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

287 related items for PubMed ID: 9073028

  • 1. Muscle histopathology in diabetes mellitus associated with mitochondrial tRNA(Leu(UUR)) mutation at position 3243.
    Suzuki Y, Goto Y, Taniyama M, Nonaka I, Murakami N, Hosokawa K, Asahina T, Atsumi Y, Matsuoka K.
    J Neurol Sci; 1997 Jan; 145(1):49-53. PubMed ID: 9073028
    [Abstract] [Full Text] [Related]

  • 2. Sporadic MERRF/MELAS overlap syndrome associated with the 3243 tRNA(Leu(UUR)) mutation of mitochondrial DNA.
    Campos Y, Martin MA, Lorenzo G, Aparicio M, Cabello A, Arenas J.
    Muscle Nerve; 1996 Feb; 19(2):187-90. PubMed ID: 8559168
    [Abstract] [Full Text] [Related]

  • 3. Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).
    Suzuki S, Hinokio Y, Hirai S, Onoda M, Matsumoto M, Ohtomo M, Kawasaki H, Satoh Y, Akai H, Abe K.
    Diabetologia; 1994 Aug; 37(8):818-25. PubMed ID: 7988784
    [Abstract] [Full Text] [Related]

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

  • 5. A MERRF/PEO overlap syndrome associated with the mitochondrial DNA 3243 mutation.
    Verma A, Moraes CT, Shebert RT, Bradley WG.
    Neurology; 1996 May; 46(5):1334-6. PubMed ID: 8628477
    [Abstract] [Full Text] [Related]

  • 6. Mitochondrial aldehyde dehydrogenase in diabetes associated with mitochondrial tRNA(Leu(UUR)) mutation at position 3243.
    Suzuki Y, Muramatsu T, Taniyama M, Atsumi Y, Suematsu M, Kawaguchi R, Higuchi S, Asahina T, Murata C, Handa M, Matsuoka K.
    Diabetes Care; 1996 Dec; 19(12):1423-5. PubMed ID: 8941476
    [Abstract] [Full Text] [Related]

  • 7. Maternally inherited diabetes and deafness is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNA(Leu(UUR)) gene.
    van den Ouweland JM, Lemkes HH, Trembath RC, Ross R, Velho G, Cohen D, Froguel P, Maassen JA.
    Diabetes; 1994 Jun; 43(6):746-51. PubMed ID: 7910800
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. [Comparison of clinical pictures of mitochondrial encephalomyopathy with tRNA(Leu(UUR)) mutation in 3243 with that in 3254].
    Mitsuoka T, Kawarai T, Watanabe C, Katayama S, Nakamura S.
    No To Shinkei; 1998 Dec; 50(12):1089-92. PubMed ID: 9989353
    [Abstract] [Full Text] [Related]

  • 10. The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study.
    Hammans SR, Sweeney MG, Hanna MG, Brockington M, Morgan-Hughes JA, Harding AE.
    Brain; 1995 Jun; 118 ( Pt 3)():721-34. PubMed ID: 7600089
    [Abstract] [Full Text] [Related]

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

  • 12. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M, Mita S, Sakuta R, Nonaka I, Araki S.
    Ann Neurol; 1993 Mar; 33(3):275-80. PubMed ID: 7684581
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA.
    Mariotti C, Savarese N, Suomalainen A, Rimoldi M, Comi G, Prelle A, Antozzi C, Servidei S, Jarre L, DiDonato S, Zeviani M.
    J Neurol; 1995 May; 242(5):304-12. PubMed ID: 7643139
    [Abstract] [Full Text] [Related]

  • 15. Phenotypic heterogeneity in a Chinese family with mitochondrial disease and A3243G mutation of mitochondrial DNA.
    Thajeb P, Lee HC, Pang CY, Jeng CM, Huang SF, Wei YH.
    Zhonghua Yi Xue Za Zhi (Taipei); 2000 Jan; 63(1):71-6. PubMed ID: 10645055
    [Abstract] [Full Text] [Related]

  • 16. The mitochondrial DNA A3243G mutation in Portugal: clinical and molecular studies in 5 families.
    Vilarinho L, Santorelli FM, Coelho I, Rodrigues L, Maia M, Barata I, Cabral P, Dionísio A, Costa A, Guimarães A, DiMauro S.
    J Neurol Sci; 1999 Mar 01; 163(2):168-74. PubMed ID: 10371079
    [Abstract] [Full Text] [Related]

  • 17. Mitochondrial DNA deletion in a patient with mitochondrial myopathy, lactic acidosis, and stroke-like episodes (MELAS) and Fanconi's syndrome.
    Campos Y, Garcia-Silva T, Barrionuevo CR, Cabello A, Muley R, Arenas J.
    Pediatr Neurol; 1995 Jul 01; 13(1):69-72. PubMed ID: 7575854
    [Abstract] [Full Text] [Related]

  • 18. [Clinical characterization of diabetes mellitus in the families with mitochondrial encephalomyopathies].
    Suzuki S.
    Nihon Rinsho; 1994 Oct 01; 52(10):2606-10. PubMed ID: 7527090
    [Abstract] [Full Text] [Related]

  • 19. Heterogeneity in the phenotypic expression of the mutation in the mitochondrial tRNA(Leu) (UUR) gene generally associated with the MELAS subset of mitochondrial encephalomyopathies.
    Jean-Francois MJ, Lertrit P, Berkovic SF, Crimmins D, Morris J, Marzuki S, Byrne E.
    Aust N Z J Med; 1994 Apr 01; 24(2):188-93. PubMed ID: 8042948
    [Abstract] [Full Text] [Related]

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

    Page: [Next] [New Search]
    of 15.