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Meier, T
Reznicek, L
Nwali, N
Coppard, N
Gallenmüller, C
Rouleau, J
Büchner, B
von Livonius, B
Yu-Wai-Man, P
Chinnery, P F
Griffiths, P G
Klopstock, T
Bailie, M
AuthorAffiliation 2 Santhera Pharmaceuticals, 4410 Liestal, Switzerland
6 Department of Ophthalmology, Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Quebec H2L 4M1, Canada
1 Department of Neurology, Friedrich-Baur-Institute, Ludwig-Maximilians-University, 80336 Munich, Germany
5 Department of Ophthalmology, Ludwig-Maximilians-University, Munich 80336, Germany
3 Departments of Neurology and Ophthalmology, Newcastle upon Tyne Foundation Hospital NHS Foundation Trust, NE1 4LP UK
4 Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, NE1 3BZ, UK
AuthorAffiliation_xml – name: 3 Departments of Neurology and Ophthalmology, Newcastle upon Tyne Foundation Hospital NHS Foundation Trust, NE1 4LP UK
– name: 5 Department of Ophthalmology, Ludwig-Maximilians-University, Munich 80336, Germany
– name: 2 Santhera Pharmaceuticals, 4410 Liestal, Switzerland
– name: 4 Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, NE1 3BZ, UK
– name: 1 Department of Neurology, Friedrich-Baur-Institute, Ludwig-Maximilians-University, 80336 Munich, Germany
– name: 6 Department of Ophthalmology, Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Quebec H2L 4M1, Canada
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  fullname: Klopstock, T
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  givenname: G
  surname: Metz
  fullname: Metz, G
– sequence: 3
  givenname: P
  surname: Yu-Wai-Man
  fullname: Yu-Wai-Man, P
– sequence: 4
  givenname: B
  surname: Büchner
  fullname: Büchner, B
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  surname: Gallenmüller
  fullname: Gallenmüller, C
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  givenname: M
  surname: Bailie
  fullname: Bailie, M
– sequence: 7
  givenname: N
  surname: Nwali
  fullname: Nwali, N
– sequence: 8
  givenname: P G
  surname: Griffiths
  fullname: Griffiths, P G
– sequence: 9
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  surname: von Livonius
  fullname: von Livonius, B
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  surname: Reznicek
  fullname: Reznicek, L
– sequence: 11
  givenname: J
  surname: Rouleau
  fullname: Rouleau, J
– sequence: 12
  givenname: N
  surname: Coppard
  fullname: Coppard, N
– sequence: 13
  givenname: T
  surname: Meier
  fullname: Meier, T
– sequence: 14
  givenname: P F
  surname: Chinnery
  fullname: Chinnery, P F
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Cites_doi 10.1016/S0022-510X(96)00311-5
10.4321/S0365-66912007000600012
10.1136/jnnp.71.6.813
10.1093/brain/awr180
10.1016/S0042-6989(97)00444-6
10.1016/S0022-510X(98)00239-1
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10.1371/journal.pone.0017963
10.1093/brain/awr170
10.1097/WNO.0b013e318241da45
10.1097/00041327-200020030-00006
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Carelli ( key 20170405101931_aws279-B3) 2011; 134
Sabet-Peyman ( key 20170405101931_aws279-B11) 2012; 32
Barnils ( key 20170405101931_aws279-B1) 2007; 82
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Carelli ( key 20170405101931_aws279-B2) 1998; 160
Carelli ( key 20170405101931_aws279-B4) 2001; 71
Mashima ( key 20170405101931_aws279-B10) 2000; 20
Haefeli ( key 20170405101931_aws279-B6) 2011; 6
Howell ( key 20170405101931_aws279-B7) 1998; 38
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SourceType Open Access Repository
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StartPage e230
SubjectTerms Adolescent
Adult
Aged
Cohort Studies
Double-Blind Method
Female
Follow-Up Studies
Humans
Letters to the Editor
Male
Middle Aged
Optic Atrophy, Hereditary, Leber - drug therapy
Optic Atrophy, Hereditary, Leber - epidemiology
Optic Atrophy, Hereditary, Leber - physiopathology
Time Factors
Treatment Outcome
Ubiquinone - analogs & derivatives
Ubiquinone - pharmacology
Ubiquinone - therapeutic use
Visual Acuity - drug effects
Visual Acuity - physiology
Young Adult
Title Persistence of the treatment effect of idebenone in Leber's hereditary optic neuropathy
URI https://www.ncbi.nlm.nih.gov/pubmed/23388409
https://pubmed.ncbi.nlm.nih.gov/PMC3572931
Volume 136
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