella J. Kirkham
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
Research in sickle cell anemia (SCA) has used, with limited race-matched control data, binary categorization of patients according to the presence or absence of silent cerebral infarction (SCI). SCI have primarily been identified using low-resolution
Externí odkaz:
https://doaj.org/article/b9b954bad2e74950bfb278ad5b115405
Autor:
Hanne Stotesbury, Patrick W. Hales, Anna M. Hood, Melanie Koelbel, Jamie M. Kawadler, Dawn E. Saunders, Sati Sahota, David C. Rees, Olu Wilkey, Mark Layton, Maria Pelidis, Baba P. D. Inusa, Jo Howard, Subarna Chakravorty, Chris A. Clark, Fenella J. Kirkham
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Previous studies have pointed to a role for regional cerebral hemodynamic stress in neurological complications in patients with sickle cell anemia (SCA), with watershed regions identified as particularly at risk of ischemic tissue injury. Using singl
Externí odkaz:
https://doaj.org/article/72f7c88f701c47aea7fb2b9583d683dc
Autor:
Laura L. Oakley, Moji Awogbade, Sarah Brien, Annette Briley, Maria Chorozoglou, Emma Drasar, Jemma Johns, Elizabeth Rhodes, Vicky Robinson, Paul Seed, Joseph Sharif, Claire Singh, Paul Telfer, Hilary Thompson, Ingrid Watt-Coote, Jo Howard, Eugene Oteng-Ntim
Publikováno v:
Trials, Vol 21, Iss 1, Pp 1-11 (2020)
Abstract Background Pregnancies in women with sickle cell disease (SCD) are associated with a higher risk of sickle and pregnancy complications. Limited options exist for treating SCD during pregnancy. Serial prophylactic exchange blood transfusion (
Externí odkaz:
https://doaj.org/article/b8c9bd9218434180a76812a14db5c657
Autor:
Anna M. Hood, Melanie Kölbel, Hanne Stotesbury, Jamie Kawadler, April Slee, Baba Inusa, Maria Pelidis, Jo Howard, Subarna Chakravorty, Sue Height, Moji Awogbade, Fenella J. Kirkham, Christina Liossi
Publikováno v:
Frontiers in Psychology, Vol 12 (2021)
Sickle cell disease (SCD) refers to a group of inherited blood disorders with considerable morbidity that causes severe pain, reduces life expectancy, and requires significant self-management. Acute painful episodes are the hallmark of SCD, but persi
Externí odkaz:
https://doaj.org/article/6740f1f1c25345b3865befa63e4c7033
Autor:
Jo Howard, Sophie A. Lee, Baba Inusa, Man Ying Edith Cheng, Cheema Bavenjit, Isabel C. Reading, Sally Ann Wakeford, Johanna C. Gavlak, Patrick B. Murphy, Nicholas Hart, Atul Gupta, Sati Sahota, Eufemia Jacob, Maria Chorozoglou, Carol Ossai, Maureen Gwam, Fenella J. Kirkham, Angela M. Wade, Christina Liossi
Publikováno v:
Trials, Vol 20, Iss 1, Pp 1-15 (2019)
Abstract Design This randomised crossover trial compared nocturnal auto-adjusting continuous positive airway pressure (APAP) and nocturnal oxygen therapy (NOT) in adults and children with sickle cell anaemia, with patient acceptability as the primary
Externí odkaz:
https://doaj.org/article/002c1b5e5a604551927164d87ae4b5c0
Autor:
Paul Telfer, Josu de la Fuente, Mamta Sohal, Ralph Brown, Perla Eleftheriou, Noémi Roy, Frédéric B. Piel, Subarna Chakravorty, Kate Gardner, Mark Velangi, Emma Drasar, Farrukh Shah, John B. Porter, Sara Trompeter, Wale Atoyebi, Richard Szydlo, Kofi A. Anie, Kate Ryan, Joseph Sharif, Josh Wright, Emma Astwood, C. Sarah Nicolle, Amy Webster, David J. Roberts, Sanne Lugthart, Banu Kaya, Moji Awogbade, David C. Rees, Rob Hollingsworth, Baba Inusa, Jo Howard, D. Mark Layton
Publikováno v:
Haematologica, Vol 105, Iss 11 (2020)
Externí odkaz:
https://doaj.org/article/6c8eb0ee441b42e3b6284c91f79e18c8
Autor:
Joanna C Willis, Moji Awogbade, Jo Howard, Cormac Breen, Allifia Abbas, Mark Harber, Ali M Shendi, Peter A Andrews, Jack Galliford, Raj Thuraisingham, Alice Gage, Sapna Shah, Claire C Sharpe
Publikováno v:
PLoS ONE, Vol 15, Iss 8, p e0236998 (2020)
There are over 12,000 people with sickle cell disease (SCD) in the UK, and 4-12% of patients who develop Sickle Cell Nephropathy (SCN) progress to End Stage Renal Disease (ESRD). Renal transplantation offers the best outcomes for these patients with
Externí odkaz:
https://doaj.org/article/e5a35882aeba4c91932063d8e2fc9482
Autor:
Kate Gardner, Tony Fulford, Nicholas Silver, Helen Rooks, Nikolaos Angelis, Marlene Allman, Siana Nkya, Julie Makani, Jo Howard, Rachel Kesse-Adu, David C. Rees, Sara Stuart-Smith, Tullie Yeghen, Moji Awogbade, Raphael Z. Sangeda, Josephine Mgaya, Hamel Patel, Stephen Newhouse, Stephan Menzel, Swee Lay Thein
Publikováno v:
Blood Advances, Vol 2, Iss 3, Pp 235-239 (2018)
Abstract: Fetal hemoglobin (HbF) is a strong modifier of sickle cell disease (SCD) severity and is associated with 3 common genetic loci. Quantifying the genetic effects of the 3 loci would specifically address the benefits of HbF increases in patien
Externí odkaz:
https://doaj.org/article/6f789b316915405c913448948a4037da