检索结果 - Mark I. Rees

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  1. 1
    Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB)

    Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glycine receptor (GLRB) 由 Mark I. Rees

    出版 2002
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  2. 2
    Localisation of glycine receptors in the human forebrain, brainstem, and cervical spinal cord: an immunohistochemical review

    Localisation of glycine receptors in the human forebrain, brainstem, and cervical spinal cord: an immunohistochemical review 由 Kristin Baer, Henry J. Waldvogel, Richard L. M. Faull, Mark I. Rees

    出版 2009
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  3. 3
    The glycinergic system in human startle disease: a genetic screening approach

    The glycinergic system in human startle disease: a genetic screening approach 由 Jeffrey S. Davies, Seo‐Kyung Chung, Rhys H. Thomas, Angela K. Robinson, Carrie L. Hammond, Jonathan G.L. Mullins, Eloisa Carta, Brian R. Pearce, Kirsten Harvey, Victoria L. Harvey, Mark I. Rees, Mark I. Rees

    出版 2010
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  4. 4
    Use of a leucocyte filter to remove tumour cells from intra‐operative cell salvage blood

    Use of a leucocyte filter to remove tumour cells from intra‐operative cell salvage blood 由 Sue Catling, Sarah I. Williams, O. Freites, Mark I. Rees, Claire M. Davies, Lynda Hopkins

    出版 2008
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  5. 5
    Weight change associated with antiepileptic drugs

    Weight change associated with antiepileptic drugs 由 William Owen Pickrell, Arron Lacey, Rhys H. Thomas, Phil E M Smith, Mark I. Rees

    出版 2012
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  6. 6
    Ghrelin inhibits LPS-induced release of IL-6 from mouse dopaminergic neurones

    Ghrelin inhibits LPS-induced release of IL-6 from mouse dopaminergic neurones 由 Amy L. Beynon, M. Rowan Brown, Rhiannon Wright, Mark I. Rees, I. Martin Sheldon, Jeffrey S. Davies

    出版 2013
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  7. 7
    Trends in the first antiepileptic drug prescribed for epilepsy between 2000 and 2010

    Trends in the first antiepileptic drug prescribed for epilepsy between 2000 and 2010 由 William Owen Pickrell, Arron Lacey, Rhys H. Thomas, Ronan A Lyons, Phil E M Smith, Mark I. Rees

    出版 2013
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  8. 8
    Dynamic changes in myelin aberrations and oligodendrocyte generation in chronic amyloidosis in mice and men

    Dynamic changes in myelin aberrations and oligodendrocyte generation in chronic amyloidosis in mice and men 由 Gwendolyn Behrendt, Kristin Baer, Annalisa Buffo, Maurice A. Curtis, Richard L. M. Faull, Mark I. Rees, Magdalena Götz, Leda Dimou

    出版 2012
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  9. 9
    Tubulin genes and malformations of cortical development

    Tubulin genes and malformations of cortical development 由 Romina Romaniello, Filippo Arrigoni, Andrew E. Fry, Maria Teresa Bassi, Mark I. Rees, Renato Borgatti, Daniela T. Pilz, Thomas D. Cushion

    出版 2018
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  10. 10
    Using natural language processing to extract structured epilepsy data from unstructured clinic letters: development and validation of the ExECT (extraction of epilepsy clinical text) system

    Using natural language processing to extract structured epilepsy data from unstructured clinic letters: development and validation of the ExECT (extraction of epilepsy clinical tex... 由 Beata Fonferko‐Shadrach, Arron Lacey, Angus Roberts, Ashley Akbari, Simon Thompson, David Ford, Ronan A Lyons, Mark I. Rees, William Owen Pickrell

    出版 2019
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  11. 11
    Incidence, Prevalence, and Health Care Outcomes in Idiopathic Intracranial Hypertension

    Incidence, Prevalence, and Health Care Outcomes in Idiopathic Intracranial Hypertension 由 Latif Miah, Huw Strafford, Beata Fonferko‐Shadrach, Joe Hollinghurst, I. M. S. Sawhney, S Hadjikoutis, Mark I. Rees, Robert Powell, Arron Lacey, William Owen Pickrell

