Kết quả tìm kiếm - Ariharan Anantharachagan

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  1. 1
    COVID-19 in patients with primary and secondary immunodeficiency: The United Kingdom experience

    COVID-19 in patients with primary and secondary immunodeficiency: The United Kingdom experience Bằng Adrian M. Shields, Siobhán O. Burns, Sinisa Savic, Alex Richter, Ariharan Anantharachagan, Gururaj Arumugakani, Kenneth F. Baker, Sameer Bahal, William Bermingham, Malini Bhole, Evon Boules, Philip Bright, Siobhán O. Burns, Betsy Cleave, John Dempster, Lisa Devlin, Fatima Dhalla, Elizabeth Drewe, C.J. Duncan, Magdalena Dziadzio, Shuayb Elkhalifa, Andrew R. Gennery, Sarah Goddard, Sofia Grigoriadou, Grant Hayman, Archana Herwadkar, Aarnoud Huissoon, Rashmi Jain, Stephen Jolles, Sarah Johnston, Lucy Leeman, Shanti Mahabir, Dylan MacLochlainn, Elizabeth McDermott, Siraj Misbah, Hadeil Morsi, Sai Murng, Sadia Noorani, Rachael O’Brien, Smita Y. Patel, Arthur Price, Alex Richter, Sinisa Savic, Suranjith L. Seneviratne, Adrian M. Shields, Anna Shrimpton, Catherine B. Stroud, Prashantha Vaitla, Nisha Verma

    Được phát hành 2020
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    Artigo
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  2. 2
    Outcomes following SARS-CoV-2 infection in patients with primary and secondary immunodeficiency in the UK

    Outcomes following SARS-CoV-2 infection in patients with primary and secondary immunodeficiency in the UK Bằng Adrian M. Shields, Ariharan Anantharachagan, Gururaj Arumugakani, Kenneth F. Baker, Sameer Bahal, Helen Baxendale, William Bermingham, Malini Bhole, Evon Boules, Philip Bright, Charu Chopra, Lucy Cliffe, Betsy Cleave, John Dempster, Lisa Devlin, Fatima Dhalla, Lavanya Diwakar, Elizabeth Drewe, C.J. Duncan, Magdalena Dziadzio, Suzanne Elcombe, Shuayb Elkhalifa, Andrew R. Gennery, Harichandrana Ghanta, Sarah Goddard, Sofia Grigoriadou, Scott Hackett, Grant Hayman, Richard Herriot, Archana Herwadkar, Aarnoud Huissoon, Rashmi Jain, Stephen Jolles, Sarah Johnston, Sujoy Khan, James Laffan, Peter J. L. Lane, Lucy Leeman, David M. Lowe, Shanti Mahabir, Dylan J. Mac Lochlainn, Elizabeth McDermott, Siraj Misbah, Fiona Moghaddas, Hadeil Morsi, Sai Murng, Sadia Noorani, Rachael O’Brien, Smita Y. Patel, Arthur Price, Tasneem Rahman, Suranjith L. Seneviratne, Anna Shrimpton, Catherine Stroud, Moira Thomas, Katie Townsend, Prashantha Vaitla, Nisha Verma, Anthony Williams, Siobhán O. Burns, Sinisa Savic, Alex Richter

    Được phát hành 2022
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    Artigo
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  3. 3
    Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma

    Autosomal Dominant STAT6 Gain of Function Causes Severe Atopy Associated with Lymphoma Bằng Ekaterina Minskaia, Jesmeen Maimaris, Persephone Jenkins, Adriana S. Albuquerque, Ying Hong, Despina Eleftheriou, Kimberly Gilmour, Richard Grace, Fernando Moreira, Bodo Grimbacher, Zoe Adhya, Hana Alachkar, Ariharan Anantharachagan, Richard Antrobus, Gururaj Arumugakani, Chiara Bacchelli, Helen Baxendale, Claire Bethune, Shahnaz Bibi, Barbara Boardman, Claire Booth, Michael Browning, Mary Brownlie, Siobhán O. Burns, Anita Chandra, Hayley Clifford, Nichola Cooper, Sophie Davies, John Dempster, Lisa Devlin, Rainer Döffinger, Elizabeth Drewe, David Edgar, William Egner, Tariq El‐Shanawany, Bobby Gaspar, Rohit Ghurye, Kimberly Gilmour, Sarah Goddard, Pavel Gordins, Sofia Grigoriadou, Scott Hackett, Rosie Hague, Lorraine Harper, Grant Hayman, Archana Herwadkar, Stephen Hughes, Aarnoud Huissoon, Stephen Jolles, Julie R. Jones, Peter Kelleher, Nigel Klein, Taco W. Kuijpers, Dinakantha Kumararatne, James Laffan, Hana Lango Allen, Sara Lear, Hilary Longhurst, Lorena Lorenzo, Jesmeen Maimaris, Ania Manson, Elizabeth McDermott, Hazel Millar, Anoop Mistry, Valerie Morrisson, Sai Murng, Iman Nasir, Sergey Nejentsev, Sadia Noorani, Eric Oksenhendler, Mark Ponsford, Waseem Qasim, Ellie Quinn, Isabella Quinti, Alexander Richter, Crina Samarghitean, Ravishankar Sargur, Sinisa Savic, Suranjith L. Seneviratne, Carrock Sewall, Fiona Shackley, Ilenia Simeoni, Kenneth G. C. Smith, Emily Staples, Hans J. Stauss, Cathal Steele, James Thaventhiran, Moira Thomas, Adrian J. Thrasher, Steve Welch, Lisa Willcocks, Sarita Workman, Austen Worth, Nigel Yeatman, Patrick Yong, Sofie Ashford, John S. Bradley, Debra Fletcher, Tracey Hammerton, Roger James

