BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

240 related articles for article (PubMed ID: 18977334)

  • 21. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.
    Nakamura M; Yabe I; Sudo A; Hosoki K; Yaguchi H; Saitoh S; Sasaki H
    J Med Genet; 2010 Oct; 47(10):659-64. PubMed ID: 20610441
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy.
    Houshmand M; Larsson NG; Holme E; Oldfors A; Tulinius MH; Andersen O
    Biochim Biophys Acta; 1994 Apr; 1226(1):49-55. PubMed ID: 8155739
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) gene.
    Shoffner JM; Bialer MG; Pavlakis SG; Lott M; Kaufman A; Dixon J; Teichberg S; Wallace DC
    Neurology; 1995 Feb; 45(2):286-92. PubMed ID: 7854527
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Ultrastructural and clinical findings of mitochondrial encephalomyopathy:report of 27 cases].
    Zhang Q; Sun YL; Zhang CP; Qu BQ; Zhang ZQ
    Zhonghua Bing Li Xue Za Zhi; 2019 Apr; 48(4):298-302. PubMed ID: 30955266
    [No Abstract]   [Full Text] [Related]  

  • 25. Defects of mitochondrial DNA.
    Zeviani M; Antozzi C
    Brain Pathol; 1992 Apr; 2(2):121-32. PubMed ID: 1341953
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Childhood encephalopathies and myopathies: a prospective study in a defined population to assess the frequency of mitochondrial disorders.
    Uusimaa J; Remes AM; Rantala H; Vainionpää L; Herva R; Vuopala K; Nuutinen M; Majamaa K; Hassinen IE
    Pediatrics; 2000 Mar; 105(3 Pt 1):598-603. PubMed ID: 10699115
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The role of complex I genes in MELAS: a novel heteroplasmic mutation 3380G>A in ND1 of mtDNA.
    Horváth R; Reilmann R; Holinski-Feder E; Ringelstein EB; Klopstock T
    Neuromuscul Disord; 2008 Jul; 18(7):553-6. PubMed ID: 18590963
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional features.
    Malfatti E; Cardaioli E; Battisti C; Da Pozzo P; Malandrini A; Rufa A; Rocchi R; Federico A
    J Neurol Sci; 2010 Oct; 297(1-2):105-8. PubMed ID: 20708751
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients.
    Del Bo R; Bordoni A; Martinelli Boneschi F; Crimi M; Sciacco M; Bresolin N; Scarlato G; Comi GP
    J Neurol Sci; 2002 Oct; 202(1-2):85-91. PubMed ID: 12220698
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Disorders associated with multiple deletions of mitochondrial DNA.
    Haltia M; Suomalainen A; Majander A; Somer H
    Brain Pathol; 1992 Apr; 2(2):133-9. PubMed ID: 1341954
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A novel mitochondrial tRNA Arg mutation resulting in an anticodon swap in a patient with mitochondrial encephalomyopathy.
    Roos S; Darin N; Kollberg G; Andersson Grönlund M; Tulinius M; Holme E; Moslemi AR; Oldfors A
    Eur J Hum Genet; 2013 May; 21(5):571-3. PubMed ID: 22781096
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Mitochondrial encephalomyopathy due to a novel mutation in the tRNAGlu of mitochondrial DNA.
    Pancrudo J; Shanske S; Bonilla E; Daras M; Akman HO; Krishna S; Malkin E; DiMauro S
    J Child Neurol; 2007 Jul; 22(7):858-62. PubMed ID: 17715279
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mitochondrial diseases.
    Nonaka I
    Curr Opin Neurol Neurosurg; 1992 Oct; 5(5):622-32. PubMed ID: 1392136
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinical phenotype, prognosis and mitochondrial DNA mutation load in mitochondrial encephalomyopathies.
    Huang CC; Kuo HC; Chu CC; Liou CW; Ma YS; Wei YH
    J Biomed Sci; 2002; 9(6 Pt 1):527-33. PubMed ID: 12372990
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy.
    Valentino ML; Barboni P; Ghelli A; Bucchi L; Rengo C; Achilli A; Torroni A; Lugaresi A; Lodi R; Barbiroli B; Dotti M; Federico A; Baruzzi A; Carelli V
    Ann Neurol; 2004 Nov; 56(5):631-41. PubMed ID: 15505787
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Site-specific somatic mitochondrial DNA point mutations in patients with thymidine phosphorylase deficiency.
    Nishigaki Y; Martí R; Copeland WC; Hirano M
    J Clin Invest; 2003 Jun; 111(12):1913-21. PubMed ID: 12813027
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Rolandic mitochondrial encephalomyelopathy and MT-ND3 mutations.
    Werner KG; Morel CF; Kirton A; Benseler SM; Shoffner JM; Addis JB; Robinson BH; Burrowes DM; Blaser SI; Epstein LG; Feigenbaum AS
    Pediatr Neurol; 2009 Jul; 41(1):27-33. PubMed ID: 19520270
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Mitochondrial DNA mutation analysis in 97 Chinese patients with mitochondrial cephalomyopathy].
    Wang ZX; Luan XH; Zhang Y; Yang YL; Qi Y; Bu DF; Yuan Y
    Zhonghua Yi Xue Za Zhi; 2008 Dec; 88(46):3254-6. PubMed ID: 19159548
    [TBL] [Abstract][Full Text] [Related]  

  • 39. A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
    Seibel P; Flierl A; Kottlors M; Reichmann H
    Biochem Biophys Res Commun; 1994 Apr; 200(2):938-42. PubMed ID: 8179630
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Myoclonus epilepsy with ragged red fibers and multiple mtDNA deletions.
    Blumenthal DT; Shanske S; Schochet SS; Santorelli FM; DiMauro S; Jaynesm M; Bodensteiner J
    Neurology; 1998 Feb; 50(2):524-5. PubMed ID: 9484389
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.