Torthaí cuardaigh - Colin G. Steward

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  1. 1
    Diagnosing haemophagocytic syndrome

    Diagnosing haemophagocytic syndrome de réir Ethan S. Sen, Colin G. Steward, Athimalaipet V Ramanan

    Foilsithe / Cruthaithe 2016
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  2. 2
    Diagnosis of invasive aspergillosis in bone marrow transplant recipients by polymerase chain reaction

    Diagnosis of invasive aspergillosis in bone marrow transplant recipients by polymerase chain reaction de réir Emma Williamson, John P. Leeming, Helen Palmer, Colin G. Steward, David W. Warnock, David I. Marks, Michael Millar

    Foilsithe / Cruthaithe 2000
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  3. 3
    Minimal residual disease analysis for the prediction of relapse in children with standard‐risk acute lymphoblastic leukaemia

    Minimal residual disease analysis for the prediction of relapse in children with standard‐risk acute lymphoblastic leukaemia de réir Nicholas J. Goulden, C. Knechtli, Russell J. Garland, Kenneth Langlands, Jeremy Hancock, Michael Potter, Colin G. Steward, A Oakhill

    Foilsithe / Cruthaithe 1998
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  4. 4
    A polymerase chain reaction study of the stability of Ig heavy-chain and T-cell receptor delta gene rearrangements between presentation and relapse of childhood B-lineage acute lymphoblastic leukemia

    A polymerase chain reaction study of the stability of Ig heavy-chain and T-cell receptor delta gene rearrangements between presentation and relapse of childhood B-lineage acute lym... de réir Colin G. Steward, NJ Goulden, F Katz, Deborah L. Baines, PG Martin, Kenneth Langlands, MN Potter, JM Chessells, A Oakhill

    Foilsithe / Cruthaithe 1994
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  5. 5
    Bloodspot Assay Using HPLC–Tandem Mass Spectrometry for Detection of Barth Syndrome

    Bloodspot Assay Using HPLC–Tandem Mass Spectrometry for Detection of Barth Syndrome de réir Willem Kulik, Henk van Lenthe, Femke S. Stet, Riekelt H. Houtkooper, Helena Kemp, Janet Stone, Colin G. Steward, Ronald J. A. Wanders, Frédéric M. Vaz

    Foilsithe / Cruthaithe 2007
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  6. 6
    The clinical features, risk factors and outcome of thrombotic thrombocytopenic purpura occurring after bone marrow transplantation

    The clinical features, risk factors and outcome of thrombotic thrombocytopenic purpura occurring after bone marrow transplantation de réir Rhian Fuge, Jennifer M. Bird, Anne Fraser, Dan Hart, Linda Hunt, Jacqueline Cornish, Nicholas Goulden, A Oakhill, Derwood Pamphilon, Colin G. Steward, David I. Marks

    Foilsithe / Cruthaithe 2001
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  7. 7
    Infections in adults undergoing unrelated donor bone marrow transplantation

    Infections in adults undergoing unrelated donor bone marrow transplantation de réir Emma Williamson, Michael Millar, Colin G. Steward, Jacqueline Cornish, A.B.M. Foot, A Oakhill, Derwood Pamphilon, B E Reeves, E O Caul, David G. Warnock, David F Marks

    Foilsithe / Cruthaithe 1999
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  8. 8
    Barth syndrome: an <b>X</b>‐linked cause of fetal cardiomyopathy and stillbirth

    Barth syndrome: an <b>X</b>‐linked cause of fetal cardiomyopathy and stillbirth de réir Colin G. Steward, RA Newbury-Ecob, Rob Hastings, Sarah Smithson, B Tsai-Goodman, OW Quarrell, Wim Kulik, Ronald Wanders, Michael Pennock, Maggie Williams, J. R. Cresswell, I. Bugallo González, Paul Brennan

    Foilsithe / Cruthaithe 2010
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  9. 9
    Adoptive transfer of cytomegalovirus-specific CTL to stem cell transplant patients after selection by HLA–peptide tetramers

    Adoptive transfer of cytomegalovirus-specific CTL to stem cell transplant patients after selection by HLA–peptide tetramers de réir Mark Cobbold, Naeem Khan, Batoul Pourgheysari, Sudhir Tauro, Dorothy McDonald, Husam Osman, Mario Assenmacher, Lucinda Billingham, Colin G. Steward, Charles Crawley, Eduardo Olavarría, John M. Goldman, Ronjon Chakraverty, Premini Mahendra, Charles Craddock, Paul Moss