    Được phát hành 2023
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    Artigo
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  4. 4
    Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

    Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans Bằng Paul Tuijnenburg, Hana Lango Allen, Siobhán O. Burns, Daniel Greene, Machiel H. Jansen, Emily Staples, Jonathan Stephens, Keren Carss, Daniele Biasci, Helen Baxendale, Moira Thomas, Anita Chandra, Sorena Kiani‐Alikhan, Hilary Longhurst, Suranjith L. Seneviratne, Eric Oksenhendler, Ilenia Simeoni, Godelieve J. de Bree, Anton T. J. Tool, Ester M. M. van Leeuwen, Eduard H.T.M. Ebberink, Alexander B. Meijer, Salih Tuna, Deborah Whitehorn, Matthew A. Brown, Ernest Turro, Adrian J. Thrasher, Kenneth G. C. Smith, James Thaventhiran, Taco W. Kuijpers, Zoe Adhya, Hana Alachkar, Ariharan Anantharachagan, Richard Antrobus, Gururaj Arumugakani, Chiara Bacchelli, Helen Baxendale, Claire Bethune, Shahnaz Bibi, Barbara Boardman, Claire Booth, Michael J. Browning, Mary Brownlie, Siobhán O. Burns, Anita Chandra, Hayley Clifford, Nichola Cooper, Sophie Davies, John Dempster, Lisa Devlin, Rainer Döffinger, Elizabeth Drewe, David Edgar, William Egner, Tariq El‐Shanawany, Bobby Gaspar, Rohit Ghurye, Kimberly Gilmour, Sarah Goddard, Pavel Gordins, Sofia Grigoriadou, Scott Hackett, Rosie Hague, Lorraine Harper, Grant Hayman, Archana Herwadkar, Stephen Hughes, Aarnoud Huissoon, Stephen Jolles, Julie R. Jones, Peter Kelleher, Nigel Klein, Taco W. Kuijpers, Dinakantha Kumararatne, James Laffan, Hana Lango Allen, Sara Lear, Hilary Longhurst, Lorena Lorenzo, Jesmeen Maimaris, Ania Manson, Elizabeth McDermott, Hazel Millar, Anoop Mistry, Valerie Morrisson, Sai Murng, Iman Nasir, Sergey Nejentsev, Sadia Noorani, Éric Oksenhendler, Mark Ponsford, Waseem Qasim, Ellie Quinn, Isabella Quinti, Alex Richter, Crina Samarghitean, Ravishankar Sargur, Sinisa Savic, Suranjith L. Seneviratne, Carrock Sewall

    Được phát hành 2018
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    Artigo
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  5. 5
    Whole-genome sequencing of a sporadic primary immunodeficiency cohort

