检索结果 - Georgina Hall

Refine Results
  1. 1
    Cerebral photosensitisation by haematoporphyrin derivative. Evidence for an endothelial site of action

    Cerebral photosensitisation by haematoporphyrin derivative. Evidence for an endothelial site of action 由 M. C. Berenbaum, Georgina Hall, A D Hoyes

    出版 1986
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  2. 2
    Anaplastic lymphoma kinase‐positive anaplastic large cell lymphoma: current and future perspectives in adult and paediatric disease

    Anaplastic lymphoma kinase‐positive anaplastic large cell lymphoma: current and future perspectives in adult and paediatric disease 由 Toby A. Eyre, Dalia Khan, Georgina Hall, Graham P. Collins

    出版 2014
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  3. 3
    Childhood and Adolescent nodular lymphocyte predominant Hodgkin lymphoma ‐ A review of clinical outcome based on the histological variants

    Childhood and Adolescent nodular lymphocyte predominant Hodgkin lymphoma ‐ A review of clinical outcome based on the histological variants 由 Ananth Shankar, Amy A. Kirkwood, Georgina Hall, Janis Hayward, Patricia O’Hare, Alan D. Ramsay

    出版 2015
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  4. 4
    Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approach

    Diagnosing the cause of bilateral paediatric cataracts: comparison of standard testing with a next-generation sequencing approach 由 Mahmoud Musleh, Georgina Hall, I. Christopher Lloyd, Rachel Gillespie, S. Waller, Sofia Douzgou, Jill Clayton‐Smith, Elias Kehdi, Graeme Black, Jane Ashworth

    出版 2016
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  5. 5
    A paradigm shift in the delivery of services for diagnosis of inherited retinal disease

    A paradigm shift in the delivery of services for diagnosis of inherited retinal disease 由 James O’Sullivan, Brendan G Mullaney, Sanjeev S. Bhaskar, Jonathan E. Dickerson, Georgina Hall, Anna O’Grady, Andrew R. Webster, Simon Ramsden, Graeme Black

    出版 2012
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  6. 6
    Treatment of bleeding episodes in haemophilia A complicated by a factor VIII inhibitor in patients receiving Emicizumab. Interim guidance from UKHCDO Inhibitor Working Party and Executive Committee

    Treatment of bleeding episodes in haemophilia A complicated by a factor VIII inhibitor in patients receiving Emicizumab. Interim guidance from UKHCDO Inhibitor Working Party and Ex... 由 Peter W. Collins, Ri Liesner, Michael Makris, Kate Talks, Pratima Chowdary, Elizabeth Chalmers, Georgina Hall, Anne Riddell, Charles Percy, C. R. M. Hay, Daniel P. Hart

    出版 2018
    获取全文
    Carta
    加到收藏夹
    Saved in:
  7. 7
    Resection alone in 58 children with limited stage, lymphocyte‐predominant Hodgkin lymphoma–experience from the European network group on pediatric Hodgkin lymphoma

    Resection alone in 58 children with limited stage, lymphocyte‐predominant Hodgkin lymphoma–experience from the European network group on pediatric Hodgkin lymphoma 由 Christine Mauz‐Körholz, S. Gorde-Grosjean, Dirk Hasenclever, Ananth Shankar, W Dörffel, William H. Wallace, G. Schellong, Alain Robert, Dieter Körholz, Odile Oberlin, Georgina Hall, Judith Landman‐Parker

    出版 2007
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  8. 8
    Quiescent leukaemic cells account for minimal residual disease in childhood lymphoblastic leukaemia

    Quiescent leukaemic cells account for minimal residual disease in childhood lymphoblastic leukaemia 由 Christoph Lutz, Petter Woll, Georgina Hall, Anders Castor, Hélène Dreau, Giovanni Cazzaniga, Jan Zuna, C. E. Jensen, Sally A. Clark, Andrea Biondi, Chris Mitchell, Helen Ferry, Anna Schuh, Veronica J. Buckle, Sten Eirik W. Jacobsen, Tariq Enver

    出版 2012
    获取全文
    Carta
    加到收藏夹
    Saved in:
  9. 9
    Guideline for the diagnosis and management of myelofibrosis

    Guideline for the diagnosis and management of myelofibrosis 由 John T. Reilly, Mary Frances McMullin, Philip Beer, Nauman M. Butt, Eibhlin Conneally, Andrew Duncombe, Anthony R. Green, N. George Michaeel, Maria Gilleece, Georgina Hall, Steven Knapper, Adam J. Mead, Ruben A. Mesa, Mallika Sekhar, Bridget S. Wilkins, Claire Harrison

