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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

149 related articles for article (PubMed ID: 18202211)

  • 1. Causes of death in pedigrees with the 3243A>G mutation in mitochondrial DNA.
    Majamaa-Voltti K; Turkka J; Kortelainen ML; Huikuri H; Majamaa K
    J Neurol Neurosurg Psychiatry; 2008 Feb; 79(2):209-11. PubMed ID: 18202211
    [TBL] [Abstract][Full Text] [Related]  

  • 2. High prevalence of impaired glucose homeostasis and myopathy in asymptomatic and oligosymptomatic 3243A>G mitochondrial DNA mutation-positive subjects.
    Frederiksen AL; Jeppesen TD; Vissing J; Schwartz M; Kyvik KO; Schmitz O; Poulsen PL; Andersen PH
    J Clin Endocrinol Metab; 2009 Aug; 94(8):2872-9. PubMed ID: 19470628
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Obstetric complications in carriers of the m.3243A>G mutation, a retrospective cohort study on maternal and fetal outcome.
    de Laat P; Fleuren LH; Bekker MN; Smeitink JA; Janssen MC
    Mitochondrion; 2015 Nov; 25():98-103. PubMed ID: 26455484
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Clinical features and heteroplasmy in blood, urine and saliva in 34 Dutch families carrying the m.3243A > G mutation.
    de Laat P; Koene S; van den Heuvel LP; Rodenburg RJ; Janssen MC; Smeitink JA
    J Inherit Metab Dis; 2012 Nov; 35(6):1059-69. PubMed ID: 22403016
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cardiomyopathy and kidney disease in a patient with maternally inherited diabetes and deafness caused by the 3243A>G mutation of mitochondrial DNA.
    Azevedo O; Vilarinho L; Almeida F; Ferreira F; Guardado J; Ferreira M; Lourenço A; Medeiros R; Almeida J
    Cardiology; 2010; 115(1):71-4. PubMed ID: 19864902
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management.
    Nesbitt V; Pitceathly RD; Turnbull DM; Taylor RW; Sweeney MG; Mudanohwo EE; Rahman S; Hanna MG; McFarland R
    J Neurol Neurosurg Psychiatry; 2013 Aug; 84(8):936-8. PubMed ID: 23355809
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children.
    Uusimaa J; Moilanen JS; Vainionpää L; Tapanainen P; Lindholm P; Nuutinen M; Löppönen T; Mäki-Torkko E; Rantala H; Majamaa K
    Ann Neurol; 2007 Sep; 62(3):278-87. PubMed ID: 17823937
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The first concurrent detection of mitochondrial DNA m.3243A>G mutation, deletion, and depletion in a family with mitochondrial diabetes.
    Tabebi M; Safi W; Felhi R; Alila Fersi O; Keskes L; Abid M; Mnif M; Fakhfakh F
    Mol Genet Genomic Med; 2020 Jul; 8(7):e1292. PubMed ID: 32394641
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults.
    Ng YS; Grady JP; Lax NZ; Bourke JP; Alston CL; Hardy SA; Falkous G; Schaefer AG; Radunovic A; Mohiddin SA; Ralph M; Alhakim A; Taylor RW; McFarland R; Turnbull DM; Gorman GS
    Eur Heart J; 2016 Aug; 37(32):2552-9. PubMed ID: 26188002
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Relative fitness of carriers of the mitochondrial DNA mutation 3243A > G.
    Moilanen JS; Majamaa K
    Eur J Hum Genet; 2001 Jan; 9(1):59-62. PubMed ID: 11175302
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mitochondrial cardiomyopathies associated with the m.3243A>G mutation in the MT-TL1 gene: two sides of the same coin.
    Gallego-Delgado M; Cobo-Marcos M; Bornstein B; Hernández-Laín A; Alonso-Pulpón L; Garcia-Pavia P
    Rev Esp Cardiol (Engl Ed); 2015 Feb; 68(2):153-5. PubMed ID: 25440178
    [No Abstract]   [Full Text] [Related]  

  • 12. Preimplantation genetic diagnosis in mitochondrial DNA disorders: challenge and success.
    Sallevelt SC; Dreesen JC; Drüsedau M; Spierts S; Coonen E; van Tienen FH; van Golde RJ; de Coo IF; Geraedts JP; de Die-Smulders CE; Smeets HJ
    J Med Genet; 2013 Feb; 50(2):125-32. PubMed ID: 23339111
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Analysis of association among clinical features and shorter leukocyte telomere length in mitochondrial diabetes with m.3243A>G mitochondrial DNA mutation.
    Zhou MC; Min R; Ji JJ; Zhang S; Tong AL; Xu JP; Li ZY; Zhang HB; Li YX
    BMC Med Genet; 2015 Oct; 16():92. PubMed ID: 26449496
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Cardiomyopathy in children with mitochondrial disease: Prognosis and genetic background.
    Imai-Okazaki A; Kishita Y; Kohda M; Mizuno Y; Fushimi T; Matsunaga A; Yatsuka Y; Hirata T; Harashima H; Takeda A; Nakaya A; Sakata Y; Kogaki S; Ohtake A; Murayama K; Okazaki Y
    Int J Cardiol; 2019 Mar; 279():115-121. PubMed ID: 30642647
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Long-term cardiac prognosis and risk stratification in 260 adults presenting with mitochondrial diseases.
    Wahbi K; Bougouin W; Béhin A; Stojkovic T; Bécane HM; Jardel C; Berber N; Mochel F; Lombès A; Eymard B; Duboc D; Laforêt P
    Eur Heart J; 2015 Nov; 36(42):2886-93. PubMed ID: 26224072
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A case with short stature and proteinuria: atypical presentation of a family with m.3243A>G mutation.
    Büyükyılmaz G; İnözü M; Çavdarlı B
    Turk J Pediatr; 2024 Oct; 66(4):490-498. PubMed ID: 39387423
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Postlingual hearing loss as a mitochondrial 3243A>G mutation phenotype.
    Iwanicka-Pronicka K; Pollak A; Skórka A; Lechowicz U; Pajdowska M; Furmanek M; Rzeski M; Korniszewski L; Skarżyński H; Płoski R
    PLoS One; 2012; 7(10):e44054. PubMed ID: 23133508
    [TBL] [Abstract][Full Text] [Related]  

  • 18. m.3243A>G mutation in mitochondrial DNA leads to decreased insulin sensitivity in skeletal muscle and to progressive beta-cell dysfunction.
    Lindroos MM; Majamaa K; Tura A; Mari A; Kalliokoski KK; Taittonen MT; Iozzo P; Nuutila P
    Diabetes; 2009 Mar; 58(3):543-9. PubMed ID: 19073775
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and Molecular Characteristics in 100 Chinese Pediatric Patients with m.3243A>G Mutation in Mitochondrial DNA.
    Xia CY; Liu Y; Liu H; Zhang YC; Ma YN; Qi Y
    Chin Med J (Engl); 2016 Aug; 129(16):1945-9. PubMed ID: 27503020
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Muscle phenotype and mutation load in 51 persons with the 3243A>G mitochondrial DNA mutation.
    Jeppesen TD; Schwartz M; Frederiksen AL; Wibrand F; Olsen DB; Vissing J
    Arch Neurol; 2006 Dec; 63(12):1701-6. PubMed ID: 17172609
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.