    Whole-genome sequencing of a sporadic primary immunodeficiency cohort Bằng James Thaventhiran, Hana Lango Allen, Oliver S. Burren, William Rae, Daniel Greene, Emily Staples, Zinan Zhang, James H. R. Farmery, Ilenia Simeoni, Elizabeth Rivers, Jesmeen Maimaris, Christopher J. Penkett, Jonathan Stephens, Sri V. V. Deevi, Alba Sanchis‐Juan, Nicholas Gleadall, Moira Thomas, Ravishankar Sargur, Pavels Gordins, Helen Baxendale, Matthew A. Brown, Paul Tuijnenburg, Austen Worth, Steven Hanson, Rachel Linger, Matthew Buckland, Paula Rayner-Matthews, Kimberly Gilmour, Crina Samarghitean, Suranjith L. Seneviratne, David M. Sansom, Andy G. Lynch, Karyn Mégy, Eva Ellinghaus, David Ellinghaus, Silje F. Jørgensen, Tom H. Karlsen, Kathleen Stirrups, Antony J. Cutler, Dinakantha Kumararatne, Anita Chandra, David Edgar, Archana Herwadkar, Nichola Cooper, Sofia Grigoriadou, Aarnoud Huissoon, Sarah Goddard, Stephen Jolles, Catharina Schuetz, Felix Boschann, Stephen Abbs, Zoe Adhya, Julian Adlard, Maryam Afzal, Irshad Ahmed, Munaza Ahmed, Saeed Ahmed, Timothy J. Aitman, Hana Alachkar, Jayanthi Alamelu, Raza Alikhan, Carl E. Allen, Louise Allen, David Allsup, Arif Alvi, Gautam Ambegaonkar, Ariharan Anantharachagan, Philip Ancliff, Julie A. Anderson, Richard Antrobus, Ruth Armstrong, Gavin Arno, Gururaj Arumugakani, Rita Arya, Sofie Ashford, William J. Astle, Anthony Attwood, Steve Austin, Yeşim Aydınok, Waqar Ayub, Christian Babbs, Chiara Bacchelli, Trevor Baglin, Tamam Bakchoul, Tadbir K. Bariana, Jonathan Barratt, Julian Barwell, John Baski, Rachel W. Bates, Joana Batista, Helen Baxendale, Gareth Baynam, David Bennett, Claire Bethune, Neha Bhatnagar, Shahnaz Bibi, Agnieszka Bierżyńska, Tina Biss, Maria Bitner‐Glindzicz, Marta Bleda

    Được phát hành 2020
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    Artigo
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  6. 6
    Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

    Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations Bằng Tiziana Lorenzini, Manfred Fliegauf, Nils Klammer, Natalie Frede, Michele Proietti, Alla Bulashevska, Nadezhda Camacho-Ordóñez, Markku Varjosalo, Matias Kinnunen, Esther de Vries, J.W.M. van der Meer, Rohan Ameratunga, Chaim M. Roifman, Yael Dinur Schejter, Robin Kobbe, Timo Hautala, Faranaz Atschekzei, Reinhold E. Schmidt, Claudia Schröder, Polina Stepensky, Bella Shadur, Luis Alberto Pedroza, Michiel van der Flier, Mónica Martínez‐Gallo, Luis Ignacio González‐Granado, Luís M. Allende, Anna Shcherbina, N. B. Kuzmenko, V.P. Zakharova, João Farela Neves, Peter Švec, Ute Fischer, Winnie Ip, Oliver Bartsch, Safa Barış, Christoph Klein, Raif S. Geha, Janet Chou, Mohammed F. Alosaimi, Lauren Weintraub, Kaan Boztuğ, Tatjana Hirschmugl, Maria Marluce dos Santos Vilela, Dirk Holzinger, Maximilian Seidl, Vassilios Lougaris, Alessandro Plebani, Laia Alsina, M. Piquer‐Gibert, Àngela Deyà‐Martínez, C Slade, Asghar Aghamohammadi, Hassan Abolhassani, Lennart Hammarström, Outi Kuismin, Merja Helminen, Hana Lango Allen, James E. Thaventhiran, Alexandra F. Freeman, Matthew Cook, Shahrzad Bakhtiar, Mette Christiansen, Charlotte Cunningham‐Rundles, Niraj Patel, William Rae, Tim Niehues, Nina Brauer, Jaana Syrjänen, Mikko Seppänen, Siobhán O. Burns, Paul Tuijnenburg, Taco W. Kuijpers, Klaus Warnatz, Bodo Grimbacher, Zoe Adhya, Hana Alachkar, Ariharan Anantharachagan, Richard Antrobus, Gururaj Arumugakani, Sofie Ashford, William J. Astle, Anthony Attwood, Chiara Bacchelli, Joana Batista, Helen Baxendale, Claire Bethune, Shahnaz Bibi, Marta Bleda, Barbara Boardman, Claire Booth, John R. Bradley, Gerome Breen, Matthew A. Brown, Michael J. Browning, Mary Brownlie, Matthew Buckland, Siobhán O. Burns, Oliver S. Burren, Keren Carss, John C. Chambers

    Được phát hành 2020
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    Artigo
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