    Foilsithe / Cruthaithe 2005
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  10. 10
    Brincidofovir is highly efficacious in controlling adenoviremia in pediatric recipients of hematopoietic cell transplant

    Brincidofovir is highly efficacious in controlling adenoviremia in pediatric recipients of hematopoietic cell transplant de réir Prashant Hiwarkar, Persis Amrolia, Ponni Sivaprakasam, Su Han Lum, Hemalatha Doss, Ciara O’Rafferty, Toni Petterson, Katharine Patrick, Juliana Silva, Mary Slatter, Sarah Lawson, Kanchan Rao, Colin G. Steward, Adam Gassas, Paul Veys, Robert Wynn

    Foilsithe / Cruthaithe 2017
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  11. 11
    Neutropenia in Barth syndrome: characteristics, risks, and management

    Neutropenia in Barth syndrome: characteristics, risks, and management de réir Colin G. Steward, Sarah Groves, Carolyn T. Taylor, Melissa K. Maisenbacher, Birgitta Versluys, Ruth Newbury‐Ecob, Hülya Özşahin, Michaela K. Damin, Valerie M. Bowen, Katherine R. McCurdy, Michael C. Mackey, Audrey Anna Bolyard, David C. Dale

    Foilsithe / Cruthaithe 2018
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  12. 12
    Tafazzin regulates neutrophil maturation and inflammatory response

    Tafazzin regulates neutrophil maturation and inflammatory response de réir Przemysław Zakrzewski, Christopher M. Rice, Kathryn Fleming, Drinalda Cela, Sarah Groves, Fernando M. Ponce-Garcia, Willem Gibbs, Kiran Roberts, Tobias Pike, Douglas Strathdee, E. S. Anderson, Angela H. Nobbs, Ashley M. Toye, Colin G. Steward, Borko Amulic

    Foilsithe / Cruthaithe 2025
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  13. 13
    Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome)

    Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome) de réir Pia Østergaard, Michael A. Simpson, Fiona Connell, Colin G. Steward, Glen Brice, Wesley J. Woollard, Dimitra Dafou, Tatjana Kilo, Sarah Smithson, Peter Lunt, Victoria A. Murday, Shirley Hodgson, Russell Keenan, Daniela T. Pilz, Inés Martínez‐Corral, Taija Mäkinen, Peter Mortimer, Steve Jeffery, Richard C. Trembath, Sahar Mansour

    Foilsithe / Cruthaithe 2011
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  14. 14
    Barth syndrome

    Barth syndrome de réir Sarah L. N. Clarke, Ann Bowron, Iris L. Gonzalez, Sarah Groves, Ruth Newbury‐Ecob, Nicol Clayton, Robin P. Martin, Beverly Tsai‐Goodman, Vanessa Garratt, Michael Ashworth, Valerie M. Bowen, Katherine R. McCurdy, Michaela K. Damin, Carolyn T. Spencer, Matthew J. Toth, Richard I. Kelley, Colin G. Steward

    Foilsithe / Cruthaithe 2013
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  15. 15
    Excellent outcome of matched unrelated donor transplantation in paediatric aplastic anaemia following failure with immunosuppressive therapy: a United Kingdom multicentre retrospective experience

    Excellent outcome of matched unrelated donor transplantation in paediatric aplastic anaemia following failure with immunosuppressive therapy: a United Kingdom multicentre retrospec... de réir Sujith Samarasinghe, Colin G. Steward, Prashant Hiwarkar, Muhammad A. Saif, Rachael Hough, David Webb, Alice Norton, Sarah Lawson, Amrana Qureshi, Philip Connor, Peter Carey, R Skinner, Ajay Vora, Maria Pelidis, Brenda Gibson, Graham Stewart, Steve Keogh, Nick Goulden, Denise Bonney, Matthew Stubbs, Persis Amrolia, Kanchan Rao, Stefan Meyer, Robert Wynn, Paul Veys

    Foilsithe / Cruthaithe 2012
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  16. 16
    Targeted busulfan-based reduced-intensity conditioning and HLA-matched HSCT cure hemophagocytic lymphohistiocytosis

    Targeted busulfan-based reduced-intensity conditioning and HLA-matched HSCT cure hemophagocytic lymphohistiocytosis de réir Matthias Felber, Colin G. Steward, Karim Kentouche, Anders Fasth, Robert Wynn, Ulrike Zeilhofer, Veronika Haunerdinger, Benjamin Volkmer, Seraina Prader, Bernd Gruhn, Stephan Ehl, Kai Lehmberg, Daniel J. Müller, Andrew R. Gennery, Michael H. Albert, Fabian Hauck, Kanchan Rao, Paul Veys, Moustapha Hassan, Arjan C. Lankester, Jana Pachlopnik Schmid, Mathias Hauri‐Hohl, Tayfun Güngör

