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pro vyhledávání: '"Feeney CL"'
Autor:
Feeney, CL, Lim, AZ, Fagan, E, Blain, A, Bright, A, Maddison, J, Devine, H, Stewart, J, Taylor, RW, Gorman, GS, Turnbull, DM, Nesbitt, V, McFarland, R
Publikováno v:
Bjog
Objective Mitochondrial disease is a disorder of energy metabolism that affects 1 in 4300 adults in the UK. Pregnancy is associated with physiological demands that have implications for energy metabolism. We were interested to know how pregnancy was
Akademický článek
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Publikováno v:
BMC Health Services Research, Vol 5, Iss 1, p 47 (2005)
Abstract Background Patient choice is a major theme in current healthcare delivery. Little is known about patients' wishes regarding the timing of medical outpatient clinics. Methods A questionnaire survey of 300 sequential patients attending cardiac
Externí odkaz:
https://doaj.org/article/64ee14b3e86443df9ed4e204522c8496
mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease.
Autor:
Grady JP; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK., Pickett SJ; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK sarah.pickett@ncl.ac.uk robert.mcfarland@ncl.ac.uk., Ng YS; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK., Alston CL; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK.; NHS Highly Specialised Mitochondrial Diagnostic Laboratory, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK., Blakely EL; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK.; NHS Highly Specialised Mitochondrial Diagnostic Laboratory, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK., Hardy SA; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK.; NHS Highly Specialised Mitochondrial Diagnostic Laboratory, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK., Feeney CL; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK., Bright AA; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK., Schaefer AM; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK., Gorman GS; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK., McNally RJ; Institute of Health and Society, Newcastle University, Newcastle upon Tyne, UK., Taylor RW; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK.; NHS Highly Specialised Mitochondrial Diagnostic Laboratory, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK., Turnbull DM; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK., McFarland R; Wellcome Centre for Mitochondrial Research, Institute of Neuroscience, Newcastle University, Newcastle upon Tyne, UK sarah.pickett@ncl.ac.uk robert.mcfarland@ncl.ac.uk.
Publikováno v:
EMBO molecular medicine [EMBO Mol Med] 2018 Jun; Vol. 10 (6).
Autor:
Nesbitt V; Wellcome Trust Centre for Mitochondrial Research, The Medical School, Institute for Ageing and Health, Newcastle University, Newcastle-upon-Tyne, UK., Alston CL; NHS Specialised Services for Rare Mitochondrial Disorders of Adults and Children UK, Oxford, UK., Blakely EL; NHS Specialised Services for Rare Mitochondrial Disorders of Adults and Children UK, Oxford, UK., Fratter C; 1] NHS Specialised Services for Rare Mitochondrial Disorders of Adults and Children UK, Oxford, UK [2] Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Trust, Oxford, UK., Feeney CL; NHS Specialised Services for Rare Mitochondrial Disorders of Adults and Children UK, Oxford, UK., Poulton J; 1] NHS Specialised Services for Rare Mitochondrial Disorders of Adults and Children UK, Oxford, UK [2] Nuffield Department of Obstetrics and Gynaecology, University of Oxford, John Radcliffe Hospital, Oxford, UK., Brown GK; 1] NHS Specialised Services for Rare Mitochondrial Disorders of Adults and Children UK, Oxford, UK [2] Department of Biochemistry, University of Oxford, Oxford, UK., Turnbull DM; 1] Wellcome Trust Centre for Mitochondrial Research, The Medical School, Institute for Ageing and Health, Newcastle University, Newcastle-upon-Tyne, UK [2] NHS Specialised Services for Rare Mitochondrial Disorders of Adults and Children UK, Oxford, UK., Taylor RW; 1] Wellcome Trust Centre for Mitochondrial Research, The Medical School, Institute for Ageing and Health, Newcastle University, Newcastle-upon-Tyne, UK [2] NHS Specialised Services for Rare Mitochondrial Disorders of Adults and Children UK, Oxford, UK., McFarland R; 1] Wellcome Trust Centre for Mitochondrial Research, The Medical School, Institute for Ageing and Health, Newcastle University, Newcastle-upon-Tyne, UK [2] NHS Specialised Services for Rare Mitochondrial Disorders of Adults and Children UK, Oxford, UK.
Publikováno v:
European journal of human genetics : EJHG [Eur J Hum Genet] 2014 Nov; Vol. 22 (11), pp. 1255-9. Date of Electronic Publication: 2014 Mar 19.