    出版 2012
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  10. 10
    Molecular findings from 537 individuals with inherited retinal disease

    Molecular findings from 537 individuals with inherited retinal disease 由 Jamie M. Ellingford, Stephanie Barton, Sanjeev S. Bhaskar, James O’Sullivan, Simon G. Williams, Janine A. Lamb, Binay Panda, Panagiotis I. Sergouniotis, Rachel Gillespie, Stephen P. Daiger, Georgina Hall, Theodora Gale, I. Christopher Lloyd, Paul N. Bishop, Simon Ramsden, Graeme Black

    出版 2016
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  11. 11
    Clinical and genetic variability in children with partial albinism

    Clinical and genetic variability in children with partial albinism 由 Patrick Campbell, Jamie M. Ellingford, Neil R. A. Parry, Tracy Fletcher, Simon Ramsden, Theodora Gale, Georgina Hall, Katherine R. Smith, Dalia Kasperavičiūtė, Ellen Thomas, Iva Lloyd, Sofia Douzgou, Jill Clayton‐Smith, Susmito Biswas, Jane Ashworth, Graeme Black, Panagiotis I. Sergouniotis

    出版 2019
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  12. 12
    Clinical utility of genetic testing in 201 preschool children with inherited eye disorders

    Clinical utility of genetic testing in 201 preschool children with inherited eye disorders 由 Eva Lenassi, Jill Clayton‐Smith, Sofia Douzgou, Simon Ramsden, Stuart Ingram, Georgina Hall, Claire Hardcastle, Tracy Fletcher, Rachel L. Taylor, Jamie M. Ellingford, William D. Newman, Cecilia Fenerty, Vinod Sharma, Iva Lloyd, Susmito Biswas, Jane Ashworth, Graeme Black, Panagiotis I. Sergouniotis

    出版 2019
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  13. 13
    Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease

    Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease 由 Jamie M. Ellingford, Stephanie Barton, Sanjeev S. Bhaskar, Simon G. Williams, Panagiotis I. Sergouniotis, James O’Sullivan, Janine A. Lamb, Rahat Perveen, Georgina Hall, William G. Newman, Paul N. Bishop, Stephen A. Roberts, Rick Leach, Rick Tearle, S. C. Bayliss, Simon Ramsden, Andrea H. Németh, Graeme Black

    出版 2016
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  14. 14
    Guideline for investigation and management of adults and children presenting with a thrombocytosis

    Guideline for investigation and management of adults and children presenting with a thrombocytosis 由 Claire Harrison, D. Bareford, Nauman M. Butt, Peter J. Campbell, Eibhlin Conneally, Mark W. Drummond, Wendy N. Erber, Tamara Everington, Anthony R. Green, Georgina Hall, Beverley J. Hunt, Christopher A. Ludlam, Richard Murrin, Catherine Nelson‐Piercy, Deepti Radia, John T. Reilly, Jon van der Walt, Bridget S. Wilkins, Mary Frances McMullin

    出版 2010
    获取全文 获取全文
    Revisão
    加到收藏夹
    Saved in:
  15. 15
    G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction

    G6PC3 mutations are associated with a major defect of glycosylation: a novel mechanism for neutrophil dysfunction 由 Bu Hayee, Aristotelis Antonopoulos, Emma J. Murphy, Farooq Rahman, Gavin W. Sewell, Bruce N. Smith, S. McCartney, Mark Furman, Georgina Hall, Stuart Bloom, Stuart M. Haslam, Howard R. Morris, Kaan Boztuğ, Christoph Klein, Bryan Winchester, Edgar Pick, David C. Linch, Rosemary E. Gale, Andrew Smith, Anne Dell, Anthony W. Segal

    出版 2011
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  16. 16
    A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias

    A novel 33‐Gene targeted resequencing panel provides accurate, clinical‐grade diagnosis and improves patient management for rare inherited anaemias 由 Noémi Roy, Edward A. Wilson, Shirley Henderson, Katherine Wray, Christian Babbs, Steven Okoli, Wale Atoyebi, Avery Mixon, Mary R. Cahill, Peter Carey, Jonathan Cullis, Julie Curtin, Hélène Dreau, David Ferguson, Brenda Gibson, Georgina Hall, Joanne Mason, Mary Morgan, Melanie Proven, Amrana Qureshi, Joaquín Sánchez‐Garcia, Nongnuch Sirachainan, Juliana Teo, Ulf Tedgård, Douglas R. Higgs, David J. Roberts, Irene Roberts, Anna Schuh

