Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Charlotte Sanders"'
Autor:
Silvia Vidali, Raffaele Gerlini, Kyle Thompson, Jill E Urquhart, Jana Meisterknecht, Juan Antonio Aguilar‐Pimentel, Oana V Amarie, Lore Becker, Catherine Breen, Julia Calzada‐Wack, Nirav F Chhabra, Yi‐Li Cho, Patricia da Silva‐Buttkus, René G Feichtinger, Kristine Gampe, Lillian Garrett, Kai P Hoefig, Sabine M Hölter, Elisabeth Jameson, Tanja Klein‐Rodewald, Stefanie Leuchtenberger, Susan Marschall, Philipp Mayer‐Kuckuk, Gregor Miller, Manuela A Oestereicher, Kristina Pfannes, Birgit Rathkolb, Jan Rozman, Charlotte Sanders, Nadine Spielmann, Claudia Stoeger, Marten Szibor, Irina Treise, John H Walter, Wolfgang Wurst, Johannes A Mayr, Helmut Fuchs, Ulrich Gärtner, Ilka Wittig, Robert W Taylor, William G Newman, Holger Prokisch, Valerie Gailus‐Durner, Martin Hrabě de Angelis
Publikováno v:
EMBO Molecular Medicine, Vol 13, Iss 12, Pp n/a-n/a (2021)
Abstract Mitochondrial disorders are clinically and genetically diverse, with isolated complex III (CIII) deficiency being relatively rare. Here, we describe two affected cousins, presenting with recurrent episodes of severe lactic acidosis, hyperamm
Externí odkaz:
https://doaj.org/article/341f02162d414b2e9fd51d3fc242e6ba
Autor:
Elisabeth Jameson, Johannes A. Mayr, Manuela A. Oestereicher, John H. Walter, Juan Antonio Aguilar-Pimentel, Wolfgang Wurst, William G. Newman, Stefanie Leuchtenberger, Patricia da Silva-Buttkus, Jill E. Urquhart, Helmut Fuchs, Ilka Wittig, Robert W. Taylor, Silvia Vidali, René G. Feichtinger, Jana Meisterknecht, Martin Hrabě de Angelis, Lore Becker, Philipp Mayer-Kuckuk, Kai P. Hoefig, Yi-Li Cho, Catherine Breen, Nadine Spielmann, Marten Szibor, Raffaele Gerlini, Irina Treise, Lillian Garrett, Nirav Florian Chhabra, Oana V. Amarie, Kyle Thompson, Charlotte Sanders, Susan Marschall, Jan Rozman, Holger Prokisch, Kristine Gampe, Birgit Rathkolb, Sabine M. Hölter, Kristina Pfannes, Gregor Miller, Tanja Klein-Rodewald, Valerie Gailus-Durner, Julia Calzada-Wack, Ulrich Gärtner, Claudia Stoeger
Publikováno v:
EMBO Molecular Medicine
Newman, W, Urquhart, J, Breen, C, Walter, J & Jameson, E 2021, ' Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes ', EMBO Molecular Medicine, vol. 13, no. 12, e14397 . https://doi.org/10.15252/emmm.202114397
EMBO Mol. Med.:e14397 (2021)
EMBO molecular medicine 13(12), e14397 (2021). doi:10.15252/emmm.202114397
EMBO Molecular Medicine, Vol 13, Iss 12, Pp n/a-n/a (2021)
Newman, W, Urquhart, J, Breen, C, Walter, J & Jameson, E 2021, ' Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes ', EMBO Molecular Medicine, vol. 13, no. 12, e14397 . https://doi.org/10.15252/emmm.202114397
EMBO Mol. Med.:e14397 (2021)
EMBO molecular medicine 13(12), e14397 (2021). doi:10.15252/emmm.202114397
EMBO Molecular Medicine, Vol 13, Iss 12, Pp n/a-n/a (2021)
Mitochondrial disorders are clinically and genetically diverse, with isolated complex III (CIII) deficiency being relatively rare. Here, we describe two affected cousins, presenting with recurrent episodes of severe lactic acidosis, hyperammonaemia,
Autor:
Charlotte L. Hall, Charlotte Sanderson, Beverly J. Brown, Per Andrén, Sophie Bennett, Liam R. Chamberlain, E. Bethan Davies, Kareem Khan, Natalie Kouzoupi, David Mataix-Cols, Caitlin McKenzie, Tara Murphy, Mark Townsend, Chris Hollis, Elizabeth Murray
Publikováno v:
Trials, Vol 21, Iss 1, Pp 1-13 (2020)
Abstract Background Despite being the gold standard of research to determine effectiveness, randomised controlled trials (RCTs) often struggle with participant recruitment, engagement and retention. These issues may be exacerbated when recruiting vul
Externí odkaz:
https://doaj.org/article/017172cbf8d548f89583c341efcf00c7