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

Journal Abstract Search


188 related items for PubMed ID: 10520236

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Leber's hereditary optic neuropathy mitochondrial DNA mutations at nucleotides 11778 and 3460 in multiple sclerosis.
    Mojon DS, Herbert J, Sadiq SA, Miller JR, Madonna M, Hirano M.
    Ophthalmologica; 1999; 213(3):171-5. PubMed ID: 10202290
    [Abstract] [Full Text] [Related]

  • 6. [Multiple sclerosis and Leber's hereditary optic neuropathy mitochondrial DNA mutations].
    Pénisson-Besnier I, Moreau C, Jacques C, Roger JC, Dubas F, Reynier P.
    Rev Neurol (Paris); 2001 May; 157(5):537-41. PubMed ID: 11438773
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Genetic analysis of Japanese pedigrees with Leber's hereditary optic neuropathy.
    Nakamura M.
    Kobe J Med Sci; 1993 Dec; 39(5-6):171-82. PubMed ID: 8182918
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. A family with Leber's hereditary optic neuropathy with mitochondrial 11778/ND4 and 4216/ND1 mutations.
    Hwang JM.
    Korean J Ophthalmol; 2000 Jun; 14(1):45-8. PubMed ID: 10933019
    [Abstract] [Full Text] [Related]

  • 13. Clinical features of Japanese Leber's hereditary optic neuropathy with 11778 mutation of mitochondrial DNA.
    Hotta Y, Fujiki K, Hayakawa M, Nakajima A, Kanai A, Mashima Y, Hiida Y, Shinoda K, Yamada K, Oguchi Y.
    Jpn J Ophthalmol; 1995 Jun; 39(1):96-108. PubMed ID: 7643491
    [Abstract] [Full Text] [Related]

  • 14. Segregation patterns and heteroplasmy prevalence in Leber's hereditary optic neuropathy.
    Jacobi FK, Leo-Kottler B, Mittelviefhaus K, Zrenner E, Meyer J, Pusch CM, Wissinger B.
    Invest Ophthalmol Vis Sci; 2001 May; 42(6):1208-14. PubMed ID: 11328729
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Leber's hereditary optic neuropathy (LHON)-related mitochondrial DNA sequence changes in italian patients presenting with sporadic bilateral optic neuritis.
    Sartore M, Grasso M, Piccolo G, Fasani R, Bergamaschi R, Malaspina A, Ceroni M, Kobayashi M, Semeraro A, Arbustini E.
    Biochem Mol Med; 1995 Oct; 56(1):45-51. PubMed ID: 8593537
    [Abstract] [Full Text] [Related]

  • 19. Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation.
    Oostra RJ, Bolhuis PA, Zorn-Ende I, de Kok-Nazaruk MM, Bleeker-Wagemakers EM.
    Hum Genet; 1994 Sep; 94(3):265-70. PubMed ID: 8076942
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 10.