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 *

421 related articles for article (PubMed ID: 11139730)

  • 21. Specific correlation between the wobble modification deficiency in mutant tRNAs and the clinical features of a human mitochondrial disease.
    Kirino Y; Goto Y; Campos Y; Arenas J; Suzuki T
    Proc Natl Acad Sci U S A; 2005 May; 102(20):7127-32. PubMed ID: 15870203
    [TBL] [Abstract][Full Text] [Related]  

  • 22. MELAS syndrome associated with both A3243G-tRNALeu mutation and multiple mitochondrial DNA deletions.
    Aharoni S; Traves TA; Melamed E; Cohen S; Silver EL
    J Neurol Sci; 2010 Sep; 296(1-2):101-3. PubMed ID: 20655066
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Absence of maternal A3243G mtDNA mutation and reversible hyperglycemia in a patient with MELAS syndrome.
    Liou CW; Huang CC; Tsai JL; Liu JY; Pang CY; Lee HC; Wang EK; Wei YH
    Acta Neurol Scand; 2000 Jan; 101(1):65-9. PubMed ID: 10660156
    [TBL] [Abstract][Full Text] [Related]  

  • 24. High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families.
    Cevoli S; Pallotti F; La Morgia C; Valentino ML; Pierangeli G; Cortelli P; Baruzzi A; Montagna P; Carelli V
    Cephalalgia; 2010 Aug; 30(8):919-27. PubMed ID: 20656703
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Wolff-Parkinson-White syndrome in Patients With MELAS.
    Sproule DM; Kaufmann P; Engelstad K; Starc TJ; Hordof AJ; De Vivo DC
    Arch Neurol; 2007 Nov; 64(11):1625-7. PubMed ID: 17998445
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. A novel mtDNA point mutation in tRNA(Val) is associated with hypertrophic cardiomyopathy and MELAS.
    Menotti F; Brega A; Diegoli M; Grasso M; Modena MG; Arbustini E
    Ital Heart J; 2004 Jun; 5(6):460-5. PubMed ID: 15320572
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Diagnosis and management of MELAS.
    Thambisetty M; Newman NJ
    Expert Rev Mol Diagn; 2004 Sep; 4(5):631-44. PubMed ID: 15347257
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Single muscle fiber analysis of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M; Mita S; Murakami T; Kumamoto T; Uchino M; Nonaka I; Ando M
    Ann Neurol; 1994 Apr; 35(4):413-9. PubMed ID: 8154867
    [TBL] [Abstract][Full Text] [Related]  

  • 30. MELAS- and Kearns-Sayre-type co-mutation [corrected] with myopathy and autoimmune polyendocrinopathy.
    Ohno K; Yamamoto M; Engel AG; Harper CM; Roberts LR; Tan GH; Fatourechi V
    Ann Neurol; 1996 Jun; 39(6):761-6. PubMed ID: 8651648
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Melas with point mutations involving tRNALeu (A3243G) and tRNAGlu(A14693g).
    Tzen CY; Thajeb P; Wu TY; Chen SC
    Muscle Nerve; 2003 Nov; 28(5):575-81. PubMed ID: 14571459
    [TBL] [Abstract][Full Text] [Related]  

  • 32. An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome.
    Ravn K; Wibrand F; Hansen FJ; Horn N; Rosenberg T; Schwartz M
    Eur J Hum Genet; 2001 Oct; 9(10):805-9. PubMed ID: 11781695
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Sequencing and quantitative assessment of mutant and wild-type mitochondrial DNA in paraffin sections from cases of MELAS.
    Love S; Nicoll JA; Kinrade E
    J Pathol; 1993 May; 170(1):9-14. PubMed ID: 8326463
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Muscle computed tomography patterns in patients with the mitochondrial DNA mutation 3243A>G.
    Kärppä M; Mahjneh I; Karttunen A; Tolonen U; Majamaa K
    J Neurol; 2004 May; 251(5):556-63. PubMed ID: 15164188
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Revelation of a new mitochondrial DNA mutation (G12147A) in a MELAS/MERFF phenotype.
    Melone MA; Tessa A; Petrini S; Lus G; Sampaolo S; di Fede G; Santorelli FM; Cotrufo R
    Arch Neurol; 2004 Feb; 61(2):269-72. PubMed ID: 14967777
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Diversity of clinical symptoms in A3243G mitochondrial DNA mutation (MELAS syndrome mutation).
    Pronicki M; Sykut-Cegielska J; Mierzewska H; Tońska K; Karczmarewicz E; Iwanicka K; Bartnik E; Pronicka E
    Med Sci Monit; 2002 Nov; 8(11):CR767-73. PubMed ID: 12444382
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Temporal bone histopathological and quantitative analysis of mitochondrial DNA in MELAS.
    Takahashi K; Merchant SN; Miyazawa T; Yamaguchi T; McKenna MJ; Kouda H; Iino Y; Someya T; Tamagawa Y; Takiyama Y; Nakano I; Saito K; Boyer P; Kitamura K
    Laryngoscope; 2003 Aug; 113(8):1362-8. PubMed ID: 12897560
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Infantile presentation of the mtDNA A3243G tRNA(Leu (UUR)) mutation.
    Okhuijsen-Kroes EJ; Trijbels JM; Sengers RC; Mariman E; van den Heuvel LP; Wendel U; Koch G; Smeitink JA
    Neuropediatrics; 2001 Aug; 32(4):183-90. PubMed ID: 11571698
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mitochondrial tRNA gene mutations in patients having mitochondrial disease with lactic acidosis.
    Ueki I; Koga Y; Povalko N; Akita Y; Nishioka J; Yatsuga S; Fukiyama R; Matsuishi T
    Mitochondrion; 2006 Feb; 6(1):29-36. PubMed ID: 16337222
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Muscle 3243A-->G mutation load and capacity of the mitochondrial energy-generating system.
    Janssen AJ; Schuelke M; Smeitink JA; Trijbels FJ; Sengers RC; Lucke B; Wintjes LT; Morava E; van Engelen BG; Smits BW; Hol FA; Siers MH; Ter Laak H; van der Knaap MS; Van Spronsen FJ; Rodenburg RJ; van den Heuvel LP
    Ann Neurol; 2008 Apr; 63(4):473-81. PubMed ID: 18306232
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 22.