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 *

160 related articles for article (PubMed ID: 38265537)

  • 1. A case of exacerbated encephalopathy with stroke-like episodes and lactic acidosis triggered by metformin in a patient with MELAS.
    Shin HJ; Na JH; Lee YM
    Neurol Sci; 2024 May; 45(5):2337-2339. PubMed ID: 38265537
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes diagnosed after metformin-triggered stroke-like episodes.
    Murakami K; Sakamoto K; Ishiguchi H; Ito H
    J Stroke Cerebrovasc Dis; 2023 May; 32(5):107080. PubMed ID: 36933522
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report.
    Fukuda M; Nagao Y
    J Med Case Rep; 2019 Oct; 13(1):313. PubMed ID: 31630688
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes due to m.3243A > G mutation in a 76-year-old woman.
    Ueki K; Wakisaka Y; Nakamura K; Shono Y; Wada S; Yoshikawa Y; Matsukuma Y; Uchiumi T; Kang D; Kitazono T; Ago T
    J Neurol Sci; 2020 May; 412():116791. PubMed ID: 32224343
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. Treatment options for mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome.
    Santa KM
    Pharmacotherapy; 2010 Nov; 30(11):1179-96. PubMed ID: 20973690
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial stroke-like episodes: The search for new therapies.
    Orsucci D; Caldarazzo Ienco E; Montano V; Siciliano G; Mancuso M
    Pharmacol Res; 2022 Jun; 180():106228. PubMed ID: 35462010
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. 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]  

  • 12. 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; 16(1):361. PubMed ID: 36210452
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [A case of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) complicated by chronic intestinal pseudo-obstruction].
    Miyanaga R; Tanaka M; Nonaka T; Shizukawa H; Shimohama S
    Rinsho Shinkeigaku; 2022 Jun; 62(6):464-468. PubMed ID: 35644578
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Letter to the Editor regarding "Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes diagnosed after metformin-triggered stroke-like episodes".
    Finsterer J
    J Stroke Cerebrovasc Dis; 2023 Jun; 32(6):107094. PubMed ID: 37085391
    [No Abstract]   [Full Text] [Related]  

  • 16. Impediments to Heart Transplantation in Adults With MELAS
    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; 80(15):1431-1443. PubMed ID: 36202533
    [TBL] [Abstract][Full Text] [Related]  

  • 17. MELAS syndrome: Clinical manifestations, pathogenesis, and treatment options.
    El-Hattab AW; Adesina AM; Jones J; Scaglia F
    Mol Genet Metab; 2015; 116(1-2):4-12. PubMed ID: 26095523
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?
    Mancuso M; Orsucci D; Angelini C; Bertini E; Carelli V; Comi GP; Donati A; Minetti C; Moggio M; Mongini T; Servidei S; Tonin P; Toscano A; Uziel G; Bruno C; Ienco EC; Filosto M; Lamperti C; Catteruccia M; Moroni I; Musumeci O; Pegoraro E; Ronchi D; Santorelli FM; Sauchelli D; Scarpelli M; Sciacco M; Valentino ML; Vercelli L; Zeviani M; Siciliano G
    J Neurol; 2014 Mar; 261(3):504-10. PubMed ID: 24375076
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An autopsy case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with a point mutation of mitochondrial DNA.
    Terauchi A; Tamagawa K; Morimatsu Y; Kobayashi M; Sano T; Yoda S
    Brain Dev; 1996; 18(3):224-9. PubMed ID: 8836506
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.