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Journal Abstract Search

180 related items for PubMed ID: 37274040

  • 1. 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 16; 11(14):3275-3281. PubMed ID: 37274040
    [Abstract] [Full Text] [Related]

  • 2. Late-onset Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes Presenting With Auditory Agnosia.
    Smith K, Chiu S, Hunt C, Chandregowda A, Babovic-Vuksanovic D, Keegan BM.
    Neurologist; 2019 May 16; 24(3):90-92. PubMed ID: 31045719
    [Abstract] [Full Text] [Related]

  • 3. Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with an MT-TL1 m.3243A>G point mutation: Neuroradiological features and their implications for underlying pathogenesis.
    Zheng H, Zhang X, Tian L, Liu B, He X, Wang L, Ding S, Guo Y, Cai J.
    Front Neurosci; 2022 May 16; 16():1028762. PubMed ID: 36685235
    [Abstract] [Full Text] [Related]

  • 4. 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; 16(7):1865-1869. PubMed ID: 34093932
    [Abstract] [Full Text] [Related]

  • 5. 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 24; 23(1):165. PubMed ID: 37095452
    [Abstract] [Full Text] [Related]

  • 6. Recurrent Stroke Events Secondary to a Late Presentation of Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-Like Symptoms (MELAS) Syndrome.
    Jameel I, Sreh A, Das P.
    Cureus; 2020 Dec 02; 12(12):e11839. PubMed ID: 33282603
    [Abstract] [Full Text] [Related]

  • 7. New Variant of MELAS Syndrome With Executive Dysfunction, Heteroplasmic Point Mutation in the MT-ND4 Gene (m.12015T>C; p.Leu419Pro) and Comorbid Polyglandular Autoimmune Syndrome Type 2.
    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 Dec 02; 10():412. PubMed ID: 30949164
    [Abstract] [Full Text] [Related]

  • 8. Delay in diagnosing a patient with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome who presented with status epilepticus and lactic acidosis: a case report.
    Alenezi AF, Almelahi MA, Fekih-Romdhana F, Jahrami HA.
    J Med Case Rep; 2022 Oct 10; 16(1):361. PubMed ID: 36210452
    [Abstract] [Full Text] [Related]

  • 9. Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature.
    Gagliardi D, Mauri E, Magri F, Velardo D, Meneri M, Abati E, Brusa R, Faravelli I, Piga D, Ronchi D, Triulzi F, Peverelli L, Sciacco M, Bresolin N, Comi GP, Corti S, Govoni A.
    Front Neurol; 2019 Oct 10; 10():38. PubMed ID: 30766507
    [Abstract] [Full Text] [Related]

  • 10. Late-onset MELAS syndrome in a 46-year-old man with initial symptom of chest tightness: a case report.
    Wang A, Zhao J, Zhao Y, Yan Y.
    Eur Heart J Case Rep; 2023 Sep 10; 7(9):ytad441. PubMed ID: 37767231
    [Abstract] [Full Text] [Related]

  • 11. 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 10; 17(7):2428-2431. PubMed ID: 35601382
    [Abstract] [Full Text] [Related]

  • 12. First Case of MELAS Syndrome Presenting with Local Brain Edema Requiring Decompressive Craniectomy.
    Yesilbas O, Sengenc E, Olbak ME, Bako D, Nizam OG, Seyithanoglu MH, Pehlivan D, Ceylaner S, Icagasioglu D, Aydin K.
    Turk Neurosurg; 2022 Jul 10; 32(1):155-159. PubMed ID: 34664704
    [Abstract] [Full Text] [Related]

  • 13. Impediments to Heart Transplantation in Adults With MELASMT-TL1:m.3243A>G Cardiomyopathy.
    Di Toro A, Urtis M, Narula N, Giuliani L, Grasso M, Pasotti M, Pellegrini C, Serio A, Pilotto A, Antoniazzi E, Rampino T, Magrassi L, Valentini A, Cavallini A, Scelsi L, Ghio S, Abelli M, Olivotto I, Porcu M, Gavazzi A, Kodama T, Arbustini E.
    J Am Coll Cardiol; 2022 Oct 11; 80(15):1431-1443. PubMed ID: 36202533
    [Abstract] [Full Text] [Related]

  • 14. 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 06; 26(4):143-148. PubMed ID: 34190208
    [Abstract] [Full Text] [Related]

  • 15. 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 06; 9():94-97. PubMed ID: 27896131
    [Abstract] [Full Text] [Related]

  • 16. Mitochondrial DNA mutation "m.3243A>G"-Heterogeneous clinical picture for cardiologists ("m.3243A>G": A phenotypic chameleon).
    Niedermayr K, Pölzl G, Scholl-Bürgi S, Fauth C, Schweigmann U, Haberlandt E, Albrecht U, Zlamy M, Sperl W, Mayr JA, Karall D.
    Congenit Heart Dis; 2018 Sep 06; 13(5):671-677. PubMed ID: 30133155
    [Abstract] [Full Text] [Related]

  • 17. 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 06; 24(5):294-303. PubMed ID: 35802497
    [Abstract] [Full Text] [Related]

  • 18. 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 Oct 06; 15():1367716. PubMed ID: 38881794
    [Abstract] [Full Text] [Related]

  • 19. [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 18; 52(5):851-855. PubMed ID: 33047718
    [Abstract] [Full Text] [Related]

  • 20. Acute encephalopathy of the temporal lobes leading to m.3243A>G. When MELAS is not always MELAS.
    Caldarazzo Ienco E, Orsucci D, Simoncini C, Montano V, LoGerfo A, Siciliano G, Bonuccelli U, Mancuso M.
    Mitochondrion; 2016 Sep 18; 30():148-50. PubMed ID: 27453332
    [Abstract] [Full Text] [Related]

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