    出版 2021
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  12. 12
    Epilepsy and deprivation, a data linkage study

    Epilepsy and deprivation, a data linkage study 由 William Owen Pickrell, Arron Lacey, Owen Bodger, Joanne Demmler, Rhys H. Thomas, Ronan A Lyons, Phil E M Smith, Mark I. Rees, Mike Kerr

    出版 2015
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  13. 13
    Complement is activated in progressive multiple sclerosis cortical grey matter lesions

    Complement is activated in progressive multiple sclerosis cortical grey matter lesions 由 Lewis M. Watkins, James Neal, Sam Loveless, Iliana Michailidou, Valeria Ramaglia, Mark I. Rees, Richard Reynolds, Neil P. Robertson, B. Paul Morgan, Owain W. Howell

    出版 2016
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  14. 14
    Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay

    Genotype-phenotype correlations in hyperekplexia: apnoeas, learning difficulties and speech delay 由 Rhys H. Thomas, Seo‐Kyung Chung, S. E. Wood, Thomas D. Cushion, Cheney Drew, Chrissy L. Hammond, Jean-François Vanbellinghen, Jonathan G.L. Mullins, Mark I. Rees

    出版 2013
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  15. 15
    Validating epilepsy diagnoses in routinely collected data

    Validating epilepsy diagnoses in routinely collected data 由 Beata Fonferko‐Shadrach, Arron Lacey, Catharine P. White, Robert Powell, I. M. S. Sawhney, Ronan A Lyons, Phil E M Smith, Mike Kerr, Mark I. Rees, William Owen Pickrell

    出版 2017
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  16. 16
    Epilepsy, antiepileptic drugs, and the risk of major cardiovascular events

    Epilepsy, antiepileptic drugs, and the risk of major cardiovascular events 由 Elinor Lee‐Lane, Fatemeh Torabi, Arron Lacey, Beata Fonferko‐Shadrach, Daniel Harris, Ashley Akbari, Ronan A Lyons, Mark I. Rees, I. M. S. Sawhney, Julian Halcox, Robert Powell, William Owen Pickrell

    出版 2021
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  17. 17
    TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins

    TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins 由 Ravinesh A. Kumar, Daniela T. Pilz, Timothy D. Babatz, Thomas D. Cushion, Kirsten Harvey, Maya Topf, Laura Yates, S. Robb, Gökhan Uyanık, G.M.S. Mancini, Mark I. Rees, Victoria L. Harvey, William B. Dobyns

    出版 2010
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  18. 18
    De Novo Mutations in the Beta-Tubulin Gene TUBB2A Cause Simplified Gyral Patterning and Infantile-Onset Epilepsy

    De Novo Mutations in the Beta-Tubulin Gene TUBB2A Cause Simplified Gyral Patterning and Infantile-Onset Epilepsy 由 Thomas D. Cushion, Alex R. Paciorkowski, Daniela T. Pilz, Jonathan G.L. Mullins, Laurie E. Seltzer, Robert W. Marion, Emily Tuttle, Dalia Ghoneim, Susan L. Christian, Seo‐Kyung Chung, Mark I. Rees, William B. Dobyns

    出版 2014
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  19. 19
    A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs

    A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs 由 Nigel Williams, Mark I. Rees, Peter Holmans, Nadine Norton, Alastair G. Cardno, Lisa Jones, Kieran C. Murphy, Robert D. Sanders, Geraldine McCarthy, M. Y. Gray, Iain Fenton, Peter McGuffin, M J Owen

    出版 1999
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  20. 20
    Meningeal inflammation and cortical demyelination in acute multiple sclerosis

    Meningeal inflammation and cortical demyelination in acute multiple sclerosis 由 Ryan J. Bevan, Rhian Evans, Lauren Griffiths, Lewis M. Watkins, Mark I. Rees, Roberta Magliozzi, Ingrid V. Allen, Gavin McDonnell, Rachael Kee, Michelle Naughton, Denise Fitzgerald, Richard Reynolds, James Neal, Owain W. Howell

    出版 2018
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