    Foilsithe / Cruthaithe 2020
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  17. 17
    The EuroChimerism concept for a standardized approach to chimerism analysis after allogeneic stem cell transplantation

    The EuroChimerism concept for a standardized approach to chimerism analysis after allogeneic stem cell transplantation de réir Thomas Lion, Franz Watzinger, Sandra Preuner, Hermann Kreyenberg, Marcel G.J. Tilanus, R de Weger, J. Van Loon, Lianne P. de Vries, Hélène Cavé, Cécile Acquaviva, Mark Lawler, Mireille Crampe, Anna Serra, B Saglio, Federica Colnaghi, Andrea Biondi, Jacques J. M. van Dongen, Mirjam van der Burg, Marcos González, Miguel Alcoceba, Gisela Barbany, Monica Hermanson, Eddy Roosnek, Colin G. Steward, J. Harvey, Florian Frommlet, Peter Bader

    Foilsithe / Cruthaithe 2012
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  18. 18
    Dynamic Cardiolipin Synthesis Is Required for CD8+ T Cell Immunity

    Dynamic Cardiolipin Synthesis Is Required for CD8+ T Cell Immunity de réir Mauro Corrado, Joy Edwards-Hicks, Matteo Villa, Lea J. Flachsmann, David E. Sanin, Maaike Jacobs, Francesc Baixauli, Michal A. Stanczak, E. S. Anderson, M. Azuma, Andrea Quintana, Jonathan D. Curtis, Thomas Clapes, Katarzyna M. Grzes, Agnieszka M. Kabat, Ryan Kyle, Annette E. Patterson, Ramon I. Klein Geltink, Borko Amulic, Colin G. Steward, Douglas Strathdee, Eirini Trompouki, David O’Sullivan, Edward J. Pearce, Erika L. Pearce

    Foilsithe / Cruthaithe 2020
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  19. 19
    Similar outcome of upfront‐unrelated and matched sibling stem cell transplantation in idiopathic paediatric aplastic anaemia. A study on behalf of the <scp>UK</scp> Paediatric <scp>BMT</scp> Working Party, Paediatric Diseases Working Party and Severe Aplastic Anaemia Working Party of <scp>EBMT</scp>

    Similar outcome of upfront‐unrelated and matched sibling stem cell transplantation in idiopathic paediatric aplastic anaemia. A study on behalf of the <scp>UK</scp> Paediatric <scp... de réir Carlo Dufour, Paul Veys, Elisa Carraro, Neha Bhatnagar, Marta Pillon, Robert Wynn, Brenda Gibson, Ajay Vora, Colin G. Steward, Anna Maria Ewins, Rachael Hough, Josu de la Fuente, Mark Velangi, Persis Amrolia, Roderick Skinner, Andrea Bacigalupo, Antonio M. Risitano, Gèrard Socié, Régis Peffault de Latour, Jakob Passweg, Alicia Rovó, André Tichelli, Hubert Schrezenmeier, Britta Höchsmann, Peter Bader, Anja van Biezen, Mahmoud Aljurf, Austin Kulasekararaj, Judith Marsh, Sujith Samarasinghe

    Foilsithe / Cruthaithe 2015
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  20. 20
    Human NK cell deficiency as a result of biallelic mutations in MCM10

    Human NK cell deficiency as a result of biallelic mutations in MCM10 de réir Emily M. Mace, Silke Paust, Matilde Immacolata Conte, Ryan M. Baxley, Megan Schmit, Sagar L. Patil, Nicole C. Guilz, Malini Mukherjee, Ashley E. Pezzi, Jolanta Chmielowiec, Swetha Tatineni, Iván K. Chinn, Zeynep Coban‐Akdemir, Shalini N. Jhangiani, Donna M. Muzny, Asbjørg Stray‐Pedersen, Rachel E. Bradley, Mo Moody, Philip Connor, Adrian Heaps, Colin G. Steward, Pinaki P. Banerjee, Richard A. Gibbs, Malgorzata Borowiak, James R. Lupski, Stephen Jolles, Anja‐Katrin Bielinsky, Jordan S. Orange

    Foilsithe / Cruthaithe 2020
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