Resultados de procura - Atif Awan

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  1. 1
    Case Report: Benefits and Challenges of Long-term Eculizumab in Atypical Hemolytic Uremic Syndrome

    Case Report: Benefits and Challenges of Long-term Eculizumab in Atypical Hemolytic Uremic Syndrome por Noelle Cullinan, Kathleen M. Gorman, Michael Riordan, Mary Waldron, Timothy H.J. Goodship, Atif Awan

    Publicado 2015
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  2. 2
    Employing a Haemodynamic Score to Predict Acute Kidney Injury in Infants With Patent Ductus Arteriosus

    Employing a Haemodynamic Score to Predict Acute Kidney Injury in Infants With Patent Ductus Arteriosus por Dermot Michael Wildes, Rachel Mullaly, Caoimhe Costigan, Atif Awan, Afif El‐Khuffash, Michael A Boyle

    Publicado 2025
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  3. 3
    Current outcomes of the Glenn bidirectional cavopulmonary connection for single ventricle palliation

    Current outcomes of the Glenn bidirectional cavopulmonary connection for single ventricle palliation por Bahaaldin Alsoufi, Cedric Manlhiot, Atif Awan, Fadel Al-Fadley, M. Al-Ahmadi, Amani Mohammad Abbad Alwadei, Brian W. McCrindle, Zohair Al‐Halees

    Publicado 2012
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  4. 4
    Assessing the supportive care needs of parents of children with rare diseases in Ireland

    Assessing the supportive care needs of parents of children with rare diseases in Ireland por Suja Somanadhan, Helen McAneney, Atif Awan, Sandra McNulty, Alison Sweeney, Niamh Buckle, Shannon Sinnott, Shirley Bracken, Amy Jayne McKnight, Thilo Kroll, Lemuel J. Pelentsov

    Publicado 2025
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  5. 5
    A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome

    A novel hybrid CFH/CFHR3 gene generated by a microhomology-mediated deletion in familial atypical hemolytic uremic syndrome por Nigel J. Francis, Bairbre McNicholas, Atif Awan, Mary Waldron, Donal Reddan, Denise M. Sadlier, David Kavanagh, Lisa Strain, Kevin J. Marchbank, Claire L. Harris, Timothy H.J. Goodship

    Publicado 2011
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  6. 6
    C3 Glomerulopathy

    C3 Glomerulopathy por Nicholas Medjeral‐Thomas, Michelle M. O’Shaughnessy, John O’Regan, Carol Traynor, Michael Flanagan, Limy Wong, Chia Wei Teoh, Atif Awan, Mary Waldron, Tom Cairns, Patrick O’Kelly, Anthony Dorman, Matthew C. Pickering, Peter J. Conlon, H. Terence Cook

    Publicado 2013
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  7. 7
    Rare Disease Research Partnership (RAinDRoP): a collaborative approach to identify research priorities for rare diseases in Ireland

    Rare Disease Research Partnership (RAinDRoP): a collaborative approach to identify research priorities for rare diseases in Ireland por Somanadhan, Suja, Nicholson, Emma, Dorris, Emma, Brinkley, Aoife, Kennan, Avril, Treacy, Eileen, Atif, Awan, Ennis, Sean, McGrath, Vicky, Mitchell, Derick, O’Sullivan, Grace, Power, Julie, Lawlor, Anne, Harkin, Paul, Lynch, Sally Ann, Watt, Philip, Daly, Avril, Donnelly, Susie, Kroll, Thilo

    Publicado 2020
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  8. 8
    Epidemiology of and Risk Factors for BK Polyomavirus Replication and Nephropathy in Pediatric Renal Transplant Recipients: An International CERTAIN Registry Study

    Epidemiology of and Risk Factors for BK Polyomavirus Replication and Nephropathy in Pediatric Renal Transplant Recipients: An International CERTAIN Registry Study por Britta Höcker, Lukas Schneble, Luisa Murer, Andrea Carraro, Lars Pape, Birgitta Kranz, Jun Oh, Matthias Zirngibl, Luca Dello Strologo, Anja Büscher, Lutz T. Weber, Atif Awan, Martin Pöhl, Martin Bald, Nikoleta Printza, Krisztina Rusai, Licia Peruzzi, Rezan Topaloĝlu, Alexander Fichtner, Kai Krupka, L. Köster, Thomas Brückner, Paul Schnitzler, Hans H. Hirsch, Burkhard Tönshoff

    Publicado 2018
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  9. 9
    Real-world use of complement inhibitors for haemolytic uraemic syndrome: an analysis of the European Rare Kidney Disease Registry cohort

    Real-world use of complement inhibitors for haemolytic uraemic syndrome: an analysis of the European Rare Kidney Disease Registry cohort por Aleksandra Vujović, Anne‐Laure Sellier‐Leclerc, Maria Cristina Mancuso, Olivia Boyer, Atif Awan, Antonio Gargiulo, Sebastian Loos, Marc Fila, Augustina Jankauskiené, Gema Ariceta, Nele Kanzelmeyer, Enrico Vidal, Maria Van Dyck, Tanja Kersnik Levart, N Simánková, Stéphane Decramer, Jonas Hofstetter, Marina Vivarelli, Savino Sciascia, Nicole C. A. J. van de Kar, Franz Schaefer

