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 *

122 related articles for article (PubMed ID: 23021505)

  • 21. Phenotypes and mitochondrial DNA substitutions in families with A3243G mutation.
    Morovvati S; Nakagawa M; Sato Y; Hamada K; Higuchi I; Osame M
    Acta Neurol Scand; 2002 Aug; 106(2):104-8. PubMed ID: 12100370
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Detection of A3243G point mutation in mitochondrial DNA from 10 cases of MELAS.
    Wang Z; Liu S; Yang Y; Yuan Y; Wu L; Qi Y; Chen Q
    Chin Med J (Engl); 2002 Jul; 115(7):995-7. PubMed ID: 12150728
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Low antioxidant content and mutation load in mitochondrial DNA A3243G mutation-related diabetes mellitus.
    Liou CW; Huang CC; Lee CF; Lin TK; Wei YH
    J Formos Med Assoc; 2003 Aug; 102(8):527-33. PubMed ID: 14569316
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Homozygous W748S mutation in the POLG1 gene in patients with juvenile-onset Alpers syndrome and status epilepticus.
    Uusimaa J; Hinttala R; Rantala H; Päivärinta M; Herva R; Röyttä M; Soini H; Moilanen JS; Remes AM; Hassinen IE; Majamaa K
    Epilepsia; 2008 Jun; 49(6):1038-45. PubMed ID: 18294203
    [TBL] [Abstract][Full Text] [Related]  

  • 25. The study of mitochondrial A3243G mutation in different samples.
    Ma Y; Fang F; Yang Y; Zou L; Zhang Y; Wang S; Xu Y; Pei P; Qi Y
    Mitochondrion; 2009 Apr; 9(2):139-43. PubMed ID: 19460298
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. MELAS: A Multigenerational Impact of the MTTL1 A3243G MELAS Mutation.
    Prasad M; Narayan B; Prasad AN; Rupar CA; Levin S; Kronick J; Ramsay D; Tay KY; Prasad C
    Can J Neurol Sci; 2014 Mar; 41(2):210-9. PubMed ID: 24534033
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation.
    Demarest ST; Whitehead MT; Turnacioglu S; Pearl PL; Gropman AL
    J Child Neurol; 2014 Sep; 29(9):1249-56. PubMed ID: 25038129
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 8-year retrospective analysis of intravenous arginine therapy for acute metabolic strokes in pediatric mitochondrial disease.
    Ganetzky RD; Falk MJ
    Mol Genet Metab; 2018 Mar; 123(3):301-308. PubMed ID: 29428506
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Clinical and pathologic features of focal segmental glomerulosclerosis with mitochondrial tRNALeu(UUR) gene mutation.
    Hotta O; Inoue CN; Miyabayashi S; Furuta T; Takeuchi A; Taguma Y
    Kidney Int; 2001 Apr; 59(4):1236-43. PubMed ID: 11260383
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Clinical features of A3243G mitochondrial tRNA mutation.
    Chae JH; Hwang H; Lim BC; Cheong HI; Hwang YS; Kim KJ
    Brain Dev; 2004 Oct; 26(7):459-62. PubMed ID: 15351082
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Clinical features of MELAS and its relation with A3243G gene point mutation.
    Zhang J; Guo J; Fang W; Jun Q; Shi K
    Int J Clin Exp Pathol; 2015; 8(10):13411-5. PubMed ID: 26722549
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Hearing impairment is common in various phenotypes of the mitochondrial DNA A3243G mutation.
    Deschauer M; Müller T; Wieser T; Schulte-Mattler W; Kornhuber M; Zierz S
    Arch Neurol; 2001 Nov; 58(11):1885-8. PubMed ID: 11708999
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Mitochondrial A3243G mutation results in corneal endothelial polymegathism.
    Bakhoum MF; Wu WP; White EC; Sengillo JD; Sanfilippo C; Morcos MM; Freund KB; Perry HD; Sarraf D; Tsang SH
    Graefes Arch Clin Exp Ophthalmol; 2018 Mar; 256(3):583-588. PubMed ID: 29376197
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Novel MTCYB mutation in a young patient with recurrent stroke-like episodes and status epilepticus.
    Mancuso M; Nesti C; Ienco EC; Orsucci D; Pizzanelli C; Chiti A; Giorgi FS; Meschini MC; Fontanini G; Santorelli FM; Logerfo A; Romano A; Siciliano G; Bonuccelli U
    Am J Med Genet A; 2014 Nov; 164A(11):2922-5. PubMed ID: 25125337
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Chorea-ballism as a dominant clinical manifestation in heteroplasmic mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome with A3251G mutation in mitochondrial genome: a case report.
    Lahiri D; Sawale VM; Banerjee S; Dubey S; Roy BK; Das SK
    J Med Case Rep; 2019 Mar; 13(1):63. PubMed ID: 30837005
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Detection of eight frequently encountered point mutations in mitochondria in Chinese patients suggestive of mitochondrial encephalomyopathies.
    Cao Y; Ma Y; Zhang Y; Li Y; Fang F; Wang S; Bu D; Xu Y; Pei P; Li L; Xiao Y; Wu H; Yang Y; Zou L; Qi Y
    Mitochondrion; 2010 Jun; 10(4):330-4. PubMed ID: 20123042
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The mitochondrial A3243G mutation involves the peripheral vestibule as well as the cochlea.
    Iwasaki S; Egami N; Fujimoto C; Chihara Y; Ushio M; Kashio A; Yamasoba T
    Laryngoscope; 2011 Aug; 121(8):1821-4. PubMed ID: 21792976
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.