These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

700 related items for PubMed ID: 11995959

  • 61. Leber's hereditary optic neuropathy and complex I deficiency in muscle.
    Larsson NG, Andersen O, Holme E, Oldfors A, Wahlström J.
    Ann Neurol; 1991 Nov; 30(5):701-8. PubMed ID: 1763894
    [Abstract] [Full Text] [Related]

  • 62. White matter changes in Leber's hereditary optic neuropathy: MRI findings.
    Küker W, Weir A, Quaghebeur G, Palace J.
    Eur J Neurol; 2007 May; 14(5):591-3. PubMed ID: 17437624
    [Abstract] [Full Text] [Related]

  • 63. Leber's hereditary optic neuropathy mutations in Korean patients with multiple sclerosis.
    Hwang JM, Chang BL, Park SS.
    Ophthalmologica; 2001 May; 215(6):398-400. PubMed ID: 11741103
    [Abstract] [Full Text] [Related]

  • 64. Reduced frequency of known mutations in a cohort of LHON patients from India.
    Sundaresan P, Kumar SM, Thompson S, Fingert JH.
    Ophthalmic Genet; 2010 Dec; 31(4):196-9. PubMed ID: 20809775
    [Abstract] [Full Text] [Related]

  • 65. Demyelinating polyneuropathy in Leber hereditary optic neuropathy.
    Gilhuis HJ, Schelhaas HJ, Cruysberg JR, Zwarts MJ.
    Neuromuscul Disord; 2006 Jun; 16(6):394-5. PubMed ID: 16690316
    [Abstract] [Full Text] [Related]

  • 66. Leber's hereditary optic neuropathy: clinical and molecular profile of a Brazilian sample.
    Maciel-Guerra AT, Zanchetta LM, Amaral Fernandes MS, Andrade PB, do Amor Divino Miranda PM, Sartorato EL.
    Ophthalmic Genet; 2010 Sep; 31(3):126-8. PubMed ID: 20565249
    [Abstract] [Full Text] [Related]

  • 67. [New mitochondrial DNA mutation in Leber's hereditary optic neuropathy: A case report].
    Thulliez M, Laudier B, Vignal-Clermont C, Hardy G, Bonicel P.
    J Fr Ophtalmol; 2018 Jun; 41(6):e293-e299. PubMed ID: 29910133
    [No Abstract] [Full Text] [Related]

  • 68. A challenging differential diagnosis - Leber's Hereditary Optic Neuropathy.
    Iorga RE, Munteanu-Dănulescu RS, Danielescu C.
    Rom J Ophthalmol; 2024 Jun; 68(1):65-71. PubMed ID: 38617721
    [Abstract] [Full Text] [Related]

  • 69. Stargardt's type maculopathy in a patient with 11778 Leber's optic neuropathy.
    Yen MY, Wei YH, Liu JH.
    J Neuroophthalmol; 1996 Jun; 16(2):120-3. PubMed ID: 8797169
    [Abstract] [Full Text] [Related]

  • 70. Leber's hereditary optic neuropathy - Case report.
    Iorga RE, Mihailovici R, Ozturk MR, Costin D.
    Rom J Ophthalmol; 2018 Jun; 62(1):64-71. PubMed ID: 29796436
    [Abstract] [Full Text] [Related]

  • 71. Leber's hereditary optic neuropathy--case report and literature review.
    Teive HA, Troiano AR, Raskin S, Werneck LC.
    Sao Paulo Med J; 2004 Nov 04; 122(6):276-9. PubMed ID: 15692724
    [Abstract] [Full Text] [Related]

  • 72. Leber's hereditary optic neuropathy mutations associated with infantile-onset myoclonic epilepsy.
    Frye RE.
    J Child Neurol; 2011 Jun 04; 26(6):782-5. PubMed ID: 21527392
    [Abstract] [Full Text] [Related]

  • 73. A case of neuromyelitis optica harboring both anti-aquaporin-4 antibodies and a pathogenic mitochondrial DNA mutation for Leber's hereditary optic neuropathy.
    Shiraishi W, Hayashi S, Kamada T, Isobe N, Yamasaki R, Murai H, Ohyagi Y, Kira J.
    Mult Scler; 2014 Feb 04; 20(2):258-60. PubMed ID: 24263387
    [Abstract] [Full Text] [Related]

  • 74. [Analysis of mutations and heteroplasmy at mitochondrial DNA 11778 using non-RI single strand conformation polymorphisms in Leber's hereditary optic neuropathy].
    Toyo-Oka Y, Wada C, Yamabe H, Inoue M, Ishigaki M, Matsuyama N, Ohnuki Y, Ichibe Y, Wakakura M, Ohtani H.
    Rinsho Byori; 1996 Jul 04; 44(7):676-80. PubMed ID: 8741498
    [Abstract] [Full Text] [Related]

  • 75. Retinal ganglion cell analysis in Leber's hereditary optic neuropathy.
    Akiyama H, Kashima T, Li D, Shimoda Y, Mukai R, Kishi S.
    Ophthalmology; 2013 Sep 04; 120(9):1943-4.e5. PubMed ID: 24001531
    [No Abstract] [Full Text] [Related]

  • 76. Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy.
    Giordano C, Iommarini L, Giordano L, Maresca A, Pisano A, Valentino ML, Caporali L, Liguori R, Deceglie S, Roberti M, Fanelli F, Fracasso F, Ross-Cisneros FN, D'Adamo P, Hudson G, Pyle A, Yu-Wai-Man P, Chinnery PF, Zeviani M, Salomao SR, Berezovsky A, Belfort R, Ventura DF, Moraes M, Moraes Filho M, Barboni P, Sadun F, De Negri A, Sadun AA, Tancredi A, Mancini M, d'Amati G, Loguercio Polosa P, Cantatore P, Carelli V.
    Brain; 2014 Feb 04; 137(Pt 2):335-53. PubMed ID: 24369379
    [Abstract] [Full Text] [Related]

  • 77. Clinical and Genetic Profile of Leber's Hereditary Optic Neuropathy in a Cohort of Patients From a Tertiary Eye Care Center.
    Bhate M, Kulkarni S, Nalawade R, Pujar A.
    J Pediatr Ophthalmol Strabismus; 2022 Feb 04; 59(5):344-349. PubMed ID: 35192383
    [Abstract] [Full Text] [Related]

  • 78. Leber hereditary optic neuropathy - historical report in comparison with the current knowledge.
    Piotrowska A, Korwin M, Bartnik E, Tońska K.
    Gene; 2015 Jan 15; 555(1):41-9. PubMed ID: 25261848
    [Abstract] [Full Text] [Related]

  • 79. [LHON (Leber's hereditary optic neuropathy)].
    Mashima Y.
    Nihon Rinsho; 2002 Apr 15; 60 Suppl 4():282-6. PubMed ID: 12013866
    [No Abstract] [Full Text] [Related]

  • 80. [Leber's hereditary optic neuropathy and its possible relation to a recent epidemic in Cuba].
    Santiesteban-Freixas R, Rodríguez-Hernández M, Hirano M, Francisco-Plasencia M, Mendoza-Santiesteban C, Carrero-Salgado M, Méndez-Larramendi I, Serrano-Verdura C, Luis-González S.
    Rev Neurol; 2002 Apr 15; 29(4):289-96. PubMed ID: 10797911
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 35.