Literature DB >> 10701903

Leber's hereditary optic neuropathy presenting as multiple sclerosis-like disease of the CNS.

R Horváth, A Abicht, E A Shoubridge, V Karcagi, C Rózsa, S Komoly, H Lochmüller.   

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Year:  2000        PMID： 10701903     DOI： 10.1007/s004150050015

Source DB:  PubMed          Journal:  J Neurol        ISSN： 0340-5354            Impact factor:   4.849


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  10 in total

1.  Magnetic resonance imaging, magnetisation transfer imaging, and diffusion weighted imaging correlates of optic nerve, brain, and cervical cord damage in Leber's hereditary optic neuropathy.

Authors:  M Inglese; M Rovaris; S Bianchi; L La Mantia; G L Mancardi; A Ghezzi; P Montagna; F Salvi; M Filippi
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-04       Impact factor: 10.154

Review 2.  Role of mitochondria in multiple sclerosis.

Authors:  Bernadette Kalman
Journal:  Curr Neurol Neurosci Rep       Date:  2006-05       Impact factor: 5.081

3.  alpha-Tocopherol/lipid ratio in blood is decreased in patients with Leber's hereditary optic neuropathy and asymptomatic carriers of the 11778 mtDNA mutation.

Authors:  P Klivenyi; E Karg; C Rozsa; R Horvath; S Komoly; I Nemeth; S Turi; L Vecsei
Journal:  J Neurol Neurosurg Psychiatry       Date:  2001-03       Impact factor: 10.154

4.  Mitochondrial DNA abnormalities in ophthalmological disease.

Authors:  Grainne S Gorman; Robert W Taylor
Journal:  Saudi J Ophthalmol       Date:  2011-02-18

5.  Leber Hereditary Optic Neuropathy and Longitudinally Extensive Transverse Myelitis.

Authors:  C Bursle; K Riney; J Stringer; D Moore; G Gole; L S Kearns; D A Mackey; D Coman
Journal:  JIMD Rep       Date:  2017-12-17

Review 6.  [The role of uveitis in demyelinating diseases of the central nervous system].

Authors:  A-M Beyer; B Rosche; U Pleyer; K P Wandinger
Journal:  Nervenarzt       Date:  2007-12       Impact factor: 1.214

7.  Leber's hereditary optic neuropathy - Case report.

Authors:  Raluca Eugenia Iorga; Ruxandra Mihailovici; Manuela Ramona Ozturk; Dănuţ Costin
Journal:  Rom J Ophthalmol       Date:  2018 Jan-Mar

8.  A Typical Case Presentation with Spontaneous Visual Recovery in Patient Diagnosed with Leber Hereditary Optic Neuropathy due to Rare Point Mutation in MT-ND4 Gene (m.11253T>C) and Literature Review.

Authors:  Rasa Liutkeviciene; Agne Sidaraite; Lina Kuliaviene; Brigita Glebauskiene; Neringa Jurkute; Lina Aluzaite-Baranauskiene; Arvydas Gelzinis; Reda Zemaitiene
Journal:  Medicina (Kaunas)       Date:  2021-02-26       Impact factor: 2.430

9.  A multiple sclerosis-like disorder in patients with OPA1 mutations.

Authors:  Patrick Yu-Wai-Man; Achillefs Spyropoulos; Holly J Duncan; Joseph V Guadagno; Patrick F Chinnery
Journal:  Ann Clin Transl Neurol       Date:  2016-07-19       Impact factor: 4.511

10.  Severe inflammatory disease activity 14 months after cessation of Natalizumab in a patient with Leber's optic neuropathy and multiple sclerosis - a case report.

Authors:  Trygve Holmøy; Antonie G Beiske; Svetozar Zarnovicky; Aija Zuleron Myro; Egil Røsjø; Emilia Kerty
Journal:  BMC Neurol       Date:  2016-10-18       Impact factor: 2.474
  10 in total

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