    Publicado 2025
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  10. 10
    Factor H autoantibody is associated with atypical hemolytic uremic syndrome in children in the United Kingdom and Ireland

    Factor H autoantibody is associated with atypical hemolytic uremic syndrome in children in the United Kingdom and Ireland por Vicky Brocklebank, Sally Johnson, Thomas P. Sheerin, Stephen D. Marks, Rodney D. Gilbert, Kay Tyerman, Meredith Kinoshita, Atif Awan, Amrit Kaur, Nicholas J.A. Webb, Shivaram Hegde, Eric Finlay, Maggie Fitzpatrick, Patrick R. Walsh, Edwin Wong, Caroline Booth, Larissa Kerecuk, Alan D. Salama, Mike Almond, Carol Inward, Timothy H.J. Goodship, Neil Sheerin, Kevin J. Marchbank, David Kavanagh

    Publicado 2017
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  11. 11
    Management of bone disease in cystinosis: Statement from an international conference

    Management of bone disease in cystinosis: Statement from an international conference por Katharina Hohenfellner, Frank Rauch, Gema Ariceta, Atif Awan, Justine Bacchetta, Carsten Bergmann, Susanne Bechtold, Noelle Cassidy, Geroges Deschenes, Ewa Elenberg, William A. Gahl, Oliver Greil, Erik Harms, Nadine Herzig, Bernd Höppe, Christian Koeppl, Malcolm Lewis, Elena Levtchenko, Galina Nesterova, Fernando Santos, Karl P. Schlingmann, Aude Servais, Neveen A. Soliman, Guenther Steidle, Clodagh Sweeney, Ulrike Treikauskas, Rezan Topaloĝlu, А.Н. Цыгин, Koenraad Veys, Rodo von Vigier, Jozef Zustin, Dieter Haffner

    Publicado 2019
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  12. 12
    The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results

    The European Rare Kidney Disease Registry (ERKReg): objectives, design and initial results por Giulia Bassanese, Tanja Wlodkowski, Aude Servais, Laurence Heidet, Dario Roccatello, Francesco Emma, Elena Levtchenko, Gema Ariceta, Justine Bacchetta, Giovambattista Capasso, Augustina Jankauskiené, Marius Miglinas, Pietro Manuel Ferraro, Giovanni Montini, Jun Oh, Stéphane Decramer, Tanja Kersnik Levart, Jack F.M. Wetzels, Marlies Cornelissen, Olivier Devuyst, Aleksandra Żurowska, Lars Pape, Anja Buescher, Dieter Haffner, Nataša Marčun Varda, Gian Marco Ghiggeri, Giuseppe Remuzzi, Martin Konrad, Germana Longo, Detlef Böckenhauer, Atif Awan, Ilze Andersone, Jaap W. Groothoff, Franz Schaefer

    Publicado 2021
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  13. 13
    HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome

    HLA-DQA1 and PLCG2 Are Candidate Risk Loci for Childhood-Onset Steroid-Sensitive Nephrotic Syndrome por Rasheed Gbadegesin, Adebowale Adeyemo, Nicholas J.A. Webb, Larry A. Greenbaum, Asiri Abeyagunawardena, Shenal Thalgahagoda, Arundhati S. Kale, Debbie S. Gipson, Tarak Srivastava, Jen-Jar Lin, Deepa H. Chand, Tracy E. Hunley, Patrick D. Brophy, Arvind Bagga, Aditi Sinha, Michelle N. Rheault, Joanna R. Ghali, Kathy Nicholls, Elizabeth Abraham, Halima S. Janjua, Abiodun Omoloja, Gina-Marie Barletta, Yi Cai, David Milford, Catherine O’Brien, Atif Awan, Vladimir Belostotsky, William E. Smoyer, Alison Homstad, Gentzon Hall, Guanghong Wu, Shashi Nagaraj, Delbert R. Wigfall, John W. Foreman, Michelle P. Winn

    Publicado 2014
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  14. 14
    Monogenic causes of chronic kidney disease in adults

    Monogenic causes of chronic kidney disease in adults por Dervla M. Connaughton, Claire Kennedy, Shirlee Shril, Nina Mann, Susan Murray, Patrick A. Williams, Eoin Conlon, Makiko Nakayama, Amelie T. van der Ven, Hadas Ityel, Franziska Kause, Caroline M. Kolvenbach, Rufeng Dai, Asaf Vivante, Daniela A. Braun, Ronen Schneider, Thomas M. Kitzler, Bróna Moloney, Conor Moran, J. Smyth, Alan Kennedy, Katherine A. Benson, Caragh P. Stapleton, Mark Denton, Colm Magee, Conall M. O’Seaghdha, William D. Plant, Matthew D. Griffin, Atif Awan, Clodagh Sweeney, Shrikant Mane, Richard P. Lifton, Brenda Walker Griffin, Sean F. Leavey, Liam Casserly, D.G. de Freitas, John Holian, Anthony Dorman, Brendan Doyle, Peter Lavin, Mark A. Little, Peter J. Conlon, Friedhelm Hildebrandt

    Publicado 2019
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