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Report provided to the Human Fertilisation and Embryology Authority, April 2011 - page 29 / 45

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Annex C: Evidence reviewed

  • 1.

    Statements/letters

    • A statement (with reference to literature) from Dr Rhiannon Lloyd, Leverhulme Early Career Research Fellow, Zoological Society of London

A letter from Dr David King, Director of Human Genetics Alert

A letter from David Thorburn, Head of Mitochondrial Research Group, Murdoch Children‟s Research Institute, Victoria, Australia

A statement from Dr Shamima Rahman & Professor Michael Hanna (National Commissioning Group funded service for Diagnosis and Management of Rare Mitochondrial Diseases in Adults and Children, Centre for Neuromuscular Diseases, National Hospital for Neurology, UCLH) and Professor Peter Clayton & Professor Francesco Muntoni (Great Ormond Street Hospital and the UCL Institute of Child Health, London)

A statement from Dr Marita Pohlschmidt, Research Director, Muscular Dystrophy Campaign

A statement from Dr Robert McFarland and Professor Robert Taylor, NCG Rare Mitochondrial Diseases Service, Newcastle University

Summary of evidence (including slides presented to the HFEA Scientific and Clinical Advances Advisory Committee in May 2010) from Lyndsey Craven, Laura Irving, Alison Murdoch, Mary Herbert, Doug Turnbull, Newcastle University

A statement from Nathan Treff with reference to four published papers

Page 29 of 45

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