Search Results - Victoria Nesbitt

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  1. 1
    Cerebellar Ataxia in Patients With Mitochondrial DNA Disease

    Cerebellar Ataxia in Patients With Mitochondrial DNA Disease by Nichola Z. Lax, Philippa D. Hepplewhite, Amy K. Reeve, Victoria Nesbitt, Robert McFarland, Evelyn Jaros, Robert W. Taylor, Douglass M. Turnbull

    Published 2012
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  2. 2
    Use of FGF-21 as a Biomarker of Mitochondrial Disease in Clinical Practice

    Use of FGF-21 as a Biomarker of Mitochondrial Disease in Clinical Practice by Alireza Morovat, Gayani Weerasinghe, Victoria Nesbitt, Monika Hofer, Thomas Agnew, G. Quaghebeur, Kate Sergeant, Carl Fratter, Nishan Guha, Mehdi Mirzazadeh, Joanna Poulton

    Published 2017
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  3. 3
    A national perspective on prenatal testing for mitochondrial disease

    A national perspective on prenatal testing for mitochondrial disease by Victoria Nesbitt, Charlotte L. Alston, Emma L. Blakely, Carl Fratter, Catherine Feeney, Joanna Poulton, Garry K. Brown, Douglass M. Turnbull, Robert W. Taylor, Robert McFarland

    Published 2014
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  4. 4
    Mitochondrial Retinopathy

    Mitochondrial Retinopathy by Johannes Birtel, C. von Landenberg, Martin Gliem, Carla Gliem, Jens Reimann, Wolfram S. Kunz, Philipp Herrmann, Christian Betz, Richard Caswell, Victoria Nesbitt, Cornelia Kornblum, Peter Charbel Issa

    Published 2021
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  5. 5
    Disease progression in patients with single, large-scale mitochondrial DNA deletions

    Disease progression in patients with single, large-scale mitochondrial DNA deletions by John P. Grady, G. Campbell, Thiloka Ratnaike, Emma L. Blakely, Gavin Falkous, Victoria Nesbitt, Andrew M. Schaefer, Richard McNally, Gráinne S. Gorman, Rachael W. Taylor, Douglass M. Turnbull, Robert McFarland

    Published 2013
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  6. 6
    Consensus-based statements for the management of mitochondrial stroke-like episodes

    Consensus-based statements for the management of mitochondrial stroke-like episodes by Yi Shiau Ng, Laurence A. Bindoff, Gráinne S. Gorman, Rita Horváth, Thomas Klopstock, Michelangelo Mancuso, Mika H. Martikainen, Robert McFarland, Victoria Nesbitt, Robert D. S. Pitceathly, Andrew M. Schaefer, Douglass M. Turnbull

    Published 2019
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  7. 7
    Epilepsy in adults with mitochondrial disease: A cohort study

    Epilepsy in adults with mitochondrial disease: A cohort study by Roger G. Whittaker, Helen Devine, Gráinne S. Gorman, Andrew M. Schaefer, Rita Horváth, Yi Shiau Ng, Victoria Nesbitt, Nichola Z. Lax, Robert McFarland, Mark O. Cunningham, Robert W. Taylor, Douglass M. Turnbull

    Published 2015
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  8. 8
    Natural disease course and genotype‐phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases

    Natural disease course and genotype‐phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases by Saskia Koene, Richard J. Rodenburg, Marjo S. van der Knaap, Michèl A.A.P. Willemsen, Wolfgang Sperl, Vincent Laugel, Elsebet Østergaard, Mark A. Tarnopolsky, Miguel A. Martı́n, Victoria Nesbitt, Janice M. Fletcher, Simon Edvardson, Vincent Procaccio, Abdelhamid Slama, Lambert P. W. J. den van Heuvel, J.A.M. Smeitink

    Published 2012
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  9. 9
    Mitochondrial disease and COVID-19: An international cohort study confirms risks and long-term outcomes

    Mitochondrial disease and COVID-19: An international cohort study confirms risks and long-term outcomes by Chiara Pizzamiglio, Hallgeir Jonvik, Stefen Brady, Patrick F. Chinnery, Lucía Galán, Gráinne S. Gorman, Alejandro Horga, Rita Horváth, Mirian C. H. Janssen, Albert Lim, Michelangelo Mancuso, Robert McFarland, Mária Judit Molnár, Olimpia Musumeci, Victoria Nesbitt, Wladimir, Guido Primiano, Ernestina Santos, Serenella Servidei, Rhys H. Thomas, Michael G. Hanna, Pedro Machado, Robert D. S. Pitceathly

    Published 2021
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  10. 10
    Diagnosis of ‘possible’ mitochondrial disease: an existential crisis

    Diagnosis of ‘possible’ mitochondrial disease: an existential crisis by Sumit Parikh, Amel Karaa, Amy Goldstein, Enrico Bertini, Patrick F. Chinnery, John Christodoulou, Bruce H. Cohen, Ryan L. Davis, Marni J. Falk, Carl Fratter, Rita Horváth, Mary Kay Koenig, M. Mancuso, Shana E. McCormack, Elizabeth M. McCormick, Robert McFarland, Victoria Nesbitt, Manuel Schiff, Hannah E. Steele, Silvia Stockler, Carolyn M. Sue, Mark A. Tarnopolsky, David R. Thorburn, Jerry Vockley, Shamima Rahman

    Published 2019
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  11. 11
    Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study

    Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study by Katherine Schon, Rita Horváth, Wei Wei, Claudia Calabrese, Arianna Tucci, Kristina Ibáñez, Thiloka Ratnaike, Robert D. S. Pitceathly, Enrico Bugiardini, Rosaline C. M. Quinlivan, Michael G. Hanna, Emma Clement, Emma Ashton, John A. Sayer, Paul M. Brennan, Dragana Josifova, Louise Izatt, Carl Fratter, Victoria Nesbitt, Timothy Barrett, Dominic J McMullen, Audrey Smith, Charulata Deshpande, Sarah Smithson, Richard Festenstein, Natalie Canham, Mark J. Caulfield, Henry Houlden, Shamima Rahman, Patrick F. Chinnery

    Published 2021
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  12. 12
    Forecasting stroke-like episodes and outcomes in mitochondrial disease

    Forecasting stroke-like episodes and outcomes in mitochondrial disease by Yi Shiau Ng, Nichola Z. Lax, Alasdair Blain, Daniel Erskine, Mark R. Baker, Tuomo Polvikoski, Rhys H. Thomas, Christopher M. Morris, Ming Lai, Roger G. Whittaker, Alasdair Gebbels, Amy Winder, Julie Hall, Catherine Feeney, Maria Elena Farrugia, Claire Hirst, Mark Roberts, Charlotte Lawthom, Alexia Chrysostomou, Kevin J. Murphy, Tracey Baird, Paul Maddison, Callum Duncan, Joanna Poulton, Victoria Nesbitt, Michael G. Hanna, Robert D. S. Pitceathly, Robert W. Taylor, Emma L. Blakely, Andrew M. Schaefer, Douglass M. Turnbull, Robert McFarland, Gráinne S. Gorman

    Published 2021
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