BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

151 related articles for article (PubMed ID: 8786027)

  • 1. Could coenzyme Q10 and L-carnitine be a treatment for diabetes secondary to 3243 mutation of mtDNA?
    Silvestre-Aillaud P; BenDahan D; Paquis-Fluckinger V; Pouget J; Pelissier JF; Desnuelle C; Cozzone PJ; Vialettes B
    Diabetologia; 1995 Dec; 38(12):1485-6. PubMed ID: 8786027
    [No Abstract]   [Full Text] [Related]  

  • 2. Diabetes mellitus associated with 3243 mitochondrial tRNA(Leu(UUR)) mutation: clinical features and coenzyme Q10 treatment.
    Suzuki Y; Taniyama M; Muramatsu T; Atsumi Y; Hosokawa K; Asahina T; Shimada A; Murata C; Matsuoka K
    Mol Aspects Med; 1997; 18 Suppl():S181-8. PubMed ID: 9266520
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The effects of coenzyme Q10 treatment on maternally inherited diabetes mellitus and deafness, and mitochondrial DNA 3243 (A to G) mutation.
    Suzuki S; Hinokio Y; Ohtomo M; Hirai M; Hirai A; Chiba M; Kasuga S; Satoh Y; Akai H; Toyota T
    Diabetologia; 1998 May; 41(5):584-8. PubMed ID: 9628277
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Insulin sensitivity in patients with NIDDM and the A-to-G mutation at nucleotide 3,243 of the mitochondrial tRNALeu(UUR) gene.
    Iwasaki N; Wasada T; Takahashi Y; Babazono T; Ohgawara H; Omori Y
    Diabetes Care; 1995 Jun; 18(6):886-8. PubMed ID: 7555525
    [No Abstract]   [Full Text] [Related]  

  • 5. [Patient with diabetes and impaired hearing].
    García E; Sánchez R; Partida M; de Mingo ML; Calatayud M; Martínez G; Hawkins F
    Endocrinol Nutr; 2012 Mar; 59(3):220-2. PubMed ID: 22153565
    [No Abstract]   [Full Text] [Related]  

  • 6. Beta-cell function in individuals carrying the mitochondrial tRNA leu (UUR) mutation.
    Salles JE; Kasamatsu TS; Dib SA; Moisés RS
    Pancreas; 2007 Jan; 34(1):133-7. PubMed ID: 17198195
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical phenotypes, insulin secretion, and insulin sensitivity in kindreds with maternally inherited diabetes and deafness due to mitochondrial tRNALeu(UUR) gene mutation.
    Velho G; Byrne MM; Clément K; Sturis J; Pueyo ME; Blanché H; Vionnet N; Fiet J; Passa P; Robert JJ; Polonsky KS; Froguel P
    Diabetes; 1996 Apr; 45(4):478-87. PubMed ID: 8603770
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Beware the thin, deaf 'type 2' diabetic: maternally inherited diabetes and deafness with systemic (mitochondrial) manifestations.
    Jones DL; Greenaway TM
    Intern Med J; 2004 Aug; 34(8):517-8. PubMed ID: 15317555
    [No Abstract]   [Full Text] [Related]  

  • 9. Myocardial dysfunction in mitochondrial diabetes treated with Coenzyme Q10.
    Salles JE; Moisés VA; Almeida DR; Chacra AR; Moisés RS
    Diabetes Res Clin Pract; 2006 Apr; 72(1):100-3. PubMed ID: 16253379
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Diminished insulin secretory response to glucose but normal insulin and glucagon secretory responses to arginine in a family with maternally inherited diabetes and deafness caused by mitochondrial tRNA(LEU(UUR)) gene mutation.
    Brändle M; Lehmann R; Maly FE; Schmid C; Spinas GA
    Diabetes Care; 2001 Jul; 24(7):1253-8. PubMed ID: 11423511
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial diabetes mellitus: a review.
    Gerbitz KD; van den Ouweland JM; Maassen JA; Jaksch M
    Biochim Biophys Acta; 1995 May; 1271(1):253-60. PubMed ID: 7599217
    [TBL] [Abstract][Full Text] [Related]  

  • 12. The effect of coenzyme Q10 administration on metabolic control in patients with type 2 diabetes mellitus.
    Eriksson JG; Forsén TJ; Mortensen SA; Rohde M
    Biofactors; 1999; 9(2-4):315-8. PubMed ID: 10416046
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Mitochondrial diabetes mellitus].
    Oka Y
    Nihon Rinsho; 2006 Sep; Suppl 3():59-63. PubMed ID: 17022500
    [No Abstract]   [Full Text] [Related]  

  • 15. Does mitochondrial genome mutation in subjects with maternally inherited diabetes and deafness decrease severity of diabetic retinopathy?
    Holmes-Walker DJ; Mitchell P; Boyages SC
    Diabet Med; 1998 Nov; 15(11):946-52. PubMed ID: 9827849
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial DNA [tRNA(Leu)(UUR)] mutation in a southern Italian diabetic population.
    Rigoli L; Di Benedetto A; Romano G; Corica F; Cucinotta D
    Diabetes Care; 1997 Apr; 20(4):674-5. PubMed ID: 9097002
    [No Abstract]   [Full Text] [Related]  

  • 17. Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNA(Leu(UUR)) gene mutation in Japanese patients.
    Katagiri H; Asano T; Ishihara H; Inukai K; Anai M; Yamanouchi T; Tsukuda K; Kikuchi M; Kitaoka H; Ohsawa N
    Diabetologia; 1994 May; 37(5):504-10. PubMed ID: 8056189
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Prevalence of maternally inherited diabetes and deafness in Australian diabetic subjects.
    Holmes-Walker DJ; Boyages SC
    Diabetologia; 1999 Aug; 42(8):1028-9. PubMed ID: 10491766
    [No Abstract]   [Full Text] [Related]  

  • 19. Maternally inherited diabetes and deafness (MIDD): a distinct subtype of diabetes associated with a mitochondrial tRNA(Leu)(UUR) gene point mutation.
    van den Ouweland JM; Lemkes HH; Gerbitz KD; Maassen JA
    Muscle Nerve Suppl; 1995; 3():S124-30. PubMed ID: 7603513
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Non-isotopic and sensitive method for diagnosis of maternally-inherited diabetes and deafness.
    Blanché H; Froguel P; Dausset J; Cohen D; Cohen N
    Diabetologia; 1994 Aug; 37(8):842. PubMed ID: 7988788
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.