BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

475 related articles for article (PubMed ID: 26517220)

  • 1. When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis?
    Lorenzoni PJ; Werneck LC; Kay CS; Silvado CE; Scola RH
    Arq Neuropsiquiatr; 2015 Nov; 73(11):959-67. PubMed ID: 26517220
    [TBL] [Abstract][Full Text] [Related]  

  • 2. An infant with a mitochondrial A3243G mutation demonstrating the MELAS phenotype.
    Kanaumi T; Hirose S; Goto Y; Naitou E; Mitsudome A
    Pediatr Neurol; 2006 Mar; 34(3):235-8. PubMed ID: 16504796
    [TBL] [Abstract][Full Text] [Related]  

  • 3. An analysis of the clinical and imaging features of mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Chen H; Hu Q; Raza HK; Chansysouphanthong T; Singh S; Rai P; Cui G; Zhang Z; Ye X; Xu C; Liu Y; Jiang H
    Somatosens Mot Res; 2020 Mar; 37(1):45-49. PubMed ID: 32000557
    [No Abstract]   [Full Text] [Related]  

  • 4. [Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children].
    Liu XL; Bao XH; Ma YN; Chang XZ; Qin J; Wu XR
    Zhonghua Er Ke Za Zhi; 2013 Feb; 51(2):130-5. PubMed ID: 23527980
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Increased mitochondrial DNA in blood vessels and ragged-red fibers in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS).
    Tokunaga M; Mita S; Sakuta R; Nonaka I; Araki S
    Ann Neurol; 1993 Mar; 33(3):275-80. PubMed ID: 7684581
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Progress in Diagnosing Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes.
    Wang YX; Le WD
    Chin Med J (Engl); 2015 Jul; 128(13):1820-5. PubMed ID: 26112726
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome: a review of treatment options.
    Scaglia F; Northrop JL
    CNS Drugs; 2006; 20(6):443-64. PubMed ID: 16734497
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [MELAS syndrome as a differential diagnosis of ischemic stroke].
    Finsterer J
    Fortschr Neurol Psychiatr; 2009 Jan; 77(1):25-31. PubMed ID: 19012224
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. When should MERRF (myoclonus epilepsy associated with ragged-red fibers) be the diagnosis?
    Lorenzoni PJ; Scola RH; Kay CS; Silvado CE; Werneck LC
    Arq Neuropsiquiatr; 2014 Oct; 72(10):803-11. PubMed ID: 25337734
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Atypical MELAS associated with mitochondrial tRNA(Lys) gene A8296G mutation.
    Sakuta R; Honzawa S; Murakami N; Goto Y; Nagai T
    Pediatr Neurol; 2002 Nov; 27(5):397-400. PubMed ID: 12504210
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Adult-onset Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke (MELAS)-like Encephalopathy Diagnosed Based on the Complete Sequencing of Mitochondrial DNA Extracted from Biopsied Muscle without any Myopathic Changes.
    Mukai M; Nagata E; Mizuma A; Yamano M; Sugaya K; Nishino I; Goto YI; Takizawa S
    Intern Med; 2017; 56(1):95-99. PubMed ID: 28050007
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Infantile encephalopathy associated with the MELAS A3243G mutation.
    Sue CM; Bruno C; Andreu AL; Cargan A; Mendell JR; Tsao CY; Luquette M; Paolicchi J; Shanske S; DiMauro S; De Vivo DC
    J Pediatr; 1999 Jun; 134(6):696-700. PubMed ID: 10356136
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Patients with MELAS with negative myopathology for characteristic ragged-red fibers.
    Lu Y; Deng J; Zhao Y; Zhang Z; Hong D; Yao S; Zhao D; Xie J; Fang H; Yuan Y; Wang Z
    J Neurol Sci; 2020 Jan; 408():116499. PubMed ID: 31726383
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [MELAS--mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome--two cases confirmed by biochemical and molecular investigations. Differential diagnosis of stroke causes].
    Mierzewska H; Mroczek K; Pronicki M; Pronicka E; Karczmarewicz E; Bartnik E; Zdzienicka E; Seniów J; Schmidt-Sidor B; Taraszewska A; Palasik W
    Neurol Neurochir Pol; 2002; 36(3):457-70. PubMed ID: 12185802
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Mitochondrial encephalomyelitis, lactic acidosis and cerebrovascular accidents (MELAS) in pediatric age with the A3243G mutation in the tRNALeu(UUR) gene of mitochondrial DNA].
    Coelho-Miranda L; Playan A; Artuch R; Vilaseca MA; Colomer J; Briones P; Coll-Cantí J; Conill J; Sans A; López de Munain A; Solano A; Alcaine MJ; Montoya J; Pineda M
    Rev Neurol; 2000 Nov 1-15; 31(9):804-11. PubMed ID: 11127079
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The A to G transition at nt 3243 of the mitochondrial tRNALeu(UUR) may cause an MERRF syndrome.
    Fabrizi GM; Cardaioli E; Grieco GS; Cavallaro T; Malandrini A; Manneschi L; Dotti MT; Federico A; Guazzi G
    J Neurol Neurosurg Psychiatry; 1996 Jul; 61(1):47-51. PubMed ID: 8676159
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [MELAS (mitochondrial myopathy, encephalopathy lactic acidosis, and stroke-like episodes): clinical features and mitochondrial DNA mutations].
    Goto Y
    Nihon Rinsho; 1993 Sep; 51(9):2373-8. PubMed ID: 8411715
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.