    出版 2016
    获取全文 获取全文
    Artigo
    加到收藏夹
    Saved in:
  17. 17
    Chemotherapy induces canalization of cell state in childhood B-cell precursor acute lymphoblastic leukemia

    Chemotherapy induces canalization of cell state in childhood B-cell precursor acute lymphoblastic leukemia 由 Virginia Turati, José Afonso Guerra‐Assunção, Nicola Potter, Rajeev Gupta, Simone Ecker, Agne Daneviciute, Maxime Tarabichi, Amy P. Webster, Chuling Ding, Gillian May, Chela James, John Brown, Lucía Conde, Lisa J. Russell, Phil Ancliff, Sarah Inglott, Giovanni Cazzaniga, Andrea Biondi, Georgina Hall, Mark Lynch, Michael Hubank, Iain C. Macaulay, Stephan Beck, Peter Van Loo, Sten Eirik W. Jacobsen, Mel Greaves, Javier Herrero, Tariq Enver

    出版 2021
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  18. 18
    GATA1-mutant clones are frequent and often unsuspected in babies with Down syndrome: identification of a population at risk of leukemia

    GATA1-mutant clones are frequent and often unsuspected in babies with Down syndrome: identification of a population at risk of leukemia 由 Irene Roberts, Kate Alford, Georgina Hall, Gaëtan Juban, Helen Richmond, Alice Norton, Grant Vallance, Kelly Perkins, Emanuele Marchi, Simon J. McGowan, Anindita Roy, Gillian Cowan, Mark Anthony, Amit Gupta, John Ho, Sabita Uthaya, Anna Curley, Shree Vishna Rasiah, Timothy J. Watts, Richard Nicholl, A Bedford-Russell, Raoul Blumberg, Angela Thomas, Brenda Gibson, Christina Halsey, Pek-Wan Lee, Sunit Godambe, Connor Sweeney, Neha Bhatnagar, Anne Goriely, Peter J. Campbell, Paresh Vyas

    出版 2013
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  19. 19
    Biallelic Mutations in the Autophagy Regulator DRAM2 Cause Retinal Dystrophy with Early Macular Involvement

    Biallelic Mutations in the Autophagy Regulator DRAM2 Cause Retinal Dystrophy with Early Macular Involvement 由 Mohammed E. El‐Asrag, Panagiotis I. Sergouniotis, Martin McKibbin, Vincent Plagnol, Eamonn Sheridan, Naushin Waseem, Zakia Abdelhamed, Declan J. McKeefry, Kristof Van Schil, James A. Poulter, Colin A. Johnson, Ian Carr, Bart P. Leroy, Elfride De Baere, Chris F. Inglehearn, Andrew R. Webster, Carmel Toomes, Manir Ali, Graeme Black, Georgina Hall, Stuart Ingram, Rachel Gillespie, Simon Ramsden, Forbes D.C. Manson, Alison J. Hardcastle, Michel Michaelides, Michael E. Cheetham, Gavin Arno, Niclas Thomas, Shomi S. Bhattacharya, Tony Moore, Andrea H. Németh, Susan M. Downes, Stefano Lise, Emma Lord

    出版 2015
    获取全文
    Artigo
    加到收藏夹
    Saved in:
  20. 20
    Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa

    Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa 由 Gavin Arno, Smriti A. Agrawal, Aiden Eblimit, James Bellingham, Mingchu Xu, Feng Wang, Christina Chakarova, David A. Parfitt, Amelia Lane, Thomas Burgoyne, Sarah Hull, Keren Carss, Alessia Fiorentino, Matthew Hayes, Peter Munro, Ralph Nicols, Nikolas Pontikos, Graham E. Holder, Chinwe Asomugha, F. Lucy Raymond, Anthony T. Moore, Vincent Plagnol, Michel Michaelides, Alison J. Hardcastle, Yumei Li, Catherine A. Cukras, Andrew R. Webster, Michael E. Cheetham, Rui Chen, Graeme Black, Georgina Hall, Stuart Ingram, Rachel Gillespie, Forbes D.C. Manson, Panagiotis I. Sergouniotis, Chris F. Inglehearn, Carmel Toomes, Manir Ali, Martin McKibbin, James A. Poulter, Kamron Khan, Emma Lord, Andrea H. Németh, Susan M. Downes, Jing Yu, Stefano Lise, Gavin Arno, Alessia Fiorentino, Nikos Ponitkos, Vincent Plagnol, Michel Michaelides, Alison J. Hardcastle, Michael E. Cheetham, Andrew R. Webster, Veronica van Heyningen

    出版 2016
    获取全文
    Artigo
    加到收藏夹
    Saved in:

检索工具: