BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 38881794)

  • 1. Case report: Late-onset MELAS syndrome with mtDNA 5783G>A mutation diagnosed by urinary sediment genetic testing.
    Cai H; Li LM; Zhang M; Zhou Y; Li P
    Front Genet; 2024; 15():1367716. PubMed ID: 38881794
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Late-onset mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with mitochondrial DNA 3243A>G mutation masquerading as autoimmune encephalitis: A case report.
    Wang JW; Yuan XB; Chen HF
    World J Clin Cases; 2023 May; 11(14):3275-3281. PubMed ID: 37274040
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Adult-onset MELAS syndrome in a 51-year-old woman without typical clinical manifestations: a case report.
    Lee SH; Lee CJ; Won D; Kang SM
    Eur Heart J Case Rep; 2023 Jan; 7(1):ytad028. PubMed ID: 36733687
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutation.
    Scarcella S; Dell'Arti L; Gagliardi D; Magri F; Govoni A; Velardo D; Mainetti C; Minorini V; Ronchi D; Piga D; Comi GP; Corti S; Meneri M
    BMC Neurol; 2023 Apr; 23(1):165. PubMed ID: 37095452
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Adult-onset mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) syndrome with progressive sensorineural hearing loss: A case report.
    Trang TM; Chien PC; Dung BT; Thu NTH; Truc NTT; Khang VNC
    Radiol Case Rep; 2021 Jul; 16(7):1865-1869. PubMed ID: 34093932
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the
    Endres D; Süß P; Maier SJ; Friedel E; Nickel K; Ziegler C; Fiebich BL; Glocker FX; Stock F; Egger K; Lange T; Dacko M; Venhoff N; Erny D; Doostkam S; Komlosi K; Domschke K; Tebartz van Elst L
    Front Immunol; 2019; 10():412. PubMed ID: 30949164
    [No Abstract]   [Full Text] [Related]  

  • 7. Case report: 5 year follow-up of adult late-onset mitochondrial encephalomyopathy with lactic acid and stroke-like episodes (MELAS).
    Sunde K; Blackburn PR; Cheema A; Gass J; Jackson J; Macklin S; Atwal PS
    Mol Genet Metab Rep; 2016 Dec; 9():94-97. PubMed ID: 27896131
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes / myoclonus epilepsy with ragged-red fibers /Leigh overlap syndrome caused by mitochondrial DNA 8344A>G mutation].
    Hou Y; Zhao XT; Xie ZY; Yuan Y; Wang ZX
    Beijing Da Xue Xue Bao Yi Xue Ban; 2020 Oct; 52(5):851-855. PubMed ID: 33047718
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Late-onset MELAS syndrome with mtDNA 14453G→A mutation masquerading as an acute encephalitis: a case report.
    Yokota Y; Hara M; Akimoto T; Mizoguchi T; Goto YI; Nishino I; Kamei S; Nakajima H
    BMC Neurol; 2020 Jun; 20(1):247. PubMed ID: 32552696
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Diagnosis of adult-onset MELAS syndrome in a 63-year-old patient with suspected recurrent strokes - a case report.
    Sinnecker T; Andelova M; Mayr M; Rüegg S; Sinnreich M; Hench J; Frank S; Schaller A; Stippich C; Wuerfel J; Bonati LH
    BMC Neurol; 2019 May; 19(1):91. PubMed ID: 31068171
    [TBL] [Abstract][Full Text] [Related]  

  • 11. MELAS and Kearns-Sayre overlap syndrome due to the mtDNA m. A3243G mutation and large-scale mtDNA deletions.
    Yu N; Zhang YF; Zhang K; Xie Y; Lin XJ; Di Q
    eNeurologicalSci; 2016 Sep; 4():15-18. PubMed ID: 29430542
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diagnosis of adult-onset MELAS with suspected recurrent strokes: A case report.
    Yang F; Peng S; Peng Q
    Exp Ther Med; 2022 Jul; 24(1):466. PubMed ID: 35747150
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
    Chakrabarty S; Govindaraj P; Sankaran BP; Nagappa M; Kabekkodu SP; Jayaram P; Mallya S; Deepha S; Ponmalar JNJ; Arivinda HR; Meena AK; Jha RK; Sinha S; Gayathri N; Taly AB; Thangaraj K; Satyamoorthy K
    J Neurol; 2021 Jun; 268(6):2192-2207. PubMed ID: 33484326
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome mimicking herpes simplex encephalitis: A case report.
    Zeng WG; Liao WM; Hu J; Chen SF; Wang Z
    Radiol Case Rep; 2022 Jul; 17(7):2428-2431. PubMed ID: 35601382
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Modeling Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome Using Patient-Derived Induced Neurons Generated by Direct Reprogramming.
    Povea-Cabello S; Villanueva-Paz M; Villalón-García I; Talaverón-Rey M; Álvarez-Cordoba M; Suárez-Rivero JM; Montes MÁ; Rodríguez-Moreno A; Andrade-Talavera Y; Armengol JA; Sánchez-Alcázar JA
    Cell Reprogram; 2022 Oct; 24(5):294-303. PubMed ID: 35802497
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) Syndrome: Frequency, Clinical Features, Imaging, Histopathologic, and Molecular Genetic Findings in a Third-level Health Care Center in Mexico.
    Galnares-Olalde JA; López-Hernández JC; Benitez-Alonso EO; de Montellano DJD; May-Mas RN; Briseño-Godínez ME; Pérez-Valdez EY; Pérez-Jovel E; Fernández-Valverde F; León-Manríquez E; Vargas-Cañas ES
    Neurologist; 2021 Jul; 26(4):143-148. PubMed ID: 34190208
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with the A3243G mutation of the tRNALeu(UUR) gene of mtDNA in native American haplogroup B2].
    Delgado-Sánchez R; Zárate-Moysen A; Monsalvo-Reyes A; Herrero MD; Ruiz-Pesini E; López-Pérez M; Montoya J; Montiel-Sosa JF
    Rev Neurol; 2007 Jan 1-15; 44(1):18-22. PubMed ID: 17199225
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Late-onset Mitochondrial Encephalomyopathy with Lactic Acidosis and Stroke-like Episodes (MELAS) Syndrome in a 63-year-old Patient.
    Abdullah H; Shah S; Husain H; Hassan F; Maqsood H
    Cureus; 2020 Apr; 12(4):e7862. PubMed ID: 32483512
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.